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dc.contributor.authorAyako Sakakibaraen_US
dc.contributor.authorKei Kohnoen_US
dc.contributor.authorNaoto Kurodaen_US
dc.contributor.authorKenji Yoritaen_US
dc.contributor.authorNirmeen A. Megaheden_US
dc.contributor.authorAhmed E. Eladlen_US
dc.contributor.authorTeerada Daroontumen_US
dc.contributor.authorEri Ishikawaen_US
dc.contributor.authorYuka Suzukien_US
dc.contributor.authorSatoko Shimadaen_US
dc.contributor.authorMasato Nakaguroen_US
dc.contributor.authorYoshie Shimoyamaen_US
dc.contributor.authorAkira Satouen_US
dc.contributor.authorSeiichi Katoen_US
dc.contributor.authorYasushi Yatabeen_US
dc.contributor.authorNaoko Asanoen_US
dc.contributor.authorShigeo Nakamuraen_US
dc.date.accessioned2018-09-05T04:35:36Z-
dc.date.available2018-09-05T04:35:36Z-
dc.date.issued2018-04-01en_US
dc.identifier.issn14401827en_US
dc.identifier.issn13205463en_US
dc.identifier.other2-s2.0-85042410761en_US
dc.identifier.other10.1111/pin.12653en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85042410761&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/58955-
dc.description.abstract© 2018 Japanese Society of Pathology and John Wiley & Sons Australia, Ltd The anaplastic variant of diffuse large B-cell lymphoma (A-DLBCL) is morphologically defined but remains an enigmatic disease in its clinicopathologic distinctiveness. Here, we report two cases involving Japanese women aged 59 years, both with A-DLBCL with the hallmark cell appearance and both indistinguishable from common and giant cell-rich patterns, respectively, of anaplastic lymphoma kinase (ALK)-positive anaplastic large cell lymphoma. Case 1 was immunohistochemically positive for CD20, CD79a and OCT-2 but not for the other pan–B-cell markers, CD30 and ALK. Case 2 showed CD20 and CD30 positivity for 50% and 20% of tumor cells in addition to strong expression of p53 and MYC. Both were positive for fascin without Epstein–Barr virus association. Our cases provide additional support for the earlier reports that A-DLBCL exhibits clinicopathologic features distinct from ordinal diffuse large B-cell lymphoma (DLBCL), and documented its broader morphologic diversity than previously recognized. They also shed light on the unique feature of absent expression of pan–B-cell markers except for CD20 and CD79a, suggesting that A-DLBCL may biologically mimic a gray zone or intermediate lymphoma between DLBCL and classic Hodgkin lymphoma.en_US
dc.subjectMedicineen_US
dc.titleAnaplastic variant of diffuse large B-cell lymphoma with hallmark cell appearance: Two cases highlighting a broad diversity in the diagnosticsen_US
dc.typeJournalen_US
article.title.sourcetitlePathology Internationalen_US
article.volume68en_US
article.stream.affiliationsNagoya University Hospitalen_US
article.stream.affiliationsOkazaki City Hospitalen_US
article.stream.affiliationsKochi Red Cross Hospitalen_US
article.stream.affiliationsMansoura University, Faculty of Medicineen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsAichi Medical Universityen_US
article.stream.affiliationsAichi Cancer Center Hospital and Research Instituteen_US
article.stream.affiliationsNagano Prefectural Suzaka Hospitalen_US
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