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        <title>Australasian Journal of Dermatology 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 'Australasian Journal of Dermatology' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Australasian+Journal+of+Dermatology&t=Australasian+Journal+of+Dermatology&s=Search&f=source]]></link>
        <lastBuildDate>Wed, 08 Feb 2012 13:12:27 +0100</lastBuildDate>
        <item>
            <title>Tinea nigra and dermoscopy: Response</title>
            <link>http://www.medworm.com/index.php?rid=5667272&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2012.00872.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5667272</comments>
            <pubDate>Wed, 01 Feb 2012 05:00:00 +0100</pubDate>
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        <item>
            <title>Tinea nigra and dermoscopy</title>
            <link>http://www.medworm.com/index.php?rid=5667271&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00858.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5667271</comments>
            <pubDate>Wed, 01 Feb 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5667271</guid>        </item>
        <item>
            <title>In other journals</title>
            <link>http://www.medworm.com/index.php?rid=5667270&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00859.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5667270</comments>
            <pubDate>Wed, 01 Feb 2012 05:00:00 +0100</pubDate>
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        <item>
            <title>Successful treatment of a severe persistent case of pemphigoid gestationis with antepartum and postpartum intravenous immunoglobulin followed by azathioprine</title>
            <link>http://www.medworm.com/index.php?rid=5667269&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00854.x</link>
            <description>We report a case of pemphigoid gestationis affecting a 37‐year‐old woman in both her pregnancies. In her second pregnancy she failed to respond to high‐dose oral prednisolone. She was treated successfully with intravenous immunoglobulin (2 g/kg each infusion cycle) as a steroid‐sparing agent during both the antepartum and postpartum period. The baby was born at the 36th week of gestation. No complications were noted for either mother or baby. After ceasing intravenous immunoglobulin, azathioprine (up to a dose of 1 mg/kg/day) was used to adequately control her pemphigoid gestationis. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5667269</comments>
            <pubDate>Wed, 01 Feb 2012 05:00:00 +0100</pubDate>
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        <item>
            <title>Sentinel lymph node biopsy in patients with Merkel cell carcinoma: An emerging role and the Westmead hospital experience</title>
            <link>http://www.medworm.com/index.php?rid=5667268&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00838.x</link>
            <description>Conclusion:  Half of our patients were upstaged and underwent nodal treatment as a result of their SLNB. Given the high rate of SLNB positivity, we believe that SLNB has a role in the management of MCC. As there is a risk of a false negative SLNB, close observation of the regional nodal basins is warranted in patients who have had a negative SLNB. Further studies are required to investigate the impact of SLNB on survival. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5667268</comments>
            <pubDate>Wed, 01 Feb 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5667268</guid>        </item>
        <item>
            <title>Accuracy in skin cancer diagnosis: A retrospective study of an Australian public hospital dermatology department</title>
            <link>http://www.medworm.com/index.php?rid=5608937&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00855.x</link>
            <description>Conclusions:  These audits are important to ensure quality of care and could aid in identifying doctors and institutions that may benefit from further training in melanoma diagnostic algorithms. These figures can be used as a benchmark to measure the impact of new vectors in skin cancer diagnosis as they are introduced. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5608937</comments>
            <pubDate>Thu, 19 Jan 2012 05:00:00 +0100</pubDate>
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        <item>
            <title>Porokeratosis in Singapore: An Asian perspective</title>
            <link>http://www.medworm.com/index.php?rid=5608936&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00856.x</link>
            <description>ABSTRACTPorokeratosis is a rare disorder of skin keratinisation characterised by a cornoid lamella. We reviewed its associations with immunosuppression and phototherapy, as well as the risks of malignant progression. This is a retrospective review on all cases of porokeratosis seen at the National Skin Centre, Singapore, between 2000 and 2010. A total of 94 patients were reviewed. Clinical and histological diagnoses were confirmed in 63% patients. Most patients were Chinese (89%) with a mean age of 51.6 years. The male to female ratio was 1.4:1. The four main clinical variants were classical porokeratosis of Mibelli (56%), disseminated superficial actinic porokeratosis (DSAP) (18%), disseminated superficial porokeratosis (DSP) (11%), and linear porokeratosis (13%). Phototherapy‐induced...</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5608936</comments>
            <pubDate>Thu, 19 Jan 2012 05:00:00 +0100</pubDate>
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        <item>
            <title>Neuropathy in a patient with lymphocytic thrombophilic arteritis</title>
            <link>http://www.medworm.com/index.php?rid=5572236&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00827.x</link>
            <description>ABSTRACTA 35‐year‐old Lebanese woman presented with a 3‐year history of persistent, localized livedo racemosa over her feet, distal legs and forearms that was associated with the development of lower limb sensorimotor neuropathy. Investigations revealed the patient was heterozygous for prothrombin gene mutation and was also found to have a T‐cell receptor gamma chain gene rearrangement. Histological examination revealed a mid‐lower dermal medium vessel lymphocytic vasculitis with prominent fibrinoid ring within its wall. These findings are consistent with a recently described condition known as lymphocytic thrombophilic arteritis. This has so far been considered to be a benign clinical condition not associated with extra cutaneous manifestations. The novel findings in the present...</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5572236</comments>
            <pubDate>Fri, 06 Jan 2012 05:00:00 +0100</pubDate>
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        <item>
            <title>Pilot study on the acceptance of mobile teledermatology for the home monitoring of high‐need patients with psoriasis</title>
            <link>http://www.medworm.com/index.php?rid=5572235&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00852.x</link>
            <description>Conclusion:  Mobile teledermatology is a valuable tool for the home monitoring of patients with psoriasis that makes a meaningful difference in their lives. It is well accepted by both patients and the physicians involved. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5572235</comments>
            <pubDate>Fri, 06 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5572235</guid>        </item>
        <item>
            <title>A single centre melanoma thickness trend (1985–2009) in relation to skin areas accessible and non‐accessible to self‐inspection</title>
            <link>http://www.medworm.com/index.php?rid=5552395&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00835.x</link>
            <description>Conclusion:  The importance of observation of the posterior parts of the body is stressed, since not only did most melanomas arise in these sites but the diagnosis of lesions in these sites is often delayed. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552395</comments>
            <pubDate>Thu, 29 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5552395</guid>        </item>
        <item>
            <title>Better, sooner, more convenient: A successful teledermoscopy service</title>
            <link>http://www.medworm.com/index.php?rid=5552394&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00836.x</link>
            <description>Conclusions:  A community‐based teledermoscopy service may allow improved management of outpatient referrals while providing a better, quicker and more convenient service. It may also provide cost savings, as teledermoscopy assessment can be cheaper than traditional assessment. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552394</comments>
            <pubDate>Thu, 29 Dec 2011 05:00:00 +0100</pubDate>
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        <item>
            <title>Topical 0.1% rapamycin for angiofibromas in paediatric patients with tuberous sclerosis: A pilot study of four patients</title>
            <link>http://www.medworm.com/index.php?rid=5552393&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00837.x</link>
            <description>We report a pilot study of topical rapamycin in four children with TSC and facial angiofibromas. Two patients were trialled on 0.1% rapamycin in petrolatum and the other two patients with 0.1% rapamycin solution (Rapamune) applied topically. Both preparations were rapidly and equally effective, however the 0.1% in petrolatum was much better tolerated. Younger patients with smaller angiofibromas had the best response with near complete clearance. Both preparations were more cost effective than pulsed dye laser under general anaesthesia. Although larger studies are needed, this treatment shows a potential to be a first‐line management for facial angiofibromas in TSC and appears safe to start in early childhood. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552393</comments>
            <pubDate>Thu, 29 Dec 2011 05:00:00 +0100</pubDate>
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        <item>
            <title>Sacroiliitis secondary to isotretinoin</title>
            <link>http://www.medworm.com/index.php?rid=5552392&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00841.x</link>
            <description>ABSTRACTReported is the case of a 17‐year old male with sacroiliitis confirmed by magnetic resonance imaging (MRI) while undergoing isotretinoin treatment for acne vulgaris. The cessation of isotretinoin and symptomatic treatment resolved the symptoms within 6 weeks, with no signs of sacroiliitis on repeat MRI 10 months later. The temporal association of disease onset and commencement of isotretinoin along with rapid recovery on withdrawal supports the role of isotretinoin in this case. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552392</comments>
            <pubDate>Thu, 29 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5552392</guid>        </item>
        <item>
            <title>The use of methotrexate in dermatology: a review</title>
            <link>http://www.medworm.com/index.php?rid=5552391&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00839.x</link>
            <description>ABSTRACTMethotrexate is a synthetic folic acid analogue valued for both its anti‐proliferative and anti‐inflammatory properties. Considered one of the original immune‐modifying agents, it is used widely for the treatment of steroid‐recalcitrant inflammatory diseases. While there are abundant studies documenting its efficacy in rheumatic diseases, the use of methotrexate for dermatological conditions, with the exception of psoriasis, has yet to be comprehensively explored. This two‐part review firstly outlines current data concerning the pharmacology of methotrexate, including its mechanism of action, side‐effect profile and recommended therapeutic approach, and, secondly, examines the emerging evidence for methotrexate's efficacy in a wide range of cutaneous disorders. (Source:...</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552391</comments>
            <pubDate>Thu, 29 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5552391</guid>        </item>
        <item>
            <title>Toxic epidermal necrolysis‐like subacute cutaneous lupus erythematosus</title>
            <link>http://www.medworm.com/index.php?rid=5552390&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00842.x</link>
            <description>This article draws attention to features that may be used to differentiate classical TEN from TEN‐like SCLE. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552390</comments>
            <pubDate>Thu, 29 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5552390</guid>        </item>
        <item>
            <title>Acute generalised exanthematous pustulosis</title>
            <link>http://www.medworm.com/index.php?rid=5552389&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00845.x</link>
            <description>ABSTRACTAcute generalised exanthematous pustulosis (AGEP) is a severe cutaneous adverse reaction and is caused by drugs in &amp;gt;90% of cases. It is rare, with an incidence of 1–5 patients per million per year. The clinical manifestations are characterised by fever and the rapid appearance of disseminated sterile pustules 3–5 days after the commencement of treatment. It is accompanied by marked neutrophilia. Mucous membranes are not typically involved. The drugs conferring the highest risk of AGEP according to the EuroSCAR study are aminopenicillins, pristinamycin, hydroxychloroquine, antibacterial sulphonamides, terbinafine and diltiazem. The pathogenesis of AGEP involves the initial influx of CD8 cytotoxic T‐cells resulting in the apoptosis of keratinocytes and formation of vesicle...</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552389</comments>
            <pubDate>Thu, 29 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5552389</guid>        </item>
        <item>
            <title>Ectodermal dysplasia‐skin fragility syndrome due to a new homozygous internal deletion mutation in the PKP1 gene</title>
            <link>http://www.medworm.com/index.php?rid=5552388&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00846.x</link>
            <description>We report a further case of this desmosomal genodermatosis. A 14‐month old child, born to consanguineous parents, presented with a history of neonatal bullae and subsequent development of dystrophic nails, sparse eyelashes and eyebrows, woolly scalp hair, abnormal dental development and a desquamating erythematous rash at sites of trauma. A clinical diagnosis of ED‐SFS was supported by skin biopsy findings of suprabasal intraepidermal clefting and a loss of immunoreactivity for PKP1. Sequencing of genomic DNA revealed a homozygous 5 base pair deletion in exon 5 of the PKP1 gene, designated c.897del5 (CAACC). This new mutation creates a frameshift, leading to a downstream premature termination codon, p.Pro299fsX61. This case highlights the clinicopathological consequences of inherited m...</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552388</comments>
            <pubDate>Thu, 29 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5552388</guid>        </item>
        <item>
            <title>Eccrine angiomatous hamartoma causing walking difficulties</title>
            <link>http://www.medworm.com/index.php?rid=5552387&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00847.x</link>
            <description>ABSTRACTEccrine angiomatous hamartoma (EAH) is a rare tumoral lesion that consists of vascular and eccrine malformation and often occurs in the distal extremities of children. Although EAH is benign, a therapeutic excision may be required for symptomatic or cosmetic considerations. We hereby report a typical case of EAH presenting as a painful and rapidly growing plaque on the right thigh. The associated symptoms of pain, hyperhidrosis and local hypertrichosis caused walking difficulties until the patient was cured by two excisional surgeries. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552387</comments>
            <pubDate>Thu, 29 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5552387</guid>        </item>
        <item>
            <title>Blastic plasmacytoid dendritic cell neoplasm</title>
            <link>http://www.medworm.com/index.php?rid=5552386&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00848.x</link>
            <description>We report a case of a 79‐year old man who had 6 months of progressive, asymptomatic BPDCN manifestations limited to the skin, before developing a leukaemic phase. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552386</comments>
            <pubDate>Thu, 29 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5552386</guid>        </item>
        <item>
            <title>Determinants of the direction of hair follicle growth after reconstruction with dissociated cells</title>
            <link>http://www.medworm.com/index.php?rid=5552385&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00849.x</link>
            <description>Conclusions:  These results indicate that developmental space provides the possibility for growth of reconstructed hair follicles and that the air–liquid interface determines the final direction of growth. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552385</comments>
            <pubDate>Thu, 29 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5552385</guid>        </item>
        <item>
            <title>Acroangiodermatitis in a lower leg amputee related to suction socket use</title>
            <link>http://www.medworm.com/index.php?rid=5408167&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00826.x</link>
            <description>We present a case of acroangiodermatitis in the stump of an amputee related to suction socket use in order to raise awareness of an unusual setting for this vascular proliferation. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5408167</comments>
            <pubDate>Tue, 15 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5408167</guid>        </item>
        <item>
            <title>Cutaneous metastasis from lung cancer: Retrospective analysis of 30 patients</title>
            <link>http://www.medworm.com/index.php?rid=5408165&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00828.x</link>
            <description>ABSTRACTLung carcinoma is one of the most frequent sources of skin metastases in male patients. Our objective was to analyse the clinical and pathological features of 30 patients with skin metastases from lung carcinoma. Cutaneous biopsies codified as ‘skin metastasis from lung carcinoma’ during 1988–2009 at Bellvitge Hospital (Barcelona, Spain) were reviewed. The histological types of 30 lung carcinomas (29 men, 1 woman) were squamous cell carcinoma (10 cases), undifferentiated carcinoma (7), adenocarcinoma (6), small cell carcinoma (5) and large cell carcinoma (2). The most frequent clinical presentation was as a solitary nodule (16 cases), and the most frequent site was the head (13 cases). Cutaneous metastases were present at the time of diagnosis of the lung primary tumour in 66...</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5408165</comments>
            <pubDate>Tue, 15 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5408165</guid>        </item>
        <item>
            <title>Recurrent endocrine mucin‐producing sweat gland carcinoma in the eyelid</title>
            <link>http://www.medworm.com/index.php?rid=5608935&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00857.x</link>
            <description>This article reviews the current literature and discusses the surgical management of EMPSGC. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5608935</comments>
            <pubDate>Tue, 01 Nov 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5608935</guid>        </item>
        <item>
            <title>The rapid onset of multiple squamous cell carcinomas in two patients commenced on ustekinumab as treatment of psoriasis</title>
            <link>http://www.medworm.com/index.php?rid=5572234&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00853.x</link>
            <description>We report the cases of two patients who developed eruptive cutaneous squamous cell carcinomas (SCC) soon after commencement of ustekinumab, as treatment of moderate to severe plaque type psoriasis. Ustekinumab is a human monoclonal antibody with a novel mechanism, selectively targeting the shared p40 subunit of interleukin‐12 (IL‐12) and IL‐23. Its efficacy has been well documented in three large phase‐III trials (PHOENIX I, PHEONIX 2, ACCEPT). Safety data on this new biological agent continue to grow. To date, no link between ustekinumab and cutaneous carcinogenesis has been demonstrated and, to our knowledge, these cases are the first of their kind. Importantly, both these patients had independent risk factors for developing non‐melanoma skin cancers; however, the specific time...</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5572234</comments>
            <pubDate>Tue, 01 Nov 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5572234</guid>        </item>
        <item>
            <title>Dermoscopic corkscrew hairs dissolve after successful therapy of Trichophyton violaceum tinea capitis: A case report</title>
            <link>http://www.medworm.com/index.php?rid=5552384&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00850.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552384</comments>
            <pubDate>Tue, 01 Nov 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5552384</guid>        </item>
        <item>
            <title>Effect of early and late mobilisation on split skin graft outcome</title>
            <link>http://www.medworm.com/index.php?rid=5408164&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00829.x</link>
            <description>Conclusion:  These results suggest that early mobilisation post‐split skin grafting of the lower limb is beneficial to patient care and is associated with lower morbidity. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5408164</comments>
            <pubDate>Tue, 01 Nov 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5408164</guid>        </item>
        <item>
            <title>Tribute to Our Reviewers</title>
            <link>http://www.medworm.com/index.php?rid=5400836&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00843.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5400836</comments>
            <pubDate>Tue, 01 Nov 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5400836</guid>        </item>
        <item>
            <title>Abstracts</title>
            <link>http://www.medworm.com/index.php?rid=5400835&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00840.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5400835</comments>
            <pubDate>Tue, 01 Nov 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5400835</guid>        </item>
        <item>
            <title>William Kenneth Amedee Paver</title>
            <link>http://www.medworm.com/index.php?rid=5400834&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00824.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5400834</comments>
            <pubDate>Tue, 01 Nov 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5400834</guid>        </item>
        <item>
            <title>Walter Barry White</title>
            <link>http://www.medworm.com/index.php?rid=5400833&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00823.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5400833</comments>
            <pubDate>Tue, 01 Nov 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5400833</guid>        </item>
        <item>
            <title>Miles Tom Havyatt</title>
            <link>http://www.medworm.com/index.php?rid=5400832&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00821.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5400832</comments>
            <pubDate>Tue, 01 Nov 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5400832</guid>        </item>
        <item>
            <title>In other journals</title>
            <link>http://www.medworm.com/index.php?rid=5400831&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00822.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5400831</comments>
            <pubDate>Tue, 01 Nov 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5400831</guid>        </item>
        <item>
            <title>Cryptococcosis presenting as upper limb cellulitis and ulceration: A case series</title>
            <link>http://www.medworm.com/index.php?rid=5400830&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00820.x</link>
            <description>We report four cases of cryptococcosis presenting as upper limb cellulitis or ulceration, or both. Three of the four patients were on long‐term prednisolone therapy at the time of presentation. In each case, the diagnosis of cryptococcosis was established by a biopsy of the skin. Only one of the four patients had conclusive evidence of disseminated disease. Our cases highlight the importance of skin biopsy in immunosuppressed individuals presenting with cellulitis, particularly when the cellulitis occurs in an atypical location and when the clinical condition fails to respond to standard antibacterial therapy. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5400830</comments>
            <pubDate>Tue, 01 Nov 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5400830</guid>        </item>
        <item>
            <title>Oral erosive lichen planus associated with thymoma treated with etretinate</title>
            <link>http://www.medworm.com/index.php?rid=5304505&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00818.x</link>
            <description>ABSTRACTA 68‐year‐old Japanese woman was referred to our hospital with a 1‐year history of multiple erosions on the oral mucosa and a few pruritic, bean‐sized, reddish‐blue plaques on the body. Based on physical examination, pathological findings, and immunofluorescence findings, a diagnosis of lichen planus (LP) was made. Computed tomography scan revealed a thymoma. After thymectomy, cutaneous LP lesions subsided spontaneously. Oral lesions responded well to oral etretinate therapy. We speculate that direct tissue injury by CD8+ T cells, activated by abnormal regulation of lymphocytes within the thymus, may cause LP. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5304505</comments>
            <pubDate>Tue, 11 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5304505</guid>        </item>
        <item>
            <title>Author Index 2011</title>
            <link>http://www.medworm.com/index.php?rid=5304507&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00811.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5304507</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5304507</guid>        </item>
        <item>
            <title>Biennial Spring Conference</title>
            <link>http://www.medworm.com/index.php?rid=5304506&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00810.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5304506</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5304506</guid>        </item>
        <item>
            <title>Reticulate eruptions: Part 2. Historical perspectives, morphology, terminology and classification</title>
            <link>http://www.medworm.com/index.php?rid=5304504&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00819.x</link>
            <description>ABSTRACTReticulate eruptions of vascular origin may represent an underlying arterial, venous, microvascular or combined pathology. In the presence of arterial pathology, individual rings are centred around ascending arterial vessels that supply the corresponding area of skin within an arterial hexagon that clinically presents with a blanched centre. Confluence of multiple arterial hexagons generates a stellate (star‐like) pattern. In the presence of a primary venous pathology, individual rings correspond to the underlying reticular veins forming multiple venous rings. Focal involvement of a limited number of vessels presents with a branched (racemosa) configuration while a generalized involvement forms a reticulate (net‐like) pattern. ‘Livedo’ refers to the colour and not the patte...</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5304504</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5304504</guid>        </item>
        <item>
            <title>Unusual presentation of herpes simplex virus infection in a boxer: ‘Boxing glove herpes’</title>
            <link>http://www.medworm.com/index.php?rid=5273983&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00815.x</link>
            <description>ABSTRACTHerein, we describe a patient with lesions of cutaneous herpes simplex virus 1 (HSV‐1) infection over the knuckles of both hands in the context of an outbreak among boxers. Interestingly, the infection had an unusually long duration (4 weeks), and was not acquired directly through skin‐to‐skin contact, as it usually does among athletes (herpes gladiatorum). In our case, transmission was acquired through the use of shared boxing gloves contaminated by HSV‐1. To the best of our knowledge, herpes gladiatorum, or wrestler's herpes, has not been described previously in boxers and infection over the knuckles is not commonly reported. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5273983</comments>
            <pubDate>Fri, 30 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5273983</guid>        </item>
        <item>
            <title>A case of erythema elevatum diutinum associated with peripheral ulcerative keratitis</title>
            <link>http://www.medworm.com/index.php?rid=5273982&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00816.x</link>
            <description>ABSTRACTA young woman with recurrent painful lesions on the dorsal aspects of her hands associated with arthralgia presented with pain and redness of both eyes. After extensive investigations, a diagnosis of erythema elevatum diutinum accompanied by peripheral ulcerative keratitis was made. The patient was treated with dapsone 50 mg, t.i.d., and responded well. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5273982</comments>
            <pubDate>Fri, 30 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5273982</guid>        </item>
        <item>
            <title>Febrile ulceronecrotic Mucha‐Habermann disease: A case with systemic symptoms managed with subcutaneous methotrexate</title>
            <link>http://www.medworm.com/index.php?rid=5237844&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00812.x</link>
            <description>We present a 10‐year‐old patient with FUMHD associated with arthritis and chronic fatigue, managed with methotrexate. Through our literature review, we also explore treatment protocols for a disease for which internationally standardized management is yet to be formulated. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5237844</comments>
            <pubDate>Tue, 20 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5237844</guid>        </item>
        <item>
            <title>A case of adrenal insufficiency secondary to syphilis and difficulties in the diagnostic work‐up</title>
            <link>http://www.medworm.com/index.php?rid=5184132&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00805.x</link>
            <description>We report a case of Addison's disease presumed to be secondary to syphilis. The patient presented with adrenal failure and a maculopapular rash on his trunk and palms. Syphilis was suspected but the non‐treponemal serological test used (the rapid plasma reagin test (RPR)) was falsely negative due to the prozone phenomenon. Treatment with benzathine penicillin resulted in normalization of adrenal function and resolution of the cutaneous findings. Repeat testing of the previously obtained serum sample showed the RPR to be positive on increasing dilutions of serum, consistent with the prozone effect. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5184132</comments>
            <pubDate>Thu, 01 Sep 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5184132</guid>        </item>
        <item>
            <title>Skin disease in the first two years of life in Aboriginal children in East Arnhem Land</title>
            <link>http://www.medworm.com/index.php?rid=5184131&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00806.x</link>
            <description>Conclusion:  Skin infections are a major reason for presentation to primary health clinics and contribute to the high disease burden experienced by children in the first 2 years of life. This high frequency of presentation provides multiple opportunities for intervention and monitoring. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5184131</comments>
            <pubDate>Thu, 01 Sep 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5184131</guid>        </item>
        <item>
            <title>Tele‐assessment of Psoriasis Area and Severity Index: A study of the accuracy of digital image capture</title>
            <link>http://www.medworm.com/index.php?rid=5143963&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00800.x</link>
            <description>Conclusion:  We demonstrate that PASI scores can be determined with moderate to good accuracy by dermatologists using standardized digital images. Our results imply the implementation of a tele‐PASI service may be a practical and effective adjunct to the dermatological care of patients with severe psoriasis where incapacity or distance prevent the realisation of face‐to‐face consultations. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5143963</comments>
            <pubDate>Tue, 16 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5143963</guid>        </item>
        <item>
            <title>Allergic contact dermatitis caused by a cell phone cover</title>
            <link>http://www.medworm.com/index.php?rid=5143962&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00801.x</link>
            <description>We describe a case of contact dermatitis to a phone cover, which was compounded by secondary allergic contact dermatitis to topical creams used. The phone cover was advertised as being composed of silicone only. Patch testing with the cover material confirmed the diagnosis. In addition, there were positive patch test reactions to a number of allergens in the plastics and glues series from Chemotechnique Diagnostics (Malmö, Sweden). The increasing use of phone covers and the multiple positive reactions to chemicals used in plastic manufacture seen in this case suggest that similar allergic reactions may occur more frequently in the future and should be considered in the differential diagnosis of facial dermatitis. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5143962</comments>
            <pubDate>Tue, 16 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5143962</guid>        </item>
        <item>
            <title>Psoriasis and type 2 diabetes risk among psoriatic patients in a Spanish population</title>
            <link>http://www.medworm.com/index.php?rid=5143961&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00802.x</link>
            <description>ABSTRACTThere is accumulating evidence showing a relationship between psoriasis and an increased risk of developing cardiovascular risk factors, including diabetes mellitus type 2 and ischemic heart disease. Our aim was to investigate if there is any difference in the diabetes risk profile among psoriatic patients based on clinical findings. To test this, we carried out a prospective and descriptive hospital‐based study. Our results suggest that the highest risk of suffering from diabetes mellitus type 2 among psoriatic patients is in patients suffering from non‐familial and late‐onset disease and in patients suffering from psoriatic arthritis. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5143961</comments>
            <pubDate>Tue, 16 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5143961</guid>        </item>
        <item>
            <title>Lipoid proteinosis presenting with an unusual nonsense Q32X mutation in exon 2 of the extracellular matrix protein 1 gene</title>
            <link>http://www.medworm.com/index.php?rid=5143960&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00803.x</link>
            <description>ABSTRACTLipoid proteinosis (LP) is a rare disorder characterized by extensive hyaline‐like deposits on the skin, mucous membranes and various internal organs with varying clinical manifestations. The disorder has been recently shown to result from loss‐of‐function mutations in the extracellular matrix protein 1 gene (ECM1) on 1Q21. The two cases reported here had typical clinical and histological features consistent with LP. Direct sequencing of amplified DNA from the second patient showed a single nucleotide substitution (C &amp;gt; T) at nucleotide 94 within exon 2 of the ECM1 gene, nonsense mutation Q32X. This is the second case reported of LP with involvement of exon 2 of ECM1. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5143960</comments>
            <pubDate>Tue, 16 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5143960</guid>        </item>
        <item>
            <title>Palmoplantar keratoderma: An adverse reaction to influenza vaccination</title>
            <link>http://www.medworm.com/index.php?rid=5273981&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00817.x</link>
            <description>ABSTRACTAcquired palmoplantar keratoderma (PPK) is a rare group of conditions with a number of aetiologies, including adverse reactions to drugs. Herein, we report a case of acquired PPK in association with influenza vaccination, confirmed by rechallenge. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5273981</comments>
            <pubDate>Mon, 01 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5273981</guid>        </item>
        <item>
            <title>Granuloma annulare‐like reaction to the bacillus Calmette‐Guerin vaccination</title>
            <link>http://www.medworm.com/index.php?rid=5237843&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00814.x</link>
            <description>We report the case of a 6‐month‐old girl with a granuloma annulare (GA)‐like reaction to the bacillus Calmette‐Guerin (BCG) vaccination. The eruption developed at the vaccination site 1 month after vaccination and the lesion gradually disseminated over the body within 2 months. A biopsy specimen of the skin lesion showed degenerated collagen bundles surrounded by imperfect palisading histiocytes, lymphocytes and epithelioid cells in the dermis, which led to a diagnosis of GA‐like reaction as a secondary reaction to BCG inoculation. The eruption at the vaccination site and the scattered GA reaction resolved after 1 month of treatment with prednisolone valerate acetate ointment, leaving only pigmentation. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5237843</comments>
            <pubDate>Mon, 01 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5237843</guid>        </item>
        <item>
            <title>Mohs' micrographic surgery as treatment for squamous dysplasia of the nail unit</title>
            <link>http://www.medworm.com/index.php?rid=5208936&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00813.x</link>
            <description>We report a series of 14 cases of nail unit squamous cell carcinoma in situ/ Bowen's disease and squamous cell carcinoma (SCC) treated with Mohs micrographic surgery (MMS). MMS has been previously reported as an ideal treatment for nail unit SCC. This series adds to the current literature substantiating this claim, and also demonstrates the good outcomes achieved with secondary intention healing. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5208936</comments>
            <pubDate>Mon, 01 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5208936</guid>        </item>
        <item>
            <title>A case of pityriasis rubra pilaris associated with membranous nephropathy</title>
            <link>http://www.medworm.com/index.php?rid=5184130&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00807.x</link>
            <description>We report a case of PRP with associated membranous nephropathy (MN), which resolved spontaneously with resolution of the dermatosis. This is only the second reported association between PRP and MN of which we are aware. Further reports of such an association will strengthen the evidence for the two conditions being linked and may thereby shed light on the pathogenesis of both PRP and MN. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5184130</comments>
            <pubDate>Sun, 31 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5184130</guid>        </item>
        <item>
            <title>Impact on the dermatology educational experience of medical students with the introduction of online teaching support modules to help address the reduction in clinical teaching</title>
            <link>http://www.medworm.com/index.php?rid=5143959&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00804.x</link>
            <description>Conclusions:  Our results suggest that the introduction of the online modules described in this paper to support learning have improved the perceived educational experience of medical students and should be incorporated as a way to improve student teaching in the face of reduced clinic teaching. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5143959</comments>
            <pubDate>Sun, 31 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5143959</guid>        </item>
        <item>
            <title>Bruce Mackie</title>
            <link>http://www.medworm.com/index.php?rid=5126427&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00795.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5126427</comments>
            <pubDate>Sun, 31 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5126427</guid>        </item>
        <item>
            <title>Letter to the editor</title>
            <link>http://www.medworm.com/index.php?rid=5126426&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00809.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5126426</comments>
            <pubDate>Sun, 31 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5126426</guid>        </item>
        <item>
            <title>In other journals</title>
            <link>http://www.medworm.com/index.php?rid=5126425&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00796.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5126425</comments>
            <pubDate>Sun, 31 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5126425</guid>        </item>
        <item>
            <title>New insights in naevogenesis: Number, distribution and dermoscopic patterns of naevi in the elderly</title>
            <link>http://www.medworm.com/index.php?rid=5079572&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00794.x</link>
            <description>Conclusions:  There is a progressive reduction in total naevus counts with advancing age with respect to a cohort aged greater than 60 years. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5079572</comments>
            <pubDate>Tue, 26 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5079572</guid>        </item>
        <item>
            <title>The use of visual language as a search pattern in dermoscopy</title>
            <link>http://www.medworm.com/index.php?rid=5079571&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00797.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5079571</comments>
            <pubDate>Tue, 26 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5079571</guid>        </item>
        <item>
            <title>Dermoscopic naevus patterns in people at high versus moderate/low melanoma risk in Queensland</title>
            <link>http://www.medworm.com/index.php?rid=5079570&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00798.x</link>
            <description>Conclusion:  Our preliminary data shows that dermoscopic naevus patterns were similar for age and body site in people at different levels of melanoma risk, suggesting high melanoma risk does not influence dermoscopic naevus patterns. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5079570</comments>
            <pubDate>Tue, 26 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5079570</guid>        </item>
        <item>
            <title>Pyoderma gangrenosum requiring inpatient management: A report of 26 cases with follow up</title>
            <link>http://www.medworm.com/index.php?rid=5039800&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00750.x</link>
            <description>We present a case series of inpatients with pyoderma gangrenosum (PG), an ulcerative neutrophilic skin condition of unknown aetiology. Twenty‐six patients were admitted with PG, nine men and 17 women. At the time of the chart review, seven patients (26.9%) had died. Patients had a mean of 2.0 active ulcerative lesions and 22 patients' ulcers (84.6%) were on the lower limb. Systemic diseases were coexistent in 15 patients (57.7%), the most common being rheumatoid arthritis (19.2%). Thirty‐eight wound cultures were taken and were positive for Staphylococcus aureus in 22 cases (57.8%) and Pseudomonas aeruginosa in 20 (52.6%). After prednisolone, cyclosporin was the next most commonly prescribed systemic therapy (34.6%). Surgical debridement was undertaken in seven cases (26.9%) and two pa...</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5039800</comments>
            <pubDate>Tue, 19 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5039800</guid>        </item>
        <item>
            <title>Changing the way we diagnose tuberculids with interferon gamma release assays</title>
            <link>http://www.medworm.com/index.php?rid=5020872&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00791.x</link>
            <description>We describe three patients with tuberculids who had no other clinical feature of tuberculosis (TB) infection and negative PCR of skin biopsies. Their diagnoses were aided by positive IGRA. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5020872</comments>
            <pubDate>Mon, 11 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5020872</guid>        </item>
        <item>
            <title>Field treatment of facial and scalp actinic keratoses with photodynamic therapy: Survey of patient perceptions of treatment satisfaction and outcomes</title>
            <link>http://www.medworm.com/index.php?rid=4977742&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00785.x</link>
            <description>Conclusions:  Overall, our results compared favourably with previously published studies using 5‐ALA or MAL PDT. However, our patient cohort experienced a greater side‐effect profile. This may have been due to our patients having greater disease burden compared to other studies and possibly due to our use of topical retinoids prior to PDT in selected patients. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4977742</comments>
            <pubDate>Tue, 28 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4977742</guid>        </item>
        <item>
            <title>Schöpf–Schulz–Passarge syndrome resulting from a homozygous nonsense mutation, p.Cys107X, in WNT10A</title>
            <link>http://www.medworm.com/index.php?rid=4977741&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00788.x</link>
            <description>This report demonstrates the molecular basis of a further case of SSPS and highlights the clinical features of this unusual ectodermal dysplasia syndrome. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4977741</comments>
            <pubDate>Tue, 28 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4977741</guid>        </item>
        <item>
            <title>Discoid lupus erythematosus at a site of previous injury</title>
            <link>http://www.medworm.com/index.php?rid=4960939&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00786.x</link>
            <description>ABSTRACTA 71‐year‐old man with three patches of discoid lupus erythematosus (DLE) confined to the right preauricular region drew our attention because of the unusual linear arrangement of the lesions. Twenty‐five years previously, the patient had suffered a trauma in the same area from falling off his motorcycle. We believe that, despite the great lapse in time, this injury may have facilitated the onset of DLE in the very same area, through long‐term destabilization of the local neuroimmune network. The case fits the recently coined concept of the immunocompromised district, a cutaneous region with altered immune control, more susceptible to harbouring opportunistic infections, tumours, and immune disorders. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4960939</comments>
            <pubDate>Wed, 22 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4960939</guid>        </item>
        <item>
            <title>Coexistence of congenital linear porokeratosis and disseminated superficial porokeratosis</title>
            <link>http://www.medworm.com/index.php?rid=4960938&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00787.x</link>
            <description>We report here on a patient exhibiting the coexistence of congenital linear porokeratosis and disseminated superficial porokeratosis. To our knowledge, this entity has been previously reported only once. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4960938</comments>
            <pubDate>Wed, 22 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4960938</guid>        </item>
        <item>
            <title>Infantile digital fibromatosis: A rare tumour of infancy. Report of five cases</title>
            <link>http://www.medworm.com/index.php?rid=4937020&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00780.x</link>
            <description>We describe the clinical history of five patients with IDF that were followed in our departments for 5 years. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4937020</comments>
            <pubDate>Sat, 11 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4937020</guid>        </item>
        <item>
            <title>Pityriasis lichenoides et varioliformis acuta: A rare association with the measles, mumps and rubella vaccine</title>
            <link>http://www.medworm.com/index.php?rid=4937019&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00781.x</link>
            <description>We report the second case of PL et varioliformis acuta (PLEVA) occurring after measles vaccination and the first following the combined measles, mumps, rubella vaccination. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4937019</comments>
            <pubDate>Sat, 11 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4937019</guid>        </item>
        <item>
            <title>Merkel cell carcinoma metastatic to the transverse colon: Disease free after six years – cure or just prolonged remission?</title>
            <link>http://www.medworm.com/index.php?rid=4937018&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00782.x</link>
            <description>We report the case of an elderly man who developed colonic metastases from a head and neck primary and with treatment has survived disease free for over 6 years. Such reports are infrequently documented and highlight the unpredictable nature of this disease. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4937018</comments>
            <pubDate>Sat, 11 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4937018</guid>        </item>
        <item>
            <title>Psoriasiform eruption triggered by a dipeptidyl peptidase IV inhibitor</title>
            <link>http://www.medworm.com/index.php?rid=4937017&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00783.x</link>
            <description>We report a psoriasiform eruption induced by sitagliptin, a DPP‐IV inhibitor. The role of DPP‐IV in the pathogenesis of DM is well established; however data on psoriatic patients is contradictory. More studies are required to elucidate the effect of DPP‐IV inhibitors and their relationship with DM and psoriasis. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4937017</comments>
            <pubDate>Sat, 11 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4937017</guid>        </item>
        <item>
            <title>A case of multicentric reticulohistiocytosis responsive to azathioprine in a patient with no underlying malignancy</title>
            <link>http://www.medworm.com/index.php?rid=4913760&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00775.x</link>
            <description>We describe the case of a 60‐year‐old man with MRH and no underlying malignancy who initially responded well to azathioprine and whose disease recurred upon cessation. A second course of azathioprine administered in conjunction with antituberculous treatment resulted in disease control. Broader associations and features of this rare disease are discussed. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4913760</comments>
            <pubDate>Wed, 08 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4913760</guid>        </item>
        <item>
            <title>Successful treatment of cyclosporine‐induced sebaceous hyperplasia with oral isotretinoin in two renal transplant recipients</title>
            <link>http://www.medworm.com/index.php?rid=4913759&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00776.x</link>
            <description>We present two cases of cyclosporine‐induced sebaceous hyperplasia in renal transplant recipients, successfully treated with isotretinoin. Both patients tolerated isotretinoin well, with no alteration in graft function. These cases provide support for the safe and effective use of oral isotretinoin in the treatment of cyclosporine‐induced sebaceous hyperplasia in the kidney transplant population. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4913759</comments>
            <pubDate>Wed, 08 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4913759</guid>        </item>
        <item>
            <title>Lymphatic malformations: Clinical course and management in 64 cases</title>
            <link>http://www.medworm.com/index.php?rid=4913758&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00777.x</link>
            <description>Conclusions:  LM are heterogenous vascular malformations that may result in significant morbidity. Diagnosis is often delayed. A multidisciplinary approach to management including dermatology, diagnostic and interventional radiology and paediatric surgery is important. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4913758</comments>
            <pubDate>Wed, 08 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4913758</guid>        </item>
        <item>
            <title>Concurrence of alopecia areata and vitiligo at the same anatomical site</title>
            <link>http://www.medworm.com/index.php?rid=4913757&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00778.x</link>
            <description>ABSTRACTBoth alopecia areata and vitiligo are common skin disorders that are considered to be caused by an autoimmune response targeted to hair follicle and melanocyte antigens, respectively. The association of these two diseases in the same patient is well known, however, coexistence of alopecia areata and vitiligo within the same lesion is very rare. Herein, we report an 8‐year‐old boy who had colocalization of alopecia areata and vitiligo on the frontal portion of his scalp. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4913757</comments>
            <pubDate>Wed, 08 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4913757</guid>        </item>
        <item>
            <title>Generalized flare of pustular psoriasis induced by PEGylated interferon‐α2b therapy for chronic hepatitis C</title>
            <link>http://www.medworm.com/index.php?rid=4885845&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00767.x</link>
            <description>ABSTRACTNew onset or exacerbation of psoriasis vulgaris has been reported in a small number of patients after interferon (IFN)‐α therapy. Herein, we report a case of generalized flare of pustular psoriasis induced by PEGylated IFN‐α2b (PEG‐IFN‐α2b) in a 59‐year‐old woman with a 15‐year history of pustular psoriasis and chronic hepatitis C. Interferon‐α therapy was discontinued and the rash resolved after treatment with cyclosporin and systemic methylprednisolone. The potential side effect of PEG‐IFN‐α2b in inducing or exacerbating psoriasis should be kept in mind when treating patients with a history of psoriasis or pustular psoriasis. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4885845</comments>
            <pubDate>Sun, 29 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4885845</guid>        </item>
        <item>
            <title>Effectiveness and limitations of reflectance confocal microscopy in detecting persistence of basal cell carcinomas: A preliminary study</title>
            <link>http://www.medworm.com/index.php?rid=4885844&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00769.x</link>
            <description>Conclusion:  The diagnosis of BCC was straightforward and reliable in the present study. Thus, RCM appears useful in assessing the early treatment response of superficial BCC treated with saucerization or curettage and cautery despite operator‐dependant limitations. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4885844</comments>
            <pubDate>Sun, 29 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4885844</guid>        </item>
        <item>
            <title>Primary localized cutaneous nodular amyloidosis successfully treated with cyclophosphamide</title>
            <link>http://www.medworm.com/index.php?rid=4885843&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00770.x</link>
            <description>We present a case of a middle‐aged woman with PLCNA associated with CREST (calcinosis, Raynaud phenomenon, oesophageal motility disorders, sclerodactyly and telangiectasia) syndrome and Sjögren's syndrome responding to cyclophosphamide with no new amyloid deposits and resolution of skin ulceration after many years of resistance to drug therapy. It is important to monitor these patients for progression into systemic amyloidosis. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4885843</comments>
            <pubDate>Sun, 29 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4885843</guid>        </item>
        <item>
            <title>Drug‐induced dermatomyositis after zoledronic acid</title>
            <link>http://www.medworm.com/index.php?rid=4885842&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00771.x</link>
            <description>ABSTRACTA 57‐year‐old woman with prior exposure to bisphosphonates developed myalgia, proximal muscle weakness and lichenoid rash over the upper extremities and face 3 days after infusion of zoledronic acid for the management of osteoporosis. The diagnosis of dermatomyositis was made on the basis of clinical, laboratory and histological findings. This is the first report of drug‐induced dermatomyositis secondary to zoledronic acid. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4885842</comments>
            <pubDate>Sun, 29 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4885842</guid>        </item>
        <item>
            <title>Allergic contact dermatitis to Myroxylon pereirae (Balsam of Peru) in papaw ointment causing cheilitis</title>
            <link>http://www.medworm.com/index.php?rid=4885841&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00772.x</link>
            <description>ABSTRACTTwo patients presented with cheilitis and perioral dermatitis. Patch testing revealed positive reactions to both Myroxylon pereirae (MP; formerly known as Balsam of Peru) and Lucas Papaw Ointment (LPO; Lucas Papaw Remedies, Bisbane, Qld, Australia). MP was not listed as an ingredient in LPO, however the manufacturer confirmed that a small amount of MP was present in LPO and we believe this to be the cause of the patients' dermatitis. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4885841</comments>
            <pubDate>Sun, 29 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4885841</guid>        </item>
        <item>
            <title>The Fixomull skin support method for wound closure in patients with fragile skin</title>
            <link>http://www.medworm.com/index.php?rid=4885840&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00773.x</link>
            <description>We report the Fixomull (BSN Medical, Hamburg, Germany) skin support technique for wound closure, a novel method for closing elliptical incisions in patients with fragile skin. After the lesion of concern is excised, a strip of Fixomull is applied to the skin adjacent to the wound edge with an approximately 2 mm gap between the Fixomull and the incision edge. The wound is then closed with interrupted sutures through the Fixomull, with care to ensure wound edge eversion. Fixomull provides extra tensile strength. The sutures are removed at approximately 14 days, and the patient given a prophylactic course of oral antibiotics only if at high risk of infection. This is a simple, time efficient, inexpensive and effective measure to avoid skin grafts and reduce skin tears and trauma in patien...</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4885840</comments>
            <pubDate>Sun, 29 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4885840</guid>        </item>
        <item>
            <title>Occupational exposure to laboratory animals causing a severe exacerbation of atopic eczema</title>
            <link>http://www.medworm.com/index.php?rid=4782621&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00754.x</link>
            <description>ABSTRACTA 24‐year‐old man with a long history of severe atopic eczema presented with a marked exacerbation requiring hospital admission. It emerged that his occupation as an animal house technician required him to work closely with laboratory animals, particularly mice and rats. Radioallergosorbent tests to mice allergens were markedly elevated. Avoidance of animal work, in conjunction with medical treatment, resulted in a marked improvement of his eczema. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4782621</comments>
            <pubDate>Wed, 04 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4782621</guid>        </item>
        <item>
            <title>Disseminated zygomycosis due to Mycocladus corymbifera with cutaneous and cerebral involvement</title>
            <link>http://www.medworm.com/index.php?rid=4782620&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00752.x</link>
            <description>We report a case of disseminated infection with Mycocladus corymbifera involving the brain, lungs, kidneys and skin in a 16‐year‐old patient with acute lymphoblastic leukaemia. The skin lesions played a significant role in the diagnosis of mucormycosis. These infections have an exceedingly high mortality rate and early recognition of cutaneous lesions is essential to successful management. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4782620</comments>
            <pubDate>Wed, 04 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4782620</guid>        </item>
        <item>
            <title>Mohs surgery histopathology concordance in Australia</title>
            <link>http://www.medworm.com/index.php?rid=4782619&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00755.x</link>
            <description>Conclusion:  An Australian Mohs surgeon is capable of correctly identifying and interpreting histopathology in non‐melanoma skin cancers, and this compares favourably to an overseas study. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4782619</comments>
            <pubDate>Wed, 04 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4782619</guid>        </item>
        <item>
            <title>Juvenile xanthogranuloma: Challenges in complicated cases</title>
            <link>http://www.medworm.com/index.php?rid=5079569&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00799.x</link>
            <description>We present challenging cases of JXG from Sydney Children's Hospital, collected over 10 years – two with multisystem involvement and concomitant urticaria, one associated with neurofibromatosis, and one case of giant JXG with an initial histopathological challenge. Although JXG has been reported with urticaria pigmentosa, in two of our cases persistent urticaria, in association with JXG is discussed. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5079569</comments>
            <pubDate>Sat, 30 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5079569</guid>        </item>
        <item>
            <title>Dermatology outpatient population profiling: Indigenous and non‐indigenous dermatoepidemiology</title>
            <link>http://www.medworm.com/index.php?rid=5039799&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00792.x</link>
            <description>Conclusions:  This data can guide strategies towards improving the provision of dermatology services for the Australian population. Particular attention is required towards improving Indigenous Australians' capacity to access dermatology services. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5039799</comments>
            <pubDate>Sat, 30 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5039799</guid>        </item>
        <item>
            <title>Dermoscopy of acquired digital fibrokeratoma</title>
            <link>http://www.medworm.com/index.php?rid=5020871&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00793.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5020871</comments>
            <pubDate>Sat, 30 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5020871</guid>        </item>
        <item>
            <title>Poor efficacy of oral tacrolimus in the treatment of severe generalized atopic eczema in adults: A small retrospective case series</title>
            <link>http://www.medworm.com/index.php?rid=4977740&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00789.x</link>
            <description>We report a small, but novel case series of four adults with severe generalized atopic eczema (AE) not responsive to several other immunomodulatory therapies, who were treated with oral tacrolimus (5 mg twice‐daily). Three of the four patients failed therapy with systemic tacrolimus, despite two of these showing an initial clinical response; the fourth patient remains on tacrolimus monotherapy with good control of skin disease. Although oral tacrolimus was well‐tolerated in this small group of adults, the clinical efficacy in this series for severe AE was poor. Tacrolimus may yet have a role in less severe disease, but larger prospective studies are required to qualify its place as a treatment option in AE. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4977740</comments>
            <pubDate>Sat, 30 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4977740</guid>        </item>
        <item>
            <title>Dermoscopy improves diagnosis of tinea nigra: A study of 50 cases</title>
            <link>http://www.medworm.com/index.php?rid=4960937&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00790.x</link>
            <description>Conclusions:  The diagnosis of tinea nigra is significantly improved by dermoscopy, the disease should be considered as a cause of palmar or plantar pigmentation. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4960937</comments>
            <pubDate>Sat, 30 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4960937</guid>        </item>
        <item>
            <title>Genitogluteal porokeratosis: An unusual clinical presentation</title>
            <link>http://www.medworm.com/index.php?rid=4937016&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00784.x</link>
            <description>ABSTRACTA 51‐year‐old man presented with a 12‐year history of an expanding, irritable rash on his buttocks, groin and scrotum. He gradually developed erythematous, annular plaques with ridged borders and depressed centres. He also had a verruciform eruption in his perianal area. A clinical diagnosis of porokeratosis confined to the genitogluteal area was confirmed histopathologically. Oral acitretin resulted in symptomatic and cosmetic improvement. He continues to be followed up to evaluate treatment outcomes. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4937016</comments>
            <pubDate>Sat, 30 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4937016</guid>        </item>
        <item>
            <title>Methotrexate toxicity presenting as ulcerated psoriatic plaques</title>
            <link>http://www.medworm.com/index.php?rid=4913756&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00779.x</link>
            <description>We describe two patients who developed painful ulcerated psoriatic plaques as an early presenting sign of methotrexate toxicity and review the risk factors associated with this manifestation. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4913756</comments>
            <pubDate>Sat, 30 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4913756</guid>        </item>
        <item>
            <title>Hydroxyurea induced dermatomyositis‐like eruption</title>
            <link>http://www.medworm.com/index.php?rid=4885839&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00774.x</link>
            <description>We present a case report and review of the literature. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4885839</comments>
            <pubDate>Sat, 30 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4885839</guid>        </item>
        <item>
            <title>Dermoscopy: An Atlas, 3rd edition</title>
            <link>http://www.medworm.com/index.php?rid=4854453&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00760.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4854453</comments>
            <pubDate>Sat, 30 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4854453</guid>        </item>
        <item>
            <title>Dermatoscopy in Clinical Practice – Beyond Pigmented Lesions (Series in Dermatological Treatment)</title>
            <link>http://www.medworm.com/index.php?rid=4854452&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00759.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4854452</comments>
            <pubDate>Sat, 30 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4854452</guid>        </item>
        <item>
            <title>The Vulva: A Clinician's Practical Handbook</title>
            <link>http://www.medworm.com/index.php?rid=4854451&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00761.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4854451</comments>
            <pubDate>Sat, 30 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4854451</guid>        </item>
        <item>
            <title>In other journals</title>
            <link>http://www.medworm.com/index.php?rid=4854450&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00762.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4854450</comments>
            <pubDate>Sat, 30 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4854450</guid>        </item>
        <item>
            <title>On isotretinoin dosing, adverse effects, and efficacy: response.</title>
            <link>http://www.medworm.com/index.php?rid=4854449&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00765.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4854449</comments>
            <pubDate>Sat, 30 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4854449</guid>        </item>
        <item>
            <title>On isotretinoin dosing, adverse effects, and efficacy</title>
            <link>http://www.medworm.com/index.php?rid=4854448&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00764.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4854448</comments>
            <pubDate>Sat, 30 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4854448</guid>        </item>
        <item>
            <title>Mutation analysis of the CYLD gene in two Chinese families with multiple familial Trichoepithelioma</title>
            <link>http://www.medworm.com/index.php?rid=4854447&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00763.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4854447</comments>
            <pubDate>Sat, 30 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4854447</guid>        </item>
        <item>
            <title>A case of autoimmune progesterone dermatitis diagnosed by progesterone pessary</title>
            <link>http://www.medworm.com/index.php?rid=4854446&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00753.x</link>
            <description>We present the case of a 34‐year‐old woman with a premenstrual papular and eczematous eruption that was exacerbated after pregnancy. Biopsy showed subacute spongiotic dermatitis. To confirm the diagnosis, we used an intravaginal progesterone pessary as a provocation challenge. There was recurrence of the rash 12 h after insertion of the pessary with spontaneous resolution thereafter. We propose that use of a progesterone pessary is an effective tool in the diagnosis of autoimmune progesterone dermatitis. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4854446</comments>
            <pubDate>Sat, 30 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4854446</guid>        </item>
        <item>
            <title>Targetoid spongiotic reaction pattern: A case series of seven paediatric patients</title>
            <link>http://www.medworm.com/index.php?rid=4854445&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00766.x</link>
            <description>We present seven cases of a targetoid eruption, clinically mimicking erythema multiforme, occurring in paediatric patients aged 12 months to 14 years. All patients presented with a pruritic targetoid eruption on body and acral sites which spared mucosal areas. All patients demonstrated a spongiotic reaction pattern on histology without lichenoid change and demonstrated excellent responses to either oral prednisolone or topical corticosteroids. We propose the term ‘targetoid spongiotic reaction pattern (TSRP)’ for our subset of paediatric patients. We review the literature regarding targetoid eruptions in the paediatric population. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4854445</comments>
            <pubDate>Sat, 30 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4854445</guid>        </item>
        <item>
            <title>First experiences using reflectance confocal microscopy on equivocal skin lesions in Queensland</title>
            <link>http://www.medworm.com/index.php?rid=4854444&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00756.x</link>
            <description>Conclusions:  Using simple techniques we found that common RCM features were readily identifiable and common artefacts could be minimized, making RCM a useful tool to aid the diagnosis of equivocal skin lesions in a clinical setting. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4854444</comments>
            <pubDate>Sat, 30 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4854444</guid>        </item>
        <item>
            <title>Mohs surgery in Australia: A survey of work practices</title>
            <link>http://www.medworm.com/index.php?rid=4782618&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00751.x</link>
            <description>Conclusion:  Australian Mohs surgeons make an important contribution to the management of skin cancer in Australia and many are skilled in laser and cosmetic procedures. The increasing number of cases performed annually and the familiarity with laser and cosmetic therapies reinforces Australian dermatologists as leaders in these important areas of dermatology. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4782618</comments>
            <pubDate>Sat, 30 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4782618</guid>        </item>
        <item>
            <title>Reticulate eruptions. Part 1: Vascular networks and physiology</title>
            <link>http://www.medworm.com/index.php?rid=4725737&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00749.x</link>
            <description>ABSTRACTReticulate pattern is one of the most important dermatological signs of a pathological process involving the superficial vascular networks. Vascular malformations, such as cutis marmorata congenita telangiectasia and benign forms of livedo reticularis, and sinister conditions, such as meningococcal meningitis or Sneddon's syndrome, can all present with a reticulate pattern. The clinical presentation and morphology is determined by the nature and extent of the underlying pathology and the involvement of a particular vascular network. This review has been divided into four instalments. In the present paper, we discuss the anatomy and physiology of the complex network of vascular structures that support the function of the skin and subcutis. (Source: Australasian Journal of Dermatolog...</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4725737</comments>
            <pubDate>Tue, 19 Apr 2011 16:32:44 +0100</pubDate>
            <guid isPermaLink="false">4725737</guid>        </item>
        <item>
            <title>Author Index 2011</title>
            <link>http://www.medworm.com/index.php?rid=4698478&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00758.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4698478</comments>
            <pubDate>Tue, 12 Apr 2011 16:01:58 +0100</pubDate>
            <guid isPermaLink="false">4698478</guid>        </item>
        <item>
            <title>44th Annual Scientific Meeting</title>
            <link>http://www.medworm.com/index.php?rid=4698477&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00757.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4698477</comments>
            <pubDate>Tue, 12 Apr 2011 16:01:57 +0100</pubDate>
            <guid isPermaLink="false">4698477</guid>        </item>
        <item>
            <title>Role of genetics and sex steroid hormones in male androgenetic alopecia and female pattern hair loss: An update of what we now know</title>
            <link>http://www.medworm.com/index.php?rid=4654436&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00745.x</link>
            <description>ABSTRACTThe role of genetic predisposition and the influence of sex steroid hormones are indisputable to the pathogenesis of male androgenetic alopecia (MAGA). The role of sex steroid hormones in female pattern hair loss (FPHL) is less known. A good knowledge of the pathophysiology underlying MAGA and FPHL empowers the clinician to confidently counsel patients and make informed therapeutic decisions. Vigorous research in recent years has provided greater insight into the role of genetics and sex steroids in physiological hair growth and cycling, as well as in hair follicle miniaturization, the histological hallmark of MAGA and FPHL. In the present review article directed towards clinicians, we discuss the current understanding of the role of androgens and oestrogens, as well as genetic ass...</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4654436</comments>
            <pubDate>Mon, 28 Mar 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4654436</guid>        </item>
        <item>
            <title>Cutaneous angiosarcoma of the leg showing radiation sensitivity</title>
            <link>http://www.medworm.com/index.php?rid=4654435&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00746.x</link>
            <description>We report a case of cutaneous angiosarcoma occurring on the leg of a 97‐year‐old Japanese woman. Considering the patient's age and general condition, she was treated with electron beam irradiation, which led to the almost complete disappearance of the tumour. Because cutaneous angiosarcoma is an aggressive tumour with a high propensity for local recurrence and distant metastases, therapy preferably involves a multimodal approach. However, monotherapy with radiation may be effective in some cases of cutaneous angiosarcoma. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4654435</comments>
            <pubDate>Mon, 28 Mar 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4654435</guid>        </item>
        <item>
            <title>Haem arginate as effective maintenance therapy for hereditary coproporphyria</title>
            <link>http://www.medworm.com/index.php?rid=4654434&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00747.x</link>
            <description>ABSTRACTA 35‐year‐old woman presented with skin fragility and photosensitivity with blisters affecting her face and hands. Other symptoms included intermittent headache, fatigue, abdominal pain and nausea. Porphyrin studies were markedly raised, with features consistent with hereditary coproporphyria (HCP). Despite strict precautions, symptoms remained significantly problematic. Regular haem arginate infusions of 3 mg/kg per day over 4 days on a monthly basis were commenced and resulted in significant improvement of the patient's symptoms and a reduction in urinary porphobilinogen. Although haem arginate infusion is known as a treatment for severe acute attacks of HCP, the effectiveness of regular infusions as maintenance therapy has not been established. This is the first report o...</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4654434</comments>
            <pubDate>Mon, 28 Mar 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4654434</guid>        </item>
        <item>
            <title>Naevus anaemicus‐like hypopigmented macules in dyskeratosis congenita</title>
            <link>http://www.medworm.com/index.php?rid=4627653&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00742.x</link>
            <description>ABSTRACTIn the present paper we report on a Taiwanese case of X‐linked recessive dyskeratosis congenita (DC), confirmed by detection of a 214 C→T mutation in the DKC1 gene, and provide a detailed description of mottled pigmentary changes of the skin, specifically numerous small, whitish macules dispersed against a background of diffuse, finely reticulated hyperpigmentation. The hypopigmented macules showed no discernible erythema upon rubbing or the local application of heat. The naevus anaemicus‐like macules may be a relatively common but under‐recognized feature in DC. More studies are required to determine the incidence and histopathology of these macules. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4627653</comments>
            <pubDate>Thu, 24 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4627653</guid>        </item>
        <item>
            <title>Pigmented spindle cell naevus of Reed: A controversial diagnostic entity in Australia</title>
            <link>http://www.medworm.com/index.php?rid=4627652&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00743.x</link>
            <description>Conclusions:  The results support our hypothesis that PSCN is under‐recognised in Australia. The results also show that despite difficulty distinguishing this lesion, management of these lesions by dermatology trainees in Australia is consistent and parallels current recommendations. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4627652</comments>
            <pubDate>Thu, 24 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4627652</guid>        </item>
        <item>
            <title>Angiolymphoid hyperplasia with eosinophilia and Kimura's disease coexisting in the same patient: Evidence for a spectrum of disease</title>
            <link>http://www.medworm.com/index.php?rid=4627651&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00744.x</link>
            <description>ABSTRACTThe relationship between angiolymphoid hyperplasia with eosinophilia (ALHE) and Kimura's disease has always been contentious. Initially, ALHE and Kimura's disease were thought to be conditions within the same disease spectrum, but it is now widely accepted that they are two separate disease entities. The two lesions may coexist in one patient. Thus, ALHE and Kimura's disease may be different manifestations of the one disease. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4627651</comments>
            <pubDate>Thu, 24 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4627651</guid>        </item>
        <item>
            <title>Birt–Hogg–Dubé syndrome with a renal angiomyolipoma: Further evidence of a relationship between Birt–Hogg–Dubé syndrome and tuberous sclerosis complex</title>
            <link>http://www.medworm.com/index.php?rid=4567058&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00738.x</link>
            <description>ABSTRACTBirt‐Hogg‐Dubé syndrome (BHDS) is an autosomal dominant condition caused by mutations in the gene which codes for folliculin (FLCN). It is characterised clinically by fibrofolliculomas, trichodiscomas, pulmonary cysts, spontaneous pneumothoraces and renal cancers. This case illustrates a patient with BHDS and a renal angiomyolipoma. Angiomyolipomas are not described as a feature of BHDS, but rather they can occur sporadically or in tuberous sclerosis complex (TSC). Recent studies suggest that clinical similarities between BHDS and TSC may be explained by FLCN and TSC proteins functioning on a common pathway, mammalian target of rapamycin. This case adds to the literature of cases with clinical similarities. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4567058</comments>
            <pubDate>Thu, 10 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4567058</guid>        </item>
        <item>
            <title>Unique brown star shape on dermatoscopy of generalized Dowling‐Degos disease</title>
            <link>http://www.medworm.com/index.php?rid=4561759&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00736.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4561759</comments>
            <pubDate>Mon, 07 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4561759</guid>        </item>
        <item>
            <title>Calcinosis cutis following contact with calcium chloride solution</title>
            <link>http://www.medworm.com/index.php?rid=4561758&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00737.x</link>
            <description>We report a 48‐year‐old white man who was dismantling a portable ice skating rink when calcium chloride solution from the pipes spilt onto his clothing. Several days later, he started to develop mildly pruritic erythematous papules, some studded with white deposits and some with umbilication over the exposed areas corresponding to the spillage of the calcium chloride solution. Histological features revealed interstitial fibrohistiocytic reaction with calcium‐encrusted degenerated collagen bundles in the dermis which was further confirmed by von Kossa stain. He was commenced on topical corticosteroid cream twice daily and the lesions cleared completely between 6 to 10 weeks. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4561758</comments>
            <pubDate>Mon, 07 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4561758</guid>        </item>
        <item>
            <title>Clofazimine‐induced enteropathy in treatment‐resistant nodular vasculitis</title>
            <link>http://www.medworm.com/index.php?rid=4561757&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00739.x</link>
            <description>We report a chronic case of nodular vasculitis that responded to oral clofazimine 300 mg daily. The condition had previously responded to moderate dose oral prednisolone, 50 mg daily, but would recur with weaning. Multiple corticosteroid‐sparing agents were trialled, however these were either ineffective or poorly tolerated. The introduction of clofazimine enabled prednisolone dose reduction, not achieved with other agents, to 22.5 mg daily, and was associated with complete suppression of disease activity. Unfortunately the patient developed a clofazimine‐induced enteropathy and the treatment was ceased after almost 2 years of therapy. Cessation of clofazimine was associated with a flare of the condition. Clofazimine should be considered as a corticosteroid‐sparing agent in r...</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4561757</comments>
            <pubDate>Mon, 07 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4561757</guid>        </item>
        <item>
            <title>X‐linked recessive polyfibromatosis manifesting with spontaneous keloid scars and Dupuytren's contracture</title>
            <link>http://www.medworm.com/index.php?rid=4561756&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00740.x</link>
            <description>We present a patient with keloid scars and Dupuytren's contracture comprising the polyfibromatosis syndrome; four members over three generations of his family are also affected. To our knowledge this is the first familial case reported of polyfibromatosis with this specific phenotypic presentation and probable X‐linked recessive inheritance. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4561756</comments>
            <pubDate>Mon, 07 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4561756</guid>        </item>
        <item>
            <title>Incipient retinal vein occlusion following immunotherapy of periorbital basal cell carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=4561755&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00741.x</link>
            <description>We report a case of retinal vein occlusion in a 54‐year‐old woman following treatment with topical imiquimod for a superficial basal cell carcinoma of the temple. Signs and symptoms resolved rapidly upon ceasing treatment. Although they are uncommon, it is important to recognise and promptly manage ophthalmic complications related to treatment with imiquimod in order to prevent serious sequelae such as macular oedema and neovascularization. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4561755</comments>
            <pubDate>Mon, 07 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4561755</guid>        </item>
        <item>
            <title>Predicting melanoma risk for the Australian population</title>
            <link>http://www.medworm.com/index.php?rid=4536758&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00727.x</link>
            <description>Conclusion:  We have developed a melanoma risk assessment tool based on the best available information (http://www.victorianmelanomaservice.org/calculator). The tool is easily modified as new information becomes available. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4536758</comments>
            <pubDate>Tue, 01 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4536758</guid>        </item>
        <item>
            <title>Dermoscopy: Ex vivo visualization of fleas head and bag of eggs confirms the diagnosis of Tungiasis</title>
            <link>http://www.medworm.com/index.php?rid=4536757&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00728.x</link>
            <description>ABSTRACTTungiasis, caused by the impregnated female sand flea Tunga penetrans, is increasingly common in returned travellers from endemic areas. Clinical suspicion is raised by the clinicodermoscopic correlation, leading to rapid treatment which involves extraction of the intact flea. Ex vivo dermoscopy demonstrates the parasite's head and distended abdomen full of eggs, confirming the diagnosis. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4536757</comments>
            <pubDate>Tue, 01 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4536757</guid>        </item>
        <item>
            <title>Dermatophytosis and Sjögren–Larsson syndrome: Foe or friend?</title>
            <link>http://www.medworm.com/index.php?rid=4536756&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00729.x</link>
            <description>We report the patchy normalization of lamellar ichthyotic skin in Sjögren–Larsson syndrome (SLS) following a cutaneous Trichophyton rubrum infection. The dermatophytosis was pruritic and pustular, requiring treatment which was followed by the return of the lamellar ichthyosis. We discuss the possible mechanism of this clinical observation, which in turn may direct future therapy for difficult to treat ichthyotic skin seen in conditions such as SLS. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4536756</comments>
            <pubDate>Tue, 01 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4536756</guid>        </item>
        <item>
            <title>Infantile myofibromatosis: Two families supporting autosomal dominant inheritance</title>
            <link>http://www.medworm.com/index.php?rid=4536755&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00730.x</link>
            <description>We present two families in whom infantile myofibromatosis affects two generations. The disease expression in these families suggests an autosomal dominant mode of inheritance. Clinical diagnosis and establishment of the inheritance pattern have important prognostic implications for the affected individual and family members and serves to guide subsequent genetic counselling. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4536755</comments>
            <pubDate>Tue, 01 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4536755</guid>        </item>
        <item>
            <title>Lymphomatoid papulosis in children: Experience of five cases and the treatment efficacy of methotrexate</title>
            <link>http://www.medworm.com/index.php?rid=4536754&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00734.x</link>
            <description>We present a case series of childhood lymphomatoid papulosis (LyP), an entity which is commonly misdiagnosed and poorly described in the paediatric dermatology literature. Clinically and histologically, the features of LyP in children can mimic insect bite reactions, with prominent dermal neutrophils and eosinophils. However, CD30 immunohistochemical staining of atypical lymphocytes within a mixed inflammatory infiltrate should point to the diagnosis of LyP. There is no consensus to guide management of childhood LyP due to its rarity and largely unknown natural course. We discuss our experience with LyP in five children and the use of methotrexate to induce rapid resolution of persistent lesions and to reduce recurrences in two children. Although none of our cases have experienced malignan...</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4536754</comments>
            <pubDate>Tue, 01 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4536754</guid>        </item>
        <item>
            <title>Treatment of female pattern hair loss with the androgen receptor antagonist flutamide</title>
            <link>http://www.medworm.com/index.php?rid=4536753&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00735.x</link>
            <description>We report a woman whose hair loss progressed while using spironolactone and topical minoxidil in combination, but reversed with flutamide, a potent androgen receptor antagonist. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4536753</comments>
            <pubDate>Tue, 01 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4536753</guid>        </item>
        <item>
            <title>Fractional filling with the microdepot technique as an alternative to bolus hyaluronic acid injections in facial volume restoration</title>
            <link>http://www.medworm.com/index.php?rid=4654433&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2011.00748.x</link>
            <description>ABSTRACTFor volume restoration of the face, hyaluronic acid is conventionally injected through long, large‐bore, 18‐gauge needles because of the higher viscosity subtypes required. These hyaluronic acids are either more highly cross‐linked or larger in particle size than the less‐viscous subtypes. The microdepot injection technique involves using the 31‐gauge BD insulin syringe (Becton‐Dickinson, North Ryde, NSW Australia) to deposit small amounts of filler (0.05–0.1 mL) throughout the area of volume loss. The procedure is extremely well tolerated, requiring only topical and ice anaesthesia. Using this method, volume restoration can be achieved naturally and progressively over a period of time. Fractional filling every 3–4 months is continued until the desired level of ...</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4654433</comments>
            <pubDate>Tue, 01 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4654433</guid>        </item>
        <item>
            <title>Ferri's fast facts in dermatology: A practical guide to skin diseases &amp; disorders, 1st edition</title>
            <link>http://www.medworm.com/index.php?rid=4502928&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00732.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4502928</comments>
            <pubDate>Tue, 01 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4502928</guid>        </item>
        <item>
            <title>Litt's D.E.R.M. Drug Eruptions &amp; Reactions Manual, 16th Edition</title>
            <link>http://www.medworm.com/index.php?rid=4502927&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00733.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4502927</comments>
            <pubDate>Tue, 01 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4502927</guid>        </item>
        <item>
            <title>In other journals</title>
            <link>http://www.medworm.com/index.php?rid=4502926&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00731.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4502926</comments>
            <pubDate>Tue, 01 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4502926</guid>        </item>
        <item>
            <title>Results of a nationwide dermoscopy survey investigating the prevalence, advantages and disadvantages of dermoscopy use among Australian dermatologists</title>
            <link>http://www.medworm.com/index.php?rid=4390152&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00708.x</link>
            <description>Conclusions:  In the sample of Australian dermatologists agreeing to be surveyed, there was a high prevalence rate of dermoscopy use. The factors supporting the use of dermoscopy are explored in this foundational database of dermoscopy use among Australian dermatologists. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4390152</comments>
            <pubDate>Sun, 23 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4390152</guid>        </item>
        <item>
            <title>Plantar verrucous carcinoma masquerading as toe web intertrigo</title>
            <link>http://www.medworm.com/index.php?rid=4339213&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00721.x</link>
            <description>ABSTRACTA 77‐year‐old man presented with a 6‐month history of intractable toe web intertrigo located in the third and fourth web spaces of his left foot. Biopsy and histological examination confirmed the presence of a verrucous carcinoma. Verrucous carcinoma of the foot has been called epithelioma cuniculatum, a case arising in the intertriginous area of the foot is presented. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4339213</comments>
            <pubDate>Wed, 12 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4339213</guid>        </item>
        <item>
            <title>Enfuvirtide injection site reactions: A clinical and histopathological appraisal</title>
            <link>http://www.medworm.com/index.php?rid=4339212&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00717.x</link>
            <description>Conclusion:  This study details histopathological changes associated with enfuvirtide ISR. We postulate that changes in DDC populations may contribute to the pathogenesis of the sclerotic process observed with enfuvirtide ISR. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4339212</comments>
            <pubDate>Wed, 12 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4339212</guid>        </item>
        <item>
            <title>Three cases of osteoma cutis occurring in infancy. A brief overview of osteoma cutis and its association with pseudo‐pseudohypoparathyroidism</title>
            <link>http://www.medworm.com/index.php?rid=4339211&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00722.x</link>
            <description>We report three cases of primary osteoma cutis in children, two of whom (siblings) were associated with Albright's hereditary osteodystrophy (AHO), manifesting as short stature with autosomal dominant inheritance from the father, but no dysmorphic features and no parathyroid hormone (PTH) resistance. Osteoma cutis can manifest as an isolated skin disease, a secondary condition to other skin diseases (such as acne), or in association with several syndromes, including AHO, which in turn may be associated with PTH resistance. The management and prognosis of patients diagnosed with osteoma cutis is determined by whether the skin manifestation has occurred in isolation, in association with a syndrome, or as a secondary skin disease. These three paediatric cases highlight the importance of under...</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
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            <pubDate>Wed, 12 Jan 2011 00:00:00 +0100</pubDate>
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            <title>Thirty‐five units of botulinum toxin type A for treatment of axillary hyperhidrosis in female patients</title>
            <link>http://www.medworm.com/index.php?rid=4339210&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00723.x</link>
            <description>We present a retrospective audit on efficacy and impact of 35 units of botulinum toxin type A per axilla on quality of life in female patients with axillary hyperhidrosis. This audit shows that 35 units of botulinum toxin type A is a reasonable starting dose and could significantly improve patients' quality of life and reduce the cost of treatment. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4339210</comments>
            <pubDate>Wed, 12 Jan 2011 00:00:00 +0100</pubDate>
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        <item>
            <title>Insights into the mechanism of Piper betle leaf‐induced contact leukomelanosis using C57BL/6 mice as the animal model and tyrosinase assays</title>
            <link>http://www.medworm.com/index.php?rid=4339209&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00724.x</link>
            <description>Conclusions:  The leukomelanosis observed in patients might be the consequence of PIH combined with a mixed reaction (hyper‐ and hypopigmenta tion), probably due to the different volatile chemicals that surface after steaming the PBL. This conflicting mixed reaction suggests that counteractive ingredients might exist in PBL. PBL, if purified, might be a promising source of a novel bleaching agent. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4339209</comments>
            <pubDate>Wed, 12 Jan 2011 00:00:00 +0100</pubDate>
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            <title>Dermatoscopy of a minute melanoma</title>
            <link>http://www.medworm.com/index.php?rid=4339208&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00725.x</link>
            <description>We present a case report of a naevoid lentigo maligna (World Health Organisation level 1 melanoma) on the nose of a 46‐year‐old man. He was under surveillance because of a past history of two melanomas and developed a new lesion. The visible lesion was 1.6 mm in maximum diameter as measured by the scale on the dermatoscope footplate. The dermatoscopic structures present were limited to dots arranged asymmetrically. We believe that the fact that some of these dots were grey provided a useful clue to the diagnosis of melanoma. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4339208</comments>
            <pubDate>Wed, 12 Jan 2011 00:00:00 +0100</pubDate>
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        <item>
            <title>Dermatofibroma and halo dermatitis</title>
            <link>http://www.medworm.com/index.php?rid=4339207&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00726.x</link>
            <description>We report a rare case of the Meyerson phenomenon occurring around a dermatofibroma in a 69‐year‐old woman. This case highlights that the phenomenon may occur in a broad range of clinical scenarios and is not limited to acquired naevi in young adults. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4339207</comments>
            <pubDate>Wed, 12 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4339207</guid>        </item>
        <item>
            <title>Prevalence of Staphylococcus aureus and antibiotic resistance in children with atopic dermatitis: A New Zealand experience</title>
            <link>http://www.medworm.com/index.php?rid=4299077&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00714.x</link>
            <description>Conclusions:  Three quarters of children with atopic dermatitis have at least one positive culture, of which the vast majority is S. aureus. The density of S. aureus colonisation correlates to severity of atopic dermatitis. Children who are S. aureus culture‐positive had no significant demographic or clinical features different to children who were culture‐negative. Only two children grew S. aureus resistant to flucloxacillin (2% resistance rate), which remains the ideal first line of treatment in our local population. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4299077</comments>
            <pubDate>Thu, 30 Dec 2010 00:00:00 +0100</pubDate>
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            <title>Facial lichen nitidus actinicus</title>
            <link>http://www.medworm.com/index.php?rid=4299076&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00716.x</link>
            <description>We report an 18‐year‐old woman with lichen nitidus with exclusive facial distribution. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4299076</comments>
            <pubDate>Thu, 30 Dec 2010 00:00:00 +0100</pubDate>
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            <title>Endothelin receptor antagonist bosentan improves the dermal sclerosis in a patient with systemic sclerosis</title>
            <link>http://www.medworm.com/index.php?rid=4208755&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00719.x</link>
            <description>We report a case of systemic sclerosis with interstitial pneumonia and severe pulmonary hypertension treated with bosentan, an endothelin receptor antagonist. Within a short period of administration of the bosentan the skin sclerosis improved. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4208755</comments>
            <pubDate>Mon, 29 Nov 2010 00:00:00 +0100</pubDate>
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            <title>Clinical effects of topical pimecrolimus in a patient with Fox–Fordyce disease</title>
            <link>http://www.medworm.com/index.php?rid=4144991&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00711.x</link>
            <description>ABSTRACTFox–Fordyce disease (FFD) is characterized by a pruritic eruption of skin‐coloured or yellowish papules in areas rich in apocrine glands. The histology comprises dilatation of follicular infundibula with hyperkeratosis, acanthosis, and spongiosis of the infundibular epithelium with perifollicular infiltration of lymphocytes and foamy histiocytes. We treated a 12‐year‐old girl with FFD with topical pimecrolimus for 12 weeks, this resulted in a complete clearance of lesions. After the therapy, the patient was followed for an additional 19 months without signs of relapse. The effects of pimecrolimus in FFD might imply that an inflammatory process inducing secondary reactive hyperkeratosis could be involved in the pathogenesis of FFD. (Source: Australasian Journal of Dermat...</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4144991</comments>
            <pubDate>Tue, 09 Nov 2010 00:00:00 +0100</pubDate>
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            <title>Porokeratosis of Mibelli: Involution and resolution with 5% imiquimod cream</title>
            <link>http://www.medworm.com/index.php?rid=4144990&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00712.x</link>
            <description>ABSTRACTAn 82‐year‐old woman presented with a longstanding, slowly enlarging annular lesion on the medial aspect of the ankle. Histology confirmed the clinical diagnosis of Porokeratosis of Mibelli. The lesion slowly involuted and resolved over 26 weeks of 5% imiquimod cream applied topically and has not recurred during a 36 month follow‐up period. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4144990</comments>
            <pubDate>Tue, 09 Nov 2010 00:00:00 +0100</pubDate>
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        <item>
            <title>The lateral pulley buried dermal suture</title>
            <link>http://www.medworm.com/index.php?rid=4144989&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00715.x</link>
            <description>ABSTRACTTo achieve complete closure of wounds under tension, the lateral pulley buried dermal suture is described. The pulley loop exists not between the two margins of the wound, but in the outer dermis. The needle entry and exit occur on the undermined undersurface of the dermis. It has mechanical advantages similar to the modified buried dermal suture and compresses less marginal tissue. The pulley suture can secure the wound under tension without creating tension on the epidermis and superficial dermis at the wound edge. (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4144989</comments>
            <pubDate>Tue, 09 Nov 2010 00:00:00 +0100</pubDate>
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        <item>
            <title>New Zealand Dermatological Society Incorporated Annual Scientific Meeting</title>
            <link>http://www.medworm.com/index.php?rid=4172806&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00707.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4172806</comments>
            <pubDate>Mon, 01 Nov 2010 00:00:00 +0100</pubDate>
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        <item>
            <title>John anthony doyle</title>
            <link>http://www.medworm.com/index.php?rid=4172805&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00706.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4172805</comments>
            <pubDate>Mon, 01 Nov 2010 00:00:00 +0100</pubDate>
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        <item>
            <title>Body contouring</title>
            <link>http://www.medworm.com/index.php?rid=4172804&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00705.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4172804</comments>
            <pubDate>Mon, 01 Nov 2010 00:00:00 +0100</pubDate>
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            <title>Flaps and grafts in dermatologic surgery</title>
            <link>http://www.medworm.com/index.php?rid=4172803&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00704.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
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            <pubDate>Mon, 01 Nov 2010 00:00:00 +0100</pubDate>
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            <title>In other journals</title>
            <link>http://www.medworm.com/index.php?rid=4172802&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00703.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4172802</comments>
            <pubDate>Mon, 01 Nov 2010 00:00:00 +0100</pubDate>
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            <title>Dermoscopic features of extraocular sebaceous carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=4062307&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00699.x</link>
            <description>(Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4062307</comments>
            <pubDate>Thu, 14 Oct 2010 00:10:32 +0100</pubDate>
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            <title>Narrowband UVB phototherapy in children: A New Zealand experience</title>
            <link>http://www.medworm.com/index.php?rid=4062306&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00701.x</link>
            <description>ABSTRACT (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4062306</comments>
            <pubDate>Thu, 14 Oct 2010 00:10:32 +0100</pubDate>
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            <title>Patients with clinically node negative extremity Merkel cell carcinoma: The importance of identifying and treating patients with microscopic nodal metastases</title>
            <link>http://www.medworm.com/index.php?rid=4062305&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00702.x</link>
            <description>ABSTRACT (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4062305</comments>
            <pubDate>Thu, 14 Oct 2010 00:10:31 +0100</pubDate>
            <guid isPermaLink="false">4062305</guid>        </item>
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            <title>Childhood actinic lichen planus: Successful treatment with antimalarials</title>
            <link>http://www.medworm.com/index.php?rid=4005315&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00695.x</link>
            <description>ABSTRACT (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4005315</comments>
            <pubDate>Wed, 29 Sep 2010 13:35:56 +0100</pubDate>
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            <title>Cutaneous larva migrans in infants in the Adelaide Hills</title>
            <link>http://www.medworm.com/index.php?rid=4005314&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00696.x</link>
            <description>ABSTRACT (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4005314</comments>
            <pubDate>Wed, 29 Sep 2010 13:35:55 +0100</pubDate>
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            <title>Folliculosebaceous cystic hamartoma of the ear and periauricular skin</title>
            <link>http://www.medworm.com/index.php?rid=4005313&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00697.x</link>
            <description>ABSTRACT (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4005313</comments>
            <pubDate>Wed, 29 Sep 2010 13:35:55 +0100</pubDate>
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            <title>Dermatophyte infections in Melbourne: Trends from 1961/64 to 2008/09</title>
            <link>http://www.medworm.com/index.php?rid=3955787&amp;cid=s_31735_12_f&amp;fid=31735&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1440-0960.2010.00678.x</link>
            <description>ABSTRACT (Source: Australasian Journal of Dermatology)</description>
            <author>Australasian Journal of Dermatology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3955787</comments>
            <pubDate>Sat, 11 Sep 2010 05:40:36 +0100</pubDate>
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