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Case report: Rare intrapulmonary malignant mesothelioma complicated with myositis

Malignant pleural mesothelioma is an uncommon aggressive tumor. Its incidence is even lower when the lung parenchyma is the primary site. Myositis is a common paraneoplastic syndrome, but it rarely presents with malignant pleural mesothelioma. This report presents a rare intrapulmonary malignant mes...

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Autores principales: Gong, Dandan, Yu, Jian, Jiang, Xiaodong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9815530/
https://www.ncbi.nlm.nih.gov/pubmed/36620605
http://dx.doi.org/10.3389/fonc.2022.1074821
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author Gong, Dandan
Yu, Jian
Jiang, Xiaodong
author_facet Gong, Dandan
Yu, Jian
Jiang, Xiaodong
author_sort Gong, Dandan
collection PubMed
description Malignant pleural mesothelioma is an uncommon aggressive tumor. Its incidence is even lower when the lung parenchyma is the primary site. Myositis is a common paraneoplastic syndrome, but it rarely presents with malignant pleural mesothelioma. This report presents a rare intrapulmonary malignant mesothelioma complicated by cancer-associated myositis. The patient presented with limb muscle weakness as the first symptom and was diagnosed with intrapulmonary malignant mesothelioma complicated by cancer-associated myositis on the basis of clinical, histological, immunohistochemical, and radiological findings. The patient responded poorly to conventional hormone therapy and died of respiratory failure within 2 months after the first presence of limb muscle weakness.
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spelling pubmed-98155302023-01-06 Case report: Rare intrapulmonary malignant mesothelioma complicated with myositis Gong, Dandan Yu, Jian Jiang, Xiaodong Front Oncol Oncology Malignant pleural mesothelioma is an uncommon aggressive tumor. Its incidence is even lower when the lung parenchyma is the primary site. Myositis is a common paraneoplastic syndrome, but it rarely presents with malignant pleural mesothelioma. This report presents a rare intrapulmonary malignant mesothelioma complicated by cancer-associated myositis. The patient presented with limb muscle weakness as the first symptom and was diagnosed with intrapulmonary malignant mesothelioma complicated by cancer-associated myositis on the basis of clinical, histological, immunohistochemical, and radiological findings. The patient responded poorly to conventional hormone therapy and died of respiratory failure within 2 months after the first presence of limb muscle weakness. Frontiers Media S.A. 2022-12-22 /pmc/articles/PMC9815530/ /pubmed/36620605 http://dx.doi.org/10.3389/fonc.2022.1074821 Text en Copyright © 2022 Gong, Yu and Jiang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Gong, Dandan
Yu, Jian
Jiang, Xiaodong
Case report: Rare intrapulmonary malignant mesothelioma complicated with myositis
title Case report: Rare intrapulmonary malignant mesothelioma complicated with myositis
title_full Case report: Rare intrapulmonary malignant mesothelioma complicated with myositis
title_fullStr Case report: Rare intrapulmonary malignant mesothelioma complicated with myositis
title_full_unstemmed Case report: Rare intrapulmonary malignant mesothelioma complicated with myositis
title_short Case report: Rare intrapulmonary malignant mesothelioma complicated with myositis
title_sort case report: rare intrapulmonary malignant mesothelioma complicated with myositis
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9815530/
https://www.ncbi.nlm.nih.gov/pubmed/36620605
http://dx.doi.org/10.3389/fonc.2022.1074821
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