Literature DB >> 27895166

T cell-rich lymphoid infiltrates with large B cells: a review of key entities and diagnostic approach.

Chee Leong Cheng1, Simon O'Connor2.   

Abstract

Accurate diagnostic interpretation of a lymphoid population composed predominantly of small T cells, together with smaller numbers of large B cells, with or without a nodular architecture, is a common problem faced by the histopathologist. The differential diagnosis of this histological pattern is wide, ranging from reactive conditions such as drug reactions and viral infections, through borderline entities such as immunodeficiency-related lymphoproliferative disorders to lymphomas. The latter includes entities where the large B cells are primarily neoplastic (classical and nodular lymphocyte-predominant Hodgkin lymphomas and T cell/histiocyte-rich large B cell lymphoma) as well as T cell lymphomas such as angioimmunoblastic T cell lymphoma where the large B cells represent an epiphenomenon and may or may not be neoplastic. Several rare variants of these conditions, and the fact that treatment can significantly modify appearances, add to the diagnostic difficulty of these pathological entities. Unlike monomorphic lymphoid infiltrates, the histological pattern of T cell-rich proliferation with large B cells requires close evaluation of the inter-relationship between B cells and T cells, follicular dendritic cells and sometimes other inflammatory cells. Epstein-Barr virus plays a key role in several of these scenarios, and interpreting not only its presence but also its distribution within cellular subgroups is essential to accurate diagnosis and the avoidance of some important diagnostic pitfalls. An understanding of normal immunoarchitecture and lymphoid maturational pathways is also fundamental to resolving these cases, as is a knowledge of their common patterns of spread, which facilitates correlation with clinical and radiological findings. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/.

Entities:  

Keywords:  HAEMATOPATHOLOGY; HISTOPATHOLOGY; HODGKINS DISEASE; LYMPH NODE PATHOLOGY; LYMPHOMA

Mesh:

Year:  2016        PMID: 27895166     DOI: 10.1136/jclinpath-2016-204065

Source DB:  PubMed          Journal:  J Clin Pathol        ISSN: 0021-9746            Impact factor:   3.411


  4 in total

1.  A Rare Case of Angioimmunoblastic T-Cell Lymphoma with Epstein-Barr Virus-Negative Reed-Sternberg-Like B-Cells, Chylous Ascites, and Chylothorax.

Authors:  Mathijs Willemsen; Arne W J H Dielis; Iryna V Samarska; Ad Koster; Arienne M van Marion
Journal:  Case Rep Hematol       Date:  2017-04-12

2.  Use of immune repertoire sequencing to resolve discordant microscopic and immunochemical findings in a case of T cell-rich large B cell lymphoma in a young dog.

Authors:  Gary Kwok Cheong Lee; Dorothee Bienzle; Stefan Matthias Keller; Mei-Hua Hwang; Nikos Darzentas; Haiyang Chang; Emily Rätsep; Rebecca Egan; Janet Beeler-Marfisi
Journal:  BMC Vet Res       Date:  2021-02-18       Impact factor: 2.741

3.  Bhlhe40 function in activated B and TFH cells restrains the GC reaction and prevents lymphomagenesis.

Authors:  René Rauschmeier; Annika Reinhardt; Charlotte Gustafsson; Vassilis Glaros; Artem V Artemov; Josefine Dunst; Reshma Taneja; Igor Adameyko; Robert Månsson; Meinrad Busslinger; Taras Kreslavsky
Journal:  J Exp Med       Date:  2021-12-17       Impact factor: 17.579

4.  Contribution of Immunocytochemistry to the Diagnosis of Usual and Unusual Lymphoma Cases.

Authors:  Dilip K Das
Journal:  J Cytol       Date:  2018 Jul-Sep       Impact factor: 1.000

  4 in total

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