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Case Reports in Radiology
Volume 2014, Article ID 291071, 4 pages
http://dx.doi.org/10.1155/2014/291071
Case Report

A Rare Anomaly of Biliary System: MRCP Evidence of a Cystic Duct Cyst

1Department of Radiology, Medical Faculty, Dicle University, Diyarbakir, Turkey
2Department of Pediatric Surgery, Medical Faculty, Dicle University, Diyarbakir, Turkey
3Department of Radiology, Yuzuncu Yil University School of Medical Science, Ercis Yolu, 65100 Van, Turkey

Received 5 March 2014; Revised 27 April 2014; Accepted 13 May 2014; Published 2 June 2014

Academic Editor: Wei-Chou Chang

Copyright © 2014 Cemil Goya et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Cystic duct cysts are a rare congenital anomaly. While the other bile duct cysts (choledochus and the intrahepatic bile ducts) are classified according to the classification described by Tadoni, there is no classification method described by the cystic duct cysts, although it is claimed that the cystic duct cysts may constitute a new “Type 6” category. Only a limited number of patients with cystic duct cysts have been reported in the literature. The diagnosis is usually made in the neonatal period or during childhood. The clinical symptoms are nonspecific and usually include pain in the right upper quadrant and jaundice. The condition may also present with biliary colic, cholangitis, cholelithiasis, or pancreatitis. In our case, the abdominal ultrasonography (US) performed on a 6-year-old female patient who presented with pain in the right upper quadrant pointed out an anechoic cyst at the neck of the gall bladder. Based on the magnetic resonance cholangiopancreatography (MRCP) results, a cystic dilatation was diagnosed in the cystic duct. The aim of this case-report presentation was to discuss the US and MRCP findings of the cystic dilatation of cystic duct, which is an extremely rare condition, in the light of the literature information.