Dilatation kystique du cholédoque associée à une dilatation kystique du canal cystique

Elabsi, M.; Amraoui, Maroc; Elouannani, Mohamed; Echarrab, M.; Faricha, A. Elalami; Errougani, A.; Moulay, R. Chkof

doi:10.1016/s0021-7697(06)73698-5

Cited by 2 publications

(1 citation statement)

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“…Its incidence varies from 1/13000 births in Japan to 1/2000000 in Europe and Africa [5][6][7]. Children and women are the most affected, particularly in Asia where 2/3 of cases are reported [8]. In Africa and the Western countries, it is generally discovered in adulthood, in the stage of complication as in our series [9,10].…”

Section: Discussionmentioning

confidence: 77%

Management of Congenital Cystic Dilation of Common Bile Duct in Dakar (Senegal)

Oumar¹,

Mamadou²,

Thiam³

et al. 2019

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Congenital cystic dilatation of common bile duct is a rare condition in Africa and the West. Its discovery is often fortuitous. The diagnosis is based on imagery. Our goal was to report 3 cases followed by a literature review. Three patients were received, most often for pain of the right hypochondrium. There were 2 women and 1 man aged between 16 and 27 years old. The physical examination was normal. The abdominal CT scan allowed us to diagnose a IA Todani cyst in all patients, including one degenerate. Cholecystectomy with resection of the bile duct, followed by hepatico-jejunal anastomosis on anseen-Y of Roux was performed in 2 patients. The immediate suites were simple. Histology showed inflammation on 2 operative specimen and cholangiocarcinoma on the 3rd. Choledochal DKC is a rare condition, often revealed in adults by complications. Bilio-pancreatic CT is an alternative to cholangio-MRI for its diagnosis with a type I Todani easily recognized. The treatment is surgical with a bad prognosis in case of degeneration.

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Section: Discussionmentioning

confidence: 77%