一名两个月大婴儿患卡罗利综合征合并常染色体隐性多囊肾病。
Caroli's syndrome with autosomal recessive polycystic kidney disease in a two month old infant.
作者信息
Kim Jeong Tae, Hur Yoon Jeong, Park Jee Min, Kim Myung Joon, Park Young Nyun, Lee Jae Seung
机构信息
Institute of Kidney Disease, Department of Pediatrics, Yonsei University College of Medicine, Seodaemun-gu, Seoul 120-752, Korea.
出版信息
Yonsei Med J. 2006 Feb 28;47(1):131-4. doi: 10.3349/ymj.2006.47.1.131.
Caroli's syndrome is a rare congenital disorder that involves intrahepatic bile duct ectasia and congenital hepatic fibrosis, frequently seen with concomitant autosomal recessive polycystic kidney disease (ARPKD). Literature on infants with ARPKD is rare. Here, we present a case of a two month old boy who was diagnosed with Caroli's syndrome and ARPKD.
卡罗里氏综合征是一种罕见的先天性疾病，涉及肝内胆管扩张和先天性肝纤维化，常伴有常染色体隐性多囊肾病（ARPKD）。关于患有ARPKD的婴儿的文献很少。在此，我们报告一例两个月大的男婴，他被诊断患有卡罗里氏综合征和ARPKD。
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