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恶性腹膜间皮瘤

Malignant peritoneal mesothelioma.

作者信息

Chun Cai-Pu, Song Lin-Xie, Zhang Hong-Pan, Guo Dan-Dan, Xu Gui-Xuan, Li Ya, Xin Xin, Cao Jiachen, Li Feng

机构信息

Department of Pathology and Medical Research Center, Beijing Chaoyang Hospital, Capital Medical University, Chaoyang District, Beijing, PR China; Department of Pathology, The Fourth Affiliated Hospital of Shihezi University, Akesu, Xinjiang, PR China.

Department of Pathology and Medical Research Center, Beijing Chaoyang Hospital, Capital Medical University, Chaoyang District, Beijing, PR China.

出版信息

Am J Med Sci. 2023 Jan;365(1):99-103. doi: 10.1016/j.amjms.2022.07.008. Epub 2022 Aug 6.

Abstract

Malignant peritoneal mesothelioma (MPM) is a rare, life-threatening malignant tumor. We present a report of a rare case of a 67-year-old male patient with MPM and severe abdominal pain, bloating, and bloody ascites as manifestations. The diagnosis was confirmed by cytology of ascites aspiration fluid and further verified by laparoscopic exploratory biopsy. The characteristics of signs and clinical manifestations in this case are less common. As everyone knows, asbestos exposure is usually associated with pleural mesothelioma, but only 6%-10% of malignant mesothelioma cases originate from the peritoneum, which is far less than pleural mesothelioma. Generally, its non-specificity provides a huge challenge to medical professionals in its diagnosis, and this is also the main reason for delayed diagnosis. Patients should be vigilant, even though no clear risk factor is observed.

摘要

恶性腹膜间皮瘤(MPM)是一种罕见的、危及生命的恶性肿瘤。我们报告一例罕见病例,一名67岁男性患者,以MPM为表现,伴有严重腹痛、腹胀和血性腹水。通过腹水穿刺液细胞学检查确诊,并经腹腔镜探查活检进一步证实。该病例的体征和临床表现特征较为少见。众所周知,石棉暴露通常与胸膜间皮瘤有关,但只有6%-10%的恶性间皮瘤病例起源于腹膜,远少于胸膜间皮瘤。一般来说,其非特异性给医学专业人员的诊断带来了巨大挑战,这也是诊断延迟的主要原因。即使未观察到明确的危险因素,患者也应保持警惕。

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