Acute abdomen and ascites as presenting features of autosomal dominant polycystic kidney disease

被引：3

作者：

Chaudhary, Sanjay ^{[1
]}

Qian, Qi ^{[1
]}

机构：

[1] Mayo Clin, Coll Med, Div Nephrol & Hypertens, Dept Med, Rochester, MN 55905 USA

来源：

WORLD JOURNAL OF HEPATOLOGY | 2012年 / 4卷 / 12期

关键词：

Autosomal dominant polycystic kidney disease; Acute abdominal pain; Ascites; polycystic liver disease;

D O I：

10.4254/wjh.v4.i12.394

中图分类号：

R57 [消化系及腹部疾病];

学科分类号：

摘要：

We describe a patient with sudden onset of abdominal pain and ascites, leading to the diagnosis of autosomal dominant polycystic kidney disease (ADPKD). Her presentation was consistent with acute liver cyst rupture as the cause of her acute illness. A review of literature on polycystic liver disease in patients with ADPKD and current management strategies are presented. This case alerts physicians that ADPKD could occasionally present as an acute abdomen; cyst rupture related to ADPKD may be considered in the differential diagnoses of acute abdomen. (C) 2012 Baishideng. All rights reserved.

引用

页码：394 / 398

页数：5

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