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        <title>Journal of Hematopathology 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 'Journal of Hematopathology' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Journal+of+Hematopathology&t=Journal+of+Hematopathology&s=Search&f=source]]></link>
        <lastBuildDate>Thu, 09 Feb 2012 00:42:17 +0100</lastBuildDate>
        <item>
            <title>Clonal antigen receptor gene PCR products outside the expected size range</title>
            <link>http://www.medworm.com/index.php?rid=5661207&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F76gn5823745r54u2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Polymerase chain reaction (PCR) of the antigen receptor genes has clinical utility in establishing clonality in lymphoproliferations,
 which is an important correlate of lymphoid neoplasia. The most frequently used procedures for this purpose were developed
 by the BIOMED-2 consortium. One of the criteria for establishing monoclonality using PCR of the antigen receptor genes is
 the finding of an abundant amplicon within a size range determined by the positions of the PCR primers and the known variability
 in size inherent in the recombination events that assemble a functional antigen receptor gene. However, several cases have
 been reported in which an amplicon outside this size range has been shown to be a valid indicator of clonality after DNA sequence
 analysis. In ...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5661207</comments>
            <pubDate>Fri, 03 Feb 2012 07:19:24 +0100</pubDate>
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        <item>
            <title>Rare case of hemolytic uremic syndrome associated with only one transient low platelet count</title>
            <link>http://www.medworm.com/index.php?rid=5639890&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq306g1332427u3g2%2F</link>
            <description>We report a second case of a young 18-year-old girl presenting with HUS and
 normal platelet counts.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-3DOI 10.1007/s12308-011-0130-8Authors
		Kalpita Hatti, Rochester General Hospital Internal Medicine Residency Program, 1425 Portland avenue, Rochester, NY 14621, USAMaria Rojas, Rochester General Hospital, 1425 Portland avenue, Rochester, NY 14621, USAPeter Kouides, Rochester General Hospital, Mary M. Gooley Hemophilia Center, Hemophilia Thrombosis Research Society, University of Rochester School of Medicine and Roswell Park Memorial Cancer Institute, 1425 Portland avenue, Rochester, NY 14621, USA
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5639890</comments>
            <pubDate>Tue, 24 Jan 2012 07:54:05 +0100</pubDate>
            <guid isPermaLink="false">5639890</guid>        </item>
        <item>
            <title>The added value of immunoglobulin Kappa light chain gene (IGK) rearrangement analysis in suspected B-cell lymphomas: three illustrative cases</title>
            <link>http://www.medworm.com/index.php?rid=5639891&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx20jr13135787hu6%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Immunoglobulin Kappa light chain gene (IGK) rearrangements are important complementary PCR targets for clonality assessment in mature B-cell proliferations in which
 detection of clonal VH-JH gene rearrangements fails. Failure to amplify VH-JH rearrangements is mainly attributable to somatic hypermutation. Detection of clonal IGK rearrangements is most relevant in the diagnosis of germinal center (GC) and post-GC B-cell lymphomas that are under a heavy
 somatic mutation process. Here we present three cases in which histology and immunophenotype of the tissue samples at time
 of diagnosis were inconclusive. PCR-based B-cell clonality assessment was performed using the standardized BIOMED-2 multiplex
 PCR protocols and Genescan analysis. No clonal VH-JH rearrangements wer...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5639891</comments>
            <pubDate>Tue, 24 Jan 2012 07:54:03 +0100</pubDate>
            <guid isPermaLink="false">5639891</guid>        </item>
        <item>
            <title>The assessment of minimal residual disease in chronic lymphocytic leukaemia: comparison of multi-colour flow cytometry and bone marrow trephine biopsy</title>
            <link>http://www.medworm.com/index.php?rid=5612006&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2524134l2122pp81%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We investigated the value and degree of agreement between a sensitive four-colour flow cytometry (FC) method and bone marrow
 trephine (BMT) biopsy for detecting minimal residual disease (MRD) in 82 chronic lymphocytic leukaemia (CLL) cases. Concordance
 was 85%, with 15% of cases discrepant (six BMT-positive/FC-negative and six BMT-negative/FC-positive cases). FC-positive/BMT-negative
 cases had a low-level MRD by FC (0.05–0.9%), whereas BMT-positive/FC-negative cases had significant residual nodular disease.
 We conclude that FC and BMT biopsy are complementary investigations for MRD assessment in CLL, and both should be considered
 in the routine setting to assess MRD in CLL.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-5DOI 10.1007/s12308-011-...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5612006</comments>
            <pubDate>Tue, 17 Jan 2012 07:07:47 +0100</pubDate>
            <guid isPermaLink="false">5612006</guid>        </item>
        <item>
            <title>Construction and implementation of a comprehensive hematopathology virtual teaching set</title>
            <link>http://www.medworm.com/index.php?rid=5612007&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F10606106t081581r%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Diagnostic hematopathology requires a multiparametric approach and integration of morphologic findings with the clinical,
 immunophenotypic, and other features. As hematopathology moves into an increasingly digital era, internet-deployed teaching
 sets consisting of whole slide images (WSI) and comprehensive ancillary information can help prepare hematopathology trainees
 for the future. Approximately 200 hematopathology conference cases over a 1-year period were de-identified, and case information
 (including clinical, microscopic and immunophenotypic features, flow cytometric histograms, and cytogenetic and molecular
 results) were entered into a database. Approximately 1,800 WSI were prepared by scanning using ×40 magnification, and WSI
 and supplemental data were s...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5612007</comments>
            <pubDate>Tue, 17 Jan 2012 07:07:46 +0100</pubDate>
            <guid isPermaLink="false">5612007</guid>        </item>
        <item>
            <title>Intratumoral heterogeneity in anaplastic large cell lymphoma of non-common subtype</title>
            <link>http://www.medworm.com/index.php?rid=5599907&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa752071k04667442%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 ALK-positive anaplastic large cell lymphoma (ALCL) with identical primary genetic aberration present with variable morphology.
 The eponymous anaplastic large cell morphology can be detected in the majority cases which are described as being of common
 type morphology. However, morphological variants displaying small tumor cells that are barely distinguishable from reactive
 lymphocytes occur often in combination with classical large tumor cells and characterize so-called non-common type ALCL. This
 subgroup has recently been shown to be associated with a weak immune response to the ALK1 protein and a poorer outcome in children. Expression of T cell markers like CD3 is often reduced or absent in these lymphomas,
 probably as a direct effect of the ALK1 protein. In non...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5599907</comments>
            <pubDate>Fri, 13 Jan 2012 16:48:46 +0100</pubDate>
            <guid isPermaLink="false">5599907</guid>        </item>
        <item>
            <title>A practical approach to diagnostic Ig/TCR clonality evaluation in clinical pathology</title>
            <link>http://www.medworm.com/index.php?rid=5585688&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx96n8284578kj8t2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The BIOMED-2 group developed and approved a set of multiplex Ig and T cell receptor PCR primers and successfully applied these
 to different well-defined WHO lymphoma entities with unprecedented high frequencies of malignant cases showing clonality.
 This approach has now become a worldwide standard of clonality testing in lymphoproliferations. While the clonality testing
 and assessment by GeneScan and/or heteroduplex analysis has become relatively easy to perform, the evaluation of the obtained
 gene rearrangement patterns can be difficult. In this review, we will address specific aspects of clonality testing, concerning
 both the practical phase as the evaluation of the obtained gene rearrangement patterns, which will help to overcome problems
 that can be encountere...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5585688</comments>
            <pubDate>Tue, 10 Jan 2012 16:57:36 +0100</pubDate>
            <guid isPermaLink="false">5585688</guid>        </item>
        <item>
            <title>CD68+ cell numbers and dendritic cell numbers and phenotype fail to predict the presence of a MYC rearrangement in aggressive B-cell lymphomas</title>
            <link>http://www.medworm.com/index.php?rid=5573446&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh834703kq3620700%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;MYC rearrangements are frequently associated with aggressive B-cell lymphomas, such as Burkitt’s lymphoma. We sought surrogate
 markers of MYC rearrangements that might obviate the need for a complex and expensive technique such as fluorescent in situ
 hybridization (FISH). We show that numbers of CD68+ macrophages/dendritic cells (DCs), DC-SIGN+ myeloid DCs and CD123+ plasmacytoid
 DCs fail to correlate with MYC rearrangement, although a starry sky appearance shows positive correlation (p = 0.003) when statistical analysis is performed on all three diagnostic groups together. We conclude that FISH is required
 to investigate the presence of a MYC rearrangement in cases of aggressive B-cell lymphoma, in order to guide the chemotherapeutic
 regime offered to the pa...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5573446</comments>
            <pubDate>Wed, 04 Jan 2012 06:58:24 +0100</pubDate>
            <guid isPermaLink="false">5573446</guid>        </item>
        <item>
            <title>Diffuse large B cell lymphoma evolving from extranodal marginal zone lymphoma as the first presentation of complicated coeliac disease: case report and review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=5546088&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fgq883354w677t299%2F</link>
            <description>Content Type Journal ArticleCategory Case ReportPages 1-5DOI 10.1007/s12308-011-0126-4Authors
		Mireille J. Hardie, PathWest Laboratory Medicine, QEII Medical Centre; and School of Pathology and Laboratory Medicine, University of Western Australia, Hospital Avenue, Nedlands, WA, AustraliaIsaac A. Thyer, Urology Department, Royal Perth Hospital, Wellington St, East Perth, WA, AustraliaTindaro Giardina, PathWest Laboratory Medicine, QEII Medical Centre, Hospital Avenue, Nedlands, WA, AustraliaMichael A. Platten, PathWest Laboratory Medicine, QEII Medical Centre, Hospital Avenue, Nedlands, WA, AustraliaMartin J. Hudson, Geraldton Regional Hospital, Shenton Street, Geraldton, WA, AustraliaPaul J. Drury, Geraldton Regional Hospital, Shenton Street, Geraldton, WA, AustraliaDominic Spagnolo, Pa...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5546088</comments>
            <pubDate>Wed, 21 Dec 2011 20:08:46 +0100</pubDate>
            <guid isPermaLink="false">5546088</guid>        </item>
        <item>
            <title>Donor-derived isolated del(20q) after hematopoietic stem cell transplantation: report of two cases and review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=5516647&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn761421610558447%2F</link>
            <description>Content Type Journal ArticleCategory Case ReportPages 1-8DOI 10.1007/s12308-011-0123-7Authors
		Rashmi Kanagal-Shamanna, Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USACarlos E. Bueso-Ramos, Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USASu S. Chen, Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USALynne V. Abruzzo, Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USAMarcos J. de Lima, Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USARachel L. Sargent, Department of Hematopathology, The University of Texas MD Anderson...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5516647</comments>
            <pubDate>Wed, 14 Dec 2011 16:30:53 +0100</pubDate>
            <guid isPermaLink="false">5516647</guid>        </item>
        <item>
            <title>ALK-positive anaplastic large cell lymphoma expressing membranous D2-40 immunopositivity and mimicking seminoma: potential diagnostic pitfall</title>
            <link>http://www.medworm.com/index.php?rid=5507285&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh7v18188r7l5m54j%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s12308-011-0127-3Authors
		Marián Švajdler, Department of pathology, L.Pasteur University Hospital, Trieda SNP 1, Košice, SlovakiaLucia Fröhlichová, Department of pathology, L.Pasteur University Hospital, Trieda SNP 1, Košice, SlovakiaMarián Benický, Department of pathology, L.Pasteur University Hospital, Trieda SNP 1, Košice, SlovakiaTomáš Torday, Department of pathology, L.Pasteur University Hospital, Trieda SNP 1, Košice, Slovakia
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5507285</comments>
            <pubDate>Mon, 12 Dec 2011 17:14:28 +0100</pubDate>
            <guid isPermaLink="false">5507285</guid>        </item>
        <item>
            <title>Multiple clonal Ig/TCR products: implications for interpretation of clonality findings</title>
            <link>http://www.medworm.com/index.php?rid=5496825&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq5653x467078h863%2F</link>
            <description>In conclusion, straightforward interpretation of clonality testing results can be hampered by the occurrence of multiple clonal
 products. Only careful consideration of immunobiological and technical explanations will prevent incorrect interpretation
 in such cases.
 
 
	Content Type Journal ArticleCategory ReviewPages 1-9DOI 10.1007/s12308-011-0129-1Authors
		Anton W. Langerak, Department of Immunology, Erasmus MC, University Medical Center Rotterdam, Dr. Molewaterplein 50, 3015 GE Rotterdam, The NetherlandsJacques J. M. van Dongen, Department of Immunology, Erasmus MC, University Medical Center Rotterdam, Dr. Molewaterplein 50, 3015 GE Rotterdam, The Netherlands
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496825</comments>
            <pubDate>Fri, 09 Dec 2011 17:05:59 +0100</pubDate>
            <guid isPermaLink="false">5496825</guid>        </item>
        <item>
            <title>A comparative analysis of protocols for detection of T cell clonality in formalin-fixed, paraffin-embedded tissue—implications for practical use</title>
            <link>http://www.medworm.com/index.php?rid=5496826&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg0847227333576n6%2F</link>
            <description>In conclusion, BIOMED-2 TCRγ and TCRβ assays show superior sensitivity for
 the detection of T cell clonality. However, the complexity of BIOMED-2 protocols requires stringent quality control and experience
 in interpreting GeneScan patterns.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-10DOI 10.1007/s12308-011-0128-2Authors
		Irina Bonzheim, Institute of Pathology, University Hospital and Comprehensive Cancer Center Tübingen, Liebermeisterstr. 8, 72076 Tübingen, GermanyFlorian Fröhlich, Institute of Pathology, University Hospital and Comprehensive Cancer Center Tübingen, Liebermeisterstr. 8, 72076 Tübingen, GermanyPatrick Adam, Institute of Pathology, University Hospital and Comprehensive Cancer Center Tübingen, Liebermeisterstr. 8, 72076 Tübingen, GermanySem...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496826</comments>
            <pubDate>Fri, 09 Dec 2011 17:05:58 +0100</pubDate>
            <guid isPermaLink="false">5496826</guid>        </item>
        <item>
            <title>Splenic marginal zone lymphoma with t(8;14)(q24.1;q32)/MYC rearrangement</title>
            <link>http://www.medworm.com/index.php?rid=5478725&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk326767m8111g83w%2F</link>
            <description>Content Type Journal ArticleCategory Case ReportPages 1-7DOI 10.1007/s12308-011-0124-6Authors
		Rebecca Sonu, Department of Pathology and Laboratory Medicine, University of California, Davis, Medical Center, PATH Bldg. 4400 V Street, Sacramento, CA 95817, USAJeffrey Gregg, Department of Pathology and Laboratory Medicine, University of California, Davis, Medical Center, PATH Bldg. 4400 V Street, Sacramento, CA 95817, USAMingyi Chen, Department of Pathology and Laboratory Medicine, University of California, Davis, Medical Center, PATH Bldg. 4400 V Street, Sacramento, CA 95817, USA
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5478725</comments>
            <pubDate>Fri, 02 Dec 2011 06:48:16 +0100</pubDate>
            <guid isPermaLink="false">5478725</guid>        </item>
        <item>
            <title>The EuroClonality website: information, education and support on clonality testing</title>
            <link>http://www.medworm.com/index.php?rid=5470570&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F771268716414686q%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Clonality assessment is an established tool in the diagnosis of malignant lymphoma; however, the evaluation of immunoglobulin/T-cell
 receptor (Ig/TCR) gene rearrangement profiles is not always straightforward. Therefore, the EuroClonality group supports and
 advises diagnostic laboratories in their clonality assessments on samples from patients suspicious for lymphoma, who are seen
 in the routine diagnostic setting. The support for clonality assessment is provided via the EuroClonality website: http://www.euroclonality.org. The features and procedures of the website are presented in this paper.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-5DOI 10.1007/s12308-011-0120-xAuthors
		Paul D. M. Rombout, Department of Pathology, Radboud University Nijmeg...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5470570</comments>
            <pubDate>Wed, 30 Nov 2011 04:56:25 +0100</pubDate>
            <guid isPermaLink="false">5470570</guid>        </item>
        <item>
            <title>Rising costs of health care and pathology: cause or solution?</title>
            <link>http://www.medworm.com/index.php?rid=5450935&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg51613w271w3xt03%2F</link>
            <description>Content Type Journal ArticleCategory EditorialPages 1-1DOI 10.1007/s12308-011-0122-8Authors
		J. Han van Krieken, Department of Pathology, Radboud University Nijmegen Medical Center, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5450935</comments>
            <pubDate>Thu, 24 Nov 2011 17:53:22 +0100</pubDate>
            <guid isPermaLink="false">5450935</guid>        </item>
        <item>
            <title>Book review: A pattern approach to lymph node diagnosis by Anthony S-Y Leong</title>
            <link>http://www.medworm.com/index.php?rid=5450936&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1m7860921j1m6736%2F</link>
            <description>Content Type Journal ArticleCategory Book ReviewPages 1-1DOI 10.1007/s12308-011-0121-9Authors
		J. Han van Krieken, Department of Pathology, Radboud University Nijmegen Medical Centre, P.O. Box 9101, 6500 Nijmegen, The Netherlands
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5450936</comments>
            <pubDate>Thu, 24 Nov 2011 06:51:25 +0100</pubDate>
            <guid isPermaLink="false">5450936</guid>        </item>
        <item>
            <title>t(14;19)(q32;q13)-associated B-cell neoplasms—a review</title>
            <link>http://www.medworm.com/index.php?rid=5433479&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp00006829u511347%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The t(14;19)(q32;q13) is a rare cytogenetic abnormality that occurs in &amp;lt;0.1% of all B-cell neoplasms. The majority of these
 cases has been categorised as “atypical” chronic lymphocytic leukaemia (CLL). Although the clinical presentation is similar
 to CLL, these patients are often younger, with a stronger male predominance and the disease is reported to have a more aggressive
 clinical course. The peripheral blood/bone marrow aspirate morphology is “atypical”, but these differences are not recognised
 on bone marrow or lymph node histology. The immunoprofile is CD5 positive and usually CD23 dim/negative with a low Matutes
 CLL score. Fluorescence in situ hybridisation confirms the presence of the translocation giving rise to IGH/BCL3 fusion. Many
 cases also...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5433479</comments>
            <pubDate>Fri, 18 Nov 2011 06:56:27 +0100</pubDate>
            <guid isPermaLink="false">5433479</guid>        </item>
        <item>
            <title>Capillary electrophoresis single-strand conformation analysis (CE-SSCA) for clonality detection in lymphoproliferative disorders</title>
            <link>http://www.medworm.com/index.php?rid=5411594&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F842tw73811412313%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Clonality analysis is a critical tool for the diagnosis of suspect lymphoproliferative disorders. Amplification of the immunoglobulin
 and T cell receptor genes on genomic DNA from the suspect samples is followed by analysis of the PCR products to distinguish
 between polyclonal and clonal rearrangements. These analyses are based on electrophoresis in polyacrylamide gels after heteroduplex
 formation, or more frequently, GeneScan analysis is performed by capillary electrophoresis in automated DNA analysers, providing
 higher resolution and sensitivity. An alternative method for clonality analysis is the use of single-strand conformation analysis;
 however, this usually required labour intensive work with polyacrylamide gels and radioactive labelling. Within the EuroClon...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5411594</comments>
            <pubDate>Mon, 14 Nov 2011 16:52:45 +0100</pubDate>
            <guid isPermaLink="false">5411594</guid>        </item>
        <item>
            <title>Emergence of JAK2-mutant primary myelofibrosis in myelodysplastic syndrome: rare case report, literature review, and implications for clonal progression</title>
            <link>http://www.medworm.com/index.php?rid=5338851&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa44n7x7433602451%2F</link>
            <description>Content Type Journal ArticleCategory Case ReportPages 1-5DOI 10.1007/s12308-011-0118-4Authors
		Michael J. Rauh, Department of Pathology and Molecular Medicine, Richardson Laboratory, Queen’s University, 88 Stuart Street, Kingston, ON K7L 3N6, CanadaJane Liesveld, Department of Medicine, University of Rochester Medical Center, Rochester, USAW. Richard Burack, Department of Pathology, Hematopathology Section, the James P. Wilmot Cancer Center, University of Rochester Medical Center, 601 Elmwood Avenue, Rochester, NY 14642, USAJohn M. Bennett, Department of Medicine, University of Rochester Medical Center, Rochester, USA
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5338851</comments>
            <pubDate>Mon, 17 Oct 2011 16:03:58 +0100</pubDate>
            <guid isPermaLink="false">5338851</guid>        </item>
        <item>
            <title>Perifollicular granulomatous inflammation in reactive lymph nodes: a possible morphologic marker for IgG4 plasmacytosis</title>
            <link>http://www.medworm.com/index.php?rid=5317332&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv464rg1441v46704%2F</link>
            <description>This study adds to the morphologic spectrum
 of IgG4-related lymphadenopathy.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s12308-011-0117-5Authors
		Imran N. Siddiqi, Department of Pathology, University of Southern California Keck School of Medicine, 2011 Zonal Ave., HMR 209, Los Angeles, CA 90033, USARussell K. Brynes, Department of Pathology, University of Southern California Keck School of Medicine, 2011 Zonal Ave., HMR 209, Los Angeles, CA 90033, USAKate Grimm, Clarient Inc./GE Healthcare, Aliso Viejo, CA, USADennis P. O’Malley, Clarient Inc./GE Healthcare, Aliso Viejo, CA, USAEndi Wang, Department of Pathology, Duke University Medical Center, Durham, NC, USA
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256 (Source: Journal of Hematopat...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5317332</comments>
            <pubDate>Tue, 11 Oct 2011 15:53:21 +0100</pubDate>
            <guid isPermaLink="false">5317332</guid>        </item>
        <item>
            <title>Transformation of double-hit large B-cell lymphoma into B-lymphoblastic lymphoma: a case report</title>
            <link>http://www.medworm.com/index.php?rid=5276590&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fnx2n3631wrlq0451%2F</link>
            <description>We describe a 55-year-old
 male who initially presented in March 2010 with significant ascites and extensive lymphadenopathy. A diagnosis of B-cell lymphoma,
 unclassifiable with features intermediate between diffuse large B-cell lymphoma and Burkitt lymphoma, was made in both peritoneal
 fluid and bone marrow. The malignant cells expressed CD10, CD19, CD20, CD45 (bright), CD79b, and monotypic kappa light chain,
 but were negative for TdT. Both IGH/BCL2 and IGL/MYC gene rearrangements were identified by FISH. Following chemotherapy,
 the patient remained in morphologic and cytogenetic remission for approximately 4&amp;nbsp;months. At relapse, a precursor B-cell lymphoma
 was detected in the diaphragm, pleural wall, and pleural effusion. The malignant cells were TdT positive and were negative
 ...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5276590</comments>
            <pubDate>Wed, 28 Sep 2011 05:51:16 +0100</pubDate>
            <guid isPermaLink="false">5276590</guid>        </item>
        <item>
            <title>Acute promyelocytic leukemia with a novel variant (15;17) rearrangement</title>
            <link>http://www.medworm.com/index.php?rid=5276591&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fwhh613j066r517w5%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-3DOI 10.1007/s12308-011-0114-8Authors
		Michael Bellone, Department of Anatomic Pathology, Stony Brook University Medical Center, Stony Brook, NY 11794, USAAnn-Leslie Zaslav, Cytogenetics, Department of Clinical Pathology, Stony Brook University Medical Center, Stony Brook, NY 11794, USABonnie Kiner-Strachan, Department of Medicine, Bone Marrow Transplant Unit, Stony Brook University Medical Center, Stony Brook, NY 11794, USAMarc Golightly, Flow Cytometry, Department of Clinical Pathology, Stony Brook University Medical Center, Stony Brook, NY 11794, USATheresa Mercado, Cytogenetics, Department of Clinical Pathology, Stony Brook University Medical Center, Stony Brook, NY 11794, USATahmeena Ahmed, Department of Anatomic Path...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5276591</comments>
            <pubDate>Wed, 28 Sep 2011 05:51:15 +0100</pubDate>
            <guid isPermaLink="false">5276591</guid>        </item>
        <item>
            <title>New developments in the pathology of malignant lymphoma. A review of the literature published from February 2011 to August 2011</title>
            <link>http://www.medworm.com/index.php?rid=5228700&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb8285776336j69n1%2F</link>
            <description>Content Type Journal ArticleCategory Review of the LiteraturePages 135-144DOI 10.1007/s12308-011-0112-xAuthors
		J. Han van Krieken, Department of Pathology, Radboud University Nijmegen Medical Centre, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256
	
		Journal Volume Volume 4
	
		Journal Issue Volume 4, Number 3 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5228700</comments>
            <pubDate>Tue, 13 Sep 2011 05:52:11 +0100</pubDate>
            <guid isPermaLink="false">5228700</guid>        </item>
        <item>
            <title>Parvovirus B19 infection associated with severe chronic aplastic anaemia—a case report</title>
            <link>http://www.medworm.com/index.php?rid=5212531&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4833366x88888r1k%2F</link>
            <description>We report a case of parvovirus B19-associated chronic aplastic anaemia in a 34-year-old female patient who presented with
 gum bleeding and ecchymotic patches over both legs and curdy vaginal discharge. She had pancytopenia on peripheral blood film
 examination and was subjected to bone marrow biopsy as the marrow aspirate showed peripheral blood only hence was not conclusive.
 Bone marrow biopsy was reported as AA, severe grade. The serological analysis performed later on revealed parvovirus B19 infection.
 Acute infection with B19V should be considered as a cause of acquired aplastic anaemia in individuals where other etiological
 factors are not elucidated.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-4DOI 10.1007/s12308-011-0113-9Authors
		Rajeev Sen, Department of Path...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5212531</comments>
            <pubDate>Fri, 09 Sep 2011 05:49:08 +0100</pubDate>
            <guid isPermaLink="false">5212531</guid>        </item>
        <item>
            <title>M.A. Proytcheva (ed): Diagnostic pediatric hematopathology</title>
            <link>http://www.medworm.com/index.php?rid=5212532&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0773g6588h776152%2F</link>
            <description>Content Type Journal ArticleCategory Book ReviewPages 1-1DOI 10.1007/s12308-011-0110-zAuthors
		Konnie Hebeda, Department of Pathology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5212532</comments>
            <pubDate>Wed, 07 Sep 2011 15:48:47 +0100</pubDate>
            <guid isPermaLink="false">5212532</guid>        </item>
        <item>
            <title>Diagnostic pathology: lymph nodes and spleen with extranodal lymphomas</title>
            <link>http://www.medworm.com/index.php?rid=5212534&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F63316871576p2566%2F</link>
            <description>Content Type Journal ArticleCategory Book ReviewPages 1-2DOI 10.1007/s12308-011-0109-5Authors
		Han van Krieken, Department of Pathology, Radboud University Nijmegen Medical Centre, P.O. Box 9101, 6500 Nijmegen, The Netherlands
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5212534</comments>
            <pubDate>Wed, 07 Sep 2011 15:48:46 +0100</pubDate>
            <guid isPermaLink="false">5212534</guid>        </item>
        <item>
            <title>Crisis? What crisis?</title>
            <link>http://www.medworm.com/index.php?rid=5212533&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff282kr86276t7x46%2F</link>
            <description>Content Type Journal ArticleCategory EditorialPages 1-1DOI 10.1007/s12308-011-0111-yAuthors
		J. Han van Krieken, Department of Pathology, Radboud University Nijmegen Medical Center, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5212533</comments>
            <pubDate>Wed, 07 Sep 2011 15:48:46 +0100</pubDate>
            <guid isPermaLink="false">5212533</guid>        </item>
        <item>
            <title>High prevalence of adverse prognostic genetic aberrations and unmutated IGHV genes in small lymphocytic lymphoma as compared to chronic lymphocytic leukemia</title>
            <link>http://www.medworm.com/index.php?rid=5186288&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp752t2473pp821px%2F</link>
            <description>In this study, we evaluated the presence of genetic abnormalities and (immunoglobulin heavy chain
 variable genes) IGHV use and mutation status in lymph node samples of patients presenting with lymphadenopathy alone and, therefore, classified
 as SLL (n = 21) or with persisting lymphadenopathy and absolute lymphocyte counts of ≥5 × 109/L and, therefore, classified as CLL/SLL (n = 17). In addition, blood samples of CLL patients were evaluated (n = 82). The majority of lymph node samples from SLL patients (66%) showed unmutated IGHV genes. This occurrence was significantly higher than in CLL (29%). Poor risk genetic aberrations (11q-, 17p-, and +12) were
 more prevalent in the SLL (45%) as compared to CLL (22%). Samples from CLL/SLL patients exhibited almost equal frequenc...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5186288</comments>
            <pubDate>Wed, 31 Aug 2011 15:56:09 +0100</pubDate>
            <guid isPermaLink="false">5186288</guid>        </item>
        <item>
            <title>Nodular lymphocyte-predominant Hodgkin lymphoma of the tonsil: a case study using immunohistochemistry and FISH analysis and review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=5149086&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fhr2036216hjk987v%2F</link>
            <description>We present a case of NLPHL arising in the tonsil of a 43-year-old man.
 The patient presented with a submucosal mass in an asymmetrically enlarged tonsil. Bilateral tonsillectomy was performed and
 histological examination showed effacement of the enlarged tonsil by nodules comprised of scattered large atypical cells having
 classic lymphocyte-predominant cell morphology in a background of benign B cells. Immunohistochemical analysis showed lack
 of CD15 and CD30 in the LP cells and strong expression of CD20, CD45, BCL-6 and epithelial membrane antigen (EMA). Interphase
 fluorescence in situ hybridization (FISH) analysis, revealed bcl-6 gene rearrangement in the LP cells. Although lymphoma is
 a common malignancy of the tonsil, there are only sporadic reports of NLPHL arising in this locat...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5149086</comments>
            <pubDate>Wed, 17 Aug 2011 05:54:23 +0100</pubDate>
            <guid isPermaLink="false">5149086</guid>        </item>
        <item>
            <title>Erratum to: Two morphologically and immunophenotypically distinct cell populations within a composite lymphoma arise from a common precursor</title>
            <link>http://www.medworm.com/index.php?rid=5127744&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fbn64u69x484ph157%2F</link>
            <description>Content Type Journal ArticlePages 1-1DOI 10.1007/s12308-011-0107-7Authors
		Harry Zhang, Department of Pathology and Laboratory Medicine, Wayne State University School of Medicine, Detroit, MI 48201, USAHossein Salimnia, Department of Pathology and Laboratory Medicine, Wayne State University School of Medicine, Detroit, MI 48201, USAGail Bentley, Department of Pathology and Laboratory Medicine, Wayne State University School of Medicine, Detroit, MI 48201, USAWeimin Liu, Department of Pathology and Laboratory Medicine, Wayne State University School of Medicine, Detroit, MI 48201, USAMichele Phillips, Detroit Medical Center University Laboratories, Detroit Medical Center, Detroit, MI 48201, USAGerald L. Feldman, Department of Pathology and Laboratory Medicine, Wayne State University School...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5127744</comments>
            <pubDate>Fri, 12 Aug 2011 06:15:13 +0100</pubDate>
            <guid isPermaLink="false">5127744</guid>        </item>
        <item>
            <title>Is relapse of mantle cell lymphoma (MCL) preceded by an “in situ” pattern in an otherwise reactive lymph node in a patient with history of MCL?</title>
            <link>http://www.medworm.com/index.php?rid=5099439&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fau2u84341347p561%2F</link>
            <description>Content Type Journal ArticlePages 1-5DOI 10.1007/s12308-011-0105-9Authors
		Changlee S. Pang, Department of Pathology, Wake Forest University School of Medicine, Medical Center Boulevard, Winston-Salem, NC 27157-1072, USAMark J. Pettenati, Department of Medical Genetics, Wake Forest University School of Medicine, Medical Center Boulevard, Winston-Salem, NC 27157-1072, USACyrus Manavi, Department of Pathology, Wake Forest University School of Medicine, Medical Center Boulevard, Winston-Salem, NC 27157-1072, USAKenneth W. Zamkoff, Department of Hematology and Oncology, Wake Forest University School of Medicine, Medical Center Boulevard, Winston-Salem, NC 27157-1072, USA
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5099439</comments>
            <pubDate>Tue, 02 Aug 2011 05:55:30 +0100</pubDate>
            <guid isPermaLink="false">5099439</guid>        </item>
        <item>
            <title>Nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL) with CD30-positive lymphocyte-predominant (LP) cells</title>
            <link>http://www.medworm.com/index.php?rid=5065421&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk272h43321857027%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL) is a distinct neoplasm within the spectrum of Hodgkin lymphomas with
 characteristic clinical, morphological, and immunohistochemical features. According to the WHO definition, lymph nodes involved
 by NLPHL should have a nodular or nodular and diffuse proliferation of scattered large neoplastic lymphocyte-predominant (LP)
 cells in a small cell background that reside in expanded follicular dendritic cell meshworks; the LP cells must also have
 a distinct immunophenotypic profile. The LP cells are monoclonal B cells that are typically CD20, BCL6, CD79a, and CD45 positive
 and are CD30 and CD15 negative. In contrast, the Reed-Sternberg cells of classical Hodgkin lymphoma (CHL) are typically positive
 for CD15 and CD...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5065421</comments>
            <pubDate>Sat, 23 Jul 2011 05:55:20 +0100</pubDate>
            <guid isPermaLink="false">5065421</guid>        </item>
        <item>
            <title>T lymphoblastic leukemia/lymphoma and human immunodeficiency virus infection</title>
            <link>http://www.medworm.com/index.php?rid=5058662&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3647083027784t46%2F</link>
            <description>Content Type Journal ArticlePages 1-3DOI 10.1007/s12308-011-0103-yAuthors
		Kamraan Z. Gill, Departments of Pathology and Cell Biology, Columbia University Medical Center and New York Presbyterian Hospital, 630 W. 168 St., VC14-229, New York, NY 10032, USAShafinaz Hussein, Departments of Pathology and Cell Biology, Columbia University Medical Center and New York Presbyterian Hospital, 630 W. 168 St., VC14-229, New York, NY 10032, USAYuxia Jia, Division of Hematology/Oncology, Columbia University Medical Center and New York Presbyterian Hospital, New York, NY, USAVundavalli V. Murty, Departments of Pathology and Cell Biology, Columbia University Medical Center and New York Presbyterian Hospital, 630 W. 168 St., VC14-229, New York, NY 10032, USAGovind Bhagat, Departments of Pathology and C...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5058662</comments>
            <pubDate>Thu, 21 Jul 2011 18:06:20 +0100</pubDate>
            <guid isPermaLink="false">5058662</guid>        </item>
        <item>
            <title>Isolated intraorbital intravascular large B-cell lymphoma: a case report</title>
            <link>http://www.medworm.com/index.php?rid=5043095&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F26x76662r4122065%2F</link>
            <description>We report the case of an 88-year-old woman who initially presented with pain, swelling, and loss of vision
 in her left eye. A left orbital mass was revealed by computed tomography, and a biopsy was performed. On histologic examination,
 large atypical lymphoid cells were present in blood vessel lumina of the intraorbital adipose tissue. No tumor cells were
 seen in the surrounding tissue. By immunohistochemistry, the tumor cells were positive for CD20, BCL-2, Bcl-6, and CD5; they
 were negative for CD10 and cyclin D1. Ki-67 revealed a proliferation rate of approximately 80–90%, and CD31 highlighted the
 vascular endothelium. These findings confirmed the diagnosis of intravascular large B-cell lymphoma. Results of bone marrow
 and cerebrospinal fluid examinations were negative for involv...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5043095</comments>
            <pubDate>Thu, 14 Jul 2011 06:00:43 +0100</pubDate>
            <guid isPermaLink="false">5043095</guid>        </item>
        <item>
            <title>Two morphologically and immunophenotypically distinct cell populations within a composite lymphoma arise from a common precursor</title>
            <link>http://www.medworm.com/index.php?rid=5012718&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe7628h8003q70268%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The term composite lymphoma defines a lymphoma consisting of two or more morphologically and immunophenotypically distinct
 lymphomas within the same lymph node or other organ. Recently, several molecular studies have shown that different components
 within a composite lymphoma may arise from a common clone. In contrast, there are also reports of biclonal cases of composite
 lymphoma. For this study, we identified five cases of composite lymphoma and analyzed them by various techniques to determine
 the clonality of the components. In four cases (1–4), a laser capture microdissection technique was used to collect separately
 each of the component lymphoma types. These were analyzed by polymerase chain reaction (PCR) to assess the rearrangement of
 the J segment of the...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5012718</comments>
            <pubDate>Fri, 08 Jul 2011 06:32:41 +0100</pubDate>
            <guid isPermaLink="false">5012718</guid>        </item>
        <item>
            <title>Bone marrow infiltration by cells resembling plasmablasts in a patient with blastic plasmacytoid dendritic cell neoplasm</title>
            <link>http://www.medworm.com/index.php?rid=4940476&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4n544536xn4h8w38%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a clinically aggressive hematologic malignancy derived from clonal
 proliferation of plasmacytoid dendritic cells. The disease has two patterns of presentation: cutaneous and leukemic. Herein
 we describe the case of a 9-year-old boy who presented with an unusual morphologic variant of leukemic BPDCN, showing bone
 marrow infiltration by medium to large cells with eccentric nuclei, regular round to oval shape, finely dispersed chromatin,
 one or more distinct nucleoli, and abundant basophilic cytoplasm, forming a pattern that resembled plasmablasts. Multiparameter
 flow cytometric immunophenotyping confirmed the diagnosis of BPDCN by identifying the expression of CD4++, CD56++, HLA-DR+++, and CD123+++ in abnormal c...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4940476</comments>
            <pubDate>Fri, 10 Jun 2011 06:39:31 +0100</pubDate>
            <guid isPermaLink="false">4940476</guid>        </item>
        <item>
            <title>Grey zone lymphoid neoplasms with features overlapping between splenic marginal zone lymphoma and hairy cell leukaemia: splenic B-cell lymphoma/leukaemia, unclassifiable</title>
            <link>http://www.medworm.com/index.php?rid=4916099&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw14v48752n1366v8%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The best characterized primary splenic B-cell lymphoma/leukaemias include splenic marginal zone lymphoma (SMZL) and hairy
 cell leukaemia (HCL). However, there are other primary splenic B-cell neoplasms that do not have the characteristic features
 of SMZL or HCL. The WHO classification has proposed a provision entity—splenic B-cell lymphoma/leukaemia, unclassifiable (SBLLu)
 to include the better-defined small B-cell clonal lymphoproliferations involving spleen that do not fall into any of the other
 types of B-cell lymphoid neoplasms. The recognized provisional entities among SBLLu include splenic diffuse red pulp small
 B-cell lymphoma (SDRPSBL) and hairy cell leukaemia variant (HCLv). The possibility of SBLLu arises when the spleen shows diffuse
 red pulp involvem...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916099</comments>
            <pubDate>Tue, 07 Jun 2011 15:51:24 +0100</pubDate>
            <guid isPermaLink="false">4916099</guid>        </item>
        <item>
            <title>Bone marrow pathology</title>
            <link>http://www.medworm.com/index.php?rid=4916100&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn1337782m4j460k3%2F</link>
            <description>Content Type Journal ArticlePages 1-1DOI 10.1007/s12308-011-0099-3

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916100</comments>
            <pubDate>Thu, 02 Jun 2011 05:59:52 +0100</pubDate>
            <guid isPermaLink="false">4916100</guid>        </item>
        <item>
            <title>Therapy-related T-cell lymphoblastic lymphoma and inv(11)(q21q23) following acute promyelocytic leukemia chemotherapy</title>
            <link>http://www.medworm.com/index.php?rid=4916101&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh3131724r84m4176%2F</link>
            <description>In this report we present therapy-related
 T-lymphoblastic lymphoma following APL treatment. The bone marrow analysis showed MLL and MAML2 genes rearrangement that can
 explain the molecular basis for the lymphoma development.
 
 
	Content Type Journal ArticlePages 1-5DOI 10.1007/s12308-011-0100-1Authors
		Alireza Torabi, Department of Pathology and Laboratory Medicine, William Beaumont Hospital, Royal Oak, MI, USAMohammad M. Chisti, Department of Medical Oncology, William Beaumont Hospital, Royal Oak, MI, USAGovinda Brahmanday, Department of Medical Oncology, William Beaumont Hospital, Royal Oak, MI, USAVonda Douglas-Nikitin, Department of Pathology and Laboratory Medicine, William Beaumont Hospital, Royal Oak, MI, USAAlaa Muslimani, Department of Medical Oncology, William Beaumont Hospit...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916101</comments>
            <pubDate>Wed, 01 Jun 2011 05:59:12 +0100</pubDate>
            <guid isPermaLink="false">4916101</guid>        </item>
        <item>
            <title>Progression of myeloproliferative neoplasms to myelofibrosis and acute leukaemia</title>
            <link>http://www.medworm.com/index.php?rid=4916102&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq41286301678636g%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Bcr-abl-negative myeloproliferative neoplasms (MPN), comprising polycythaemia vera (PV), primary myelofibrosis (PMF) and essential
 thrombocythaemia (ET), usually follow a biphasic course. From a phase which is characterized by excess production of mature
 haematopoietic cells of one or more lineages, many, but not all MPN, progress to haematopoietic insufficiency with cytopenia
 affecting two or three lineages. The latter may be the result of either fibrosis, blastic transformation or both. An intermediate
 stage of variable duration is called acceleration. Unlike bcr-abl-positive chronic myeloid leukaemia (CML), acceleration in
 MPN is not homogeneously defined. Long-lasting PV may progress to a PMF-like myelofibrosis, labelled spent phase. Less frequently,
 PV develo...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916102</comments>
            <pubDate>Mon, 30 May 2011 16:43:25 +0100</pubDate>
            <guid isPermaLink="false">4916102</guid>        </item>
        <item>
            <title>Eosinophil, basophil, and mast cell infiltrates in the bone marrow: crossing the boundaries of diagnosis</title>
            <link>http://www.medworm.com/index.php?rid=4916103&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4513774682mv2t65%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;An increase in eosinophils, basophils, and/or mast cells in the bone marrow may pose considerable diagnostic problems for
 the hematopathologist. In a first step, it is crucial to classify these changes as either being reactive or neoplastic. A
 slight increase in eosinophils is often seen in reactive states of myeloid hyperplasia while an increase in basophils is usually
 indicative of a neoplastic hematologic disorder. Regarding mast cells, the presence of compact infiltrates is the major criterion
 for systemic mastocytosis whereas a diffuse interstitial increase is often encountered in reactive states of mast cell hyperplasia.
 When a neoplastic disorder is diagnosed, definitive classification depends on immunohistochemical, molecular, and cytogenetic
 markers. The ...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916103</comments>
            <pubDate>Fri, 27 May 2011 18:15:09 +0100</pubDate>
            <guid isPermaLink="false">4916103</guid>        </item>
        <item>
            <title>The AML–MDS interface—leukemic transformation in myelodysplastic syndromes</title>
            <link>http://www.medworm.com/index.php?rid=4916104&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg58802621062k88k%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;On average, 30% of patients with myelodysplastic syndrome (MDS) develop overt acute myeloid leukemia (AML) during the course
 of the disease. There is a continuous search for the best model of individual risk assessment for MDS patients. In this review,
 we summarize current findings on factors that have been associated with increased risk of AML transformation. These include
 laboratory values such as high lactate dehydrogenase levels, complex karyotypes, numbers and aberrant immunophenotype of bone
 marrow blasts, bone marrow-related features such as numbers and distribution of CD34+ cells, and recently established molecular
 markers. A wide range of described molecular aberrations in MDS, including various gene mutations, chromosomal instability,
 short telomeres, hi...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916104</comments>
            <pubDate>Wed, 25 May 2011 16:06:35 +0100</pubDate>
            <guid isPermaLink="false">4916104</guid>        </item>
        <item>
            <title>The first special issue of the Journal of Hematopathology</title>
            <link>http://www.medworm.com/index.php?rid=4916105&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy4r2062618733171%2F</link>
            <description>Content Type Journal ArticlePages 1-1DOI 10.1007/s12308-011-0095-7Authors
		Han van Krieken, Department of Pathology, Radboud University Nijimegen Medical Center, Postbus 9101, 6500 HB Nijimegen, The Netherlands
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916105</comments>
            <pubDate>Wed, 25 May 2011 16:06:33 +0100</pubDate>
            <guid isPermaLink="false">4916105</guid>        </item>
        <item>
            <title>The hematopathologist as detective</title>
            <link>http://www.medworm.com/index.php?rid=4916106&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F331513g187q75q11%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The skills required of a physician are akin to those of a detective, fictional or real. The diagnostic process is based on
 observation, deduction, and inference. We may thus see the hematopathologist as using the same skills as a detective. Sometimes,
 the hematopathologist is involved, usually inadvertently, in the detection of actual crime or other illicit activity. More
 often, the skills of a detective are being applied in the normal diagnostic process.
 
 
	Content Type Journal ArticlePages 1-4DOI 10.1007/s12308-011-0098-4Authors
		Barbara J. Bain, Department of Haematology, St Mary’s Hospital Campus of Imperial College Faculty of Medicine, St Mary’s Hospital, Praed Street, London, W2 1NY UK
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256 (Source...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916106</comments>
            <pubDate>Tue, 24 May 2011 16:04:32 +0100</pubDate>
            <guid isPermaLink="false">4916106</guid>        </item>
        <item>
            <title>Chronic myelogenous leukemia in the age of imatinib: assessing response, acceleration, and blast phase</title>
            <link>http://www.medworm.com/index.php?rid=4916107&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh1n8045p3431u504%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Chronic myelogenous leukemia, BCR-ABL1+ (CML) is a myeloproliferative neoplasm defined by the presence of the BCR-ABL fusion gene and a t(9;22)(q34;q11) cytogenetic abnormality. Its natural history is that of inexorable progression to an acute
 leukemia (blast crisis) after a prolonged chronic phase. The recent development of imatinib and other inhibitors of BCR-ABL tyrosine kinase activity has dramatically altered the clinical course of CML, with long-term remissions in most patients
 treated early in the course of the disease. Monitoring of resistance to therapy and progression on therapy are critical in
 the current management of the disease. Problems facing the diagnostic pathologist in this “Age of Imatinib” include accurate
 diagnosis and determination of CML ...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916107</comments>
            <pubDate>Fri, 20 May 2011 16:16:04 +0100</pubDate>
            <guid isPermaLink="false">4916107</guid>        </item>
        <item>
            <title>Acute myeloid leukemia with an unusual histologic pattern mimicking metastatic carcinoma in bone marrow: a diagnostic pitfall</title>
            <link>http://www.medworm.com/index.php?rid=4916108&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F81412v3418241105%2F</link>
            <description>We describe two cases of acute myeloid leukemia with an unusual histological pattern mimicking metastatic non-hematopoietic
 neoplasm, leading to diagnostic difficulties. Both patients presented with pancytopenia and absence of circulating blasts.
 Bone marrow aspirations were not successful. Bone marrow core biopsies contained neoplastic cells arranged in cohesive sheets
 or single file patterns with prominent myxoid stroma resembling metastatic carcinoma. The accompanying bone marrow touch imprints
 showed clusters of immature cells with monocytoid features. The cell lineage was further revealed by immunohistochemical analysis
 of bone marrow core biopsy sections. The neoplastic cells showed strong reactivity for myeloperoxidase, CD33, CD43, CD45,
 and CD68, indicating a myeloid cell ori...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916108</comments>
            <pubDate>Mon, 16 May 2011 15:47:28 +0100</pubDate>
            <guid isPermaLink="false">4916108</guid>        </item>
        <item>
            <title>New insights into the pathobiology of chronic lymphocytic leukemia</title>
            <link>http://www.medworm.com/index.php?rid=4916109&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0j210205n5k26710%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Chronic lymphocytic leukemia (CLL) is a heterogeneous disease with a varying clinical outcome; however, the pathogenic mechanisms
 involved in disease development have remained largely unknown. In recent years, novel biomarkers, such as certain recurrent
 genomic alterations and the immunoglobulin heavy variable gene mutational status, have significantly improved the subdivision
 of the disease along with the prognostic assessment of individual patients. Advanced molecular studies have also revealed
 important genetic/epigenetic events and potential susceptibility loci for CLL, as well as implicating antigens in CLL development.
 Furthermore, the presence of monoclonal B cell lymphocytosis (MBL) has been demonstrated to precede CLL and appears to be
 a pre-leukemic cond...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916109</comments>
            <pubDate>Mon, 16 May 2011 15:47:27 +0100</pubDate>
            <guid isPermaLink="false">4916109</guid>        </item>
        <item>
            <title>Inherited bone marrow failure syndromes</title>
            <link>http://www.medworm.com/index.php?rid=4916110&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft040027148t21194%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The inherited bone marrow failure syndromes are a diverse group of disorders characterized by BM failure usually in association
 with one or more somatic/physical abnormality. Over the last two decades, the genes responsible for many of these have been
 identified. The significant advances in their molecular basis have provided insights into several biological pathways, such
 as DNA repair and telomere maintenance, of importance in human physiology. They have also provided a link between the inherited
 and idiopathic forms of bone marrow failure syndromes; for example, some patients with idiopathic forms of aplastic anemia
 have mutations in genes first identified in the classic forms of dyskeratosis congenita. Clinical similarities (bone marrow
 failure, developmental ...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916110</comments>
            <pubDate>Thu, 12 May 2011 16:45:38 +0100</pubDate>
            <guid isPermaLink="false">4916110</guid>        </item>
        <item>
            <title>Audit of the value of bone marrow aspirates when a bone marrow trephine is used for lymphoma staging</title>
            <link>http://www.medworm.com/index.php?rid=4916111&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg443767x822q6mr8%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Bone marrow involvement is assessed in lymphoma staging/restaging following treatment/relapse by a combination of an aspirate
 and trephine biopsy. Of 262 consecutive cases staged by aspirate and trephine, the aspirate yielded a diagnosis when a trephine
 did not in only 11.8%. Trephine biopsies were positive in 34.7% cases and equivocal/insufficient in 14.9%, while aspirates
 were positive in 11.1% cases and equivocal/insufficient in 21%. We suggest that in the majority of cases, it may be acceptable
 either to store an aspirate for reporting only if the trephine is inconclusive or to take a trephine biopsy without an aspirate.
 
 
	Content Type Journal ArticlePages 1-4DOI 10.1007/s12308-011-0087-7Authors
		Zanna J. Voysey, Oxford University Medical School, Oxford, UKE...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916111</comments>
            <pubDate>Tue, 12 Apr 2011 21:37:16 +0100</pubDate>
            <guid isPermaLink="false">4916111</guid>        </item>
        <item>
            <title>New developments in the pathology of malignant lymphoma: a review of the literature published from November 2010–January 2011</title>
            <link>http://www.medworm.com/index.php?rid=4916112&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F33104h36048488r0%2F</link>
            <description>Content Type Journal ArticlePages 31-43DOI 10.1007/s12308-011-0086-8Authors
		J. Han van Krieken, Department of Pathology, Radboud University Nijmegen Medical Centre, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256
	
		Journal Volume Volume 4
	
		Journal Issue Volume 4, Number 1 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916112</comments>
            <pubDate>Wed, 02 Mar 2011 07:46:07 +0100</pubDate>
            <guid isPermaLink="false">4916112</guid>        </item>
        <item>
            <title>The times they are a-changin'</title>
            <link>http://www.medworm.com/index.php?rid=4916113&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj30471q0778264w0%2F</link>
            <description>Content Type Journal ArticlePages 1-1DOI 10.1007/s12308-011-0085-9Authors
		J. H. van Krieken, Department of Pathology, Radboud University Nijmegen Medical Centre, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256
	
		Journal Volume Volume 4
	
		Journal Issue Volume 4, Number 1 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916113</comments>
            <pubDate>Wed, 02 Mar 2011 07:46:06 +0100</pubDate>
            <guid isPermaLink="false">4916113</guid>        </item>
        <item>
            <title>Mantle cell lymphoma with features of marginal-zone lymphoma</title>
            <link>http://www.medworm.com/index.php?rid=4916114&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr627r80536802888%2F</link>
            <description>We present seven cases of mantle cell lymphoma with morphological features of marginal-zone lymphoma. Of particular interest,
 four of the patients had predominant involvement of the gastrointestinal tract. All cases displayed the translocation t(11;14)(q13;q32)
 and expressed cyclin D1. Cytogenetic analysis revealed trisomy 3 in one case and somatic hypermutation of immunoglobulin heavy
 genes could be demonstrated in two out of four cases. The latter features are reminiscent of marginal-zone lymphoma. The localization
 of these lymphomas mainly in the gastrointestinal tract and the higher exposure to antigens in this area may explain why this
 variant of mantle cell lymphoma harbours features of marginal-zone lymphoma.
 
 
	Content Type Journal ArticlePages 7-11DOI 10.1007/s12308-011-008...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916114</comments>
            <pubDate>Wed, 02 Mar 2011 07:46:05 +0100</pubDate>
            <guid isPermaLink="false">4916114</guid>        </item>
        <item>
            <title>Commentary on the WHO 2008 classification of immunodeficiency-associated lymphoproliferative disorders</title>
            <link>http://www.medworm.com/index.php?rid=4916115&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc72u676258418j74%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The 2008 WHO update of Classification of Tumours of Hematopoietic and Lymphoid Tissues revised the classification of immunodeficiency-associated
 lymphoproliferative disorders with the aim to better define these heterogeneous entities to better distinguish between reactive
 and neoplastic lesions, further refine some entities (plasmablastic lymphoma, monomorphic post-transplant lymphoproliferative
 disorders and other iatrogenic immunodeficiency-associated lymphoproliferative disorders), and introduce a new lymphoma entity
 (large B-cell lymphoma arising in HHV8-associated multicentric Castleman disease). The purpose of this review is to highlight
 the changes in the 2008 WHO classification of immunodeficiency-associated lymphoproliferative disorders.
 
 
	Content Type ...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916115</comments>
            <pubDate>Sat, 19 Feb 2011 07:05:31 +0100</pubDate>
            <guid isPermaLink="false">4916115</guid>        </item>
        <item>
            <title>A case of pediatric anaplastic large cell lymphoma with hemophagocytic lymphohistiocytosis mimicking juvenile myelomonocytic leukemia</title>
            <link>http://www.medworm.com/index.php?rid=4916116&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F26v1442ruw7l1052%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening inflammatory syndrome characterized by reactive proliferation
 of histiocytes in hematopoietic tissues, with accompanying hemophagocytosis. A number of primary and secondary triggers have
 been identified, including some hematolymphoid neoplasms. We submit the case of an 11-year-old female who presented with HLH
 and met diagnostic criteria for juvenile myelomonocytic leukemia, which included the apparently non-recurrent clonal cytogenetic
 abnormality t(5;12)(q35;q24.1). The diagnosis was eventually revised to systemic anaplastic large cell lymphoma with cryptic
 NPM-ALK fusion. We review the previously reported cases of pediatric HLH triggered by systemic ALCL and find that the marked neutrophilia,
 monocy...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916116</comments>
            <pubDate>Wed, 26 Jan 2011 19:39:58 +0100</pubDate>
            <guid isPermaLink="false">4916116</guid>        </item>
        <item>
            <title>New developments in the pathology of malignant lymphoma. A review of the literature published from August 2010–October 2010</title>
            <link>http://www.medworm.com/index.php?rid=4916117&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn417308g61565544%2F</link>
            <description>Content Type Journal ArticlePages 167-174DOI 10.1007/s12308-010-0078-0Authors
		J. Han van Krieken, Department of Pathology, Radboud University Nijmegen, Medical Center, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256
	
		Journal Volume Volume 3
	
		Journal Issue Volume 3, Number 4 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916117</comments>
            <pubDate>Tue, 30 Nov 2010 08:18:00 +0100</pubDate>
            <guid isPermaLink="false">4916117</guid>        </item>
        <item>
            <title>Recent advances in bone marrow biopsy pathology</title>
            <link>http://www.medworm.com/index.php?rid=4916118&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5385204322176678%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The 2010 has seen steady advances in bone marrow biopsy (BMB) pathology. The following publications are a personal selection
 of publications that advance the understanding of the pathobiology of the bone marrow and the interpretation of the BMB.
 
 
	Content Type Journal ArticlePages 129-136DOI 10.1007/s12308-010-0075-3Authors
		Jon van der Walt, Department of Histopathology, St Thomas’ Hospital, Westminster Bridge Road, London, SE1 7EH UK
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256
	
		Journal Volume Volume 3
	
		Journal Issue Volume 3, Number 4 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916118</comments>
            <pubDate>Tue, 30 Nov 2010 08:17:58 +0100</pubDate>
            <guid isPermaLink="false">4916118</guid>        </item>
        <item>
            <title>Editorial</title>
            <link>http://www.medworm.com/index.php?rid=4916119&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv83810h17q4xqr27%2F</link>
            <description>Content Type Journal ArticlePages 127-127DOI 10.1007/s12308-010-0081-5Authors
		J. Han van Krieken, Department of Pathology, Radboud University Nijmegen Medical Centre, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256
	
		Journal Volume Volume 3
	
		Journal Issue Volume 3, Number 4 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916119</comments>
            <pubDate>Tue, 30 Nov 2010 08:17:57 +0100</pubDate>
            <guid isPermaLink="false">4916119</guid>        </item>
        <item>
            <title>Anaplastic large cell lymphoma (monomorphic post-transplant lymphoproliferative disorder) presenting in gallbladder</title>
            <link>http://www.medworm.com/index.php?rid=4916120&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn2xv525323k453j4%2F</link>
            <description>We report a case of ALCL (monomorphic PTLD) in a 45-year-old male lung transplant recipient.
 Within the first year post-transplant, the patient presented with sepsis and acalculous cholecystitis. The patient ultimately
 underwent an open cholecystectomy and was subsequently found to have ALCL of the gallbladder. Despite aggressive treatment
 of septic shock, renal failure, and coagulopathy, the patient died 5&amp;nbsp;days after presentation.
 
 
	Content Type Journal ArticlePages 17-20DOI 10.1007/s12308-010-0080-6Authors
		Elizabeth Ann Wey, Department of Pathology, University of Michigan, 1301 Catherine Road, Ann Arbor, MI 48109, USALauren B. Smith, Department of Pathology, University of Michigan, 1301 Catherine Road, Ann Arbor, MI 48109, USA
	

	
		Journal Journal of HematopathologyPrint I...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916120</comments>
            <pubDate>Tue, 23 Nov 2010 18:17:17 +0100</pubDate>
            <guid isPermaLink="false">4916120</guid>        </item>
        <item>
            <title>PNH clone assessment by flow cytometry and its clinical correlation in PNH and aplastic anemia</title>
            <link>http://www.medworm.com/index.php?rid=4916121&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe347m78671140117%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Flow cytometry is the most sensitive and specific diagnostic modality for paroxysmal nocturnal hemoglobinuria (PNH) clone
 assessment in PNH and other bone marrow failure states. A total of 101 samples included 23 PNH, 46 aplastic anemia (AA), seven
 myelodysplastic syndrome (MDS) cases, and 25 normal controls. Flow cytometry was performed using CD55, CD59, and stain–lyse–wash
 method, and the PNH clone size was correlated with the severity of disease. The PNH clone size on granulocytes in PNH patients
 varied from 7% to 97% detected with a sensitivity of 0.2% and correlated with the clone on monocytes (r = 0.563; p &amp;lt; 0.01). In PNH patients, a significant correlation was seen between PNH clone and the hemoglobin of patient (r = −0.523; p &amp;lt; 0....</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916121</comments>
            <pubDate>Tue, 23 Nov 2010 07:08:49 +0100</pubDate>
            <guid isPermaLink="false">4916121</guid>        </item>
        <item>
            <title>Intravascular extranodal NK/T-cell lymphoma, nasal type, presenting as acute abdomen</title>
            <link>http://www.medworm.com/index.php?rid=4916122&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff5177278n611171w%2F</link>
            <description>We present a case of intravascular extranodal NK/T-cell lymphoma (ENKTCL),
 nasal type, in a 37-year-old Hispanic man admitted for severe abdominal pain. Intraoperative evaluation revealed necrotic
 small bowel and multiple mesenteric venous thromboses. Initial histologic examination demonstrated classic changes of ischemic
 bowel without evidence of dense lymphoid infiltrates or other mass lesions. However closer review of the mesenteric vasculature
 exposed an angioinvasive and angiodestructive process comprised of lymphomatous cells which were positive by immunohistochemistry
 for CD2, CD3, CD8, BCL2, TIA-1, Granzyme B, and Epstein-Barr virus (EBV) EBER in situ hybridization. Although exceedingly
 rare, isolated intravascular ENKTCL, nasal type, may present without a mass; such lesions ...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916122</comments>
            <pubDate>Mon, 22 Nov 2010 16:47:14 +0100</pubDate>
            <guid isPermaLink="false">4916122</guid>        </item>
        <item>
            <title>Congenital dyserythropoietic anemia type II (CDA II) diagnosed in an adult patient</title>
            <link>http://www.medworm.com/index.php?rid=4916123&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fuv0r0r642072326l%2F</link>
            <description>We report a case of CDA II diagnosed in a 48-year-old woman
 with a longstanding history of anemia of unknown etiology.
 
 
	Content Type Journal ArticlePages 149-153DOI 10.1007/s12308-010-0073-5Authors
		Bevan Tandon, Department of Pathology, Northwestern University Feinberg School of Medicine, 251 E. Huron, Feinberg 7-209A, Chicago, IL 60611, USALoAnn C. Peterson, Department of Pathology, Northwestern University Feinberg School of Medicine, 251 E. Huron, Feinberg 7-209A, Chicago, IL 60611, USAStephanie Norwood, Department of Pathology, Northwestern University Feinberg School of Medicine, 251 E. Huron, Feinberg 7-209A, Chicago, IL 60611, USAAnaadriana Zakarija, Division of Hematology/Oncology, Department of Internal Medicine, Northwestern University Feinberg School of Medicine, Chicago, I...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916123</comments>
            <pubDate>Thu, 18 Nov 2010 17:57:15 +0100</pubDate>
            <guid isPermaLink="false">4916123</guid>        </item>
        <item>
            <title>Hairy cell leukemia variant</title>
            <link>http://www.medworm.com/index.php?rid=4916124&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk8560154w8436337%2F</link>
            <description>In this report we aim to add a description of the splenic histology, and extend our knowledge
 of HCLv. We describe one case of this entity for which a splenic histology was available. It fulfilled all the diagnostic
 criteria for HCLv, exhibiting a characteristic pattern of splenic infiltration, and responded favorably to treatment. The
 case described seems to fit well with HCLv where neither morphology nor immunophenotype bears any relation with hairy cell
 leukemia.
 
 
	Content Type Journal ArticlePages 13-16DOI 10.1007/s12308-010-0077-1Authors
		George Kanellis, Haematopathology Department, Evangelismos Hospital, Perikleus 11, 17343 Athens, GreeceLuis Garcia-Alonso, Department of Haematology, Hospital Universitario de Getafe, Madrid, SpainFrancisca I. Camacho, Department of Pathology...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916124</comments>
            <pubDate>Thu, 18 Nov 2010 17:57:14 +0100</pubDate>
            <guid isPermaLink="false">4916124</guid>        </item>
        <item>
            <title>Clear cell myeloma. Report of two cases with comments on morphogenesis and ubiquitin expression</title>
            <link>http://www.medworm.com/index.php?rid=4916125&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy7642510704242mj%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Three bone marrow trephine biopsies from two multiple myeloma patients were involved by a diffuse infiltrate of microvacuolated
 plasma cells with a variable number of signet ring cells, CD138, κ-light chains, and ubiquitin positive. The vacuoles remained
 clear on PAS and in May–Grünwald–Giemsa-stained bone marrow aspirates. Differential diagnosis on conventional stains included
 malignant epithelial and mesenchymal tumors, non-neoplastic histiocytes, and fixation artifacts. Electron microscopy revealed
 translucent vacuoles with no apparent membrane and a fuzzy internal surface occasionally merging with smaller membrane-delineated
 spaces filled with granular material, without communication with cisternae of rough endoplasmic reticulum. Rare multivesicular
 bodi...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916125</comments>
            <pubDate>Tue, 16 Nov 2010 19:31:24 +0100</pubDate>
            <guid isPermaLink="false">4916125</guid>        </item>
        <item>
            <title>Diffuse large B-cell lymphoma with both CD5 and cyclin D1 expression—a case report and review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=4916126&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk741156v4l123042%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Diffuse large B-cell lymphoma (DLBCL) is the most common type of non-Hodgkin’s lymphoma (NHL), representing approximately
 25–30% of newly diagnosed adult NHL in Western countries. CD5-positive DLBCL has been reported in 10% of cases in some series.
 DLBCL with cyclin D1 expression has also been reported in the literature. These cases may sometimes be confused with mantle
 cell lymphoma (MCL), especially blastoid variant MCL, morphologically and immunophenotypically. Herein, we present an unusual
 case of a 41-year-old female without significant medical history who presented with a right facial/parotid mass. Morphologically,
 the tumor showed a diffuse growth pattern of large lymphoid cells with vesicular nuclei, consistent with a DLBCL. Immunostains,
 however, show...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916126</comments>
            <pubDate>Fri, 05 Nov 2010 11:06:53 +0100</pubDate>
            <guid isPermaLink="false">4916126</guid>        </item>
        <item>
            <title>Are we making progress?</title>
            <link>http://www.medworm.com/index.php?rid=4916127&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F05vp002w647505h7%2F</link>
            <description>Content Type Journal ArticlePages 59-59DOI 10.1007/s12308-010-0071-7Authors
		Han van Krieken, Department of Pathology, Radboud University Nijmegen Medical Center, Postbus 9101, 6500 HB Nijmegen, The Netherlands
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256
	
		Journal Volume Volume 3
	
		Journal Issue Volume 3, Numbers 2-3 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916127</comments>
            <pubDate>Tue, 05 Oct 2010 05:50:38 +0100</pubDate>
            <guid isPermaLink="false">4916127</guid>        </item>
        <item>
            <title>New developments in the pathology of malignant lymphoma: a review of the literature published from April 2010–July 2010</title>
            <link>http://www.medworm.com/index.php?rid=4916128&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp5618682724x2u49%2F</link>
            <description>Content Type Journal ArticlePages 117-126DOI 10.1007/s12308-010-0069-1Authors
		J. Han van Krieken, Department of Pathology, Radboud University Nijmegen, Medical Center, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256
	
		Journal Volume Volume 3
	
		Journal Issue Volume 3, Numbers 2-3 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916128</comments>
            <pubDate>Tue, 05 Oct 2010 05:50:37 +0100</pubDate>
            <guid isPermaLink="false">4916128</guid>        </item>
        <item>
            <title>p53 protein overexpression in bone marrow biopsies from chronic lymphocytic leukaemia is associated with TP53 deletion and resistance to fludarabine</title>
            <link>http://www.medworm.com/index.php?rid=4916129&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0132x77580461155%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Abnormalities of the TP53 gene in chronic lymphocytic leukaemia (CLL) are associated with large cell transformation, short survival and resistance
 to purine analogue therapy. Deletion of one allele and somatic mutation of the remaining allele have been described as the
 main mechanism of TP53 inactivation in CLL, but its relationship with p53 protein expression remains unclear. We studied 103 CLL patients using
 fluorescence in situ hybridisation (FISH) to detect allelic loss at chromosome 17p and immunohistochemistry (IHC) to test
 for p53 protein overexpression. TP53 deletion (≥10% of cells) was found in 21 cases (20.4%) and no deletion in 82 (79.6%). By IHC, 16 cases (15.5%) showed p53
 protein expression and 87 (84.5%) were negative. There was a good correlation ...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916129</comments>
            <pubDate>Mon, 04 Oct 2010 13:19:44 +0100</pubDate>
            <guid isPermaLink="false">4916129</guid>        </item>
        <item>
            <title>Inflammatory pseudotumor-like follicular dendritic cell tumor of the liver with expression of estrogen receptor suggests a pathogenic mechanism: a case report and review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=4916130&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5821787714733108%2F</link>
            <description>We report the case of a 59-year-old woman who presented with a 6-cm mass in the liver. Histological examination
 showed spindle cells with a storiform pattern and prominent inflammatory infiltrate mimicking inflammatory pseudotumor. Spindle
 cells expressed follicular dendritic cell markers CD21 and CD35, and were positive for Epstein–Barr virus-encoded RNA and
 LMP-1 protein. In addition, neoplastic cells expressed estrogen receptor (ER). Fifteen cases of inflammatory pseudotumor-like
 follicular dendritic cell tumor of the liver including the case we describe here have been reported in the literature. A review
 of the literature disclosed that normal follicular dendritic cells may express ER; however, extensive testing has not been
 previously reported in follicular dendritic cell sarc...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916130</comments>
            <pubDate>Mon, 27 Sep 2010 16:53:00 +0100</pubDate>
            <guid isPermaLink="false">4916130</guid>        </item>
        <item>
            <title>Leukemic phase of hepatosplenic T cell lymphoma: a case report and review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=4916131&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv2452746t88lvv54%2F</link>
            <description>Content Type Journal ArticlePages 101-107DOI 10.1007/s12308-010-0066-4Authors
		Elizabeth Kehr, Department of Pathology, Oregon Health &amp; Science University, L-471, 3181 Sam Jackson Park Road, Portland, OR 97239-3098, USAPeter Stenzel, Department of Pathology, Oregon Health &amp; Science University, L-471, 3181 Sam Jackson Park Road, Portland, OR 97239-3098, USAGang Xu, Department of Pathology, Oregon Health &amp; Science University, L-471, 3181 Sam Jackson Park Road, Portland, OR 97239-3098, USAKatalin Kelemen, Department of Pathology, Oregon Health &amp; Science University, L-471, 3181 Sam Jackson Park Road, Portland, OR 97239-3098, USA
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256
	
		Journal Volume Volume 3
	
		Journal Issue Volume 3, Numbers 2-3 (Source: Journal of Hematopatholog...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916131</comments>
            <pubDate>Tue, 21 Sep 2010 04:11:06 +0100</pubDate>
            <guid isPermaLink="false">4916131</guid>        </item>
        <item>
            <title>An unusual case of cyclin-D1-positive peripheral T cell lymphoma with a 11:14 translocation</title>
            <link>http://www.medworm.com/index.php?rid=4916132&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fkr10pk36076g3720%2F</link>
            <description>We describe an unusual case of high-grade T cell lymphoma, presenting as rapidly
 enlarging, painless lymphadenopathy in an 80-year-old female. She died 13&amp;nbsp;months after presentation, having relapsed after
 chemotherapy. The lymph node showed diffuse effacement by blastic lymphoid cells, positive for T cell markers and cyclin D1.
 Molecular genetics investigations found t(11:14) translocation. There was definite T cell clonality demonstrating clonal rearrangement
 of both T cell receptor gamma and beta genes but no convincing evidence of B cell clonality. These data represent the first
 documented case where deregulation of the cyclin D1 expression has been implicated in human T cell lymphoreticular malignancy.
 
 
	Content Type Journal ArticlePages 77-81DOI 10.1007/s12308-010-0063-7Au...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916132</comments>
            <pubDate>Fri, 16 Jul 2010 19:48:35 +0100</pubDate>
            <guid isPermaLink="false">4916132</guid>        </item>
        <item>
            <title>Mantle cell lymphoma and chronic lymphocytic leukemia: report of a rare disease association and review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=4916133&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff07141j8rv258772%2F</link>
            <description>We report the case of an 86-year-old female who presented with lymphadenopathy, lymphocytosis, and thrombocytopenia. Peripheral
 blood immunophenotypic analysis identified two lymphoid B cell populations that differ in CD23, CD200, and CD43 expression
 and in the intensity of CD5, CD20, CD79b, and kappa light chain. By fluorescence in situ hybridization (FISH) analysis, approximately
 30% of the mononuclear cells were positive for the t(11;14)(q13;q32) and 40% for trisomy 12; analysis of the two populations
 separated by fluorescence activated cell sorting showed that t(11;14) occurs exclusively in CD23−/CD200−/CD43− cells and trisomy
 12 in the CD23+/CD200+/CD43+ population. Lymph node biopsy showed a typical small lymphocytic lymphoma morphology, with an
 effaced architecture and a...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916133</comments>
            <pubDate>Tue, 06 Jul 2010 17:07:39 +0100</pubDate>
            <guid isPermaLink="false">4916133</guid>        </item>
        <item>
            <title>EBV-positive diffuse large B-cell lymphoma of the elderly with dual genotype and aberrant TIA-1 expression: a case report and review of literature</title>
            <link>http://www.medworm.com/index.php?rid=4916134&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq171514027g26r2q%2F</link>
            <description>We report a case of EBV-positive diffuse large B-cell lymphoma (DLBCL) of the elderly with aberrant expression of TIA-1. The
 patient was an 84-year-old man with a history of progressively enlarged left parotid mass and mild facial paresis for 2&amp;nbsp;months.
 The incisional biopsy revealed sheets of medium to large lymphoma cells with focal angiocentricity and extensive tumor necrosis;
 only a few scattered small lymphocytes were noted among the lymphoma cells. Immunohistochemistry in formalin-fixed paraffin-embedded
 tissue demonstrated that the lymphoma cells marked with CD20, CD30, CD45 (focal), CD79a, BCL2 (focal and weak), PAX5, Oct2,
 BOB.1, IRF4/MUM1, EBV-LMP1, and TIA-1, but they did not mark with CD3, CD4, CD5, CD7, CD8, CD10, CD15, CD23, CD56, CD57, CD138,
 kappa and lambda immun...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916134</comments>
            <pubDate>Mon, 28 Jun 2010 17:01:16 +0100</pubDate>
            <guid isPermaLink="false">4916134</guid>        </item>
        <item>
            <title>Hodgkin lymphoma in a young child contributing to a diagnosis of ataxia telangiectasia: review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=4916135&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp10860h635742872%2F</link>
            <description>We report the clinical, histopathologic, and molecular features of a 6-year-old child who presented with EBV-positive Hodgkin
 lymphoma (HL), which led to the diagnosis of ataxia telangiectasia. The diagnosis of HL at this unusually young age prompted
 further clinical, immunologic and cytogenetic evaluations, all of which supported a diagnosis of A-T. Because A-T patients
 are exquisitely sensitive to radiation, the patient was put on a modified chemotherapeutic regimen; however, 14&amp;nbsp;months later,
 he experienced a relapse and passed away by age 9. Classical HL is relatively rare among A-T patients, and this is the first
 documented case of an EBER-1 positive Hodgkin lymphoma in an ataxia telangiectasia patient. A review of the literature examining
 cases of HL in A-T is provided.
 
 ...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916135</comments>
            <pubDate>Wed, 16 Jun 2010 07:19:51 +0100</pubDate>
            <guid isPermaLink="false">4916135</guid>        </item>
        <item>
            <title>New developments in the pathology of malignant lymphoma: a review of the literature published from October 2009 to January 2010</title>
            <link>http://www.medworm.com/index.php?rid=4916136&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fct642jm355077570%2F</link>
            <description>Content Type Journal ArticlePages 47-58DOI 10.1007/s12308-010-0060-xAuthors
		J. Han van Krieken, Radboud University Nijmegen Medical Centre Department of Pathology P.O. Box 9101 6500 HB Nijmegen The Netherlands
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256
	
		Journal Volume Volume 3
	
		Journal Issue Volume 3, Number 1 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916136</comments>
            <pubDate>Wed, 02 Jun 2010 14:10:13 +0100</pubDate>
            <guid isPermaLink="false">4916136</guid>        </item>
        <item>
            <title>Epstein–Barr virus and Hodgkin’s lymphoma in Cairo, Egypt</title>
            <link>http://www.medworm.com/index.php?rid=4916137&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F71l83r577w6hv726%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Fifty-five consecutive cases of Hodgkin’s lymphoma (HL), collected between 1996 and 1998 from Cairo, Egypt, were histologically
 subtyped, phenotyped, and then studied for the presence of Epstein–Barr virus (EBV). We used immunohistochemical stains for
 EBV latent membrane protein 1 (LMP-1) and in situ hybridization stains for EBV-encoded small RNA (EBER-1) transcripts. Forty-five
 cases (82%) had classic HL (cHL), and ten cases (18%) had nodular lymphocyte predominant HL (NLPHL), with each group expressing
 its typical phenotype. LMP-1 stains were positive in 63% and 0% of cHL and NLPHL cases, respectively. EBER-positive Reed–Sternberg
 cells and variants were also present in 62% and 0% of each group, respectively. The cHL cases showed variable EBER positivity:
 ...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916137</comments>
            <pubDate>Thu, 27 May 2010 16:58:16 +0100</pubDate>
            <guid isPermaLink="false">4916137</guid>        </item>
        <item>
            <title>Hematopathology in the new decade: what to expect</title>
            <link>http://www.medworm.com/index.php?rid=4916138&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc7338h6565217521%2F</link>
            <description>Content Type Journal ArticlePages 1-1DOI 10.1007/s12308-010-0061-9Authors
		J. Han van Krieken, Radboud University Nijmegen Medical Centre Department of Pathology P.O. Box 9101 6500 HB Nijmegen The Netherlands
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256
	
		Journal Volume Volume 3
	
		Journal Issue Volume 3, Number 1 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916138</comments>
            <pubDate>Wed, 19 May 2010 11:23:59 +0100</pubDate>
            <guid isPermaLink="false">4916138</guid>        </item>
        <item>
            <title>Therapy-related myelodysplastic syndrome presenting as fulminant heart failure secondary to myeloid sarcoma</title>
            <link>http://www.medworm.com/index.php?rid=4916139&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff17t21u45qk11751%2F</link>
            <description>We present an unusual case that was caused by a diffuse infiltration of the
 myocardium with leukemic cells (myeloid sarcoma). The patient presented with episodic shortness of breath, he was anemic and
 thrombocytopenic, and his bone marrow biopsy revealed myelodysplastic syndrome from treatment for oligodendroglioma. His clinical
 course was characterized by a chronic leak of cardiac enzymes, a new right bundle branch block, and a large pericardial effusion
 causing tamponade and death from fulminant heart failure and ventricular arrhythmias within 2&amp;nbsp;weeks. At autopsy, the heart
 was massively infiltrated with myeloblasts and other immature myeloid cells. There was no evidence of acute leukemia in the
 bone marrow or peripheral blood. Cardiac infiltration in a patient with myelodyspl...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916139</comments>
            <pubDate>Wed, 05 May 2010 07:59:10 +0100</pubDate>
            <guid isPermaLink="false">4916139</guid>        </item>
        <item>
            <title>NK cell lymphoma, nasal type, with massive lung involvement: a case report</title>
            <link>http://www.medworm.com/index.php?rid=4916141&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp51766t2204p3106%2F</link>
            <description>We describe the unusual case of a 41-year-old male with NK cell lymphoma, nasal type, who presented with massive secondary
 lung involvement 2.5&amp;nbsp;years after the detection of a retroperitoneal mass. The diagnosis was made by open lung biopsy. Despite
 aggressive treatment, the patient died shortly after the initiation of therapy. Lung involvement by NK/T cell lymphoma occurs
 most commonly as part of widely disseminated disease and carries a poor prognosis for the patient. Novel agents and innovative
 therapies need to be developed for this aggressive lymphoma.
 
 
	Content Type Journal ArticlePages 19-22DOI 10.1007/s12308-009-0050-zAuthors
		Anamarija Morovic, University of Cincinnati College of Medicine Department of Pathology and Laboratory Medicine 231 Albert Sabin Way Cincinnati O...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916141</comments>
            <pubDate>Tue, 23 Mar 2010 18:08:57 +0100</pubDate>
            <guid isPermaLink="false">4916141</guid>        </item>
        <item>
            <title>Small intestinal presentation of nodular lymphocyte-predominant Hodgkin lymphoma with T cell/histiocyte-rich B cell lymphoma-like areas—with review of literature on extranodal presentation of this disease</title>
            <link>http://www.medworm.com/index.php?rid=4916140&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg7665p65t4426558%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL), accounts for ∼5% of all cases of Hodgkin lymphoma and is characterized
 by involvement of the peripheral lymph nodes. NLPHL occurs in young adults and is associated with frequent relapses. In 3%
 to 7% of cases, NLPHL progresses to a diffuse large B cell lymphoma. Furthermore, a proportion of NLPHL also have areas with
 features of T cell/histiocyte-rich large B cell lymphoma (THRLBCL), either at presentation or on follow-up. Here, we describe
 a 32-year-old man who presented to the emergency department with small bowel perforation. The resected small bowel showed
 full-thickness mural ulceration and involvement by a lymphoma with features of NLPHL that also had areas resembling THRLBCL.
 The patient had axillar...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916140</comments>
            <pubDate>Tue, 23 Mar 2010 18:08:57 +0100</pubDate>
            <guid isPermaLink="false">4916140</guid>        </item>
        <item>
            <title>NK cell lymphoma, nasal type, with massive lung involvement: a case report</title>
            <link>http://www.medworm.com/index.php?rid=3401400&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fspringerlink.com%2Fcontent%2Fp51766t2204p3106%2F</link>
            <description>We describe the unusual case of a 41-year-old male with NK cell lymphoma, nasal type, who presented with massive secondary
 lung involvement 2.5&amp;nbsp;years after the detection of a retroperitoneal mass. The diagnosis was made by open lung biopsy. Despite
 aggressive treatment, the patient died shortly after the initiation of therapy. Lung involvement by NK/T cell lymphoma occurs
 most commonly as part of widely disseminated disease and carries a poor prognosis for the patient. Novel agents and innovative
 therapies need to be developed for this aggressive lymphoma.
 
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s12308-009-0050-zAuthors
		Anamarija Morovic, University of Cincinnati College of Medicine Department of Pathology and Laboratory Medicine 231 Albert Sabin Way Cin...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3401400</comments>
            <pubDate>Tue, 23 Mar 2010 18:08:57 +0100</pubDate>
            <guid isPermaLink="false">3401400</guid>        </item>
        <item>
            <title>Small intestinal presentation of nodular lymphocyte-predominant Hodgkin lymphoma with T cell/histiocyte-rich B cell lymphoma-like areas—with review of literature on extranodal presentation of this disease</title>
            <link>http://www.medworm.com/index.php?rid=3401399&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fspringerlink.com%2Fcontent%2Fg7665p65t4426558%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL), accounts for ∼5% of all cases of Hodgkin lymphoma and is characterized
 by involvement of the peripheral lymph nodes. NLPHL occurs in young adults and is associated with frequent relapses. In 3%
 to 7% of cases, NLPHL progresses to a diffuse large B cell lymphoma. Furthermore, a proportion of NLPHL also have areas with
 features of T cell/histiocyte-rich large B cell lymphoma (THRLBCL), either at presentation or on follow-up. Here, we describe
 a 32-year-old man who presented to the emergency department with small bowel perforation. The resected small bowel showed
 full-thickness mural ulceration and involvement by a lymphoma with features of NLPHL that also had areas resembling THRLBCL.
 The patient had axillar...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3401399</comments>
            <pubDate>Tue, 23 Mar 2010 18:08:57 +0100</pubDate>
            <guid isPermaLink="false">3401399</guid>        </item>
        <item>
            <title>NK/T cell non-Hodgkin lymphoma in a HIV-positive patient</title>
            <link>http://www.medworm.com/index.php?rid=4916142&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu1543h2536641534%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;NK/T lymphomas have rarely been reported in HIV/AIDS patients. Here we report a case of a 37-year-old woman, with AIDS and
 a recent diagnosis of Kaposi sarcoma in a mesenteric lymph node, who presented with extra-ocular nerve palsies and gastrointestinal
 bleeding. A small intestine resection specimen revealed an extra-nodal NK/T cell lymphoma, nasal type. The unique presentation
 of this rare and aggressive lymphoma in the setting of AIDS and Kaposi sarcoma underscores the importance of maintaining a
 broad differential diagnosis when evaluating a malignant neoplasm from a HIV-positive patient.
 
 
	Content Type Journal ArticlePages 35-40DOI 10.1007/s12308-010-0057-5Authors
		Nicole C. Panarelli, Weill Cornell Medical College Department of Pathology and Laboratory Med...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916142</comments>
            <pubDate>Wed, 10 Mar 2010 16:08:50 +0100</pubDate>
            <guid isPermaLink="false">4916142</guid>        </item>
        <item>
            <title>Cytotoxic peripheral T cell lymphoma arising in a patient with nodular lymphocyte predominant Hodgkin lymphoma: a case report</title>
            <link>http://www.medworm.com/index.php?rid=4916143&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb414454583064623%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In this paper, we describe a case of nodular lymphocyte predominant Hodgkin lymphoma with the subsequent development of a
 peripheral T cell lymphoma. This case is unusual in that the sheets of atypical and small to intermediate-sized T cells in
 the diffuse component were CD8 positive and expressed cytotoxic proteins. The diagnosis of peripheral T cell lymphoma was
 supported by the demonstration of a clonal T cell receptor beta chain gene rearrangement by Southern blot analysis. Peripheral
 T cell lymphoma with a cytotoxic phenotype is a rare entity with an aggressive clinical behavior. As such, this report emphasizes
 the need to consider a diagnosis of coexisting peripheral T cell lymphoma in cases of nodular lymphocyte predominant Hodgkin
 lymphoma with atypical fe...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916143</comments>
            <pubDate>Wed, 10 Mar 2010 16:08:49 +0100</pubDate>
            <guid isPermaLink="false">4916143</guid>        </item>
        <item>
            <title>Immunoexpression of Survivin in non-neoplastic lymphoid tissues and malignant lymphomas using a new monoclonal antibody reactive on paraffin sections</title>
            <link>http://www.medworm.com/index.php?rid=4916144&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn32523266177080t%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Survivin is a member of the inhibitor of apoptosis gene family, which is also implicated in mitosis regulation. Most reports
 in the literature impute poor prognosis to neoplasms with overexpression of this protein. The purpose of the present study
 is to validate and compare the immunohistochemical reactivity of malignant lymphomas and reactive lymphoid tissue using a
 new mouse monoclonal antibody to Survivin produced in our laboratory, 6-78. Survivin was detected by immunohistochemistry
 on tissue microarrays. It was shown that the antibody anti-Survivin 6-78 reliably stains formalin-fixed, paraffin-embedded
 reactive and neoplastic lymphoid tissues, mostly in a nuclear pattern. We confirmed using this novel antibody that Survivin
 immunostaining has a tendency to be...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916144</comments>
            <pubDate>Sat, 30 Jan 2010 18:16:30 +0100</pubDate>
            <guid isPermaLink="false">4916144</guid>        </item>
        <item>
            <title>Gray zones around diffuse large B cell lymphoma. Conclusions based on the workshop of the XIV meeting of the European Association for Hematopathology and the Society of Hematopathology in Bordeaux, France</title>
            <link>http://www.medworm.com/index.php?rid=4916145&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5h78192g55q32315%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The term “gray-zone” lymphoma has been used to denote a group of lymphomas with overlapping histological, biological, and
 clinical features between various types of lymphomas. It has been used in the context of Hodgkin lymphomas (HL) and non-Hodgkin
 lymphomas (NHL), including classical HL (CHL), and primary mediastinal large B cell lymphoma, cases with overlapping features
 between nodular lymphocyte predominant Hodgkin lymphoma and T-cell/histiocyte-rich large B cell lymphoma, CHL, and Epstein–Barr-virus-positive
 lymphoproliferative disorders, and peripheral T cell lymphomas simulating CHL. A second group of gray-zone lymphomas includes
 B cell NHL with intermediate features between diffuse large B cell lymphoma and classical Burkitt lymphoma. In order to revi...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916145</comments>
            <pubDate>Mon, 21 Dec 2009 23:05:38 +0100</pubDate>
            <guid isPermaLink="false">4916145</guid>        </item>
        <item>
            <title>Hematopathology: a decade into the new millennium</title>
            <link>http://www.medworm.com/index.php?rid=4916146&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1u3lj01227574262%2F</link>
            <description>Content Type Journal ArticlePages 185-185DOI 10.1007/s12308-009-0051-yAuthors
		J. Han van Krieken, Radboud University Nijmegen Medical Centre Department of Pathology P.O. Box 9101 6500 HB Nijmegen The Netherlands
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256
	
		Journal Volume Volume 2
	
		Journal Issue Volume 2, Number 4 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916146</comments>
            <pubDate>Fri, 18 Dec 2009 16:30:49 +0100</pubDate>
            <guid isPermaLink="false">4916146</guid>        </item>
        <item>
            <title>New developments in the pathology of malignant lymphoma: a review of the literature published from August to November 2009</title>
            <link>http://www.medworm.com/index.php?rid=4916147&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ftg2464376w035279%2F</link>
            <description>Content Type Journal ArticlePages 245-251DOI 10.1007/s12308-009-0052-xAuthors
		J. Han van Krieken, Radboud University Nijmegen Medical Centre Department of Pathology P.O. Box 9101 6500 HB Nijmegen The Netherlands
	

	
		Journal Journal of HematopathologyPrint ISSN 1868-9256
	
		Journal Volume Volume 2
	
		Journal Issue Volume 2, Number 4 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916147</comments>
            <pubDate>Thu, 17 Dec 2009 07:08:26 +0100</pubDate>
            <guid isPermaLink="false">4916147</guid>        </item>
        <item>
            <title>P38 mitogen activated protein kinase expression and regulation by interleukin-4 in human B cell non-Hodgkin lymphomas</title>
            <link>http://www.medworm.com/index.php?rid=4916148&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F527t575158m982u5%2F</link>
            <description>In conclusion, there is constitutive expression and activation of p38 MAPK in a large number of B-lymphoma-derived
 cell lines and primary lymphoma tissues, supportive of its role in lymphomagenesis. The differential IL-4 regulation of p38
 MAPK expression in cell lines derived from DLBCL may relate to the cellular origin of these neoplasms.
 
	Content Type Journal ArticlePages 195-204DOI 10.1007/s12308-009-0049-5Authors
		Hu Ding, University of Utah Health Sciences Center Salt Lake City UT USAAli M. Gabali, University of Michigan Department of Pathology 4061 BSRB, 109 Zina Pitcher Place Ann Arbor MI 48109 USAStephen D. Jenson, University of Utah Health Sciences Center Salt Lake City UT USAMegan S. Lim, University of Michigan Department of Pathology 4061 BSRB, 109 Zina Pitcher Place Ann Ar...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4916148</comments>
            <pubDate>Wed, 21 Oct 2009 09:06:27 +0100</pubDate>
            <guid isPermaLink="false">4916148</guid>        </item>
        <item>
            <title>Changed concepts and definitions of myeloproliferative neoplasms (MPN), myelodysplastic syndromes (MDS) and myelodysplastic/myeloproliferative neoplasms (MDS/MPN) in the updated 2008 WHO classification</title>
            <link>http://www.medworm.com/index.php?rid=2849117&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fspringerlink.com%2Fcontent%2F101218846q6574j1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The purpose of this overview is to discuss the changes in the 2008 WHO classification of myeloid neoplasms, with exclusion
 of acute myeloid leukaemia. Specific mutations or rearrangements leading to constitutive activation of growth factor receptors
 or cytoplasmic tyrosine kinases are now recognised as recurrent genetic events characterising the group of myeloproliferative
 neoplasms (MPN). A newly introduced subgroup consists of patients with persistent eosinophilia and myeloid or lymphoid proliferations
 harbouring specific genetic changes involving platelet-derived growth factor receptors alpha and beta (PDGFRA and PDGFRB) or fibroblast growth factor receptor 1 (FGFR1). The clinical relevance of recognising myeloid neoplasms with aberrant tyrosine kinase activity i...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2849117</comments>
            <pubDate>Mon, 28 Sep 2009 14:58:13 +0100</pubDate>
            <guid isPermaLink="false">2849117</guid>        </item>
        <item>
            <title>Journal of Hematopathology listed in PubMed!</title>
            <link>http://www.medworm.com/index.php?rid=2849118&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fspringerlink.com%2Fcontent%2Fg9tt8623804r0241%2F</link>
            <description>Content Type Journal ArticleCategory EditorialDOI 10.1007/s12308-009-0047-7Authors
		J. Han van Krieken, Radboud University Nijmegen Medical Centre Department of Pathology P.O. Box 9101 6500 HB Nijmegen The Netherlands
	

	
		Journal Journal of HematopathologyPrint ISSN 1865-5785 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2849118</comments>
            <pubDate>Mon, 28 Sep 2009 14:58:11 +0100</pubDate>
            <guid isPermaLink="false">2849118</guid>        </item>
        <item>
            <title>Recent advances in bone marrow biopsy pathology</title>
            <link>http://www.medworm.com/index.php?rid=2849119&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fspringerlink.com%2Fcontent%2F048480266w166481%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The second quarter of 2009 saw steady advances in bone marrow biopsy (BMB) pathology. The following publications are a personal
 selection of the highlights. Quality issues in diagnostic immunohistochemistry for BMB have largely been ignored in external
 quality assurance programmes, and this issue is highlighted. In other areas, publications reflecting advances in flow cytometry
 and aspirate morphology are discussed where translation to the BMB is possible. Classifications undergo constant change, and
 several publications address the redefinition of the cut off points between malignancy, benign, and normal. Lastly, current
 scientific research is presented where it is relevant to the understanding of BMB pathobiology.
 
	Content Type Journal ArticleCategory Review Ar...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2849119</comments>
            <pubDate>Mon, 28 Sep 2009 14:58:10 +0100</pubDate>
            <guid isPermaLink="false">2849119</guid>        </item>
        <item>
            <title>New developments in the pathology of malignant lymphoma: a review of the literature published from January to August 2009</title>
            <link>http://www.medworm.com/index.php?rid=2849120&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fspringerlink.com%2Fcontent%2Fp67u9725vj10x852%2F</link>
            <description>Content Type Journal ArticleCategory Review of the LiteratureDOI 10.1007/s12308-009-0046-8Authors
		J. Han van Krieken, Radboud University Nijmegen Medical Centre Department of Pathology P.O. Box 9101 6500 HB Nijmegen The Netherlands
	

	
		Journal Journal of HematopathologyPrint ISSN 1865-5785 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2849120</comments>
            <pubDate>Mon, 28 Sep 2009 14:58:07 +0100</pubDate>
            <guid isPermaLink="false">2849120</guid>        </item>
        <item>
            <title>A cytomorphological and immunohistochemical profile of aggressive B-cell lymphoma: high clinical impact of a cumulative immunohistochemical outcome predictor score</title>
            <link>http://www.medworm.com/index.php?rid=2767741&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fspringerlink.com%2Fcontent%2Fv4121710206541hn%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We analyzed morphological and immunohistochemical features in 174 aggressive B-cell lymphomas of nodal and extranodal origin.
 Morphological features included presence or absence of a follicular component and cytologic criteria according to the Kiel
 classification, whereas immunohistochemical studies included expression of CD10, BCL-2, BCL-6, IRF4/MUM1, HLA-DR, p53, Ki-67
 and the assessment of plasmacytoid differentiation. Patients were treated with a CHOP-like regimen. While the presence or
 absence of either CD10, BCL-6 and IRF4/MUM1 reactivity or plasmacytoid differentiation did not identify particular cytomorphologic
 or site-specific subtypes, we found that expression of CD10 and BCL-6, and a low reactivity for IRF4/MUM1 were favourable
 prognostic indicators. In...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2767741</comments>
            <pubDate>Thu, 03 Sep 2009 05:59:31 +0100</pubDate>
            <guid isPermaLink="false">2767741</guid>        </item>
        <item>
            <title>Rare lymphoid malignancies of the breast: a report of two cases illustrating potential diagnostic pitfalls</title>
            <link>http://www.medworm.com/index.php?rid=2722239&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fspringerlink.com%2Fcontent%2Fg274195p18396272%2F</link>
            <description>We describe two cases of lymphoid malignancies predominantly
 involving the breast, both presenting diagnostic dilemmas. The first case, ALK-negative anaplastic large-cell lymphoma involving
 a seroma associated with a breast implant, is an emerging clinicopathologic entity. Anaplastic large-cell lymphoma has been
 identified in association with breast implants and seroma formation relatively recently. The second case, hairy cell leukemia
 involving the breast and ipsilateral axillary sentinel lymph node, is, to our knowledge, the first reported case of hairy
 cell leukemia involving the breast at the time of diagnosis. While a localized bone lesion was present at time of diagnosis,
 bone marrow involvement was relatively mild in comparison to that seen in the breast and lymph node. In the...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2722239</comments>
            <pubDate>Thu, 20 Aug 2009 08:31:19 +0100</pubDate>
            <guid isPermaLink="false">2722239</guid>        </item>
        <item>
            <title>The 2008 WHO-classification: small and big changes!</title>
            <link>http://www.medworm.com/index.php?rid=2661767&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fspringerlink.com%2Fcontent%2Fd833tv4285002322%2F</link>
            <description>Content Type Journal ArticleCategory EditorialDOI 10.1007/s12308-009-0042-zAuthors
		J. H. van Krieken, Radboud University Nijmegen Medical Centre Department of Pathology P.O. Box 9101 6500 HB Nijmegen The Netherlands
	

	
		Journal Journal of HematopathologyPrint ISSN 1865-5785 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2661767</comments>
            <pubDate>Thu, 30 Jul 2009 18:47:36 +0100</pubDate>
            <guid isPermaLink="false">2661767</guid>        </item>
        <item>
            <title>Carcinoma and multiple lymphomas in one patient: establishing the diagnoses and analyzing risk factors</title>
            <link>http://www.medworm.com/index.php?rid=2661768&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fspringerlink.com%2Fcontent%2Fl3651n7vwv50927q%2F</link>
            <description>We report the case of a patient who showed the sequential occurrence of four different lymphoid neoplasms together
 with a squamous cell carcinoma of the lung. A 62-year-old man with adenopathy was admitted to the hospital, and lymph node
 biopsy was positive for low-grade follicular lymphoma. He achieved a partial remission with chemotherapy. Two years later,
 a PET-CT scan showed a left hilar mass in the lung; biopsy showed a squamous cell carcinoma. Simultaneously, he was diagnosed
 with diffuse large B cell lymphoma in a neck lymph node; after chemo- and radiotherapy, he achieved a complete response. A
 restaging PET-CT scan 2&amp;nbsp;years later revealed a retroperitoneal nodule, and biopsy again showed a low-grade follicular lymphoma,
 while a biopsy of a cutaneous scalp lesion showed a...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2661768</comments>
            <pubDate>Thu, 30 Jul 2009 18:47:33 +0100</pubDate>
            <guid isPermaLink="false">2661768</guid>        </item>
        <item>
            <title>Commentary on the WHO 2008 classification of neoplasms arising from histiocytic and other accessory cells</title>
            <link>http://www.medworm.com/index.php?rid=2661769&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fspringerlink.com%2Fcontent%2Fc2u35532j3kv1437%2F</link>
            <description>Content Type Journal ArticleCategory CommentDOI 10.1007/s12308-009-0035-yAuthors
		Megan S. Lim, University of Michigan Medical School Department of Pathology M5242D, Med Sci I, 1301 Catherine Road Ann Arbor MI 48109 USA
	

	
		Journal Journal of HematopathologyPrint ISSN 1865-5785 (Source: Journal of Hematopathology)</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2661769</comments>
            <pubDate>Thu, 30 Jul 2009 18:47:32 +0100</pubDate>
            <guid isPermaLink="false">2661769</guid>        </item>
        <item>
            <title>UK-based real-time lymphoproliferative disorder diagnostic service to improve the management of patients in Ghana</title>
            <link>http://www.medworm.com/index.php?rid=2592515&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fspringerlink.com%2Fcontent%2Fm664411631245260%2F</link>
            <description>This study confirmed
 findings from wealthy countries that a specialised haematopathology service can improve LPD diagnosis. This model of Ghana–UK
 collaboration provides a platform on which to build local capacity to operate an international quality diagnostic service
 for LPDs.
 
	Content Type Journal ArticleCategory Original ArticleDOI 10.1007/s12308-009-0032-1Authors
		Elizabeth Parkins, Royal Cornwall Hospital Trust Truro TR1 3LJ UKRoger G. Owen, St James’s Institute of Oncology HMDS Laboratory Beckett Street Leeds LS9 7TF UKGeorge Bedu-Addo, Kwame Nkrumah University of Science and Technology Komfo Anokye Teaching Hospital and School of Medical Sciences P. O. Box 1934 Kumasi GhanaOhene Opare Sem, Kwame Nkrumah University of Science and Technology Komfo Anokye Teaching Hospital an...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2592515</comments>
            <pubDate>Thu, 09 Jul 2009 12:17:09 +0100</pubDate>
            <guid isPermaLink="false">2592515</guid>        </item>
        <item>
            <title>Myelofibrosis involving lymph node: a novel cytogenetic abnormality in a mimicker of mesenchymal neoplasm</title>
            <link>http://www.medworm.com/index.php?rid=2566086&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fspringerlink.com%2Fcontent%2Fm89474834v694795%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A case of primary myelofibrosis involving lymph node and with a novel cytogenetic abnormality [del (18) (p11.2-3)] is reported.
 The abnormalities are identical among specimens from the lymph node, peripheral blood, and bone marrow that were analyzed
 years apart. Additionally, we show that the infiltrate by dysplastic megakaryocytes in the lymph node morphologically mimics
 a metastatic mesenchymal neoplasm, even when the clinical history myelofibrosis was known.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s12308-009-0040-1Authors
		Youjun Hu, Stony Brook University Hospital Department of Pathology Stony Brook NY 11794 USAAnn-Leslie Zaslav, Stony Brook University Hospital Department of Pathology Stony Brook NY 11794 USANeetu Radhakrishnan, Stony Broo...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2566086</comments>
            <pubDate>Tue, 30 Jun 2009 15:41:38 +0100</pubDate>
            <guid isPermaLink="false">2566086</guid>        </item>
        <item>
            <title>Commentary on the 2008 WHO classification of mature T- and NK-cell neoplasms</title>
            <link>http://www.medworm.com/index.php?rid=2558542&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fspringerlink.com%2Fcontent%2Fj473485p1425xp67%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In 2008, the World Health Organization (WHO) published a revised and updated edition of the classification of tumors of the
 hematopoietic and lymphoid tissues. The aims of the fourth edition of the WHO classification was to incorporate new scientific
 and clinical information in order to refine diagnostic criteria for previously described neoplasms and to introduce newly
 recognized disease entities. The recognition that T-cell lymphomas are related to the innate and adaptive immune system, as
 well as enhanced understanding of other T-cell subsets, such as the regulatory T-cell and follicular helper T-cells, has contributed
 to our understanding of the morphologic, histologic, and immunophenotypic features of T- and NK-cell neoplasms. The purpose
 of this review is to...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
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            <pubDate>Mon, 29 Jun 2009 10:30:36 +0100</pubDate>
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            <title>Commentary on the WHO classification of tumors of lymphoid tissues (2008): “Gray zone” lymphomas overlapping with Burkitt lymphoma or classical Hodgkin lymphoma</title>
            <link>http://www.medworm.com/index.php?rid=2558543&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fspringerlink.com%2Fcontent%2F2k0810314201tg68%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The 2008 WHO Classification of Tumors of Haematopoietic and Lymphoid Tissues has introduced two new categories of high-grade
 B-cell lymphomas: entities in which features of diffuse large B-cell lymphoma (DLBCL) overlap with Burkitt lymphoma (DLBCL/BL)
 or classical Hodgkin lymphoma (DLBCL/HL). The DLBCL/BL category encompasses cases that resemble Burkitt lymphoma morphologically,
 but have one or more immunophenotypic or molecular genetic deviations that would exclude it from the BL category; conversely,
 some cases have immunophenotypic and/or genetic features of BL, but display cytologic variability unacceptable for BL. Many
 of the cases in the DLBCL/BL category contain a translocation of MYC as well as either BCL2 or BCL6 (so-called double-hit lymphomas) and have a...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
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            <pubDate>Mon, 29 Jun 2009 10:30:30 +0100</pubDate>
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            <title>Commentary on the WHO classification of tumors of lymphoid tissues (2008): indolent B cell lymphomas</title>
            <link>http://www.medworm.com/index.php?rid=2549757&amp;cid=s_37296_32_f&amp;fid=37296&amp;url=http%3A%2F%2Fspringerlink.com%2Fcontent%2Fr1k2073k301j6h1h%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The 4th edition of the World Health Organization classification of tumors of hematopoietic and lymphoid tissues introduces
 many new items to the classification scheme of the so-called indolent B cell lymphomas. New proposed entities, such as splenic B cell lymphoma/leukemia, unclassifiable, splenic diffuse red pulp small B cell lymphoma, hairy cell leukemia variant,
 pediatric follicular lymphoma, and pediatric marginal zone lymphoma have been coined, and some definitions of established diseases, such as chronic lymphocytic leukemia or Waldenström’s macroglobulinemia
 have been revised. One aspect of major importance is the recent description of small clonal B cell populations, in part with
 a CLL phenotype, and their relationship to B-CLL. Some new subtypes or vari...</description>
            <author>Journal of Hematopathology</author>
            <type>journals</type>
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            <pubDate>Thu, 25 Jun 2009 06:54:35 +0100</pubDate>
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