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1例唐氏综合征患儿原发性心脏肿瘤的罕见病例。

A rare case of pediatric primary cardiac tumor in a patient with Down syndrome.

作者信息

Okada Kimiaki, Masuoka Ayumu, Hotoda Kentaro, Uno Yoshimasa, Suzuki Takaaki

机构信息

Department of Pediatric Cardiac Surgery, Saitama Medical University, International Medical Center, Hidaka City, Saitama, Japan.

出版信息

Asian Cardiovasc Thorac Ann. 2017 Nov;25(9):630-632. doi: 10.1177/0218492317721788. Epub 2017 Jul 13.

Abstract

Although hematological malignancies are a known complication of Down syndrome, few reports have described cases involving solid tumors. We describe the case of a 3-year-old Down syndrome girl with a primary solid cardiac tumor. Outpatient echocardiography after intracardiac repair of a ventricular septal defect at 6 months of age revealed a highly mobile pedunculated mass (8 × 9 mm) on the free wall of the right atrium. Due to potential incarceration of the mass in the tricuspid orifice, it was excised under extracorporeal circulation and cardiac arrest. Macroscopically, the tumor closely resembled a papillary fibroelastoma, although histopathological tests were inconclusive.

摘要

虽然血液系统恶性肿瘤是唐氏综合征已知的并发症,但很少有报告描述涉及实体瘤的病例。我们描述了一名3岁患有原发性心脏实体瘤的唐氏综合征女孩的病例。该女孩6个月大时进行室间隔缺损心内修复术后门诊超声心动图检查显示,右心房游离壁有一个高度活动的带蒂肿块(8×9毫米)。由于肿块可能嵌顿于三尖瓣口,遂在体外循环和心脏停搏下将其切除。大体上,该肿瘤很像乳头状纤维弹性瘤,不过组织病理学检查结果不明确。

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