首页> 美国卫生研究院文献>BMJ Case Reports >Rare disease: Gallbladder agenesis with choledochal cyst—a rare association: a case report and review of possible genetic or embryological links
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Rare disease: Gallbladder agenesis with choledochal cyst—a rare association: a case report and review of possible genetic or embryological links

机译:罕见疾病:胆囊囊性胆囊发育不全-罕见的病例:病例报告和可能的遗传或胚胎学联系回顾

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摘要

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.
机译:胆囊发育不全是一种罕见的先天性异常。胆总管囊肿并不常见。据报道,这两个实体在56岁的女性中结合在一起。一位先前健康的女性,向急诊科介绍了3天的腹痛病史。术前影像学检查和术中发现证实胆囊发育不全和I型胆总管囊肿。没有其他异常。她接受了胆总管囊肿切除术,并进行了肝空肠吻合术。

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