Malignant Pleural Mesothelioma: A Rare Case Report

Q4 Medicine
Benita Soundar Raj, Mohamed Sulaiman G, Monika Peter, Mousigan M.V
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引用次数: 0

Abstract

Malignant pleural mesothelioma (MPM) is a rare and extremely aggressive intrathoracic neoplasm that emerges from the mesothelial cells that line the ribs and the membrane that envelopes the lungs. We present the case of a 68-year-old male with complaints of breathlessness and fatigue. He had no history of exposure to asbestos and no association with familial exposure either. He was evaluated with a PET-CT scan, pleural cytology, and immunohistochemistry and was diagnosed with Malignant Pleural Mesothelioma. The patient was managed with chemotherapy, radiotherapy, and palliative care. A detailed report of malignant pleural mesothelioma was presented in this study.
恶性胸膜间皮瘤1例报告
恶性胸膜间皮瘤(Malignant pleural mesothelioma, MPM)是一种罕见且极具侵袭性的胸腔内肿瘤,起源于肋骨和肺膜的间皮瘤细胞。我们提出的情况下,68岁的男性抱怨呼吸困难和疲劳。他没有石棉接触史,也没有家族接触史。通过PET-CT扫描、胸膜细胞学检查和免疫组织化学检查,诊断为恶性胸膜间皮瘤。患者接受化疗、放疗和姑息治疗。本文报告一例恶性胸膜间皮瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.50
自引率
0.00%
发文量
12
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