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原发性恶性心包间皮瘤:一例报告。

Primary malignant pericardial mesothelioma: a case report.

机构信息

Cardiology Department, Habib Bourguiba University Hospital, Medenine, Tunisia.

出版信息

Pan Afr Med J. 2020 Aug 31;36:375. doi: 10.11604/pamj.2020.36.375.25336. eCollection 2020.

Abstract

Metastases to the heart and pericardium are much more common than primary malignant neoplasms. Primary malignant pericardial mesothelioma is a rare tumor that arises from the mesothelial cells of the pericardium. It is usually characterized by a delayed diagnosis, a low response to treatment, and a poor prognosis with an overall survival up to six months after the onset of symptoms. We report a rare case of a 32-year-old woman with primary pericardial malignant mesothelioma that was diagnosed 4 months after the onset of pericardial effusion as the first clinical manifestation.

摘要

心脏和心包转移瘤比原发性恶性肿瘤更为常见。原发性恶性心包间皮瘤是一种罕见的肿瘤,起源于心包的间皮细胞。它通常表现为诊断延迟、对治疗反应差以及预后不良,症状出现后总生存时间长达 6 个月。我们报告了 1 例罕见的 32 岁女性患者,以心包积液为首发临床表现,在出现心包积液 4 个月后被诊断为原发性心包恶性间皮瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8353/7666705/2602d914fb9f/PAMJ-36-375-g001.jpg

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