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谢伊综合征(I型黏多糖贮积症)的手术治疗:两例报告

Surgical treatment for Scheie's syndrome (mucopolysaccharidosis type I-S): report of two cases.

作者信息

Minakata K, Konishi Y, Matsumoto M, Miwa S

机构信息

Department of Cardiovascular Surgery, Japanese Red Cross Society, Wakayama Medical Center, Wakayama-city.

出版信息

Jpn Circ J. 1998 Sep;62(9):700-3. doi: 10.1253/jcj.62.700.

Abstract

Scheie's syndrome (mucopolysaccharidosis type I-S) is a rare genetic lysosomal storage disease affecting mucopolysaccharide metabolism, and is known to include cardiovascular disease. Surgical treatment was carried out in 2 patients with Scheie's syndrome. Patient 1 was a 56-year-old man with triple-vessel coronary artery disease, who successfully underwent coronary artery bypass grafting. Patient 2 was a 52-year-old man with aortic and mitral valve stenosis, who successfully underwent combined aortic and mitral valve replacement. The literature on Scheie's syndrome associated with valvular and coronary artery disease is also reviewed.

摘要

谢伊综合征(黏多糖贮积症I-S型)是一种罕见的影响黏多糖代谢的遗传性溶酶体贮积病,已知其会引发心血管疾病。对2例谢伊综合征患者实施了外科治疗。患者1为一名56岁男性,患有三支冠状动脉疾病,成功接受了冠状动脉搭桥手术。患者2为一名52岁男性,患有主动脉瓣和二尖瓣狭窄,成功接受了主动脉瓣和二尖瓣联合置换术。本文还对与瓣膜和冠状动脉疾病相关的谢伊综合征的文献进行了综述。

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