A woman in her early 30s was referred for assessment of a midline cystic mass in her 22-week fetus that was discovered on a routine detailed sonogram. Sonography and magnetic resonance imaging confirmed a midline cystic mass separate from the fetal bladder and stomach in an otherwise normal fetus. The diagnosis of a type I choledochal cyst was made.
Suchy FJ: Biliary atresia and other disorders of the extrahepatic bile ducts , in: Suchy FJ, Sokol RJ, Balisteri WF (eds): Liver Disease in Children. Philadelphia, Lippincott Williams & Wilkins, 2001, pp 267—271.
2.
Jiexiong F., Minju L., Hongfeng T., Weizhing G., Shaoyong Y.: Clinical and pathological characteristics of cystic lesions of extrahepatic bile duct in neonates. Acta Paediatr2003;92:1183—1189.
3.
Stringer M.: Choledochal cysts, in: Howard ER, Stringer MD, Columbani PM (eds): Surgery of the Liver, Bile Ducts and Pancreas in Children. 2nd ed. London, Arnold, 2002, pp 149—164.
4.
Bianchi DW, Crombleholme TM, D'Alton ME: Fetology Diagnosis & Management of the Fetal Patient. New York: McGraw-Hill Medical Publishing , 2000.
5.
Siddiqui M., Grier D., Cusick E.: Postnatal rupture of an antenatally diagnosed choledochal cyst: first case report. Acta Paediatrica2006;95:115—117.
6.
Woo R., Le D., Albanese CT, Kim SS: Robot assisted laparoscopic resection of a type I choledochal cyst in a child . J Laparoendosc Adv Surg Tech A2006;16:179—183.
