先天性肺发育不全行经脐单孔腹腔镜胆囊切除术1例报告  

Single-port transumbilical laparoscopic cholecystectomy in an adult patient with congenital pulmonary hypoplasia:a case report

作　　者：秦佳升[1] 高毅[1] 潘明新[1] 

机构地区：[1]南方医科大学珠江医院肝胆二科,广东广州510282

出　　处：《南方医科大学学报》2011年第8期1334-1335,共2页Journal of Southern Medical University

摘　　要：目的先天性肺发育不全是一种罕见的肺发育异常疾病,全球发病率为五百万分之一,临床上多数患者在出生后因呼吸功能不全而夭折,成人患者罕见。我院于2011年5月收治1例先天性左肺发育不全合并胆囊管结石患者,行经脐单孔腹腔镜胆囊切除术,取得了与常规腹腔镜胆囊切除术同样满意的临床效果。Objective Congenital pulmonary hypoplasia is a rare developmental abnormality of the lung with an incidence rate of around 1/5000 000.As a fatal condition associated with respiratory insufficiency after birth,this disease is rare in adults.We treated a 29-year-old female patient with congenital pulmonary hypoplasia and concurrent of cystic duct calculus in May,2011 using single-port transumbilical laparoscopic cholecystectomy,which resulted in a good therapeutic effect comparable to that by routine laparoscopic cholecystectomy.

关 键 词：先天性肺发育不全 胆囊管结石 经脐单孔腹腔镜胆囊切除术 

分 类 号：R657.4[医药卫生—外科学]