Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/68520
Title: Giant choledochal cyst and infantile polycystic kidneys as prenatal sonographic features of Caroli syndrome
Authors: Kuntharee Traisrisilp
Fuanglada Tongprasert
Komson Wannasai
Theera Tongsong
Keywords: Medicine
Issue Date: 1-Jan-2020
Abstract: © 2019 Wiley Periodicals, Inc. Caroli syndrome is a developmental disorder caused by complete or partial arrest of ductal plate remodeling, leading to dilated bile ducts along with fibrosis surrounding the portal tracts. It is most commonly associated with autosomal recessive polycystic kidney (ARPKD). We report a unique case of Caroli syndrome, diagnosed prenatally at 24 weeks of gestation in a 29-year-old Thai woman. Ultrasound findings revealed the association of a fetal giant choledochal cyst with ARPKD. Autopsy findings showed ductal plate malformation, typical of Caroli syndrome, associated with giant choledocal cyst and ARPKD.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85073977450&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/68520
ISSN: 10970096
00912751
Appears in Collections:CMUL: Journal Articles

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