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一例以心脏转移为表现的尤因肉瘤病例。

A Case of Ewing Sarcoma Presenting With Cardiac Metastasis.

作者信息

Murad Ruba, Bakkar Rimaa, Sukkar Rehab, Mahmoud Fadi, Al-Dairy Alwaleed

机构信息

Department of Cardiology, Damascus University Cardiac Surgery Hospital, Damascus, Syria.

Damascus University Cardiac Surgery Hospital, Damascus, Syria.

出版信息

World J Pediatr Congenit Heart Surg. 2019 Sep;10(5):632-634. doi: 10.1177/2150135119846047.

Abstract

Ewing sarcoma is the second most prevalent primary malignant bone tumor. Metastases from Ewing sarcoma to the heart are very rare. Herein, we present a case of undiagnosed Ewing sarcoma in a 12-year-old boy who presented with metastasis to the left atrium. The mass was prolapsing across the mitral valve. In view of the potential risk of embolization, urgent cardiac surgery was performed before the establishment of a definitive diagnosis. Histopathology was consistent with Ewing sarcoma. Subsequent magnetic resonance imaging revealed a mass in his left fibula. The patient was referred to the oncology center and received chemotherapy. One year later, he is alive with no evidence of recurrent cardiac involvement.

摘要

尤因肉瘤是第二常见的原发性恶性骨肿瘤。尤因肉瘤转移至心脏极为罕见。在此,我们报告一例12岁男孩,患有未被诊断出的尤因肉瘤,且已出现左心房转移。肿块经二尖瓣脱垂。鉴于存在栓塞的潜在风险,在明确诊断之前就进行了紧急心脏手术。组织病理学结果与尤因肉瘤相符。随后的磁共振成像显示其左侧腓骨有一肿块。该患者被转诊至肿瘤中心并接受了化疗。一年后,他仍存活,且无心脏受累复发的迹象。

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