Toyama Rosai Hospital, Uozu, Japan
Hokkaido Chuo Rosai Hospital, Iwamizawa, Hokkaido, Japan.
BMJ Case Rep. 2024 Feb 10;17(2):e257618. doi: 10.1136/bcr-2023-257618.
Sarcomatoid mesothelioma is difficult to differentiate from other mesotheliomas. Here, we describe the case of a man in his early 80s with sarcomatoid mesothelioma and a history of asbestos exposure. He initially presented with right-sided chest pain and was examined. Right-sided pleural effusion was detected; therefore, he was hospitalised. Based on the observed pleural effusion and biopsy result, the presence of a malignant tumour was excluded; hence, he was diagnosed with benign asbestos pleurisy. He subsequently developed left-sided pleural effusion, masses and lung nodules, and died 9.5 months after the initial examination. A definitive diagnosis of sarcomatoid mesothelioma with rapid systemic progression was established after detailed investigations using autopsy specimens. This rare case of mesothelioma-without deletion (detected using fluorescence in situ hybridisation)-presented differently from the usual sarcomatoid mesothelioma.
肉瘤样间皮瘤难以与其他间皮瘤区分。在这里,我们描述了一位 80 多岁的男性患者,他患有肉瘤样间皮瘤且有石棉暴露史。他最初表现为右侧胸痛并接受了检查。发现右侧胸腔积液,因此住院治疗。根据观察到的胸腔积液和活检结果,排除了恶性肿瘤的存在;因此,诊断为良性石棉性胸膜炎。随后他出现左侧胸腔积液、肿块和肺结节,并在初次检查后 9.5 个月死亡。详细的尸检标本检查后,明确诊断为肉瘤样间皮瘤伴快速全身进展。这种罕见的间皮瘤(未通过荧光原位杂交检测到)的表现与通常的肉瘤样间皮瘤不同。