【右心房破裂致心脏血管肉瘤合并心包填塞1例】。

Q4 Medicine
Atsushi Kawakami, Yutaka Kobayashi, Ikumi Osawa, Masatoshi Sunada, Gaku Uchino, Shuta Kitaoka, Naomichi Uchida
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引用次数: 0

摘要

原发性心脏血管肉瘤极为罕见,预后较差。一名39岁男子因发烧及心包疼痛向医生求诊,并转介至我科接受进一步治疗。患者经心包穿刺后病情稳定,但入院时仍未确定心包填塞的原因。经食管超声心动图和心电图同步增强计算机断层扫描(CT)显示疑似右心房出血,需要开胸手术。术前影像学未见肿瘤,但术中发现疑似右心房肿瘤,切除后用牛心包补片修复。组织病理检查证实为血管肉瘤。血管肉瘤在早期诊断通常具有挑战性,多次检查对早期诊断和治疗很重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Cardiac Angiosarcoma with Cardiac Tamponade due to Ruptured Right Atrium:Report of a Case].

Primary angiosarcoma of the heart is extremely rare with poor prognosis. A 39-year-old man presented to his physician for evaluation of fever and pericardial pain and was referred to our department for further management. The patient's condition stabilized after pericardiocentesis;however, the cause of cardiac tamponade remained undetermined on admission. Transesophageal echocardiography and electrocardiography-synchronized contrast-enhanced computed tomography (CT) revealed a suspected source of bleeding in the right atrium, necessitating open chest surgery. Preoperative imaging showed no evidence of a tumor;however, intraoperatively, we observed a suspected right atrial tumor, which was resected, followed by repair using a bovine pericardial patch. Histopathological examination confirmed diagnosis of angiosarcoma. Angiosarcoma is often diagnostically challenging in the early stages, and multiple examinations are important for early diagnosis and treatment.

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