Publication:
Aberrant antigenic expression in extranodal NK/T-cell lymphoma: a multi-parameter study from Thailand

dc.contributor.authorTawatchai Pongpruttipanen_US
dc.contributor.authorTanawan Kummalueen_US
dc.contributor.authorAnan Bedavanijaen_US
dc.contributor.authorArchrob Khuhapinanten_US
dc.contributor.authorKoichi Ohshimaen_US
dc.contributor.authorFumiko Arakawaen_US
dc.contributor.authorDaisuke Niinoen_US
dc.contributor.authorSanya Sukpanichnanten_US
dc.contributor.otherMahidol University. Faculty of Medicine Siriraj Hospital. Department of Pathologyen_US
dc.date.accessioned2017-08-03T23:59:43Z
dc.date.available2017-08-03T23:59:43Z
dc.date.created2017-08-04
dc.date.issued2011
dc.description.abstractBackground: Extranodal NK/T-cell lymphoma, nasal type (ENKTL) is not common worldwide, but it is the most common T- and NK-cell lymphomas in many Asian countries. Immunophenotypic profiles were studied based on limited series. The authors, therefore, studied on ENKTL according to characterize immunophenotypic profiles as well as the distribution of EBV subtype and LMP-1 gene deletion. Methods: By using tissue microarray (TMA), immunohistochemical study and EBV encoded RNA (EBER) in situ hybridization were performed. T-cell receptor (TCR) gene rearrangement, EBV subtyping, and LMP-1 gene deletion were studied on the available cases. Results: There were 22 cases eligible for TMA. ENKTL were positive for CD3 (91%), CD5 (9%), CD7 (32%), CD4 (14%), CD56 (82%), TIA-1 (100%), granzyme B (95%), perforin (86%), CD45 (83%), CD30 (75%), Oct2 (25%), and IRF4/ MUM1 (33%). None of them was positive for bF1, CD8, or CD57. TCR gene rearrangement was negative in all 18 tested cases. EBV was subtype A in all 15 tested cases, with 87% deleted LMP-1 gene. Cases lacking perforin expression demonstrated a significantly poorer survival outcome (p = 0.008). Conclusions: The present study demonstrated TIA-1 and EBER as the two most sensitive markers. There were a few CD3 and/or CD56 negative cases noted. Interestingly, losses of CD45 and/or CD7 were not uncommon while Oct2 and IRF4/MUM1 could be positive in a subset of cases. Based on the present study in conjunction with the literature review, determination of PCR-based TCR gene rearrangement analysis might not be a useful technique for making diagnosis of ENKTL.en_US
dc.identifier.citationDiagnostic Pathology. Vol. 6, (2011), 79en_US
dc.identifier.doi10.1186/1746-1596-6-79
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/2640
dc.language.isoengen_US
dc.rightsMahidol Universityen_US
dc.rights.holderBioMed Centralen_US
dc.subjectOpen Access articleen_US
dc.subjectExtranodal NK/T-cell lymphomaen_US
dc.subjectpathologyen_US
dc.subjectimmunophenotypeen_US
dc.subjectEBVen_US
dc.subjectLMP-1 geneen_US
dc.subjectTCR geneen_US
dc.titleAberrant antigenic expression in extranodal NK/T-cell lymphoma: a multi-parameter study from Thailanden_US
dc.typeResearch Articleen_US
dspace.entity.typePublication
mods.location.urlhttp://www.diagnosticpathology.org/content/6/1/79en_US

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