Primary epiglottic follicular variant of peripheral T-cell lymphoma

The follicular variant of peripheral T-cell lymphoma, not otherwise specified, is very rare. Primary epiglottic follicular variant of peripheral T-cell lymphoma is extremely rare in clinical practice. Here, we report the first case of a follicular variant of peripheral T-cell lymphoma not otherwise...

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Main Authors: Jienan Kong, Lin Zhong, Xue Gao, Wenjing Qi, Lizhi Zhang, Zhenhua Lin
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2019-01-01
Series:Indian Journal of Pathology and Microbiology
Subjects:
Online Access:http://www.ijpmonline.org/article.asp?issn=0377-4929;year=2019;volume=62;issue=4;spage=586;epage=588;aulast=Kong
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spelling doaj-e5287de62bb34201aabaf215d76bb0a22020-11-25T02:39:24ZengWolters Kluwer Medknow PublicationsIndian Journal of Pathology and Microbiology0377-49292019-01-0162458658810.4103/IJPM.IJPM_849_18Primary epiglottic follicular variant of peripheral T-cell lymphomaJienan KongLin ZhongXue GaoWenjing QiLizhi ZhangZhenhua LinThe follicular variant of peripheral T-cell lymphoma, not otherwise specified, is very rare. Primary epiglottic follicular variant of peripheral T-cell lymphoma is extremely rare in clinical practice. Here, we report the first case of a follicular variant of peripheral T-cell lymphoma not otherwise specified in a 44-year-old Chinese man, who presented with a tumor in the middle of the epiglottis tongue surface. Microscopically, the tumor had a vague nodular growth pattern and the morphology of the nodules was different from each other at low power. Atypical lymphoid cells were medium to large in size and had round nuclei, with an irregular nuclear membrane, distinct nucleoli, and rapid mitotic activity. Plasma cells were found surrounding the nodules. The tumor cells were positive for follicular helper T-cell markers (CD10, PD-1, CXCL13, and BCL-6). The EBER was negative by in situ hybridization. Polymerase chain reaction-based analysis showed monoclonal rearrangements of TCRβ, TCRγ, and polyclonal rearrangements of IgH, IgK, and IgL. The clinical and imaging features and the prognostic factors of FV PTCL-NOS remain poorly understood. Thus, investigation of more cases and longer follow-up is necessary to understand the disease and to identify the best treatment to improve prognosis.http://www.ijpmonline.org/article.asp?issn=0377-4929;year=2019;volume=62;issue=4;spage=586;epage=588;aulast=KongEpiglottisfollicular T-helper cellsfollicular variant PTCL
collection DOAJ
language English
format Article
sources DOAJ
author Jienan Kong
Lin Zhong
Xue Gao
Wenjing Qi
Lizhi Zhang
Zhenhua Lin
spellingShingle Jienan Kong
Lin Zhong
Xue Gao
Wenjing Qi
Lizhi Zhang
Zhenhua Lin
Primary epiglottic follicular variant of peripheral T-cell lymphoma
Indian Journal of Pathology and Microbiology
Epiglottis
follicular T-helper cells
follicular variant PTCL
author_facet Jienan Kong
Lin Zhong
Xue Gao
Wenjing Qi
Lizhi Zhang
Zhenhua Lin
author_sort Jienan Kong
title Primary epiglottic follicular variant of peripheral T-cell lymphoma
title_short Primary epiglottic follicular variant of peripheral T-cell lymphoma
title_full Primary epiglottic follicular variant of peripheral T-cell lymphoma
title_fullStr Primary epiglottic follicular variant of peripheral T-cell lymphoma
title_full_unstemmed Primary epiglottic follicular variant of peripheral T-cell lymphoma
title_sort primary epiglottic follicular variant of peripheral t-cell lymphoma
publisher Wolters Kluwer Medknow Publications
series Indian Journal of Pathology and Microbiology
issn 0377-4929
publishDate 2019-01-01
description The follicular variant of peripheral T-cell lymphoma, not otherwise specified, is very rare. Primary epiglottic follicular variant of peripheral T-cell lymphoma is extremely rare in clinical practice. Here, we report the first case of a follicular variant of peripheral T-cell lymphoma not otherwise specified in a 44-year-old Chinese man, who presented with a tumor in the middle of the epiglottis tongue surface. Microscopically, the tumor had a vague nodular growth pattern and the morphology of the nodules was different from each other at low power. Atypical lymphoid cells were medium to large in size and had round nuclei, with an irregular nuclear membrane, distinct nucleoli, and rapid mitotic activity. Plasma cells were found surrounding the nodules. The tumor cells were positive for follicular helper T-cell markers (CD10, PD-1, CXCL13, and BCL-6). The EBER was negative by in situ hybridization. Polymerase chain reaction-based analysis showed monoclonal rearrangements of TCRβ, TCRγ, and polyclonal rearrangements of IgH, IgK, and IgL. The clinical and imaging features and the prognostic factors of FV PTCL-NOS remain poorly understood. Thus, investigation of more cases and longer follow-up is necessary to understand the disease and to identify the best treatment to improve prognosis.
topic Epiglottis
follicular T-helper cells
follicular variant PTCL
url http://www.ijpmonline.org/article.asp?issn=0377-4929;year=2019;volume=62;issue=4;spage=586;epage=588;aulast=Kong
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