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布加综合征患儿经颈静脉肝内门体分流术后心脏压塞的成功外科治疗:一种潜在的危及生命的情况。

Successful surgical management of cardiac tamponade following direct intrahepatic portosystemic shunt in a child with Budd-Chiari syndrome: A potentially life-threatening situation.

作者信息

Mishra Anand Kumar, Mandal Meenakshi, Mohamed Irshad R, Lal Sadhna, Bhujade Harish

机构信息

Department of Cardiothoracic and Vascular Surgery, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

Department of Gastroenterology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

出版信息

Ann Pediatr Cardiol. 2023 Sep-Oct;16(5):370-373. doi: 10.4103/apc.apc_107_23. Epub 2024 Apr 1.

Abstract

Direct intrahepatic portosystemic shunt is a technique of portocaval shunting performed through the percutaneous route in patients with Budd-Chiari syndrome. Stent migration into right-sided heart chambers or perforations causing hemopericardium and cardiac tamponade is rare and underreported. In a child with a coexisting decompensated liver disease, surgical intervention and cardiopulmonary bypass can be challenging. However, surgical management in these life-threatening situations is better than redo interventions.

摘要

直接肝内门体分流术是一种通过经皮途径对布加综合征患者进行门腔分流的技术。支架移入右侧心腔或穿孔导致心包积血和心脏压塞的情况罕见且报道较少。对于一名同时患有失代偿性肝病的儿童,手术干预和体外循环可能具有挑战性。然而,在这些危及生命的情况下进行手术管理比再次干预更好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54f6/11098295/010cc0b00419/APC-16-370-g001.jpg

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