心脏手术治疗 Andersen-Tawil 综合征患者。

Cardiac surgery for a patient with Andersen-Tawil syndrome.

机构信息

Department of Cardiovascular Surgery, Ehime Prefectural Central Hospital, Matsuyama City, Ehime, Japan.

出版信息

Ann Thorac Surg. 2010 Jul;90(1):285-7. doi: 10.1016/j.athoracsur.2009.12.045.

DOI:10.1016/j.athoracsur.2009.12.045

PMID:20609799

Abstract

Andersen-Tawil syndrome is an uncommon inherited autosomal disorder characterized by a prolonged QT interval, periodic paralysis, and dysmorphic features. The deleterious effects of cardioplegia on periodic paralysis and cardiac arrhythmia are unknown, and no studies have reported the performance of cardiac surgery in patients with Andersen-Tawil syndrome. We present a case of successful cardiac surgery in a patient with Andersen-Tawil syndrome, without using cardioplegia.

摘要

Andersen-Tawil 综合征是一种罕见的遗传性常染色体疾病，其特征为 QT 间期延长、周期性瘫痪和发育异常。心脏停搏液对周期性瘫痪和心律失常的有害影响尚不清楚，也没有研究报道过 Andersen-Tawil 综合征患者行心脏手术的情况。我们报告了 1 例成功施行心脏手术而未使用心脏停搏液的 Andersen-Tawil 综合征患者。