Case Report: Rupture of a gastric varix in liver cirrhosis associated with glycogen storage disease type III

被引:4
|
作者
Hashimoto, M
Watanabe, G
Yokoyama, T
Tsutsumi, K
Dohi, T
Matsuda, M
Okubo, M
Nakamura, N
Tsurumaru, M
机构
[1] Toranomon Gen Hosp, Dept Digest Surg, Minato Ku, Tokyo 105, Japan
[2] Toranomon Gen Hosp, Dept Endocrinol & Metab, Tokyo, Japan
[3] Univ Tsukuba, Dept Pediat, Ibaragi, Japan
关键词
debranching enzyme deficiency; glycogen storage disease type III; Hassab's operation; liver cirrhosis; oesophagogastric varix; portal hypertension;
D O I
10.1111/j.1440-1746.1998.tb00643.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Glycogen storage disease type III, or Cori's disease, is caused by a deficiency of amylo-1,6-glucosidase (debranching enzyme), which leads to the storage of an abnormal glycogen in the liver and in skeletal and heart muscle. Glycogen storage disease type III is usually characterized by hepatic symptoms, growth failure and myopathy. Even though liver cirrhosis is reported, portal hypertension is a rare complication of this disease. We describe the ease of a glycogen storage disease type III patient who was diagnosed at 3 years of age and developed complications (liver cirrhosis and rupture of a gastric varix) at 31 gears of age. We discuss the histological progression to cirrhosis of the liver and describe the liver enzyme profile at 3 and 31 years of age.
引用
收藏
页码:232 / 235
页数:4
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