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先天性胆道闭锁临床研究现状 预览 被引量:5

Current Condition of Clinical Research of Congenital Biliary Atresia
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摘要 胆道闭锁是一种肝外胆管部分或全部发生闭锁的畸形。临床主要表现为进行性外科梗阻性黄疸。现就其病因学研究,尤其是病毒感染和胆管基板异常学说进行简要介绍,同时对胆道闭锁有关诊断、Kasai手术后并发症处理、治疗结果等现状进行阐述。
作者 施诚仁 SHI Cheng - ren (Department of Pediatric Surgery, Xinhua Hospital Affiliated to Medical College, Shanghai Jiaotong University, Shanghai 200092, China)
出处 《实用儿科临床杂志》 CAS CSCD 北大核心 2008年第23期 1802-1803,共2页 Journal of Applied Clinical Pediatrics
作者简介 施诚仁,男,主任医师,教授,硕士学位,博士生导师,研究方向为小儿外科疾病。
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