Nodular Lymphocyte Predominant Hodgkin Lymphoma versus T-Cell-Histiocyte-Rich Large B-Cell Lymphoma: A Diagnostic ChallengeReport as inadecuate




Nodular Lymphocyte Predominant Hodgkin Lymphoma versus T-Cell-Histiocyte-Rich Large B-Cell Lymphoma: A Diagnostic Challenge - Download this document for free, or read online. Document in PDF available to download.

Case Reports in PathologyVolume 2014 2014, Article ID 956217, 5 pages

Case ReportDepartment of Pathology, State University of New York Downstate Medical Center, 450 Clarkson Avenue, Brooklyn, NY 11203, USA

Received 1 May 2014; Accepted 25 June 2014; Published 7 July 2014

Academic Editor: Piero Tosi

Copyright © 2014 Anton V. Rets and Susan R. S. Gottesman. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Lymphomas with overlapping histological features of two distinct entities cause difficulty in classification. Their classification is of particular significance when the two alternatives require different treatment modalities. We present a diagnostically challenging case of a nodular lymphocyte predominant Hodgkin lymphoma NLPHL with features of T-cell-histiocyte-rich large B-cell lymphoma THRLBCL. Our patient is a 39-year-old woman who presented with painless subclavicular and axillary lymphadenopathy. The biopsied lymph node showed diffuse architectural effacement and scattered large neoplastic cells with large irregular nuclei and prominent nucleoli. These cells were positive for CD20 and Bcl-6 and negative for CD15, CD30, IgD, and Bcl-2. The background cells were predominantly T lymphocytes, whereas B cells were markedly depleted. The lymph node was interpreted as NLPHL, consistent with THRLBCL-like variant. NLPHL, especially THRLBC-like variant, and de novo THRLBCL are characterized by significant morphologic and immunophenotypic overlap. Our case demonstrates a rare predominance of background T-cells in NLPHL and emphasizes the importance of thorough evaluation of multiple morphologic and immunophenotypic features as an essential approach for arriving at the correct diagnosis.





Author: Anton V. Rets and Susan R. S. Gottesman

Source: https://www.hindawi.com/



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