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一名患有进展迅速的肉瘤样胸膜间皮瘤的患者的详细临床过程,该患者无 p16 缺失,伴有全身血源性软组织转移。

Detailed clinical course of a patient with rapidly progressing sarcomatoid pleural mesothelioma without p16 deletion with systemic haematogenous metastasis to soft tissues.

机构信息

Toyama Rosai Hospital, Uozu, Japan

Hokkaido Chuo Rosai Hospital, Iwamizawa, Hokkaido, Japan.

出版信息

BMJ Case Rep. 2024 Feb 10;17(2):e257618. doi: 10.1136/bcr-2023-257618.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7e0/10862345/8728a3c255aa/bcr-2023-257618f01.jpg

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