Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/19062
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dc.contributor.authorKanavaros, P.en
dc.contributor.authorLavergne, A.en
dc.contributor.authorGalian, A.en
dc.contributor.authorHoudart, R.en
dc.contributor.authorBernard, J. F.en
dc.date.accessioned2015-11-24T18:56:34Z-
dc.date.available2015-11-24T18:56:34Z-
dc.identifier.issn0008-543X-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/19062-
dc.rightsDefault Licence-
dc.subjectAntigens, Neoplasm/*analysisen
dc.subjectDiagnosis, Differentialen
dc.subjectHumansen
dc.subjectLymphoma/analysis/diagnosis/*pathologyen
dc.subjectMaleen
dc.subjectMiddle Ageden
dc.subjectNeoplasm Proteins/*analysisen
dc.subjectPhenotypeen
dc.subjectPhosphopyruvate Hydratase/analysisen
dc.subjectStomach Neoplasms/analysis/diagnosis/*pathologyen
dc.subjectT-Lymphocytes/analysis/*pathologyen
dc.subjectT-Lymphocytes, Helper-Inducer/analysis/*pathologyen
dc.titlePrimary gastric peripheral T-cell malignant lymphoma with helper/inducer phenotype. First case report with a complete histological ultrastructural and immunochemical studyen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/2964894-
heal.identifier.secondaryhttp://onlinelibrary.wiley.com/store/10.1002/1097-0142(19880415)61:8<1602::AID-CNCR2820610818>3.0.CO;2-P/asset/2820610818_ftp.pdf?v=1&t=h0exlgwb&s=83468f6e07d495455fa75d647d83f9d6ff730aaa-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate1988-
heal.abstractPrimary gastrointestinal T-cell malignant lymphomas (T-ML) are very rare. In this case report we describe a primary gastric tumor with local lymph node involvement. On the basis of histologic, immunohistochemical, and electron microscopic studies, the authors classified this tumor as a pleomorphic T-ML, large cell variant with peripheral helper/inducer T-cell phenotype (Leu1/CD5+, Leu4/CD3+, Leu5/CD2+, Leu9/CD7+, and Leu3/CD4+). The extreme pleomorphism of lymphoma cells, the numerous giant cells, and the presence of tumor nodules with two or three concentric layers were the three striking morphologic features of our case. Tumor cells showed an inconstant but true positive staining with anti-LeuM1/CD15 and LeuM3/CD14 antibodies. Vimentin positivity could be related to the presence of intermediate filaments at ultrastructural level. Neuron-specific enolase reactivity was a peculiar but unexplained feature. Furthermore, the positivity of the surface markers Ki-1/CD30, anti-Tac/CD25 and HLA-DR, and the nuclear marker Ki-67 suggested an activation state and a high proliferative activity of the tumor cells. This study emphasizes the usefulness of combined pathologic methods in order to rule other diagnoses such as undifferentiated carcinoma, malignant melanoma, malignant histiocytosis, B-cell lymphoma and interdigitating reticulum cells sarcoma, in view of an extremely polymorph tumor proliferation. This is apparently the first completely documented case report of a primary gastric pleomorphic T-ML of peripheral T-cell origin.en
heal.journalNameCanceren
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ

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