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Common Bile Duct Cysts Leading to Cholestasis and Jaundice: A Rare Case Report
Department of Visceral Surgery, Hassan II Teaching Hospital, Fes, Morocco
Department of Visceral Surgery, Hassan II Teaching Hospital, Fes, Morocco
Department of Radiology, Hassan II Teaching Hospital, Fes, Morocco
Department of Visceral Surgery, Hassan II Teaching Hospital, Fes, Morocco
Department of Visceral Surgery, Hassan II Teaching Hospital, Fes, Morocco
Department of Radiology, Hassan II Teaching Hospital, Fes, Morocco
Department of Radiology, Hassan II Teaching Hospital, Fes, Morocco
Department of Visceral Surgery, Hassan II Teaching Hospital, Fes, Morocco
Department of Visceral Surgery, Hassan II Teaching Hospital, Fes, Morocco
Department of Visceral Surgery, Hassan II Teaching Hospital, Fes, Morocco
- 1 Department of Visceral Surgery, Hassan II Teaching Hospital, Fes, Morocco
- 2 Department of Visceral Surgery, Hassan II Teaching Hospital, Fes, Morocco
- 3 Department of Radiology, Hassan II Teaching Hospital, Fes, Morocco
- 4 Department of Visceral Surgery, Hassan II Teaching Hospital, Fes, Morocco
- 5 Department of Visceral Surgery, Hassan II Teaching Hospital, Fes, Morocco
- 6 Department of Radiology, Hassan II Teaching Hospital, Fes, Morocco
- 7 Department of Radiology, Hassan II Teaching Hospital, Fes, Morocco
- 8 Department of Visceral Surgery, Hassan II Teaching Hospital, Fes, Morocco
- 9 Department of Visceral Surgery, Hassan II Teaching Hospital, Fes, Morocco
- 10 Department of Visceral Surgery, Hassan II Teaching Hospital, Fes, Morocco
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Abstract
Cystic dilatation of the common bile duct constitutes a rare congenital malformation prevalent in people of Asian origin with a female predominance. Its classification follows that of Todani. The commonest form, found in 80% of cases, is type I. Common bile duct cysts are often diagnosed in 2 out of 3 cases, during childhood with adult forms often rare. We hereby report the case of a cystic dilatation of the bile duct in a 75-year-old patient without significant history of disease.
KeywordsDilatationCystCommon Bile DuctJaundiceAdult
- Yamaguchi, M. (1980) Congenital Choledochal Cyst: Analysis on 1433 Patients in the Japanese Literature. The American Journal of Surgery, 140, 653-657. http://dx.doi.org/10.1016/0002-9610(80)90051-3
- Lopez, R.R., Pinson, W., Campbell, J.R., Harrison, M. and Katou, R.M. (1991) Variation on Management Bases on Type of Choledochal Cyst. The American Journal of Surgery, 161, 612-615. http://dx.doi.org/10.1016/0002-9610(91)90911-V
- Alonso-Lej, et al. (1959) Congenital Choledocal Cyst, with Report of 2, and Analysis of 94, Cases. International Journal of Surgery, 108, 1-30.
- Todani, T., Watanable, Y., Narusue, M., Tabuchi, K. and Okajima, K. (1977) Congenital Bile Duct Cysts: Classification, Operative Procedures, and Review of Thirty-Seven Cases Including Cancer Arising from Choledochal Cyst. The American Journal of Surgery, 134, 263-269. http://dx.doi.org/10.1016/0002-9610(77)90359-2
- Banerjee Jesudason, S.R., Ranjan Jesudason, M., Paul Mukha, R., Vyas, F.L., Govil, S. and Muthusami, J.C. (2006) Management of Adult Choledochal Cysts—A 15-Year Experience. The Official Journal of the International HepatoPancreato Biliary Association (Oxford), 8, 299-305.
- Ammori, J.B. and Mulholland, M.W. (2009) Adult Type I Choledochal Cyst Resection. Journal of Gastrointestinal Surgery, 13, 363-367. http://dx.doi.org/10.1007/s11605-008-0521-z