<?xml version="1.0" encoding="UTF-8"?>
<!-- generator="FeedCreator 1.7.2" -->
<rss version="2.0">
    <channel>
        <title>Dermatol Online J via MedWorm.com</title>
        <description>MedWorm.com provides a medical RSS filtering service. Over 6000 RSS medical sources are combined and output via different filters. This feed contains the latest items from the 'Dermatol Online J' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Dermatol+Online+J&t=Dermatol+Online+J&s=Search&f=source]]></link>
        <lastBuildDate>Tue, 16 Mar 2010 14:29:22 +0100</lastBuildDate>
        <item>
            <title>A review of home phototherapy for psoriasis.</title>
            <link>http://www.medworm.com/index.php?rid=3312437&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20178697%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Home phototherapy is a well-tolerated, efficacious, economical and patient friendly therapeutic option. Advantages of home phototherapy include improved quality of life, greater convenience, lower cost, and less time lost from work and social activities. Dermatologists should strongly consider home phototherapy as a first-line treatment option for appropriately selected psoriasis patients.
    PMID: 20178697 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3312437</comments>
            <pubDate>Sat, 27 Feb 2010 11:58:02 +0100</pubDate>
            <guid isPermaLink="false">3312437</guid>        </item>
        <item>
            <title>Psoriasis: Can statins play a dual role?</title>
            <link>http://www.medworm.com/index.php?rid=3312436&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20178698%26dopt%3DAbstract</link>
            <description>Authors: Rajpara AN, Goldner R, Gaspari A
    Recently, a strong association between &quot;psoriasis&quot; and &quot;atherosclerosis&quot; has emerged. Psoriasis patients have an increased prevalence of atherosclerotic disease including coronary artery, cerebrovascular, and peripheral vascular diseases. The exact connection between psoriasis and atherosclerosis remains unclear, but it is thought that inflammation, which plays an important role in both diseases, may be the causative link. Nevertheless, psoriasis patients suffer from an increased burden of atherosclerotic disease and most commonly die from &quot;coronary artery disease&quot; (CAD). Psoriatic patients have an increased prevalence of CAD risk factors and an increased risk of myocardial infarction (MI). One CAD risk factor in psoriasis patients that can eas...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3312436</comments>
            <pubDate>Sat, 27 Feb 2010 11:58:02 +0100</pubDate>
            <guid isPermaLink="false">3312436</guid>        </item>
        <item>
            <title>Does D matter? The role of vitamin D in hair disorders and hair follicle cycling.</title>
            <link>http://www.medworm.com/index.php?rid=3312435&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20178699%26dopt%3DAbstract</link>
            <description>CONCLUSION: Additional studies to evaluate the role of vitamin D in the hair cycle should be done. Treatments that up regulate the vitamin D receptor may be successful in treating hair disorders and are a potential area of further study.
    PMID: 20178699 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3312435</comments>
            <pubDate>Sat, 27 Feb 2010 11:58:02 +0100</pubDate>
            <guid isPermaLink="false">3312435</guid>        </item>
        <item>
            <title>Reliability of self-assessed reading of skin tests: A possible approach in research and clinical practice?</title>
            <link>http://www.medworm.com/index.php?rid=3312434&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20178700%26dopt%3DAbstract</link>
            <description>Authors: Falk M, Anderson C
    In the investigation and management of skin disease, various testing protocols are of importance. The extent to which clinical judgments and decisions on therapy are supported by the performance of such testing can be affected negatively by the lack of time and resources for the performance of tests. In the present study, the possibility of utilizing self-reporting by subjects is investigated. Determination of irritation threshold for sodium lauryl sulphate (SLS) and minimal erythema dose for ultraviolet B were chosen as suitable self-reading protocols. Test reading by 26 subjects instructed in &quot;present&quot; or &quot;absent&quot; reporting of test reactions were compared to trained observer reading. Absolute agreement was found in 76.9 percent of the SLS reactions and in ...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3312434</comments>
            <pubDate>Sat, 27 Feb 2010 11:58:02 +0100</pubDate>
            <guid isPermaLink="false">3312434</guid>        </item>
        <item>
            <title>Scrotal calcinosis: Idiopathic or dystrophic?</title>
            <link>http://www.medworm.com/index.php?rid=3312433&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20178701%26dopt%3DAbstract</link>
            <description>Authors: Dubey S, Sharma R, Maheshwari V
    Scrotal calcinosis is a rare benign local process characterized by multiple, painless, hard scrotal nodules in the absence of any systemic metabolic disorder. Histological examination reveals extensive deposition of calcium in the dermis, which may be surrounded by histiocytes and an inflammatory giant cell reaction. Numerous theories have been propounded to explain the pathogenesis of this condition, but the principal debate revolves around whether the calcium is deposited at the site of previous epithelial cysts or the calcified nodules are purely idiopathic. This is the largest study of scrotal calcinosis to date with 100 cases, on which clinical, biochemical, radiological, cytopathological, and histopathological examinations were conducted. ...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3312433</comments>
            <pubDate>Sat, 27 Feb 2010 11:58:02 +0100</pubDate>
            <guid isPermaLink="false">3312433</guid>        </item>
        <item>
            <title>An unusual ulcer in an 8-year-old girl.</title>
            <link>http://www.medworm.com/index.php?rid=3312432&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20178702%26dopt%3DAbstract</link>
            <description>Authors: Friedman A, Abadi M, Wu K, Fisher M, Abadi J
    
    PMID: 20178702 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3312432</comments>
            <pubDate>Sat, 27 Feb 2010 11:58:02 +0100</pubDate>
            <guid isPermaLink="false">3312432</guid>        </item>
        <item>
            <title>A teen-ager with linear atrophoderma of Moulin.</title>
            <link>http://www.medworm.com/index.php?rid=3312431&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20178703%26dopt%3DAbstract</link>
            <description>We present here a peculiar case of linear atrophoderma affecting a teenager.
    PMID: 20178703 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3312431</comments>
            <pubDate>Sat, 27 Feb 2010 11:58:02 +0100</pubDate>
            <guid isPermaLink="false">3312431</guid>        </item>
        <item>
            <title>Verrucous carcinoma of the foot affecting the bone: Utility of the computed tomography scanner.</title>
            <link>http://www.medworm.com/index.php?rid=3312430&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20178704%26dopt%3DAbstract</link>
            <description>Authors: Garc&amp;#xED;a-Gav&amp;#xED;n J, Gonz&amp;#xE1;lez-Vilas D, Rodr&amp;#xED;guez-Pazos L, S&amp;#xE1;nchez-Aguilar D, Toribio J
    Verrucous Carcinoma (VC) of the foot often affects deep structures such as tendons, muscles or bone. The complete removal of the tumor is essential to avoid recurrences. Radiological studies should be performed before surgical planning in order to determine the extent of the tumor. A 54-year-old man presented with a VC of the foot. Magnetic resonance imaging (MRI) demonstrated a soft-tissue mass affecting the plantar aponeurosis and the sole muscles, without evidence of bone invasion. Computed tomography (CT) showed a lytic area with cortical disruption in the fourth metatarsal neck. A transmetatarsal amputation was performed. Histopathological examination confirmed the b...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3312430</comments>
            <pubDate>Sat, 27 Feb 2010 11:58:02 +0100</pubDate>
            <guid isPermaLink="false">3312430</guid>        </item>
        <item>
            <title>Atypical melanocytic nevi of genital type: A distinctive pigmented lesion of the genital tract often confused with malignant melanoma.</title>
            <link>http://www.medworm.com/index.php?rid=3312429&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20178705%26dopt%3DAbstract</link>
            <description>Authors: Quddus MR, Rashid LB, Sung CJ, Robinson-Bostom L, Lawrence WD
    A 30-year-old female presented with a 0.3 cm slightly raised tan-brown papule with somewhat irregular borders on her right labia minora. The papule was detected by her gynecologist during an annual gynecologic visit. Excision of the lesion revealed an atypical melanocytic nevus of genital type (AMNGT). This nevus is often confused with other pigmented lesions especially dysplastic nevus or even malignant melanoma. This distinctive melanocytic nevus often causes significant concern to pathologists and dermatologists. The diagnostic criteria and differentiating features from dysplastic nevi and malignant melanoma are discussed.
    PMID: 20178705 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3312429</comments>
            <pubDate>Sat, 27 Feb 2010 11:58:02 +0100</pubDate>
            <guid isPermaLink="false">3312429</guid>        </item>
        <item>
            <title>Cutaneous metastasis of renal cell carcinoma through percutaneous fine needle aspiration biopsy: Case report.</title>
            <link>http://www.medworm.com/index.php?rid=3312428&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20178706%26dopt%3DAbstract</link>
            <description>Authors: Jilani G, Mohamed D, Wadia H, Ramzi K, Meriem J, Houssem L, Samir G, Nawfel BR
    A 39-year-old man, who had undergone left nephrectomy for renal cell carcinoma of clear cell type, was noted to have a solitary nodular shadow in the right lung on chest X-ray. Percutaneous needle biopsy of the lung was performed via the right anterior chest wall and the histologic findings showed metastasis from renal carcinoma. Six month later, the patient presented with a cutaneous nodule at the site of puncture of the lung needle biopsy. Histological examination of a biopsy of the skin tumor revealed features of metastatic renal cell carcinoma of clear cell type. Surgical excision of the cutaneous nodule was performed, followed by radiotherapy at the site of the skin lesion on the chest wall. Af...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3312428</comments>
            <pubDate>Sat, 27 Feb 2010 11:58:02 +0100</pubDate>
            <guid isPermaLink="false">3312428</guid>        </item>
        <item>
            <title>Unknown: A firm plaque on the back of a newborn.</title>
            <link>http://www.medworm.com/index.php?rid=3312427&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20178707%26dopt%3DAbstract</link>
            <description>We report a case of subcutaneous fat necrosis of the newborn (SCFN), a rare disorder in term or post-term neonates. Although it is often associated with hematological abnormalities such as anemia and hypercalcemia, SCFN in this patient presented with hyperbilirubinemia. The course of SCFN is generally benign and self-limiting, though may be associated with complications secondary to hypercalcemia.
    PMID: 20178707 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3312427</comments>
            <pubDate>Sat, 27 Feb 2010 11:58:02 +0100</pubDate>
            <guid isPermaLink="false">3312427</guid>        </item>
        <item>
            <title>Epidemiology and outcomes of dermatology in-patient consultations in a Midwestern U.S. university hospital.</title>
            <link>http://www.medworm.com/index.php?rid=3312426&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20178708%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Our results suggest that common skin conditions account for a large majority of dermatologic consultations in a University hospital setting. Modern hospital ward teams continue to struggle with accurately recognizing and appropriately managing common skin problems resulting in inappropriate treatment, wasted resources, and prolonged hospitalization. Increasing medical student and house staff knowledge and experience in the diagnosis and management of common skin disorders could help address this problem.
    PMID: 20178708 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3312426</comments>
            <pubDate>Sat, 27 Feb 2010 11:58:02 +0100</pubDate>
            <guid isPermaLink="false">3312426</guid>        </item>
        <item>
            <title>A case of aseptic pleuropericarditis in a patient with chronic plaque psoriasis under methotrexate therapy.</title>
            <link>http://www.medworm.com/index.php?rid=3312425&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20178709%26dopt%3DAbstract</link>
            <description>We report here a rare case of pleuropericarditis due to methotrexate. The effusion resolved after the withdrawal of the drug and the beginning of anti-inflammatory therapy; there was no relapse during a 10-month follow-up.
    PMID: 20178709 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3312425</comments>
            <pubDate>Sat, 27 Feb 2010 11:58:02 +0100</pubDate>
            <guid isPermaLink="false">3312425</guid>        </item>
        <item>
            <title>Guidelines needed for academic titles within dermatology.</title>
            <link>http://www.medworm.com/index.php?rid=3312424&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20178710%26dopt%3DAbstract</link>
            <description>Authors: Wu JJ
    The system of giving academic titles to those outside of full-time academic practice should be re-evaluated.
    PMID: 20178710 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3312424</comments>
            <pubDate>Sat, 27 Feb 2010 11:58:02 +0100</pubDate>
            <guid isPermaLink="false">3312424</guid>        </item>
        <item>
            <title>Basal cell carcinoma on the toe.</title>
            <link>http://www.medworm.com/index.php?rid=3312423&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20178711%26dopt%3DAbstract</link>
            <description>Authors: Suzuki Y, Nakamura-Wakatsuki T, Satoh M, Nishibu A, Kawakami Y, Oyama N, Yamamoto T
    
    PMID: 20178711 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3312423</comments>
            <pubDate>Sat, 27 Feb 2010 11:58:02 +0100</pubDate>
            <guid isPermaLink="false">3312423</guid>        </item>
        <item>
            <title>The role of radiotherapy in the treatment of hidradenitis suppurativa: Case report and review of the literature.</title>
            <link>http://www.medworm.com/index.php?rid=3312422&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20178712%26dopt%3DAbstract</link>
            <description>Authors: Trombetta M, Werts ED, Parda D
    
    PMID: 20178712 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3312422</comments>
            <pubDate>Sat, 27 Feb 2010 11:58:02 +0100</pubDate>
            <guid isPermaLink="false">3312422</guid>        </item>
        <item>
            <title>Sorafenib-associated remission of psoriasis in hypernephroma: Case report.</title>
            <link>http://www.medworm.com/index.php?rid=3312421&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20178713%26dopt%3DAbstract</link>
            <description>Authors: Fournier C, Tisman G
    Psoriasis is a disease characterized by epidermal hyperproliferation that results in the formation of lesional plaques covered by scale. Psoriasis is thought to be angiogenesis dependent. Clear cell renal cell carcinoma is a hypervascularized solid tumor associated with loss of function of the von Hippel-Lindau (VHL) tumor suppressor gene and increased Raf-1 activity. A 68-year-old man who suffered from recalcitrant psoriasis for over 50 years was treated with sorafenib for metastatic clear cell renal carcinoma. One month later, his psoriasis, previously 8 x 6 cm on the mid posterior thorax, completely resolved. Sorafenib works by inhibiting several receptor tyrosine kinases (RTKs), such as vascular endothelial growth factor (VEGFR) and platelet-derived gr...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3312421</comments>
            <pubDate>Sat, 27 Feb 2010 11:58:02 +0100</pubDate>
            <guid isPermaLink="false">3312421</guid>        </item>
        <item>
            <title>The pendulum's swing: Cause and effect relationship.</title>
            <link>http://www.medworm.com/index.php?rid=3312420&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20178714%26dopt%3DAbstract</link>
            <description>Authors: Goihman-Yahr M
    
    PMID: 20178714 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3312420</comments>
            <pubDate>Sat, 27 Feb 2010 11:58:02 +0100</pubDate>
            <guid isPermaLink="false">3312420</guid>        </item>
        <item>
            <title>Clinical and epidemiological aspects of subtypes of melanocytic nevi (Flat nevi, Miescher nevi, Unna nevi).</title>
            <link>http://www.medworm.com/index.php?rid=3257217&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20137743%26dopt%3DAbstract</link>
            <description>Authors: Witt C, Krengel S
    The term &quot;melanocytic nevus&quot; comprises a group of clinically and pathologically distinct subtypes. In this prospective clinical study we evaluated the frequency, localization, and age and gender distribution of flat nevi (FN), Miescher nevi (MN), and Unna nevi (UN) in a caucasian population. Nevi were counted in 400 patients, of which 47 had a history of melanoma. Additionally, the patients answered to a detailed UV questionnaire. Flat nevi represented the most common type of melanocytic nevi, with a peak in the 3rd decade of life. They were mostly found on the extremities and on the trunk. Miescher nevi were most common in the 6th decade and were predominantly found in the head and neck region. Unna nevi showed a maximum in the 8th decade and they were mainl...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3257217</comments>
            <pubDate>Wed, 10 Feb 2010 15:16:03 +0100</pubDate>
            <guid isPermaLink="false">3257217</guid>        </item>
        <item>
            <title>Linear IgA bullous dermatosis: The more frequent bullous dermatosis of children.</title>
            <link>http://www.medworm.com/index.php?rid=3257216&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20137744%26dopt%3DAbstract</link>
            <description>CONCLUSION: This study confirms that LAD is the most common AIBD in children in Tunisia and it frequently occurs in preschool-aged males. Independently of the medication chosen for treatment, a long term remission is frequently observed.
    PMID: 20137744 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3257216</comments>
            <pubDate>Wed, 10 Feb 2010 15:16:03 +0100</pubDate>
            <guid isPermaLink="false">3257216</guid>        </item>
        <item>
            <title>Patient safety in dermatology: A review of the literature.</title>
            <link>http://www.medworm.com/index.php?rid=3257215&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20137745%26dopt%3DAbstract</link>
            <description>CONCLUSION: Our review reveals few studies on dermatologic patient safety, supporting the pressing need for such studies and reports in the future.
    PMID: 20137745 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3257215</comments>
            <pubDate>Wed, 10 Feb 2010 15:16:03 +0100</pubDate>
            <guid isPermaLink="false">3257215</guid>        </item>
        <item>
            <title>Topical delivery of active principles: The field of dermatological research.</title>
            <link>http://www.medworm.com/index.php?rid=3257214&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20137746%26dopt%3DAbstract</link>
            <description>Authors: Nino M, Calabr&amp;#xF2; G, Santoianni P
    To be effective an active drug or principle must cross the stratum corneum barrier; this process can be influenced to obtain better functional and therapeutical effects. In spite of the wide variety of the methods studied in order to improve the transdermal transfer to obtain systemic effects, the applicability is limited in this field. Attention to the epidermal barrier and penetration of active principles has been reported mostly in studies concerning dermocosmetics. Studies regarding methods of penetration are gaining experimental and clinical interest. Cutaneous bioavailability of most commercially available dermatological formulations is low. Increase of intradermal delivery can relate to chemical, biochemical, or physical manipulation...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3257214</comments>
            <pubDate>Wed, 10 Feb 2010 15:16:03 +0100</pubDate>
            <guid isPermaLink="false">3257214</guid>        </item>
        <item>
            <title>Patients are happy to be informed of their final non-melanoma skin cancer results by post.</title>
            <link>http://www.medworm.com/index.php?rid=3257213&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20137747%26dopt%3DAbstract</link>
            <description>Authors: Thomson P, Palamaras I, Hill V, Robles W, Stevens H
    During the past year, because of increasing pressure to see more patients, we have started to write to our patients informing them in a letter of their final skin cancer histology results following surgery for non-melanoma skin cancers: basal cell carcinoma and squamous cell carcinoma only. A questionnaire-based study was carried out to assess whether patients were happy to receive information concerning their non-melanoma skin cancer diagnosis in a carefully worded letter. One-hundred fifty patients were involved with a diagnosis of &quot;completely excised non-melanoma skin cancer (NMSC)&quot; that had previously received their final diagnosis by post. Seventy-seven (51.3%) patients responded to the questionnaire. Eighty-seven percen...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3257213</comments>
            <pubDate>Wed, 10 Feb 2010 15:16:03 +0100</pubDate>
            <guid isPermaLink="false">3257213</guid>        </item>
        <item>
            <title>Verrucous plaque on the face: What is your diagnosis?</title>
            <link>http://www.medworm.com/index.php?rid=3257212&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20137748%26dopt%3DAbstract</link>
            <description>Authors: De A, Gharami RC, Datta PK
    A 46-year-old male patient presented with hyperpigmented verrucous plaques and papules mainly on the left cheek and malar region that had evolved over a 7 month period. Histopathology demonstrated the presence of a large number of classical copper penny bodies or muriform bodies and a predominantly neutrophilic dermal infiltrate that confirmed the diagnosis of chromoblastomycosis.
    PMID: 20137748 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3257212</comments>
            <pubDate>Wed, 10 Feb 2010 15:16:03 +0100</pubDate>
            <guid isPermaLink="false">3257212</guid>        </item>
        <item>
            <title>Cowden syndrome.</title>
            <link>http://www.medworm.com/index.php?rid=3257211&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20137749%26dopt%3DAbstract</link>
            <description>We report the case of a 22-year-old man with oral and cutaneous papules and a past history of thyroid malignancy. It is important to recognize oral manifestations of CS; they can lead to early diagnosis of the condition.
    PMID: 20137749 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3257211</comments>
            <pubDate>Wed, 10 Feb 2010 15:16:03 +0100</pubDate>
            <guid isPermaLink="false">3257211</guid>        </item>
        <item>
            <title>Type 2 segmental glomangiomas.</title>
            <link>http://www.medworm.com/index.php?rid=3257210&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20137750%26dopt%3DAbstract</link>
            <description>In this report we describe a 39-year-old man who developed unilateral segmental GVMs on his trunk in early childhood, with the histological features of glomangiomas. As several satellite lesions emerged at distant skin sites later in life, our case probably represents type 2 segmental GVMs, caused by localized loss of heterozygosity in an individual carrying a heterozygous germline mutation in the glomulin gene.
    PMID: 20137750 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3257210</comments>
            <pubDate>Wed, 10 Feb 2010 15:16:03 +0100</pubDate>
            <guid isPermaLink="false">3257210</guid>        </item>
        <item>
            <title>A toddler with facial nodules: A case of idiopathic facial aseptic granuloma.</title>
            <link>http://www.medworm.com/index.php?rid=3257209&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20137751%26dopt%3DAbstract</link>
            <description>We describe the case of a 3-year-old boy who presented with several asymptomatic facial nodules present for six months. A skin biopsy obtained from the nodules showed a moderately well-defined granuloma in the superficial and deep dermis. A squamous epithelial lined cyst, extravasated keratin, or shadow cells were not identified. Bartonella henselae titers and the Coccidioidomycosis immitis immunodiffusion test were negative; a Tuberculin Skin Test was non-reactive. Fite, Periodic acid-Schiff (PAS) and Gomori-Grocott methenamine silver (GMS) stains failed to identify microorganisms. In addition, tissue cultures for bacteria, fungus, and acid fast bacilli were negative. In light of the clinical findings, histology, and negative cultures, a diagnosis of idiopathic facial aseptic granuloma (I...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3257209</comments>
            <pubDate>Wed, 10 Feb 2010 15:16:03 +0100</pubDate>
            <guid isPermaLink="false">3257209</guid>        </item>
        <item>
            <title>Perianal cutaneous malakoplakia in an immunocompetent patient.</title>
            <link>http://www.medworm.com/index.php?rid=3257207&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20137752%26dopt%3DAbstract</link>
            <description>We describe a case of an isolated perianal cutaneous malakoplakia in an immunocompetent 23-year-old Syrian male.
    PMID: 20137752 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3257207</comments>
            <pubDate>Wed, 10 Feb 2010 15:16:03 +0100</pubDate>
            <guid isPermaLink="false">3257207</guid>        </item>
        <item>
            <title>Piebaldism and neurofibromatosis type 1: family report.</title>
            <link>http://www.medworm.com/index.php?rid=3257206&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20137753%26dopt%3DAbstract</link>
            <description>Authors: Duarte AF, Mota A, Baudrier T, Morais P, Santos A, Cerqueira R, Tavares P, Azevedo F
    Piebaldism is a rare disorder present at birth and inherited as an autosomal dominant trait. It results from a mutation in the c-kit proto-oncogene and is associated with a defect in the migration and differentiation of melanoblasts from the neural crest. Clinical manifestations and phenotypic severity strongly correlates with the site of mutation within the KIT gene. Here we report a 3-year-old boy and his 33-year-old father with leukoderma and poliosis associated with clinical criteria for Neurofibromatosis type 1. Genetic study of both revealed a p.Gly610Asp mutation in the KIT gene. This familiar mutation has not yet been reported in the literature. There are rare reports of piebaldism in ...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3257206</comments>
            <pubDate>Wed, 10 Feb 2010 15:16:03 +0100</pubDate>
            <guid isPermaLink="false">3257206</guid>        </item>
        <item>
            <title>Bilateral retro-auricular milia en plaque: A case report and review of the literature.</title>
            <link>http://www.medworm.com/index.php?rid=3257205&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20137754%26dopt%3DAbstract</link>
            <description>Authors: Hallaji Z, Akhyani M, Jamshidi S, Modabbernia A, Kamyab K
    Milia en plaque, a rare inflammatory plaque type of milia is generally located in the periauricular area. Bilateral retroauricular milia en plaque is very rarely reported. Here, we report another case of bilateral retroauricular milia en plaque and review the previous cases.
    PMID: 20137754 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3257205</comments>
            <pubDate>Wed, 10 Feb 2010 15:16:03 +0100</pubDate>
            <guid isPermaLink="false">3257205</guid>        </item>
        <item>
            <title>Punctate porokeratotic keratoderma.</title>
            <link>http://www.medworm.com/index.php?rid=3257204&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20137755%26dopt%3DAbstract</link>
            <description>We report a 29-year-old woman with multiple small keratotic papules on her lateral fingers and first and second toes. Histopathology revealed a compact parakeratotic column with a poorly developed stratum granulosum, indicating punctate porokeratotic keratoderma (PPK). We discuss demographics, etiology, histopathology, differential diagnosis, and treatment of this disease.
    PMID: 20137755 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3257204</comments>
            <pubDate>Wed, 10 Feb 2010 15:16:03 +0100</pubDate>
            <guid isPermaLink="false">3257204</guid>        </item>
        <item>
            <title>Infundibulomatosis: A case report with immunohistochemical study and literature review.</title>
            <link>http://www.medworm.com/index.php?rid=3257203&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20137756%26dopt%3DAbstract</link>
            <description>Authors: Cardoso JC, Reis JP, Figueiredo P, Tellechea O
    Tumor of the follicular infundibulum was first described in 1961 by Mehregan and Butler in a patient presenting with multiple papules. It is more frequent, however, as an isolated lesion affecting mainly the face, neck, and upper trunk. Clinical presentation is variable, requiring histology for the diagnosis, which reveals typically a plate-like proliferation of keratinocytes in continuity with the epidermis and hair follicles; some morphological features are reminiscent of the outer root sheath of the hair follicle. A well defined network of elastic fibers surrounding the tumor is usually present using the appropriate staining and this finding is specific because it is not found in other benign follicular tumors. Multiple infundi...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3257203</comments>
            <pubDate>Wed, 10 Feb 2010 15:16:03 +0100</pubDate>
            <guid isPermaLink="false">3257203</guid>        </item>
        <item>
            <title>Case report: Prolonged collodion membrane causing constrictive bands of the digits and treatment.</title>
            <link>http://www.medworm.com/index.php?rid=3257202&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20137757%26dopt%3DAbstract</link>
            <description>We describe a 2-month-old female with lamellar ichthyosis and prolonged collodion membrane with two constrictive bands of the fingers causing significant erythema, edema, and pain. We suggest prompt release of these constrictive bands with an 11-blade and closely follow up of collodion babies until their membrane has fully desquamated.
    PMID: 20137757 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3257202</comments>
            <pubDate>Wed, 10 Feb 2010 15:16:03 +0100</pubDate>
            <guid isPermaLink="false">3257202</guid>        </item>
        <item>
            <title>A review of the practices and results of the UTMB to South Pole teledermatology program over the past six years.</title>
            <link>http://www.medworm.com/index.php?rid=3257201&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20137758%26dopt%3DAbstract</link>
            <description>We present the practices and results of the UTMB to the South Pole teledermatology program over the past six years, from 2003 to 2008. Issues encountered include logistics of sending out biopsies for pathologic diagnosis, limited bandwidth, and satellite availability for data transmission. The UTMB to the South Pole teledermatology program demonstrates the clinical practicality of telemedicine in providing dermatologic care to remote populations in extreme climate conditions.
    PMID: 20137758 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3257201</comments>
            <pubDate>Wed, 10 Feb 2010 15:16:03 +0100</pubDate>
            <guid isPermaLink="false">3257201</guid>        </item>
        <item>
            <title>Important risk factors in melanoma from the Dermato-Oncologic Unit of Brescia, Italy.</title>
            <link>http://www.medworm.com/index.php?rid=3257200&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20137759%26dopt%3DAbstract</link>
            <description>We reported the experience of the Dermato-Oncologic Unit of Brescia, Italy.
    PMID: 20137759 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3257200</comments>
            <pubDate>Wed, 10 Feb 2010 15:16:03 +0100</pubDate>
            <guid isPermaLink="false">3257200</guid>        </item>
        <item>
            <title>Symmetrical bilateral Becker melanosis: A rare presentation.</title>
            <link>http://www.medworm.com/index.php?rid=3133387&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20040251%26dopt%3DAbstract</link>
            <description>Authors: Grim KD, Wasko CA
    Becker melanosis, also known as Becker nevus, is a relatively common cutaneous hamartoma. The condition is classically characterized by a unilateral, hyperpigmented patch with varying degrees of hypertrichosis on a peripubertal individual. As Becker nevi are generally singular in a given individual, there are very few reported cases of multiple or bilateral lesions. We herein report a rare case of bilateral, symmetrical, non-syndromic Becker melanosis and we discuss possible pathogenesis and current treatment options.
    PMID: 20040251 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3133387</comments>
            <pubDate>Thu, 31 Dec 2009 16:04:02 +0100</pubDate>
            <guid isPermaLink="false">3133387</guid>        </item>
        <item>
            <title>Acquired dermal melanocytosis of the hand at the site of treated psoriasis.</title>
            <link>http://www.medworm.com/index.php?rid=3133386&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20040252%26dopt%3DAbstract</link>
            <description>We report a case of acquired dermal melanocytosis occurring in a 42-year-old Hispanic man with psoriasis treated with infliximab for 9 months. The patient presented with an isolated pigmented patch on his left dorsal hand. Histopathologic examination of the skin revealed numerous dendritic, heavily pigmented melanocytes in the papillary and upper reticular dermis. We review the literature and discuss the pathogenesis of acquired dermal melanocytosis.
    PMID: 20040252 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3133386</comments>
            <pubDate>Thu, 31 Dec 2009 16:04:02 +0100</pubDate>
            <guid isPermaLink="false">3133386</guid>        </item>
        <item>
            <title>Granuloma faciale: Case report and review.</title>
            <link>http://www.medworm.com/index.php?rid=3133384&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20040253%26dopt%3DAbstract</link>
            <description>We present an illustrative case of GF and briefly review available treatment options.
    PMID: 20040253 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3133384</comments>
            <pubDate>Thu, 31 Dec 2009 16:04:02 +0100</pubDate>
            <guid isPermaLink="false">3133384</guid>        </item>
        <item>
            <title>Interferon induced sarcoidosis with cutaneous involvement along lines of venous drainage in a former intravenous drug user.</title>
            <link>http://www.medworm.com/index.php?rid=3133381&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20040254%26dopt%3DAbstract</link>
            <description>Authors: Shuja F, Kavoussi SC, Mir MR, Jogi RP, Rosen T
    
    PMID: 20040254 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3133381</comments>
            <pubDate>Thu, 31 Dec 2009 16:04:02 +0100</pubDate>
            <guid isPermaLink="false">3133381</guid>        </item>
        <item>
            <title>Two pediatric cases of Blau syndrome.</title>
            <link>http://www.medworm.com/index.php?rid=3133376&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20040255%26dopt%3DAbstract</link>
            <description>Authors: Glass DA, Maender J, Metry D
    
    PMID: 20040255 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3133376</comments>
            <pubDate>Thu, 31 Dec 2009 16:04:02 +0100</pubDate>
            <guid isPermaLink="false">3133376</guid>        </item>
        <item>
            <title>A case of Kaposi sarcoma mimicking nephrogenic systemic fibrosis.</title>
            <link>http://www.medworm.com/index.php?rid=3133375&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20040256%26dopt%3DAbstract</link>
            <description>We present an unusual case of AIDS-associated Kaposi sarcoma mimicking nephrogenic systemic fibrosis.
    PMID: 20040256 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3133375</comments>
            <pubDate>Thu, 31 Dec 2009 16:04:02 +0100</pubDate>
            <guid isPermaLink="false">3133375</guid>        </item>
        <item>
            <title>Clinical pearl for the diagnosis of Hansen disease.</title>
            <link>http://www.medworm.com/index.php?rid=3133374&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20040257%26dopt%3DAbstract</link>
            <description>Authors: Bhuchar S, Chan CS, Mir MR, Subrt P, Tschen JA, Collins WE, Hsu S
    
    PMID: 20040257 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3133374</comments>
            <pubDate>Thu, 31 Dec 2009 16:04:02 +0100</pubDate>
            <guid isPermaLink="false">3133374</guid>        </item>
        <item>
            <title>Fluoroquinolone-induced generalized fixed drug eruption.</title>
            <link>http://www.medworm.com/index.php?rid=3133373&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20040258%26dopt%3DAbstract</link>
            <description>Authors: Hager JL, Mir MR, Hsu S
    
    PMID: 20040258 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3133373</comments>
            <pubDate>Thu, 31 Dec 2009 16:04:02 +0100</pubDate>
            <guid isPermaLink="false">3133373</guid>        </item>
        <item>
            <title>Primary cutaneous CD30+ large-cell lymphoma presenting as a scrotal plaque.</title>
            <link>http://www.medworm.com/index.php?rid=3133372&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20040259%26dopt%3DAbstract</link>
            <description>We report a patient with a one-year history of an enlarging scrotal plaque. Skin biopsy stained positive for CD30, and after thorough systemic evaluation, a diagnosis of primary cutaneous CD30+ LCL was made. Most commonly CD30+ LCL presents on the extremities and trunk. We present the first case to our knowledge of a patient initially presenting with a solitary scrotal nodule. When primary cutaneous CD30+ LCL is suspected, it is important to conduct a thorough systemic evaluation for systemic LCL and immunohistological studies for CD30- types. Ruling these conditions out will prevent unnecessarily aggressive treatment for primary cutaneous CD30+ LCL, an indolent disease with a favorable prognosis.
    PMID: 20040259 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3133372</comments>
            <pubDate>Thu, 31 Dec 2009 16:04:02 +0100</pubDate>
            <guid isPermaLink="false">3133372</guid>        </item>
        <item>
            <title>Vogt-Koyanagi-Harada syndrome: Association with alopecia areata.</title>
            <link>http://www.medworm.com/index.php?rid=3133371&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20040260%26dopt%3DAbstract</link>
            <description>We present a case of VKH syndrome and propose that the alopecia and poliosis described in the original reports by ophthalmologists could instead be alopecia areata with re-growth of white hair.
    PMID: 20040260 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3133371</comments>
            <pubDate>Thu, 31 Dec 2009 16:04:02 +0100</pubDate>
            <guid isPermaLink="false">3133371</guid>        </item>
        <item>
            <title>Transfer contact dermatitis caused by rosin use in bowling.</title>
            <link>http://www.medworm.com/index.php?rid=3133370&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20040261%26dopt%3DAbstract</link>
            <description>We present a case of transfer contact dermatitis of the face due to rosin use in bowling.
    PMID: 20040261 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3133370</comments>
            <pubDate>Thu, 31 Dec 2009 16:04:02 +0100</pubDate>
            <guid isPermaLink="false">3133370</guid>        </item>
        <item>
            <title>Treatment of necrobiosis lipoidica with etanercept and adalimumab.</title>
            <link>http://www.medworm.com/index.php?rid=3133367&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20040262%26dopt%3DAbstract</link>
            <description>Authors: Zhang KS, Quan LT, Hsu S
    
    PMID: 20040262 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3133367</comments>
            <pubDate>Thu, 31 Dec 2009 16:04:02 +0100</pubDate>
            <guid isPermaLink="false">3133367</guid>        </item>
        <item>
            <title>Treatment of pityriasis amiantacea with infliximab.</title>
            <link>http://www.medworm.com/index.php?rid=3133366&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20040263%26dopt%3DAbstract</link>
            <description>Authors: Pham RK, Chan CS, Hsu S
    
    PMID: 20040263 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3133366</comments>
            <pubDate>Thu, 31 Dec 2009 16:04:02 +0100</pubDate>
            <guid isPermaLink="false">3133366</guid>        </item>
        <item>
            <title>Two cases of photocontact allergy to the new sun filter octocrylene.</title>
            <link>http://www.medworm.com/index.php?rid=3133365&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20040264%26dopt%3DAbstract</link>
            <description>We report two cases of photocontact allergy to a cinnamate sun filter, octocrylene. In the last few years octocrylene has been broadly used in the manufacturing of many cosmetics and UV filters, hence the importance of octocrylene as an emerging cause of contact and photocontact allergy.
    PMID: 20040264 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3133365</comments>
            <pubDate>Thu, 31 Dec 2009 16:04:02 +0100</pubDate>
            <guid isPermaLink="false">3133365</guid>        </item>
        <item>
            <title>Persistent cutaneous hyperpigmentation due to hydroxychloroquinone one year after therapy discontinuation.</title>
            <link>http://www.medworm.com/index.php?rid=3133363&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20040265%26dopt%3DAbstract</link>
            <description>We report a case of HCQ induced dyschromia diffusely involving the extremities, with minimal resolution one year after treatment discontinuation.
    PMID: 20040265 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3133363</comments>
            <pubDate>Thu, 31 Dec 2009 16:04:02 +0100</pubDate>
            <guid isPermaLink="false">3133363</guid>        </item>
        <item>
            <title>Whitish bullae on the fingers: what is the diagnosis? Tophaceous gout.</title>
            <link>http://www.medworm.com/index.php?rid=3120888&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19723483%26dopt%3DAbstract</link>
            <description>Authors: Nogueira A, Duarte AF, Morais P, Magina S, Azevedo F
    A 56-year-old woman presented with a 6 month history of bullae and whitish plaques of the fingers. She had chronic renal failure, but no joint pains or evidence of arthritis. An aspirate of fluid from a bulla revealed uric acid crystals and serum uric acid was elevated at 16.2 mg/dL. A diagnosis of tophaceous gout was made.
    PMID: 19723483 [PubMed - indexed for MEDLINE] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3120888</comments>
            <pubDate>Sat, 26 Dec 2009 02:30:03 +0100</pubDate>
            <guid isPermaLink="false">3120888</guid>        </item>
        <item>
            <title>A man with erythematous nodules: what is the diagnosis? Lepromatous leprosy.</title>
            <link>http://www.medworm.com/index.php?rid=3120887&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19723484%26dopt%3DAbstract</link>
            <description>Authors: Santos AP, Selles BR, Ayres EL, Xavier MH, Rochael MC
    A 65-year-old man presented with an approximately 5-year history of cutaneous nodules of the arms and legs. In addition, physical examination revealed bilateral thickening of ulnar and tibial nerves, distal weakness with hallux extension and finger abduction, and distal hypoesthesia of the left hallux. Histopathological analysis of the skin biopsy specimen showed a dense inflammatory infiltrate in the hypodermis, characterized by vacuolated macrophages containing multiple organisms. The Fite stain was positive confirming the diagnosis of multibacillary leprosy.
    PMID: 19723484 [PubMed - indexed for MEDLINE] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3120887</comments>
            <pubDate>Sat, 26 Dec 2009 02:30:03 +0100</pubDate>
            <guid isPermaLink="false">3120887</guid>        </item>
        <item>
            <title>Parable: When the gods howled.</title>
            <link>http://www.medworm.com/index.php?rid=3093081&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19723485%26dopt%3DAbstract</link>
            <description>Authors: Goihman-Yahr M
    
    PMID: 19723485 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3093081</comments>
            <pubDate>Wed, 16 Dec 2009 20:06:03 +0100</pubDate>
            <guid isPermaLink="false">3093081</guid>        </item>
        <item>
            <title>The &quot;away&quot; dermatology elective for visiting medical students: Educational opportunities and barriers.</title>
            <link>http://www.medworm.com/index.php?rid=3052761&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951619%26dopt%3DAbstract</link>
            <description>Authors: Philips RC, Dhingra N, Uchida T, Wagner RF
    Dermatology electives allow medical students an opportunity to explore the field of dermatology. In order to gain greater exposure to the specialty of dermatology, some medical students have an interest in taking &quot;away&quot; dermatology electives at other U.S. medical schools. A telephone survey was conducted to better understand the opportunities and barriers that exist for visiting medical students to take an elective in dermatology. Areas of focus in the survey included dermatology elective offerings, institutional policies toward visiting students, academic requirements for visiting students, timing of electives, financial costs of electives incurred by the student and institutional and regional preferences of the host medical school. ...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052761</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052761</guid>        </item>
        <item>
            <title>A national survey to determine an optimal fourth year curriculum for dermatology candidates.</title>
            <link>http://www.medworm.com/index.php?rid=3052760&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951620%26dopt%3DAbstract</link>
            <description>Authors: Alikhan A, Ledo L, Armstrong AW
    
    PMID: 19951620 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052760</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052760</guid>        </item>
        <item>
            <title>Advice for fourth year medical students beginning the dermatology residency application process: Perspectives from interns who matched.</title>
            <link>http://www.medworm.com/index.php?rid=3052759&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951621%26dopt%3DAbstract</link>
            <description>Authors: Alikahn A, Sivamani RK, Mutizwa MM, Felsten LM
    
    PMID: 19951621 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052759</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052759</guid>        </item>
        <item>
            <title>Basal cell carcinoma with neuroendocrine differentiation arising in a scar: A case report.</title>
            <link>http://www.medworm.com/index.php?rid=3052758&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951622%26dopt%3DAbstract</link>
            <description>Authors: Krokowski M, Hoch J, Feller AC, Bernd HW, Thorns C, Krueger S
    Basal cell carcinoma (BCC), the most common cutaneous malignant tumor, may display neuroendocrine differentiation in very rare instances. We here describe a case of a BCC with neuroendocrine differentiation that arose in a scar resulting from a trauma 75 years earlier. Neuroendocrine differentiation was proven by immunohistochemistry and electron microscopy. The simultaneous occurrence of BCC development in a scar and neuroendocrine differentiation is quite rare.
    PMID: 19951622 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052758</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052758</guid>        </item>
        <item>
            <title>Disseminated fusariosis presenting as panniculitis-like lesions on the legs of a neutropenic girl with acute lymphoblastic leukemia.</title>
            <link>http://www.medworm.com/index.php?rid=3052757&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951623%26dopt%3DAbstract</link>
            <description>We present a case of fusariosis in an 11-year-old neutropenic patient with acute lymphoblastic leukemia whose only symptom of the fungal infection consisted of painful, indurated nodules and plaques on her legs. The diagnosis and treatment of this invasive fungal infection is also discussed.
    PMID: 19951623 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052757</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052757</guid>        </item>
        <item>
            <title>Alopecia syphilitica-report of a patient with secondary syphilis presenting as moth-eaten alopecia and a review of its common mimickers.</title>
            <link>http://www.medworm.com/index.php?rid=3052756&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951624%26dopt%3DAbstract</link>
            <description>Authors: Bi MY, Cohen PR, Robinson FW, Gray JM
    Alopecia syphilitica is an uncommon manifestation of secondary syphilis, occurring in only 4 percent of these individuals. It is non-inflammatory and non-cicatricial hair loss that can present in a diffuse pattern, a moth-eaten pattern, or a combination of both. A 38-year-old, otherwise asymptomatic, homosexual man is described whose initial presentation of syphilis was patchy, moth-eaten, alopecia. In addition, differentiating features of alopecia syphilitica and other similar appearing non-cicatricial alopecias are reviewed. Conditions that mimic moth-eaten alopecia include other localized and non-cicatricial alopecias, such as alopecia areata, alopecia neoplastica, tinea capitis, and trichotillomania. The distinguishing clinical and lab...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052756</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052756</guid>        </item>
        <item>
            <title>Epidermal nevus syndrome associated with polyostotic fibrous dysplasia, CNS lipoma, and aplasia cutis.</title>
            <link>http://www.medworm.com/index.php?rid=3052755&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951625%26dopt%3DAbstract</link>
            <description>We describe a patient with an extensive epidermal nevus associated with various organ abnormalities, particularly polyostotic fibrous dysplasia, central nervous system lipoma, and aplasia cutis. Our patient demonstrates the polymorphic spectrum of involvement in epidermal nevus syndrome.
    PMID: 19951625 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052755</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052755</guid>        </item>
        <item>
            <title>Cutaneous pseudallescheria boydii infection in a renal transplant patient: A case report.</title>
            <link>http://www.medworm.com/index.php?rid=3052754&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951626%26dopt%3DAbstract</link>
            <description>We describe the case of a 59-year-old male renal transplant recipient who presented with a 1 month history of nodular, erythematous, and crusted lesions on the anterior surface of the left leg. There was no history of trauma. The patient had no systemic signs or symptoms. A skin biopsy revealed evidence of a deep fungal infection, with septate and branching hyphae amongst the dermal inflammatory infiltrate, but the culture was negative. Initial treatment with itraconazole proved ineffective and new lesions appeared. New tissue samples were obtained for culture, allowing the isolation of Pseudallescheria boydii. The patient underwent surgical excision of the lesions combined with voriconazole 400 mg/day for 2 months. After this period no new lesions appeared and the patient has remained wit...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052754</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052754</guid>        </item>
        <item>
            <title>Unilesional pemphigus vulgaris of the scalp.</title>
            <link>http://www.medworm.com/index.php?rid=3052753&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951627%26dopt%3DAbstract</link>
            <description>Authors: Ferrara G, Massone C, Zalaudek I, Argenziano G
    
    PMID: 19951627 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052753</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052753</guid>        </item>
        <item>
            <title>Pyogenic granuloma clinically and dermoscopically mimicking pigmented melanoma.</title>
            <link>http://www.medworm.com/index.php?rid=3052752&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951628%26dopt%3DAbstract</link>
            <description>We report the case of an 18-year-old male who presented with a round, purple-black nodule with hemorrhagic crust, 1 cm in diameter, located on the lower part of the thorax. Dermoscopic evaluation revealed the presence of a blue-white veil, a black blotch, polymorphous atypical vessels, milky-red areas, and hemorrhagic crusts. The subsequent histopathological examination revealed a pyogenic granuloma. We present a case of pyogenic granuloma clinically and dermoscopically indistinguisable from a pigmented malignant melanoma.
    PMID: 19951628 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052752</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052752</guid>        </item>
        <item>
            <title>Longitudinal melanonychia induced by capecitabine.</title>
            <link>http://www.medworm.com/index.php?rid=3052751&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951629%26dopt%3DAbstract</link>
            <description>Authors: Paravar T, Hymes SR
    Capecitabine is an oral prodrug of 5-fluorouracil (5-FU), used in the treatment of metastatic colon and breast cancers; it is also under investigation for use in gastric cancers. Multiple cutaneous adverse effects have been reported with the use of capecitabine including acral erythema, pyogenic granulomas, inflammation of actinic keratoses, cutaneous and mucosal hyperpigmentation, leopardlike vitiligo, radiation recall, onycholysis, onychomadesis, and subacute cutaneous lupus. To our knowledge, no cases of capecitabine-induced linear melanonychia have been reported to date in the literature.
    PMID: 19951629 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052751</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052751</guid>        </item>
        <item>
            <title>Palmar filiform parakeratotic hyperkeratosis: A report of 2 cases.</title>
            <link>http://www.medworm.com/index.php?rid=3052750&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951630%26dopt%3DAbstract</link>
            <description>We report two new cases of this entity without systemic pathology associated.
    PMID: 19951630 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052750</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052750</guid>        </item>
        <item>
            <title>Fissure leishmaniasis: A new variant of cutaneous leishmaniasis.</title>
            <link>http://www.medworm.com/index.php?rid=3052749&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951631%26dopt%3DAbstract</link>
            <description>We report two cases of CL who presented as cutaneous fissures (on lower lip in one patient and dorsum of finger in another). They were diagnosed by demonstrating leishmania parasites in skin smear preparations and were treated accordingly.
    PMID: 19951631 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052749</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052749</guid>        </item>
        <item>
            <title>Eruptive angiokeratomas on the glans penis.</title>
            <link>http://www.medworm.com/index.php?rid=3052748&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951632%26dopt%3DAbstract</link>
            <description>Authors: Feramisco JD, Fournier JB, Venna SS
    Angiokeratomas are benign proliferations of dilated thin-walled blood vessels in the upper dermis with overlying epidermal hyperkeratosis. There are several clinical variants of angiokeratomas: 1. Fordyce: smooth reddish-purple papules on scrotum or vulva; 2. Mibelli: hyperkeratotic papules on fingers or toes, solitary, multiple, or circumscriptum (grouped papules usually on an extremity); 4. angiokeratoma corporis diffusum, widespread papules that are a manifestation of one of several inherited lysozomal storage diseases. Herein, we report a rare case of multiple angiokeratomas of Fordyce on the corona of the glans penis.
    PMID: 19951632 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052748</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052748</guid>        </item>
        <item>
            <title>Multiple lentigines confined to a resolving psoriatic plaque.</title>
            <link>http://www.medworm.com/index.php?rid=3052747&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951633%26dopt%3DAbstract</link>
            <description>We report the case of patient who developed nevus spilus-like lentigines following therapy with topical calcipotriol on psoriatic plaques. We consider that the mechanism of production of lentigines is an unusual form of postinflammatory hyperpigmentation.
    PMID: 19951633 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052747</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052747</guid>        </item>
        <item>
            <title>Bowen disease over photoprotected site in an Indian male.</title>
            <link>http://www.medworm.com/index.php?rid=3052746&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951634%26dopt%3DAbstract</link>
            <description>Authors: Gupta S, Nutan N, Dogra S, Kanwar AJ
    Bowen Disease is squamous cell carcinoma in situ in which the basement membrane is intact on histopathology. Lesions are usually solitary but may be multiple in 10-20 percent of cases. About three-quarters of these lesions are situated on the lower limb. It typically presents as an erythematous enlarging plaque having irregular borders with scaling and crusting. Our patient presented with a lesion on the chest that was not sun exposed thus leading to a diagnostic dilemma.
    PMID: 19951634 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052746</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052746</guid>        </item>
        <item>
            <title>Treatment of crusted scabies with albendazole: A case report.</title>
            <link>http://www.medworm.com/index.php?rid=3052745&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951635%26dopt%3DAbstract</link>
            <description>We describe a 22-year-old Syrian immunocompetent female who had hyperkeratotic psoriasiform plaques and hyperkeratosis without itching. She was treated with oral albendazol and topical crotamiton with salicylic acid 5 percent.
    PMID: 19951635 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052745</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052745</guid>        </item>
        <item>
            <title>Adult onset eccrine angiomatous hamartoma.</title>
            <link>http://www.medworm.com/index.php?rid=3052744&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951636%26dopt%3DAbstract</link>
            <description>We report a patient with onset in adulthood.
    PMID: 19951636 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052744</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052744</guid>        </item>
        <item>
            <title>Melanoma costs: A dynamic model comparing estimated overall costs of various clinical stages.</title>
            <link>http://www.medworm.com/index.php?rid=3052743&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951637%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: There is a significant cost decrement when melanoma is diagnosed at an earlier stage, with a T4b lesion being approximately 2200 percent more expensive to diagnose and treat than an early in situ melanoma and 1000 percent more expensive than a stage T1a tumor. Although a direct comparison with other cancers would require the use of the same dynamic model, it is apparent that the high costs of melanoma care places it at the top of the most expensive cancers to diagnose, follow, and treat. These high costs for advanced-stage melanoma warrant an increased emphasis on developing effective strategies for its early diagnosis and treatment.
    PMID: 19951637 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052743</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052743</guid>        </item>
        <item>
            <title>Hand-foot syndrome and seborrheic dermatitis-like eruption induced by erlotinib.</title>
            <link>http://www.medworm.com/index.php?rid=3052742&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951638%26dopt%3DAbstract</link>
            <description>We report a case of hand-foot syndrome associated with a papulo-pustular and seborrheic dermatitis-like eruption of the face in a 61-year-old patient treated with erlotinib for lung cancer.
    PMID: 19951638 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052742</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052742</guid>        </item>
        <item>
            <title>Linear IgA bullous dermatosis following influenza vaccination.</title>
            <link>http://www.medworm.com/index.php?rid=3052741&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951639%26dopt%3DAbstract</link>
            <description>We report the case of a 54-year-old woman who developed LABD shortly after receiving an influenza vaccination.
    PMID: 19951639 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052741</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052741</guid>        </item>
        <item>
            <title>Naproxen-induced generalized bullous fixed drug eruption.</title>
            <link>http://www.medworm.com/index.php?rid=3052740&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951640%26dopt%3DAbstract</link>
            <description>We present a case of naproxen-induced generalized bullous FDE in a 50-year-old woman.
    PMID: 19951640 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052740</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052740</guid>        </item>
        <item>
            <title>Hyper- and hypopigmented macules over palms and soles since birth - a case of dyschromatosis symmetrica hereditaria.</title>
            <link>http://www.medworm.com/index.php?rid=3052739&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951641%26dopt%3DAbstract</link>
            <description>We report a case of a 4-year-old girl with DSH and review the pertinent features of this genodermatosis.
    PMID: 19951641 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052739</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052739</guid>        </item>
        <item>
            <title>Oto-Rhino-Laryngology (ORL) tumor presentation in a case of systemic AA amyloidosis.</title>
            <link>http://www.medworm.com/index.php?rid=3052738&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951642%26dopt%3DAbstract</link>
            <description>Authors: Khoudri I, Marcil T, Elmeknassi I, Kzadri M, Ismaili N, Afifi Y, Senouci K, Hassam B
    A 64-year-old male with no underlying disease presented with the development of multiple skin nodules, loss of sensation in the extremities, hoarseness, macroglossia, and pain in the oral cavity. Direct laryngoscopy showed nodules involving the oral cavity, oropharynx, supraglottic region, and vocal cords. Biopsy from skin nodules showed amyloid deposits staining with Congo red. Immunohistochemical staining was used for AA protein and was positive. Biopsy from the oral floor was also positive for amyloid. Oto-Rhino-Laryngology (ORL) involvement has been reported in approximately 40 percent of AL amyloidosis patients, but does not appear to be frequent in AA amyloidosis. Cutaneous manifestation...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052738</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052738</guid>        </item>
        <item>
            <title>An unusual vascular tumor: Verrucous hemangioma.</title>
            <link>http://www.medworm.com/index.php?rid=3052737&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951643%26dopt%3DAbstract</link>
            <description>Authors: Koc M, Kavala M, Kocat&amp;#xFC;rk E, Zemheri E, Zindanci I, Sudogan S, Kural E
    Verrucous hemangioma is an uncommon capillary or cavernous hemangioma with reactive epidermal changes of hyperkeratosis, acanthosis, and papillomatosis. These growths are usually located on the lower extremities and involvement is generally unilateral. A diagnosis of verrucous hemangioma should be considered in lesions especially with a hyperkeratotic nodular appearance located on the lower extremities.
    PMID: 19951643 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052737</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052737</guid>        </item>
        <item>
            <title>Severe 20-nail psoriasis successfully treated by low dose methotrexate.</title>
            <link>http://www.medworm.com/index.php?rid=3052736&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951644%26dopt%3DAbstract</link>
            <description>We report a case of severe psoriatic nail dystrophy involving all 20 nails successfully treated by low dose MTX. A previously healthy 11-year-old girl presented with painful deformity involving all 20 nails that developed over a one-month period. Examination revealed geographic and fissured tongue, as well as severe nail dystrophy of all 20 nails characterized by erythematous swelling of the nail folds, yellowish discoloration of nail plates with pitting, severe crumbling and destruction, transverse depressions, prominent oil spots, and swelling of proximal nail. Topical clobetasol propionate and calcipotriol were tried first but the nail dystrophy continued to progress. Low dose of MTX (5 mg per week) was initiated. The response was fairly satisfactory with emergence of normal plate proxi...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052736</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052736</guid>        </item>
        <item>
            <title>Syringocystoadenoma papilliferum associated with apocrine hidrocystoma and verruca.</title>
            <link>http://www.medworm.com/index.php?rid=3052735&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951645%26dopt%3DAbstract</link>
            <description>Authors: Arias-Santiago S, Aceituno-Madera P, Aneiros-Fern&amp;#xE1;ndez J, Guti&amp;#xE9;rrez-Salmer&amp;#xF3;n MT, Naranjo-Sintes R
    Syringocystoadenoma papilliferum is a benign adnexal tumor usually located in head and neck that occurs during childhood or adolescence. A case of a syringocystoadema papilliferum associated with apocrine hydrocystoma and verruca is presented. It is unusual to see the occurrence of three histopathologic types of tumors coexisting in one cutaneous lesion.
    PMID: 19951645 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052735</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052735</guid>        </item>
        <item>
            <title>Psoriasis in a 3-month-old infant with Kawasaki disease.</title>
            <link>http://www.medworm.com/index.php?rid=3052734&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951646%26dopt%3DAbstract</link>
            <description>Authors: Liao YC, Lee JY
    Kawasaki disease (KD) or mucocutaneous lymph node syndrome is a systemic vasculitis of unknown etiology affecting young children. Typical cutaneous manifestations of KD are polymorphous, including maculopapular or morbilliform rash and erythroderma. Occurrence of psoriasis following KD is rare. Herein we report a case of new onset of psoriasis in a 3-month-old that flared after a typical clinical case of KD, manifesting spiking fever, diffuse redness and fissuring of the lips, bilateral conjunctiva injection, injected throat, left cervical lymphadenopathy, erythema and desquamation of the lips, cheeks, hands, feet and perianal area, and a generalized maculopapular eruption. In addition, erythema and induration of the BCG vaccination site and coronary artery dil...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052734</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052734</guid>        </item>
        <item>
            <title>Is a cystic sebaceous neoplasm always marker for Muir-Torre syndrome?</title>
            <link>http://www.medworm.com/index.php?rid=3052733&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951647%26dopt%3DAbstract</link>
            <description>We present a 73-year-old man with a cystic sebaceous neoplasm on his arm, clinically not associated with Muir-Torre syndrome.
    PMID: 19951647 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052733</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052733</guid>        </item>
        <item>
            <title>Hypomelanosis of Ito with hemimegalencephaly.</title>
            <link>http://www.medworm.com/index.php?rid=3052732&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951648%26dopt%3DAbstract</link>
            <description>We present a 3-month-old male infant with Hypomelanosis of Ito, hemi-hypertrophy and hemi-megalencephaly.
    PMID: 19951648 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052732</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052732</guid>        </item>
        <item>
            <title>Kaiser Permanente: A new model for academic dermatology.</title>
            <link>http://www.medworm.com/index.php?rid=3052731&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951649%26dopt%3DAbstract</link>
            <description>We describe this model from within Kaiser Permanente Los Angeles Medical Center.
    PMID: 19951649 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052731</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052731</guid>        </item>
        <item>
            <title>Localized cutaneous T cell lymphoma presenting as disfiguring facial lesions.</title>
            <link>http://www.medworm.com/index.php?rid=3052730&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951650%26dopt%3DAbstract</link>
            <description>We report a case of a 27-year-old male patient with localized cutaneous T cell lymphoma presenting as disfiguring lesions on the face.
    PMID: 19951650 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052730</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052730</guid>        </item>
        <item>
            <title>Rare presentation of a congenital neuroblastoma.</title>
            <link>http://www.medworm.com/index.php?rid=3052729&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951651%26dopt%3DAbstract</link>
            <description>Authors: D'souza IE, Patidar RC, Mani R, Shamseldeen M
    A term neonate born by caesarian section was found to have multiple shiny, pinkish purple, fleshy nodules all over the body in addition to the bluish subcutaneous nodules with massive hepatomegaly. Computerized tomography of the chest revealed a posterior mediastinal mass at the right paravertebral region; abdominal CT showed multiple hypodense lesions in the liver. A biopsy from one of these skin nodules confirmed the diagnosis of neuroblastoma. Multiple skin nodules are a rare presentation of congenital neuroblastoma.
    PMID: 19951651 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052729</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052729</guid>        </item>
        <item>
            <title>Stevens-Johnson syndrome related to ciprofloxacin, possibly enhanced by overadministration of levothyroxine.</title>
            <link>http://www.medworm.com/index.php?rid=3052728&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951652%26dopt%3DAbstract</link>
            <description>Authors: Cholongitas E, Georgousaki C, Spyrou S, Katsogridakis K, Dasenaki M
    A 66-year-old woman is presented who developed Stevens-Johnson syndrome related to ciprofloxacin. It is postulated that overdose of levothyroxine could have reduced cytochrome activity required for the metabolism of ciprofloxacin and that this could have contributed to the development of the drug reaction.
    PMID: 19951652 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052728</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052728</guid>        </item>
        <item>
            <title>Pool palms.</title>
            <link>http://www.medworm.com/index.php?rid=3052727&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19951653%26dopt%3DAbstract</link>
            <description>This article reviews the clinical features of this entity.
    PMID: 19951653 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3052727</comments>
            <pubDate>Thu, 03 Dec 2009 20:46:04 +0100</pubDate>
            <guid isPermaLink="false">3052727</guid>        </item>
        <item>
            <title>A survey of dermatology residency program directors' views on mentorship.</title>
            <link>http://www.medworm.com/index.php?rid=3027191&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19930988%26dopt%3DAbstract</link>
            <description>Conclusion: Program Directors viewed mentoring as an important resource for their residents' professional development. A need was identified for additional strategies to help residents find mentors.
    PMID: 19930988 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3027191</comments>
            <pubDate>Thu, 26 Nov 2009 11:14:02 +0100</pubDate>
            <guid isPermaLink="false">3027191</guid>        </item>
        <item>
            <title>Risk factors in pediatric dermatologic surgery.</title>
            <link>http://www.medworm.com/index.php?rid=3027190&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19930989%26dopt%3DAbstract</link>
            <description>CONCLUSION: General anesthesia is safe in pediatric dermatology in the hands of experienced pediatric anesthetists. The most frequent surgical complication was scar stretching. Limb location and use of absorbable continuous intradermal suture in the upper closures should be taken into account as possible risk factors when informing parents and performing these procedures.
    PMID: 19930989 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3027190</comments>
            <pubDate>Thu, 26 Nov 2009 11:14:02 +0100</pubDate>
            <guid isPermaLink="false">3027190</guid>        </item>
        <item>
            <title>Case of mistaken identity: Bullous congenital ichthyosiform erythroderma mistaken as epidermolysis bullosa simplex.</title>
            <link>http://www.medworm.com/index.php?rid=3027189&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19930990%26dopt%3DAbstract</link>
            <description>We present a case of BCIE misdiagnosed as EBS and review characteristic clinical and histopathological features of each disorder as well as the basic approach to treatment.
    PMID: 19930990 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3027189</comments>
            <pubDate>Thu, 26 Nov 2009 11:14:02 +0100</pubDate>
            <guid isPermaLink="false">3027189</guid>        </item>
        <item>
            <title>Lichen sclerosus et atrophicus-like graft versus host disease post stem cell transplant.</title>
            <link>http://www.medworm.com/index.php?rid=3027188&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19930991%26dopt%3DAbstract</link>
            <description>We describe two cases of lichen sclerosus et atrophicus-like cGVHD developing in patients after hematopoietic stem cell transplantation. Both patients presented clinically with patches of pigmentary changes and scaling that displayed classic histologic features of lichen sclerosus et atrophicus. The skin is a frequent target organ of cGVHD and often the presenting location of the disease, making dermatologists key in recognition and management. It has been proposed that cutaneous cGVHD is a spectrum of disease and the lesions may evolve through various stages. Lichen sclerosus et atrophicus-like cGVHD may represent a phase in this continuum or a distinct sub-type of disease. Remaining cognizant of the potential manifestations of disease is key for prompt recognition and proper treatment.
 ...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3027188</comments>
            <pubDate>Thu, 26 Nov 2009 11:14:02 +0100</pubDate>
            <guid isPermaLink="false">3027188</guid>        </item>
        <item>
            <title>Flat type verruciform xanthoma of the tongue and its differential diagnosis.</title>
            <link>http://www.medworm.com/index.php?rid=3027187&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19930992%26dopt%3DAbstract</link>
            <description>We present herein a case of oral verruciform xanthoma (VX) in order to discuss this relatively rare entity in light of current information. A 38-year-old woman, non-smoker, presented with a lesion at the left ventral surface of the tongue. The lesion is characterized by a mild epithelial proliferation and sub-epithelial accumulation of foam cells, which were positive for CD68, and negative for CD1a and S-100 protein. Human papillomavirus (HPV) DNA typing for low, intermediate, and high-risk groups was also performed and no etiological link between HPV and this lesion was found. The past medical history of the patient was unremarkable and further investigations did not reveal any biochemical abnormalities or systemic disease. Verruciform xanthoma is an uncommon benign lesion of undetermined...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3027187</comments>
            <pubDate>Thu, 26 Nov 2009 11:14:02 +0100</pubDate>
            <guid isPermaLink="false">3027187</guid>        </item>
        <item>
            <title>Eccrine angiomatous hamartoma: A rare multifocal variant with features suggesting trauma.</title>
            <link>http://www.medworm.com/index.php?rid=3027186&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19930993%26dopt%3DAbstract</link>
            <description>We report a rare case of the multifocal variant of EAH in a 13-year-old girl, with histological features suggesting trauma. Clinically, this condition must be differentiated from other angiomatoses and a definitive diagnosis is based upon histology. Eccrine angiomatous hamartoma is a benign slowly growing lesion for which aggressive treatment is not indicated. Simple excision is reserved for painful or cosmetically disfiguring examples.
    PMID: 19930993 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3027186</comments>
            <pubDate>Thu, 26 Nov 2009 11:14:02 +0100</pubDate>
            <guid isPermaLink="false">3027186</guid>        </item>
        <item>
            <title>S100, HMB-45, and Melan-A negative primary melanoma.</title>
            <link>http://www.medworm.com/index.php?rid=3027185&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19930994%26dopt%3DAbstract</link>
            <description>We report a case of melanoma with loss of staining for S100 protein, HMB-45, and Melan-A, with retained expression of tyrosinase. Regional lymph node metastases showed positive S100 protein staining. Although the loss of phenotypic markers including S100 protein has been reported in metastatic melanoma, loss of S100 in primary melanoma is rare. Discordant staining between primary and metastatic lesions further emphasizes the protean nature of melanoma.
    PMID: 19930994 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3027185</comments>
            <pubDate>Thu, 26 Nov 2009 11:14:02 +0100</pubDate>
            <guid isPermaLink="false">3027185</guid>        </item>
        <item>
            <title>Terbinafine-induced acute generalized exanthematous pustulosis (AGEP) responsive to high dose intravenous corticosteroid.</title>
            <link>http://www.medworm.com/index.php?rid=3027184&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19930995%26dopt%3DAbstract</link>
            <description>Authors: Ibrahimi OA, Gunawardane N, Sepehr A, Reynolds RV
    Acute generalized exanthematous pustulosis (AGEP) is a febrile pustular drug eruption. Terbinafine, an allylamine fungicidial agent, is the most common anti-mycotic associated with AGEP. Here, we report a case of terbinafine-induced AGEP that was recalcitrant to oral corticosteroid but responsive to high-dose intravenous corticosteroid.
    PMID: 19930995 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3027184</comments>
            <pubDate>Thu, 26 Nov 2009 11:14:02 +0100</pubDate>
            <guid isPermaLink="false">3027184</guid>        </item>
        <item>
            <title>Erosions on a prolapsed uterine in an old woman: an unusual manifestation of pemphigus vulgaris.</title>
            <link>http://www.medworm.com/index.php?rid=3027183&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19930996%26dopt%3DAbstract</link>
            <description>We describe a patient with pemphigus vulgaris who had pemphigus erosions on a prolapsed uterus (i.e., on the everted surface of vagina). The patient had widespread lesions of pemphigus in other mucosal and cutaneous sites. Biopsy, antibodies against desmoglein 1 and 3, and direct and indirect immunofluorescence were confirming. The erosions on the prolapsed uterus were resistant to treatment; other mucosal and cutaneous lesions responded rapidly to prednisolone and azathioprine. After lowering the dose of prednisolone the patient was referred to a gynecologist for a vaginal hysterectomy. This case was unique because her vaginal lesions could be easily examined and followed.
    PMID: 19930996 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3027183</comments>
            <pubDate>Thu, 26 Nov 2009 11:14:02 +0100</pubDate>
            <guid isPermaLink="false">3027183</guid>        </item>
        <item>
            <title>Frostbite injury of the foot from portable fire extinguisher.</title>
            <link>http://www.medworm.com/index.php?rid=3027182&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19930997%26dopt%3DAbstract</link>
            <description>We present a case of sudden frostbite burn of the left foot caused by carbon dioxide. The circumstances of this injury and preventive measures are discussed.
    PMID: 19930997 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3027182</comments>
            <pubDate>Thu, 26 Nov 2009 11:14:02 +0100</pubDate>
            <guid isPermaLink="false">3027182</guid>        </item>
        <item>
            <title>Furuncular myiasis: Unusual case of African Dermatobia hominis.</title>
            <link>http://www.medworm.com/index.php?rid=3027181&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19930998%26dopt%3DAbstract</link>
            <description>We present an unusual patient with myiasis infestation of the leg caused by Dermatobia hominis, which manifested after returning from the Democratic Republic of Congo. This particular infestation has not been reported in Morocco prior to this case. Furuncular cutaneous miyasis must be considered when travellers exhibit draining nodules. Medical treatment consists of occlusion of the furuncular punctum with vaseline to stimulate extrusion of the larva or surgical debridement under local anesthesia.
    PMID: 19930998 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3027181</comments>
            <pubDate>Thu, 26 Nov 2009 11:14:02 +0100</pubDate>
            <guid isPermaLink="false">3027181</guid>        </item>
        <item>
            <title>Cryptococcal meningitis with an antecedent cutaneous Cryptococcal lesion.</title>
            <link>http://www.medworm.com/index.php?rid=3027180&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19930999%26dopt%3DAbstract</link>
            <description>Authors: Tilak R, Prakash P, Nigam C, Tilak V, Gambhir IS, Gulati AK
    Cutaneous cryptococcosis, caused by an encapsulated yeast, Cryptococcus neoformans, is generally associated with concomitant systemic infection. Here we report a case of primary cutaneous cryptococcosis with spread to central nervous system in an HIV seronegative young boy. In the present case, a 17-year-old boy who was suffering from a non-healing ulcer on his right great toe for 5 months, presented with the signs and symptoms of meningitis. Cryptococcus neoformans var. gattii was isolated from the CSF of the patient. Amphotericin B administration produced recovery from the meningitis as well as from the ulcer. This case study suggests that primary cutaneous cryptococcosis can be diagnosed provisionally by a simple G...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3027180</comments>
            <pubDate>Thu, 26 Nov 2009 11:14:02 +0100</pubDate>
            <guid isPermaLink="false">3027180</guid>        </item>
        <item>
            <title>Lymphangioma-like Kaposi sarcoma: Case report.</title>
            <link>http://www.medworm.com/index.php?rid=3027179&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19931000%26dopt%3DAbstract</link>
            <description>We report the case of a 76-year-old woman, HIV negative, with a 4-year history of classic Kaposi sarcoma treated with cryotherapy who developed new bullous lesions on her lower extremities. Biopsy revealed histologic findings of lymphangioma-like KS (LLKS), together with areas of classic KS; HHV-8 staining was positive. Diagnosis of LLKS was made and the patient was proposed for radiotherapy. The lymphangioma-like Kaposi sarcoma is a rare morphologic expression of KS characterized by dilated and bizarrely shaped vascular channels lined by flattened endothelium permeating the dermis. &quot;Bulla-like&quot; lesions have been considered as a clinical hallmark of this variant. Its histologic appearance suggests a lymphatic origin of KS and it may resemble other vascular tumors. Findings of areas of typi...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3027179</comments>
            <pubDate>Thu, 26 Nov 2009 11:14:02 +0100</pubDate>
            <guid isPermaLink="false">3027179</guid>        </item>
        <item>
            <title>Unknown: Eyebrow papule in an elderly man.</title>
            <link>http://www.medworm.com/index.php?rid=3027178&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19931001%26dopt%3DAbstract</link>
            <description>Authors: Clark FL, Somoano B, Taube J, Egbert B, Kim J
    A 70-year-old Caucasian man presented with a several-month history of a solitary, asymptomatic papule on the left eyebrow. His medical history included stage 1A lentigo maligna melanoma and multiple non-melanoma skin cancers. Physical examination demonstrated a solitary 5-mm smooth, dome-shaped skin colored papule with subtle central erosion on the left eyebrow. No overlying telangiectasias were noted.
    PMID: 19931001 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3027178</comments>
            <pubDate>Thu, 26 Nov 2009 11:14:02 +0100</pubDate>
            <guid isPermaLink="false">3027178</guid>        </item>
        <item>
            <title>Síndrome de Down: ¿otra causa de inmunosupresión asociada con dermatofibromas eruptivos múltiples?</title>
            <link>http://www.medworm.com/index.php?rid=3027177&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19931002%26dopt%3DAbstract</link>
            <description>We report three patients with Down syndrome. One patient had psoriatic arthritis under treatment with methotrexate, one had Graves-Basedow disease, and one had hypercholesterolemia. All three patients developed multiple eruptive dermatofibromas. We suggest that the immunologic disturbances associated with Down syndrome, together with other underlying conditions present in these patients, could trigger the development of cutaneous lesions. Espa&amp;#xF1;ol: El t&amp;#xE9;rmino &quot;dermatofibromas eruptivos m&amp;#xFA;ltiples&quot; se emplea actualmente para definir la aparici&amp;#xF3;n de 5 a 8 lesiones en menos de 4 meses. Suele presentarse en estados de inmunodeficiencia causados por enfermedades autoinmunes en tratamiento con f&amp;#xE1;rmacos inmunosupresores, neoplasias hematol&amp;#xF3;gicas, infecci&amp;#xF3;n por el ...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3027177</comments>
            <pubDate>Thu, 26 Nov 2009 11:14:02 +0100</pubDate>
            <guid isPermaLink="false">3027177</guid>        </item>
        <item>
            <title>If at first you don't succeed: A difficult case of Linear IgA.</title>
            <link>http://www.medworm.com/index.php?rid=3027176&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19931003%26dopt%3DAbstract</link>
            <description>We present a patient with Linear IgA who was both difficult to diagnose and treat. Numerous biopsies were needed before a positive result could be returned. Trials of multiple systemic agents failed. Eventually, a second trial of dapsone was successful and well-tolerated. The case exemplifies the determination and perseverance that is often required by both patient and physician in pursuit of symptom relief.
    PMID: 19931003 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3027176</comments>
            <pubDate>Thu, 26 Nov 2009 11:14:02 +0100</pubDate>
            <guid isPermaLink="false">3027176</guid>        </item>
        <item>
            <title>Parable: What is this noise?</title>
            <link>http://www.medworm.com/index.php?rid=3027175&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19931004%26dopt%3DAbstract</link>
            <description>Authors: Goihman-Yahr M
    
    PMID: 19931004 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3027175</comments>
            <pubDate>Thu, 26 Nov 2009 11:14:02 +0100</pubDate>
            <guid isPermaLink="false">3027175</guid>        </item>
        <item>
            <title>Satisfying patient expectations with soft-tissue augmentation.</title>
            <link>http://www.medworm.com/index.php?rid=2985878&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19903429%26dopt%3DAbstract</link>
            <description>This article suggests a series of steps to help determine the most appropriate approach for volume restoration with injectable devices for satisfying patient treatment expectations.
    PMID: 19903429 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2985878</comments>
            <pubDate>Fri, 13 Nov 2009 12:06:04 +0100</pubDate>
            <guid isPermaLink="false">2985878</guid>        </item>
        <item>
            <title>Nail disease in pemphigus vulgaris.</title>
            <link>http://www.medworm.com/index.php?rid=2985877&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19903430%26dopt%3DAbstract</link>
            <description>Authors: Serratos BD, Rashid RM
    Patients affected by pemphigus vulgaris will occasionally present with associated and characteristic nail changes. This manuscript was prepared as a review of this unique presentation of pemphigus. Articles describing pemphigus vulgaris of the nail were compiled and reviewed and pertinent information was extracted to provide a concise analysis. The literature on this topic is still maturing. Publications to date suggest the incidence of nail and periungal involvement may correlate with the severity of mucocutaneous symptoms and the duration of the disease. The most common nail manifestations reported were acute or chronic paronychia and onychomadesis, and involvement of the fingernails. The nail changes may precede or develop concurrently with the mucocu...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2985877</comments>
            <pubDate>Fri, 13 Nov 2009 12:06:04 +0100</pubDate>
            <guid isPermaLink="false">2985877</guid>        </item>
        <item>
            <title>Pioderma gangrenoso - Abordagem clínica, laboratorial e terapêutica: Revisão de 28 casos.</title>
            <link>http://www.medworm.com/index.php?rid=2985876&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19903431%26dopt%3DAbstract</link>
            <description>We present a retrospective study of 28 patients, admitted to Hospital de S&amp;#xE3;o Jo&amp;#xE3;o, EPE, between January of 1990 and June of 2008. Pyoderma gangrenosum was observed more frequently in middle age adults, in the ulcerated form, and predominantly localized in the lower limbs. Pediatric presentation was very rare. In 50 percent of these cases a systemic disease was present and the most frequent was Crohn disease (14% of patients).
    PMID: 19903431 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2985876</comments>
            <pubDate>Fri, 13 Nov 2009 12:06:04 +0100</pubDate>
            <guid isPermaLink="false">2985876</guid>        </item>
        <item>
            <title>Advice for medical students interested in dermatology: Perspectives from fourth year students who matched.</title>
            <link>http://www.medworm.com/index.php?rid=2985875&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19903432%26dopt%3DAbstract</link>
            <description>We present perspectives from four fourth year medical students who matched into dermatology that highlight the factors they believed helped them most. The purpose is to offer advice to medical students interested in dermatology. We divide the paper into four areas of discussion: academics, extracurricular activities, research, and mentorship. All four factors are crucial for a strong dermatology application. We believe the paper provides valuable suggestions and guidance to students considering a career in dermatology.
    PMID: 19903432 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2985875</comments>
            <pubDate>Fri, 13 Nov 2009 12:06:04 +0100</pubDate>
            <guid isPermaLink="false">2985875</guid>        </item>
        <item>
            <title>A case of bullous disease limited to the skin illustrates the spectrum of neoplasia induced autoimmunity.</title>
            <link>http://www.medworm.com/index.php?rid=2985874&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19903433%26dopt%3DAbstract</link>
            <description>We describe a patient with fatal autoimmune blistering disease with absence of mucous membrane lesions. The pattern of complement indirect immunofluoresence helped identify the prognosis prospectively. This case illustrates yet another presentation of the neoplasia-induced autoimmunity.
    PMID: 19903433 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2985874</comments>
            <pubDate>Fri, 13 Nov 2009 12:06:04 +0100</pubDate>
            <guid isPermaLink="false">2985874</guid>        </item>
        <item>
            <title>A case of primary cutaneous B cell lymphoma of the knee.</title>
            <link>http://www.medworm.com/index.php?rid=2985873&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19903434%26dopt%3DAbstract</link>
            <description>We report the case of a gentleman with a primary cutaneous B cell lymphoma of the leg who underwent an amputation and later died. This is an uncommon type of cutaneous lymphoma with poor prognosis and the case demonstrates how aggressive the tumor can become.
    PMID: 19903434 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2985873</comments>
            <pubDate>Fri, 13 Nov 2009 12:06:04 +0100</pubDate>
            <guid isPermaLink="false">2985873</guid>        </item>
        <item>
            <title>Pseudoxanthoma elasticum-like syndrome and thalassemia: An update.</title>
            <link>http://www.medworm.com/index.php?rid=2985872&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19903435%26dopt%3DAbstract</link>
            <description>We describe three cases of the acquired PXE-like syndrome that often occurs in association with hemolytic anemias, in particular the hemoglobinopathies, and review the literature on the subject. The pathogenesis of the acquired PXE-like lesions is not yet completely understood. None of the mutations observed in the inherited form has been detected in the syndrome accompanying thalassemia. The cardiovascular complications could be life-threatening. Therefore, an close surveillance of these patients is mandatory.
    PMID: 19903435 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2985872</comments>
            <pubDate>Fri, 13 Nov 2009 12:06:04 +0100</pubDate>
            <guid isPermaLink="false">2985872</guid>        </item>
        <item>
            <title>Mucoceles not - Oral cysticercosis and minor salivary gland adenocarcinoma: Two case reports.</title>
            <link>http://www.medworm.com/index.php?rid=2985871&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19903436%26dopt%3DAbstract</link>
            <description>We present two cases that were clinically diagnosed as mucoceles that were removed because of patient anxiety. However, histological examination revealed dissimilar and medically significant pathologies. Oral cysticercosis and salivary gland adenocarcinoma are rare diseases of the oral mucosa. It is important to consider these and other uncommon diagnoses when evaluating an oral nodule presumed to be a mucocele. We will discuss the natural history and pathogenesis of these disease processes.
    PMID: 19903436 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2985871</comments>
            <pubDate>Fri, 13 Nov 2009 12:06:04 +0100</pubDate>
            <guid isPermaLink="false">2985871</guid>        </item>
        <item>
            <title>Keratoacanthoma in a tattoo.</title>
            <link>http://www.medworm.com/index.php?rid=2985870&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19903437%26dopt%3DAbstract</link>
            <description>We report a keratoacanthoma arising in a recent tattoo. A 60-year-old woman presented with a tumor on her right leg, over an area of red pigment in a professional tattoo. Histological analysis confirmed the clinical diagnosis of keratoacanthoma. Although the association between malignancy and tattoos is very uncommon dermatologists and dermatologic surgeons should be attentive to this possibility.
    PMID: 19903437 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2985870</comments>
            <pubDate>Fri, 13 Nov 2009 12:06:04 +0100</pubDate>
            <guid isPermaLink="false">2985870</guid>        </item>
        <item>
            <title>A remarkable case of cutaneous metastatic breast carcinoma.</title>
            <link>http://www.medworm.com/index.php?rid=2985869&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19903438%26dopt%3DAbstract</link>
            <description>We describe a 50-year-old woman with a 5-month history of multiple asymptomatic papulonodular lesions on the left chest area. Biopsy was consistent with cutaneous metastases from a ductal breast carcinoma. No distant metastatic lesions were detected. The patient was referred to the Gynecologic Oncology Department. Treatment included chemotherapy, radiotherapy and surgery. At present the patient is well with no signs of recurrence. This case reports a clinically remarkable cutaneous metastatic breast carcinoma.
    PMID: 19903438 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2985869</comments>
            <pubDate>Fri, 13 Nov 2009 12:06:04 +0100</pubDate>
            <guid isPermaLink="false">2985869</guid>        </item>
        <item>
            <title>Title.</title>
            <link>http://www.medworm.com/index.php?rid=2985868&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19903439%26dopt%3DAbstract</link>
            <description>TITLE.
    Dermatol Online J. 2009;15(7):11
    Authors: Last FM, Last FM, Last FM
    ABSTRACT.
    PMID: 19903439 [PubMed - as supplied by publisher] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2985868</comments>
            <pubDate>Fri, 13 Nov 2009 12:06:04 +0100</pubDate>
            <guid isPermaLink="false">2985868</guid>        </item>
        <item>
            <title>Autologous &quot;foreign body&quot; as a sequel of improper cutting of an ingrowing toe nail?</title>
            <link>http://www.medworm.com/index.php?rid=2985867&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19903440%26dopt%3DAbstract</link>
            <description>We report on a 63-year-old male who suffered from an ingrown toenail affecting the left first digit for several years. Medical history revealed that repeated vigorous nail plate trimming by the patient relieve the red, painful swelling of his great toe. Furthermore, Emmert onychoplasty as well as non-invasive procedures did not achieve improvement. A thorough surgical exploration of the affected area detected a nail spicule in the deeper paronychium. This was likely caused by improper cutting of the nail plate. Removal of the fragment in combination with partial nail plate excision, followed by phenol cauterization of the matrix resulted in full recovery.
    PMID: 19903440 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2985867</comments>
            <pubDate>Fri, 13 Nov 2009 12:06:04 +0100</pubDate>
            <guid isPermaLink="false">2985867</guid>        </item>
        <item>
            <title>Saphenous vein harvesting site dermatoses in eastern India.</title>
            <link>http://www.medworm.com/index.php?rid=2985866&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19903441%26dopt%3DAbstract</link>
            <description>We report the cutaneous effects at the saphenous vein harvesting sites in 21 patients who underwent CABG.
    PMID: 19903441 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2985866</comments>
            <pubDate>Fri, 13 Nov 2009 12:06:04 +0100</pubDate>
            <guid isPermaLink="false">2985866</guid>        </item>
        <item>
            <title>Drug-induced pruritic micropapular eruption: anastrozole, a commonly used aromatase inhibitor.</title>
            <link>http://www.medworm.com/index.php?rid=2985865&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19903442%26dopt%3DAbstract</link>
            <description>Authors: Bremec T, Demsar J, Luzar B, Pavlovi&amp;#x107; MD
    Anastrozole, a selective nonsteroidal aromatase inhibitor is widely used as an adjuvant therapy for postmenopausal women with early hormone-sensitive breast cancer. There are few reports on cutaneous side effects of anastrozole. It may induce subacute cutaneous lupus erythematosus, erythema nodosum, cutaneous vasculitis, and nondescript skin eruptions. A 68-year-old woman was prescribed anastrozole after surgical removal of her breast cancer and adjuvant radiation therapy. Two months later she experienced a generalized pruritic micropapular eruption. History, clinical presentation, histology and inadvertent re-exposure to the drug confirmed that anastrozole triggered the exanthem. Pruritic micropapular eruption is a typical patter...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2985865</comments>
            <pubDate>Fri, 13 Nov 2009 12:06:04 +0100</pubDate>
            <guid isPermaLink="false">2985865</guid>        </item>
        <item>
            <title>Adalimumab in the management of palmoplantar psoriasis.</title>
            <link>http://www.medworm.com/index.php?rid=2985864&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19903443%26dopt%3DAbstract</link>
            <description>Authors: Ghate JV, Alspaugh CD
    Palmoplantar pustular psoriasis (PPP) is an uncommon form of chronic psoriasis. Characterized by sterile, intraepidermal pustules located on the palms and soles, it is highly resistant to treatment. Our patient presented with palmar inflammation and throbbing joint pain in his hands, as well as erythematous, pustular, and micaceous scaling skin on his right foot, legs, elbows, and hands. Approximately 4 percent of his body surface area was involved and he was diagnosed with PPP after skin biopsy. After conventional therapy failed, the patient underwent treatment with adalimumab and the majority of his symptoms resolved after 16 weeks of therapy. Adalimumab may be effective for the treatment of PPP. Adalimumab, a fully human immunoglobulin G1 monoclonal an...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2985864</comments>
            <pubDate>Fri, 13 Nov 2009 12:06:04 +0100</pubDate>
            <guid isPermaLink="false">2985864</guid>        </item>
        <item>
            <title>Rowell syndrome (systemic lupus erythematosus + erythema multiforme).</title>
            <link>http://www.medworm.com/index.php?rid=2970681&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19891909%26dopt%3DAbstract</link>
            <description>Authors: Lee A, Batra P, Furer V, Cheung W, Wang N, Franks A
    A 61-year-old woman with a history of chilblains and systemic lupus erythematosus (SLE) for 15 years presented with annular, erythematous, scaly papules and plaques on her face, neck, chest, abdomen, back, arms, and legs. A biopsy specimen showed a destructive interface dermatitis with extensive epithelial cell necrosis, which was consistent with lupus erythematosus with combined subacute cutaneous lupus and erythema multiforme-like features. These findings are most compatible with a diagnosis of Rowell syndrome. Rowell syndrome and its relation to lupus erythematosus and erythema multiforme are discussed.
    PMID: 19891909 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2970681</comments>
            <pubDate>Sat, 07 Nov 2009 22:36:03 +0100</pubDate>
            <guid isPermaLink="false">2970681</guid>        </item>
        <item>
            <title>Eosinophilic fasciitis/generalized morphea overlap.</title>
            <link>http://www.medworm.com/index.php?rid=2970680&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19891910%26dopt%3DAbstract</link>
            <description>Authors: Heidary N, Cheung W, Wang N, Kamino H, Franks AG
    A 50-year-old woman presented with a three-month history of violaceous, non-tender, indurated plaques on the chest, abdomen, breasts, and proximal portions of the arms and legs. An incisional biopsy specimen showed changes consistent with a diagnosis of inflammatory morphea. Over the course of one year, the patient began to develop signs and symptoms suggestive of a diagnosis of eosinophilic fasciitis, which included the characteristic groove sign on the upper extremities. Although our patient did not exhibit peripheral or histopathologic evidence of eosinophilia, the diagnosis of eosinophilic fasciitis could still be made because the aforementioned phenomena are not required for diagnosis. Multitude treatment regimes have been ...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2970680</comments>
            <pubDate>Sat, 07 Nov 2009 22:36:03 +0100</pubDate>
            <guid isPermaLink="false">2970680</guid>        </item>
        <item>
            <title>Systemic drug-related intertriginous and flexural exanthema (SDRIFE).</title>
            <link>http://www.medworm.com/index.php?rid=2970679&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19891911%26dopt%3DAbstract</link>
            <description>Authors: Elmariah SB, Cheung W, Wang N, Kamino H, Pomeranz MK
    A 72-year-old man with a history of metastatic melanoma presented with a two-day history of erythematous and edematous plaques, with scattered bullae on the neck, chest, axillae, and inguinal and gluteal folds, which began five days after infusion of an experimental drug. The clinical and histopathologic findings were consistent with systemic drug-related intertriginous and flexural exanthema (SDRIFE), which is an uncommon drug reaction that results in symmetric erythema that affects the buttocks, groin, and/or thighs as well other flexural folds. The clinical manifestations of SDRIFE are highly characteristic and include distinctive primary cutaneous lesions with a specific distribution and course; however, heterogeneity ex...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2970679</comments>
            <pubDate>Sat, 07 Nov 2009 22:36:03 +0100</pubDate>
            <guid isPermaLink="false">2970679</guid>        </item>
        <item>
            <title>Linear psoriasis.</title>
            <link>http://www.medworm.com/index.php?rid=2970678&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19891912%26dopt%3DAbstract</link>
            <description>Authors: Chien P, Rosenman K, Cheung W, Wang N, Sanchez M
    A 33-year-old man presented with verrucous, red-brown papules, which coalesced into linear plaques on the right buttock, waist, thigh, and genitals. A skin biopsy was consistent with psoriasis, and the unilateral distribution in a linear pattern led to a diagnosis of linear psoriasis, which is a rare variant of psoriasis. Although histopathologically it can be difficult to distinguish from inflammatory linear verrucous epidermal nevus (ILVEN), linear psoriasis presents in adulthood and responds to conventional topical antipsoriatic therapies.
    PMID: 19891912 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2970678</comments>
            <pubDate>Sat, 07 Nov 2009 22:36:03 +0100</pubDate>
            <guid isPermaLink="false">2970678</guid>        </item>
        <item>
            <title>Fixed cutaneous sporotrichosis.</title>
            <link>http://www.medworm.com/index.php?rid=2970677&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19891913%26dopt%3DAbstract</link>
            <description>We present a patient with fixed cutaneous sporotrichosis whose delayed diagnosis led to appreciable scars and morbidity.
    PMID: 19891913 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2970677</comments>
            <pubDate>Sat, 07 Nov 2009 22:36:03 +0100</pubDate>
            <guid isPermaLink="false">2970677</guid>        </item>
        <item>
            <title>Generalized eruptive keratoacanthomas of Grzybowski.</title>
            <link>http://www.medworm.com/index.php?rid=2970676&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19891914%26dopt%3DAbstract</link>
            <description>Authors: Lu PD, Lee A, Cassetty CT, Cheung W, Wang N, Halpern AC, Cohen DE
    A 48-year-old man presented with a two-year history of a generalized, pruritic eruption that was associated with numerous, dome-shaped papules and nodulocystic lesions. Biopsy specimens have shown keratoacanthomas and a lichenoid dermatitis. Evaluation for malignant conditions has been negative. Owing to the constellation of findings, a diagnosis of generalized eruptive keratoacanthomas of Grzybowski associated with lichenoid dermatitis and acneiform lesions is favored. The patient is currently on a trial of acitretin.
    PMID: 19891914 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2970676</comments>
            <pubDate>Sat, 07 Nov 2009 22:36:03 +0100</pubDate>
            <guid isPermaLink="false">2970676</guid>        </item>
        <item>
            <title>Lymphedema praecox.</title>
            <link>http://www.medworm.com/index.php?rid=2970675&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19891915%26dopt%3DAbstract</link>
            <description>Authors: Rizzo C, Gruson LM, Wainwright BD
    A 57-year-old man presented with the post-pubertal onset of asymptomatic swelling of the left arm and legs that had been complicated by recurrent bouts of cellulitis. The presentation and disease course are consistent with lymphedema praecox, which is a subtype of primary lymphedema with onset at puberty and a slowly progressive course. The subtypes of lymphedema, pathogenesis, and treatment are reviewed.
    PMID: 19891915 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2970675</comments>
            <pubDate>Sat, 07 Nov 2009 22:36:03 +0100</pubDate>
            <guid isPermaLink="false">2970675</guid>        </item>
        <item>
            <title>Porokeratosis palmaris et plantaris disseminata or a disseminated late-onset variant of porokeratotic eccrine ostial and dermal ductal nevus (PEODDN) with follicular involvement.</title>
            <link>http://www.medworm.com/index.php?rid=2970674&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19891916%26dopt%3DAbstract</link>
            <description>Authors: Hartman R, Rizzo C, Patel R, Kamino H, Shupack JL
    A 48-year-old woman presented with a four-year history of pruritic, hyperkeratotic, spiny papules that began on her chest and spread to her extremities, groin, palms, face, and scalp where it caused non-scarring alopecia. Histopathologic features included cornoid lamella, which is the hallmark of porokeratosis. However, the patient's constellation of findings does not meet diagnostic criteria for any of the five clinical variants of porokeratosis. Her presentation is most compatible with either porokeratosis palmaris et plantaris disseminata (PPPD), which is a rare variant of punctate porokeratosis that can involve any area of the body or late-onset porokeratotic eccrine ostial and dermal ductal nevus (PEODDN), which is a rare,...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2970674</comments>
            <pubDate>Sat, 07 Nov 2009 22:36:03 +0100</pubDate>
            <guid isPermaLink="false">2970674</guid>        </item>
        <item>
            <title>POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes).</title>
            <link>http://www.medworm.com/index.php?rid=2970673&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19891917%26dopt%3DAbstract</link>
            <description>Authors: Liang C, Gonzalez M, Patel R, Meehan S, Kamino H, Franks AG
    A 62-year-old woman with hypothyroidism presented with a seven-year history of paresthesias, itching, and edema of the skin. Physical examination showed indurated, edematous plaques on the lower extremities. A biopsy specimen showed increased mucin deposition that was consistent with myxedema, and monoclonal IgM was observed on immunofixation. The constellation of findings, which included paresthesias, endocrinopathy, monoclonal gammopathy, and skin changes was consistent with POEMS (polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes) syndrome, which is a rare multisystemic disease that is associated with an underlying plasma-cell dyscrasia.
    PMID: 19891917 [PubMed - in process] (...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2970673</comments>
            <pubDate>Sat, 07 Nov 2009 22:36:03 +0100</pubDate>
            <guid isPermaLink="false">2970673</guid>        </item>
        <item>
            <title>Cutaneous piloleiomyomata.</title>
            <link>http://www.medworm.com/index.php?rid=2970672&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19891918%26dopt%3DAbstract</link>
            <description>Authors: Smith G, Heidary N, Patel R, Rosenman K, Meehan SA, Kamino H, Sanchez M
    A 49-year-old man presented with an eight-month history of intermittently painful, subcutaneous nodules that were increasing in size, number, and pain intensity. A biopsy specimen showed smooth muscle proliferation, which also stained positive for actin, and was consistent with piloleiomyoma. The patient was placed initially on gabapentin and then nifedipine with very limited success in pain control. The lesions continued to proliferate, and the patient was referred to surgery for excision.
    PMID: 19891918 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2970672</comments>
            <pubDate>Sat, 07 Nov 2009 22:36:03 +0100</pubDate>
            <guid isPermaLink="false">2970672</guid>        </item>
        <item>
            <title>Keratitis-ichthyosis-deafness (KID) syndrome.</title>
            <link>http://www.medworm.com/index.php?rid=2970671&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19891919%26dopt%3DAbstract</link>
            <description>This report draws attention to inflammatory nodules (representing ruptured folliculitis), cysts, and recurrent infections on the scalp as manifestations of KID syndrome and reviews the increasingly recognized risk of follicular tumors and squamous-cell carcinomas in patients with this conditions.
    PMID: 19891919 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2970671</comments>
            <pubDate>Sat, 07 Nov 2009 22:36:03 +0100</pubDate>
            <guid isPermaLink="false">2970671</guid>        </item>
        <item>
            <title>Acquired smooth-muscle hamartoma.</title>
            <link>http://www.medworm.com/index.php?rid=2970670&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19891920%26dopt%3DAbstract</link>
            <description>Authors: Yancovitz M, Gonzalez ME, Votava HJ, Walters R, Kundu R, Shupack JL
    A 52-year-old woman presented with an occasionally pruritic, hyperpigmented and hypertrichotic, indurated plaque on the left upper arm that initially developed during childhood. Histopathologic examination showed changes that were consistent with a smooth-muscle hamartoma. Cutaneous smooth-muscle hamartomas are uncommon benign neoplasms. Most lesions are congenital, but there have been a few reports of acquired lesions. These lesions have been described as part of a spectrum of neoplasms that include Becker nevi since they share many clinical and histopathologic features.
    PMID: 19891920 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2970670</comments>
            <pubDate>Sat, 07 Nov 2009 22:36:03 +0100</pubDate>
            <guid isPermaLink="false">2970670</guid>        </item>
        <item>
            <title>Lichenoid drug eruption.</title>
            <link>http://www.medworm.com/index.php?rid=2970669&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19891921%26dopt%3DAbstract</link>
            <description>Authors: Brauer J, Votava HJ, Meehan S, Soter NA
    A 78-year-old man presented with an eight-month history of folliculocentric, pink, hyperkeratotic papules and plaques with thick white scale that involved the entire body, with confluence on the buttocks and genitalia. A biopsy specimen demonstrated superficial and focal, mild perivascular and perifollicular, band-like lymphocytic infiltrate and eosinophils. There were lymphocytes extending to the dermo-epidermal junction with vacuolar changes. A diagnosis of lichenoid drug eruption secondary to a proton-pump inhibitor was made. To the best of our knowledge, only one other case of lichenoid drug eruption secondary to a proton-pump inhibitor has been reported.
    PMID: 19891921 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2970669</comments>
            <pubDate>Sat, 07 Nov 2009 22:36:03 +0100</pubDate>
            <guid isPermaLink="false">2970669</guid>        </item>
        <item>
            <title>Pityriasis rotunda.</title>
            <link>http://www.medworm.com/index.php?rid=2970668&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19891922%26dopt%3DAbstract</link>
            <description>Authors: Batra P, Cheung W, Meehan SA, Pomeranz M
    A 42-year-old man presented with asymptomatic, sharply-demarcated, round, scaly lesions on his forearms that had been present for several months. A skin biopsy specimen was consistent with pityriasis rotunda. Pityriasis rotunda is a disorder of keratinization, which is thought to be a form of acquired ichthyosis, a delayed presentation of congenital ichthyosis, or a cutaneous manifestation of systemic disease. Patients with pityriasis rotunda may be classified into one of two groups, which are based on ethnicity, number of lesions, family history, and association with systemic diseases. Treatment is challenging, but the use of lactic acid lotion and oral vitamin A has shown some promise.
    PMID: 19891922 [PubMed - in process] (Source:...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2970668</comments>
            <pubDate>Sat, 07 Nov 2009 22:36:03 +0100</pubDate>
            <guid isPermaLink="false">2970668</guid>        </item>
        <item>
            <title>Familial benign chronic pemphigus (Hailey-Hailey disease).</title>
            <link>http://www.medworm.com/index.php?rid=2970667&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19891923%26dopt%3DAbstract</link>
            <description>Authors: Warycha M, Patel R, Meehan S, Merola JF
    A 57-year-old woman presented with a 27-year history of vesicles and crusted erosions of the intertriginous folds. Prior treatments had included topical glucocorticoids, mupirocin, and minocycline, all of which provided minimal relief. A skin biopsy specimen was consistent with Hailey-Hailey disease. Hailey-Hailey disease is the result of mutations in the ATP2C1 gene and is characterized by recurrent vesicles and erosions in intertriginous areas. Whereas topical and/or systemic antibiotic/antifungal agents in combination with topical glucocorticoids is the mainstay of treatment, case reports have documented dramatic improvement with oral retinoids, calcitriol, and tacrolimus.
    PMID: 19891923 [PubMed - in process] (Source: Dermatol Onl...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2970667</comments>
            <pubDate>Sat, 07 Nov 2009 22:36:03 +0100</pubDate>
            <guid isPermaLink="false">2970667</guid>        </item>
        <item>
            <title>Hyperimmunoglobulin E syndrome with a novel STAT3 mutation.</title>
            <link>http://www.medworm.com/index.php?rid=2970666&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19891924%26dopt%3DAbstract</link>
            <description>Authors: Anolik R, Elmariah S, Lehrhoff S, Votava HJ, Martiniuk FT, Levis W
    A 35-year-old man with severe eczematous dermatitis and recurrent staphylococcal skin infections, some of which required hospitalization, is presented. Other medical concerns include recurrent oral staphylococcal infections, otitis media, ocular herpes simplex virus keratitis, asthma, steroid-induced gastritis, steroid-induced cataracts, recurrent upper respiratory infections, and acute pharyngitis. Past medical history includes retained dentition of six primary teeth, two episodes of childhood pneumonia that required hospitalization, and three wrist and ankle fractures. Laboratory data showed an eosinophil count of 2,400 cells/ml; the highest IgE level was 17,028 IU/mL. Considering the clinical and laboratory ...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2970666</comments>
            <pubDate>Sat, 07 Nov 2009 22:36:03 +0100</pubDate>
            <guid isPermaLink="false">2970666</guid>        </item>
        <item>
            <title>Pseudoxanthoma elasticum.</title>
            <link>http://www.medworm.com/index.php?rid=2970665&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19891925%26dopt%3DAbstract</link>
            <description>We present two siblings with pseudoxanthoma elasticum, who have considerable differences in disease related morbidity, which highlights intra-familiar phenotypic heterogeneity.
    PMID: 19891925 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2970665</comments>
            <pubDate>Sat, 07 Nov 2009 22:36:03 +0100</pubDate>
            <guid isPermaLink="false">2970665</guid>        </item>
        <item>
            <title>Generalized discoid lupus erythematosus.</title>
            <link>http://www.medworm.com/index.php?rid=2970664&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19891926%26dopt%3DAbstract</link>
            <description>Authors: Farley-Loftus R, Mahlberg M, Merola JF, Votava HJ, Meehan S, Stein J, Shupack JL
    A 79-year-old woman presented with a four-year history of generalized, erythematous, indurated plaques on the malar areas, back, and extremities. The lesions had been recalcitrant in the past to topical glucocorticoid therapy. A skin biopsy specimen was diagnostic of discoid lupus erythematosus (DLE). A minority of patients with DLE progress to develop systemic lupus erythematosus although generalized DLE is more frequently associated with systemic involvement than is limited disease. Standard therapy of cutaneous lupus includes broad spectrum sunscreens, topical and intralesional glucocorticoids, and antimalarial agents.
    PMID: 19891926 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2970664</comments>
            <pubDate>Sat, 07 Nov 2009 22:36:03 +0100</pubDate>
            <guid isPermaLink="false">2970664</guid>        </item>
        <item>
            <title>Mixed immunobullous disorder most consistent with the IgA-form of epidermolysis bullosa acquisita.</title>
            <link>http://www.medworm.com/index.php?rid=2970663&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19891927%26dopt%3DAbstract</link>
            <description>We describe a case of non-scarring, generalized, cutaneous and mucosal subepidermal bullous dermatosis that is characterized histopathologically by a neutrophilic infiltrate and strong linear staining with both IgA and IgG along the basement-membrane zone. Autoantibodies to collagen VII of both the IgA and IgG4 subtypes were detected by indirect immunofluorescence test, which led led to a diagnosis of epidermolysis bullosa aquisita (EBA). EBA is a subepidermal bullous disorder that is mediated by autoantibodies, which are directed against type VII collagen. The distinct clinical presentations of EBA are reviewed and discussed in the context of the unique autoantibody profile of this case.
    PMID: 19891927 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2970663</comments>
            <pubDate>Sat, 07 Nov 2009 22:36:03 +0100</pubDate>
            <guid isPermaLink="false">2970663</guid>        </item>
        <item>
            <title>Multiple eruptive milia.</title>
            <link>http://www.medworm.com/index.php?rid=2970662&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19891928%26dopt%3DAbstract</link>
            <description>Authors: Batra P, Tsou HC, Warycha M, Votava HJ, Stein J
    A 61-year-old-man presented with a sudden onset of multiple, hyperpigmented papules with a central punctum on the face, chest, upper back, and arms. Histopathologic examination showed infundibular cysts. These findings are consistent with a diagnosis of multiple eruptive milia, which is a rare disorder that is characterized by the sudden development of crops of milia over weeks to months. They are more extensive in number and distribution than they are in primary milia. Milia may present spontaneously without a known cause, as part of an inherited familial condition, or as part of a genodermatosis. The etiologies are uncertain, and treatment options are varied.
    PMID: 19891928 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2970662</comments>
            <pubDate>Sat, 07 Nov 2009 22:36:03 +0100</pubDate>
            <guid isPermaLink="false">2970662</guid>        </item>
        <item>
            <title>Neurovascular hamartoma.</title>
            <link>http://www.medworm.com/index.php?rid=2970661&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19891929%26dopt%3DAbstract</link>
            <description>Authors: Lee A, Heidary N, Altiner A, Votava H, Kamino H, Sanchez M
    A 29-year-old man presented with a large, asymptomatic, brown, hyperpigmented, depressed plaque over his left upper back, which included the scapular area, since childhood. Histopathological analyses of the biopsy specimens was consistent with a rare entity known as neurovascular hamartoma. This uncommon lesion has been reported in two publications, either as a possible marker of the malignant rhabdoid tumor or as a hamartomatous tongue lesion in children. Due to its possible association with the aggressive and often fatal rhabdoid tumor, periodic examination of this lesion may be warranted.
    PMID: 19891929 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2970661</comments>
            <pubDate>Sat, 07 Nov 2009 22:36:03 +0100</pubDate>
            <guid isPermaLink="false">2970661</guid>        </item>
        <item>
            <title>Interstitial granulomatous dermatitis with arthritis.</title>
            <link>http://www.medworm.com/index.php?rid=2970660&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19891930%26dopt%3DAbstract</link>
            <description>Authors: Jabbari A, Cheung W, Kamino H, Soter NA
    A 54-year-old woman with a history of arthritis presented for a long-standing history of symmetric, indurated plaques on her thighs and lateral aspects of the trunk. Histopathologic examination of skin biopsy specimens was consistent with interstitial granulomatous dermatitis, and a diagnosis of interstitial granulomatous dermatitis with arthritis was made. Administration of topical potent glucocorticoids, intralesional glucocorticoids, and narrow-band ultraviolet B phototherapy, in addition to continuation of systemic glucocorticoids and methotrexate, resulted in improvement of her cutaneous and musculoskeletal disease.
    PMID: 19891930 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2970660</comments>
            <pubDate>Sat, 07 Nov 2009 22:36:03 +0100</pubDate>
            <guid isPermaLink="false">2970660</guid>        </item>
        <item>
            <title>Genital porokeratosis.</title>
            <link>http://www.medworm.com/index.php?rid=2970659&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19891931%26dopt%3DAbstract</link>
            <description>Authors: Liang C, Batra P, Patel R, Kamino H
    A 22-year-old man presented with a two-year history of warts on the penis, scrotum, and thighs. Physical examination showed multiple annular plaques with thin, threadlike borders on the penis and scrotum. The biopsy specimen showed a cornoid lamella with underlying dyskeratotic cells that was consistent with porokeratosis. Genital porokeratosis is a rare condition that may be misdiagnosed as a sexually transmitted disease.
    PMID: 19891931 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2970659</comments>
            <pubDate>Sat, 07 Nov 2009 22:36:03 +0100</pubDate>
            <guid isPermaLink="false">2970659</guid>        </item>
        <item>
            <title>Graduates-of-foreign-dermatology residencies and military dermatology residencies and women in academic dermatology.</title>
            <link>http://www.medworm.com/index.php?rid=2856431&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19624980%26dopt%3DAbstract</link>
            <description>CONCLUSION: GFDRs, GMDRs, and women comprise important proportions of full-time faculty members at U.S. dermatology residency programs.
    PMID: 19624980 [PubMed - indexed for MEDLINE] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2856431</comments>
            <pubDate>Sat, 03 Oct 2009 15:52:03 +0100</pubDate>
            <guid isPermaLink="false">2856431</guid>        </item>
        <item>
            <title>[Stevens-Johnson syndrome plus intrahepatic cholestasis caused by clindamycin or chlorpheniramine]</title>
            <link>http://www.medworm.com/index.php?rid=2856430&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19624990%26dopt%3DAbstract</link>
            <description>We present a discussion of this case and review the main characteristics of the Stevens Johnson Syndrome.
    PMID: 19624990 [PubMed - indexed for MEDLINE] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2856430</comments>
            <pubDate>Sat, 03 Oct 2009 15:52:03 +0100</pubDate>
            <guid isPermaLink="false">2856430</guid>        </item>
        <item>
            <title>Melanoma screening with serial whole body photographic change detection using Melanoscan technology.</title>
            <link>http://www.medworm.com/index.php?rid=2762673&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19723475%26dopt%3DAbstract</link>
            <description>Authors: Drugge RJ, Nguyen C, Drugge ED, Gliga L, Broderick PA, McClain SA, Brown CC
    The use of an automated, whole-body, diffusely lit digital imaging enclosure to produce serial images, which were then compared, using an astrophysics image display method, enabled a private practice dermatologist to detect melanoma at significantly thinner Breslow depths compared to all other clinical detection paradigms examined in this study. The patients were triaged to scanning using a melanoma risk survey system. The system employed a 24 camera semicircular imaging wall, with front and back views. 10,000 whole body photographic scans were obtained. Privacy was maintained with 128-bit image encryption and off-line storage. Image to image comparison of whole body digital photography was combined wi...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2762673</comments>
            <pubDate>Fri, 04 Sep 2009 06:02:04 +0100</pubDate>
            <guid isPermaLink="false">2762673</guid>        </item>
        <item>
            <title>Pearls for perfecting the mastoid interpolation flap.</title>
            <link>http://www.medworm.com/index.php?rid=2762672&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19723476%26dopt%3DAbstract</link>
            <description>We present our suggestions for performing these reconstructions. Ways to optimize results, potential pitfalls, and postoperative care instructions are discussed. Step by step videos are included with this manuscript.
    PMID: 19723476 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2762672</comments>
            <pubDate>Fri, 04 Sep 2009 06:02:04 +0100</pubDate>
            <guid isPermaLink="false">2762672</guid>        </item>
        <item>
            <title>Juvenile dermatomyositis in an 8-year-old boy.</title>
            <link>http://www.medworm.com/index.php?rid=2762671&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19723477%26dopt%3DAbstract</link>
            <description>In this report we describe an 8-year-old boy who, besides myopathy, presented with an uncommonly broad spectrum of skin findings that had evolved after summer holidays at the Mediterranean Sea. Upon treatment with intravenous methylprednisolone the patient's condition considerably improved. Our case report illustrates that JDM requires comprehensive evaluation and multidisciplinary management.
    PMID: 19723477 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2762671</comments>
            <pubDate>Fri, 04 Sep 2009 06:02:04 +0100</pubDate>
            <guid isPermaLink="false">2762671</guid>        </item>
        <item>
            <title>Anti-phospholipid syndrome preceding a diagnosis of lepromatous leprosy.</title>
            <link>http://www.medworm.com/index.php?rid=2762670&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19723478%26dopt%3DAbstract</link>
            <description>We present this as a case of APS, preceding a diagnosis of lepromatous leprosy.
    PMID: 19723478 [PubMed - in process] (Source: Dermatol Online J)</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2762670</comments>
            <pubDate>Fri, 04 Sep 2009 06:02:04 +0100</pubDate>
            <guid isPermaLink="false">2762670</guid>        </item>
        <item>
            <title>Two cases of primary endonasal leishmaniasis in Sardinia (Italy).</title>
            <link>http://www.medworm.com/index.php?rid=2762669&amp;cid=s_31723_12_f&amp;fid=31723&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19723479%26dopt%3DAbstract</link>
            <description>We report two cases of endonasal primary Leishmaniasis, which is a very rare event in adult men who are immunocompetent, born in, and residents of Sardinia. The diagnosis was confirmed by the presence of intra and extracellular Leishmania amastigotes in the histological smear. Isoenzymatic characterization identified Leishmania infantum zymodeme MON-111 in both cases. Laboratory and instrumental investigations excluded visceral involvement. Treatment with meglumine antimoniate (Glucantim) intralesional administration, 1 ml weekly for 4-5 weeks, led to complete resolution. The unusual location is likely a reflection an uncommon site of inoculation of the protozoa, transmitted by flying vectors. The patients were a shepherd and a farmer, respectively, both professions at high risk of infecti...</description>
            <author>Dermatol Online J</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2762669</comments>
            <pubDate>Fri, 04 Sep 2009 06:02:04 +0100</pubDate>
            <guid isPermaLink="false">2762669</guid>        </item>
    </channel>
</rss>
