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进行性家族性肝内胆汁淤积症胆汁内分流术后结肠镜观察1例

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摘要 进行性家族性肝内胆汁淤积症(progressive familial intra—hepatic holestasis,PFIC)是一种严重的胆汁淤积性肝病,为常染色体隐性遗传性疾病。作者近期对1例PFIC部分胆汁内分流术后再发黄染的患儿进行结肠镜检查,现汇报如下:患儿,女,2岁3个月,因进行性家族性肝内胆汁淤积症行胆囊结肠吻合术后8个月,再发黄染,经口服利胆药无好转,渐加重20d人院。体查:皮肤巩膜黄染,伴全身瘙痒,躯干四肢多处有抓痕,腹胀腹软,可见手术瘢痕,肝肋下3em,
出处 《临床小儿外科杂志》 CAS 2013年第1期78-78,共1页 Journal of Clinical Pediatric Surgery
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