T- and NK-Cell Lymphomas and Systemic Lymphoproliferative Disorders and the Immunodeficiency Setting: 2015 SH/EAHP Workshop Report-Part 4.

TitleT- and NK-Cell Lymphomas and Systemic Lymphoproliferative Disorders and the Immunodeficiency Setting: 2015 SH/EAHP Workshop Report-Part 4.
Publication TypeJournal Article
Year of Publication2017
AuthorsGratzinger D, de Jong D, Jaffe ES, Chadburn A, Chan JKC, Goodlad JR, Said J, Natkunam Y
JournalAm J Clin Pathol
Volume147
Issue2
Pagination188-203
Date Published2017 Feb 01
ISSN1943-7722
KeywordsEducation, Epstein-Barr Virus Infections, Female, Humans, Immunologic Deficiency Syndromes, Lymphoma, Extranodal NK-T-Cell, Lymphoma, T-Cell, Lymphoproliferative Disorders, Male
Abstract

Objectives: The 2015 Workshop of the Society for Hematopathology/European Association for Haematopathology aimed to review immunodeficiency-related T- and natural killer (NK)-cell lymphoproliferations.

Methods: The Workshop Panel reviewed 88 T- or NK-cell lymphoproliferations and rendered consensus diagnoses.

Results: Hyperplasias of T-cell subsets may be clonal; retained architecture and the clinical setting support a benign diagnosis. Specific associations include hepatosplenic T-cell lymphoma with iatrogenic immunosuppression and breast implants with an indolent variant of anaplastic large cell lymphoma. Epstein-Barr virus (EBV)-positive T-cell lymphomas rarely occur in the acquired immunodeficiency setting. Systemic T- and NK-cell lymphoma of childhood overlaps with chronic active EBV and reversible hemophagocytic lymphohistiocytosis-related T-cell lymphoproliferations.

Conclusions: Immunodeficiencies predispose to T-cell hyperplasias, which must not be overdiagnosed as lymphoma. Many T-cell lymphomas in the immunodeficiency setting are likely coincidental, with specific exceptions. Systemic T- or NK-cell lymphomas are part of a spectrum of EBV+ T or NK lymphoproliferations and can present in the acquired immunodeficiency setting.

DOI10.1093/ajcp/aqw213
Alternate JournalAm J Clin Pathol
PubMed ID28395105
PubMed Central IDPMC6248696
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