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病例报告:原发性心包血管肉瘤,一种导致心脏压塞的罕见病因。

Case report: Primary pericardial angiosarcoma, a rare cause of cardiac tamponade.

作者信息

Kong Ling-Yun, Cui Xiao-Zheng, Xiang Wei, Wang Xiu-Juan, Liu Fang

机构信息

Cardiovascular Center, School of Clinical Medicine, Beijing Tsinghua Changgung Hospital, Tsinghua University, Beijing, China.

出版信息

Front Cardiovasc Med. 2024 Feb 13;11:1344975. doi: 10.3389/fcvm.2024.1344975. eCollection 2024.

Abstract

Primary pericardial angiosarcoma is a rare malignancy of the pericardium with variable clinical features and imaging characteristics. Herein, we report a case of histopathologically confirmed pericardial angiosarcoma in a 66-year-old man. The patient developed cardiac tamponade in a short time period. The transthoracic echocardiography showed the presence of multiple irregular echodensities, heterogeneous in echogenicity, encasing the apex of both ventricles in the pericardial space, initially misinterpreted as pericardial effusion. The patient died of cardiogenic shock despite undergoing a surgical pericardiectomy. Pericardial angiosarcoma can manifest as a mass obliterating the pericardial sac, rather than the typical pericardial effusion observed on echocardiography. Multimodality imaging studies aid in diagnosing primary pericardial angiosarcoma, but the final diagnosis relies on tissue histopathology.

摘要

原发性心包血管肉瘤是一种罕见的心包恶性肿瘤,具有多样的临床特征和影像学表现。在此,我们报告一例经组织病理学确诊的66岁男性心包血管肉瘤病例。该患者在短时间内出现了心脏压塞。经胸超声心动图显示心包腔内存在多个不规则回声密度,回声不均匀,包绕着双心室的心尖部,最初被误诊为心包积液。尽管接受了心包切除术,但患者最终死于心源性休克。心包血管肉瘤可表现为填充心包腔的肿块,而非超声心动图上典型的心包积液。多模态影像学检查有助于原发性心包血管肉瘤的诊断,但最终诊断仍依赖于组织病理学检查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba24/10897014/8153855ab9f2/fcvm-11-1344975-g001.jpg

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