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儿童布加综合征血管成形术随访26年

Angioplasty for Budd-Chiari Syndrome in a Child with 26-Year Follow-up.

作者信息

Gao Xixiang, Tong Zhu, Guo Lianrui, Li Jianxin, Zhang Jian, Gu Yongquan

机构信息

Department of Vascular Surgery, Xuan Wu Hospital and Institute of Vascular Surgery, Capital Medical University, Beijing, China.

Department of Vascular Surgery, Xuan Wu Hospital and Institute of Vascular Surgery, Capital Medical University, Beijing, China.

出版信息

Ann Vasc Surg. 2018 Aug;51:328.e7-328.e12. doi: 10.1016/j.avsg.2018.03.004. Epub 2018 May 17.

Abstract

Budd-Chiari syndrome (BCS) is a rare but life-threatening disease. If not treated promptly, it is almost always lethal with progressive liver failure, severe nutritional depletion, and renal failure at the late stage. We report the successful treatment of a 5-year-old boy with BCS due to a stenosis of the inferior vena cava (IVC) with a 26-year follow-up. We performed a percutaneous transluminal angioplasty, which resulted in a great improvement of BCS and the disappearance of ascites. Restenosis occurred at 25 years after the initial angioplasty, for which balloon angioplasty was repeatedly performed. The IVC was patent at 1-year follow-up after the second angioplasty.

摘要

布加综合征(BCS)是一种罕见但危及生命的疾病。如果不及时治疗,几乎总会因晚期进行性肝衰竭、严重营养消耗和肾衰竭而致命。我们报告了一名5岁因下腔静脉(IVC)狭窄导致布加综合征的男孩的成功治疗,并进行了26年的随访。我们进行了经皮腔内血管成形术,这使布加综合征有了很大改善,腹水消失。初次血管成形术后25年出现再狭窄,对此反复进行了球囊血管成形术。第二次血管成形术后1年随访时,下腔静脉通畅。

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