先天性胆管囊肿研究进展  

Research Progress of Congenital Choledochal Cyst

作　　者：路景绍 吴璇昭[2] 

机构地区：[1]贵州医科大学,贵州贵阳550004 [2]贵阳医学院附属医院小儿外科,贵州贵阳550004

出　　处：《中外医疗》2016年第5期196-198,共3页China & Foreign Medical Treatment

摘　　要：先天性胆管囊肿,亦称先天性胆管囊状扩张症,该病具有分型复杂、症状无特异性、手术难度大、并发症多等特点。因该病临床症状不典型,且常合并肝、胆、胰疾病,极易被误诊或者漏诊,严重威胁患者生命、健康。随临床诊疗技术的不断更新,该病在病理、形态、病因、诊断及治疗方面均有所发展,该综述通过其病因、分型着手,对近年来先天性胆管囊肿的诊断、治疗方面内容进行综述。Congenital choledochal cyst is also known as congenital cystic dilatation of bile duct, the disease has the characteristics such as complex type, aspecific symptom, difficult operation and many complications, misdiagnosis and missed diagnosis of the disease can easily occur because of its atypical clinical symptoms and also because it was often with hepatic, biliary and pancreas diseases, which seriously threatens the patient＇s life and health, with the constant update of clinical diagnosis and treatment technology, the disease has some developments in the aspects such as pathology, form, pathogeny, diagnosis and treatment, this paper summarizes the diagnosis and treatment of congenital choledochal cyst？in recent years starting from its pathogeny and type.

关 键 词：先天性胆管囊肿 诊断 治疗 进展 

分 类 号：R575.7[医药卫生—消化系统]