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Caroli's disease misdiagnosed as intraductal papillary neoplasm of the bile duct

Authors
Gu D.H.Park M.S.Jung C.H.Yoo Y.J.Cho J.Y.Lee Y.H.Seo Y.S.Yim H.J.Um S.H.Ryu H.S.
Issue Date
Jun-2015
Publisher
대한간학회
Keywords
Caroli's disease; Intraductal papillary neoplasm of the bile duct; Segmentectomy
Citation
Clinical and Molecular Hepatology, v.21, no.2, pp 175 - 179
Pages
5
Indexed
SCOPUS
KCI
Journal Title
Clinical and Molecular Hepatology
Volume
21
Number
2
Start Page
175
End Page
179
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/30159
DOI
10.3350/cmh.2015.21.2.175
ISSN
2287-2728
2287-285X
Abstract
Caroli's disease is a rare autosomal-recessive disorder caused by malformation of the ductal plate during embryonic development. Although it is present at birth, Caroli's disease is typically not diagnosed until between the second and fourth decades of life, as it was in the present patient. Here we report a rare case of Caroli's disease limited to one liver segment, which was initially misdiagnosed as an intraductal papillary neoplasm of the bile duct. The asymptomatic patient was treated with liver segmentectomy.
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2. Clinical Science > Department of Internal Medicine > 1. Journal Articles
2. Clinical Science > Department of Gastroenterology and Hepatology > 1. Journal Articles
2. Clinical Science > Department of Endocrinology and Metabolism > 1. Journal Articles

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Anam Hospital (Department of Internal Medicine, Anam Hospital)
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