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成人先天性肝纤维化3例报告

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摘要 先天性肝纤维化(CHF)是一种多发生于儿童的常染色体隐性遗传性疾病,是一种罕见的、与胆管板畸形相关的肝内胆管遗传发育障碍疾病[1,2]。本病的发病率极低,有文献报道约为1/10000至1/20000[3],而在成年人中更为少见,因其临床表现无特异性,诊断方法主要依靠病理活组织检查,故对于临床诊断CHF尤为困难。本文报道十堰市太和医院感染科收治的3例成人先天性肝纤维化患者。
出处 《中西医结合肝病杂志》 CAS 2023年第9期854-856,共3页 Chinese Journal of Integrated Traditional and Western Medicine on Liver Diseases
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  • 2赵新颜,王宝恩,贾继东.36例先天性肝纤维化的临床病理特点[J].中华消化杂志,2005,25(12):748-749. 被引量:19
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