摘要
目的探讨先天性胆总管囊肿的诊断与治疗方法。方法对我院2002年1月～2007年1月收治的52例先天性胆总管囊肿患儿进行回顾性分析。结果52例均经B超、CT、MRCP等检查诊断为先天性胆总管囊肿,并行手术治疗,手术方式为胆总管囊肿切除、肝门空肠Roux-Y型吻合术。全组无死亡病例,无重大并发症,预后良好。结论B超是诊断先天性胆总管囊肿的首选方法,胆总管囊肿切除、肝门空肠Roux-Y型吻合术是治疗先天性胆总管囊肿的首选方法。
Objective To study the diagnosis and treatment of children suffered from congenital choledochocyst. Methods From January 2002 to January 2007,52 cases children with congenital choldochal cyst were used for this study. Results All the 52 cases underwent B-ultrasound, computer tomography （CT）, magnetic resonance cholangiopancreatography （MRCP） examination. They were diagnosed as choledochocyst and were treated with operation. Operative method included choledochocystectomy, cholecystectomy and Roux-Y cholangiojejunostomy. All cases were cured. There was no serious complication and without death case. Conclusion B-ultrasound examination is the best method to diagnose the congenital choledochocyst. CT and Roux-Y cholangiojejunostomy are also effective for treating the disease.
出处
《临床小儿外科杂志》
CAS
2007年第3期17-18,共2页
Journal of Clinical Pediatric Surgery
