新医学Issue(12)：844-846,3.DOI:10.3969/g.issn.0253-9802.2014.12.016
先天性胆囊缺如一例
Congenital absence of gallbladder:one case report
査晓华1
作者信息
- 1. 442200 竹山，湖北竹山县人民医院普外科
- 折叠
摘要
Abstract
Congenital absence of gallbladder is rarely seen and difficult to be diagnosed. The misdi-agnosis rate is relatively high. In this paper,we reported one case diagnosed with cholelithiasis by gastrointesti-nal symptoms and explicit ultrasonic examination. The patient underwent cholecystectomy and common bile duct exploration. Intraoperatively,no gall bladder was detected whereas common bile duct stone was complicated. Clinical symptoms disappeared after surgery. This case prompted that understanding of congenital absence of gallbladder assisted the clinicians to identify the suspected cases and analyze the problems during the diagnosis and treatment,thereby avoiding unnecessary surgical exploration and reducing the risk of postoperative compli-cations.关键词
先天性胆囊缺如/诊断/治疗Key words
Congenital absence of gallbladder/Diagnosis/Treatment引用本文复制引用
査晓华..先天性胆囊缺如一例[J].新医学,2014,(12):844-846,3.
