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Hodgkin Lymphoma: Biology and Differential Diagnostic Problem

Hodgkin lymphomas (HLs) are lymphoid neoplasms that are morphologically defined as being composed of dysplastic cells, namely, Hodgkin and Reed–Sternberg cells, in a reactive inflammatory background. The biological nature of HLs has long been unclear; however, our understanding of HL-related genetic...

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Autores principales: Takahara, Taishi, Satou, Akira, Tsuzuki, Toyonori, Nakamura, Shigeo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9221773/
https://www.ncbi.nlm.nih.gov/pubmed/35741318
http://dx.doi.org/10.3390/diagnostics12061507
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author Takahara, Taishi
Satou, Akira
Tsuzuki, Toyonori
Nakamura, Shigeo
author_facet Takahara, Taishi
Satou, Akira
Tsuzuki, Toyonori
Nakamura, Shigeo
author_sort Takahara, Taishi
collection PubMed
description Hodgkin lymphomas (HLs) are lymphoid neoplasms that are morphologically defined as being composed of dysplastic cells, namely, Hodgkin and Reed–Sternberg cells, in a reactive inflammatory background. The biological nature of HLs has long been unclear; however, our understanding of HL-related genetics and tumor microenvironment interactions is rapidly expanding. For example, cell surface overexpression of programmed cell death 1 ligand 1 (CD274/PD-L1) is now considered a defining feature of an HL subset, and targeting such immune checkpoint molecules is a promising therapeutic option. Still, HLs comprise multiple disease subtypes, and some HL features may overlap with its morphological mimics, posing challenging diagnostic and therapeutic problems. In this review, we summarize the recent advances in understanding the biology of HLs, and discuss approaches to differentiating HL and its mimics.
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spelling pubmed-92217732022-06-24 Hodgkin Lymphoma: Biology and Differential Diagnostic Problem Takahara, Taishi Satou, Akira Tsuzuki, Toyonori Nakamura, Shigeo Diagnostics (Basel) Review Hodgkin lymphomas (HLs) are lymphoid neoplasms that are morphologically defined as being composed of dysplastic cells, namely, Hodgkin and Reed–Sternberg cells, in a reactive inflammatory background. The biological nature of HLs has long been unclear; however, our understanding of HL-related genetics and tumor microenvironment interactions is rapidly expanding. For example, cell surface overexpression of programmed cell death 1 ligand 1 (CD274/PD-L1) is now considered a defining feature of an HL subset, and targeting such immune checkpoint molecules is a promising therapeutic option. Still, HLs comprise multiple disease subtypes, and some HL features may overlap with its morphological mimics, posing challenging diagnostic and therapeutic problems. In this review, we summarize the recent advances in understanding the biology of HLs, and discuss approaches to differentiating HL and its mimics. MDPI 2022-06-20 /pmc/articles/PMC9221773/ /pubmed/35741318 http://dx.doi.org/10.3390/diagnostics12061507 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Takahara, Taishi
Satou, Akira
Tsuzuki, Toyonori
Nakamura, Shigeo
Hodgkin Lymphoma: Biology and Differential Diagnostic Problem
title Hodgkin Lymphoma: Biology and Differential Diagnostic Problem
title_full Hodgkin Lymphoma: Biology and Differential Diagnostic Problem
title_fullStr Hodgkin Lymphoma: Biology and Differential Diagnostic Problem
title_full_unstemmed Hodgkin Lymphoma: Biology and Differential Diagnostic Problem
title_short Hodgkin Lymphoma: Biology and Differential Diagnostic Problem
title_sort hodgkin lymphoma: biology and differential diagnostic problem
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9221773/
https://www.ncbi.nlm.nih.gov/pubmed/35741318
http://dx.doi.org/10.3390/diagnostics12061507
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