Metzger Patrick Bastos, Costa Kamilla Rosales, Silva Simone Lessa E, Dos Santos Valter Ribeiro, Nunes Vinicius, Freire Murilo Quadro Berbert, Mello Milton Oliveira de Albuquerque
Escola Bahiana de Medicina e Saúde Pública - EBMSP, Salvador, BA, Brasil.
Hospital Santo Antônio, Obra Sociais Irmã Dulce - OSID, Salvador, BA, Brasil.
J Vasc Bras. 2021 Aug 2;20:e20200133. doi: 10.1590/1677-5449.200133. eCollection 2021.
The Budd-Chiari syndrome is a rare hepatic venous disease. It is more prevalent in young adults and may present in acute, subacute, or chronic forms, causing portal hypertension. Traditional treatment consists of thrombolysis techniques and transjugular intrahepatic portosystemic shunt, as a bridge to liver transplantation. Recently, use of balloon or stent angioplasty techniques has been reported for treatment of this condition. In this article, we report and discuss a case of BCS by membranous obstruction in the hepatic vein outflow tract, with middle hepatic vein thrombosis, in a 24-year-old patient. The treatment chosen and employed was transjugular balloon angioplasty, which achieved satisfactory results and good clinical evolution.
布加综合征是一种罕见的肝静脉疾病。它在年轻成年人中更为常见,可呈现急性、亚急性或慢性形式,导致门静脉高压。传统治疗包括溶栓技术和经颈静脉肝内门体分流术,作为肝移植的桥梁。最近,有报道使用球囊或支架血管成形术技术来治疗这种疾病。在本文中,我们报告并讨论了一名24岁患者因肝静脉流出道膜性梗阻伴肝中静脉血栓形成而导致布加综合征的病例。所选择并采用的治疗方法是经颈静脉球囊血管成形术,取得了满意的效果和良好的临床进展。