胆囊缺如合并胆总管囊肿——一种罕见的关联：一例病例报告及对可能的遗传或胚胎学联系的综述
Gallbladder agenesis with choledochal cyst--a rare association: a case report and review of possible genetic or embryological links.
作者信息
Bedi Nishant, Bond-Smith Giles, Kumar Senthil, Hutchins Robert
机构信息
Department of Surgery, Royal London Hospital, London, UK.
出版信息
BMJ Case Rep. 2013 Jan 9;2013:bcr2012006786. doi: 10.1136/bcr-2012-006786.
Abstract
Gallbladder agenesis is a rare congenital anomaly. Choledochal cysts are uncommon. The combination of both these entities in a 56-year-old woman is reported. A previously fit and well woman, presented to the emergency department with a 3-day history of abdominal pain. Preoperative imaging and intraoperative findings confirmed gallbladder agenesis and a type I choledochal cyst. There were no other anomalies. She underwent a resection of the choledochal cyst and reconstruction by hepaticojejunostomy.
摘要
胆囊缺如是一种罕见的先天性异常。胆总管囊肿并不常见。本文报道了一名56岁女性同时存在这两种情况。一名既往健康的女性因腹痛3天就诊于急诊科。术前影像学检查和术中发现证实为胆囊缺如及I型胆总管囊肿。无其他异常。她接受了胆总管囊肿切除术及肝空肠吻合术重建。
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