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Primary Skeletal Muscle Peripheral T-cell Lymphoma: An Autopsy Case Report and Review of the Literature

Primary skeletal muscle lymphoma is extremely uncommon, and there have only been eight previous case reports on primary skeletal muscle peripheral T-cell lymphoma, not otherwise specified (PSM-PTCL, NOS). We herein report an autopsy case of a 71-year-old woman with PSM-PTCL, NOS, who had a 24-year h...

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Autores principales: Iizuka, Hiroko, Harada, Sakiko, Iwao, Noriaki, Koike, Michiaki, Noguchi, Masaaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8580759/
https://www.ncbi.nlm.nih.gov/pubmed/33967141
http://dx.doi.org/10.2169/internalmedicine.7391-21
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author Iizuka, Hiroko
Harada, Sakiko
Iwao, Noriaki
Koike, Michiaki
Noguchi, Masaaki
author_facet Iizuka, Hiroko
Harada, Sakiko
Iwao, Noriaki
Koike, Michiaki
Noguchi, Masaaki
author_sort Iizuka, Hiroko
collection PubMed
description Primary skeletal muscle lymphoma is extremely uncommon, and there have only been eight previous case reports on primary skeletal muscle peripheral T-cell lymphoma, not otherwise specified (PSM-PTCL, NOS). We herein report an autopsy case of a 71-year-old woman with PSM-PTCL, NOS, who had a 24-year history of systemic sclerosis treated with immunosuppressive drugs. A post-mortem examination revealed infiltration of lymphoma cells positive for T-cell markers, cytotoxic markers, and p53. This case was considered to be one of other iatrogenic immunodeficiency-associated lymphoproliferative disorder (OIIA-LPD). This is the first case categorized under both PSM-PTCL, NOS, and OIIA-LPD.
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spelling pubmed-85807592021-11-19 Primary Skeletal Muscle Peripheral T-cell Lymphoma: An Autopsy Case Report and Review of the Literature Iizuka, Hiroko Harada, Sakiko Iwao, Noriaki Koike, Michiaki Noguchi, Masaaki Intern Med Case Report Primary skeletal muscle lymphoma is extremely uncommon, and there have only been eight previous case reports on primary skeletal muscle peripheral T-cell lymphoma, not otherwise specified (PSM-PTCL, NOS). We herein report an autopsy case of a 71-year-old woman with PSM-PTCL, NOS, who had a 24-year history of systemic sclerosis treated with immunosuppressive drugs. A post-mortem examination revealed infiltration of lymphoma cells positive for T-cell markers, cytotoxic markers, and p53. This case was considered to be one of other iatrogenic immunodeficiency-associated lymphoproliferative disorder (OIIA-LPD). This is the first case categorized under both PSM-PTCL, NOS, and OIIA-LPD. The Japanese Society of Internal Medicine 2021-05-07 2021-10-15 /pmc/articles/PMC8580759/ /pubmed/33967141 http://dx.doi.org/10.2169/internalmedicine.7391-21 Text en Copyright © 2021 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/The Internal Medicine is an Open Access journal distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Iizuka, Hiroko
Harada, Sakiko
Iwao, Noriaki
Koike, Michiaki
Noguchi, Masaaki
Primary Skeletal Muscle Peripheral T-cell Lymphoma: An Autopsy Case Report and Review of the Literature
title Primary Skeletal Muscle Peripheral T-cell Lymphoma: An Autopsy Case Report and Review of the Literature
title_full Primary Skeletal Muscle Peripheral T-cell Lymphoma: An Autopsy Case Report and Review of the Literature
title_fullStr Primary Skeletal Muscle Peripheral T-cell Lymphoma: An Autopsy Case Report and Review of the Literature
title_full_unstemmed Primary Skeletal Muscle Peripheral T-cell Lymphoma: An Autopsy Case Report and Review of the Literature
title_short Primary Skeletal Muscle Peripheral T-cell Lymphoma: An Autopsy Case Report and Review of the Literature
title_sort primary skeletal muscle peripheral t-cell lymphoma: an autopsy case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8580759/
https://www.ncbi.nlm.nih.gov/pubmed/33967141
http://dx.doi.org/10.2169/internalmedicine.7391-21
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