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 anse-en-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.
| Published in | Journal of Surgery (Volume 7, Issue 6) |
| DOI | 10.11648/j.js.20190706.11 |
| Page(s) | 154-157 |
| Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
| Copyright |
Copyright © The Author(s), 2024. Published by Science Publishing Group |
Cystic Dilatation, Bile Duct, CT Scan, MRI, Surgery
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APA Style
Toure Alpha Oumar, Seck Mamadou, Thiam Ousmane, Sylla Mohamed, Ka Ibrahima, et al. (2019). Management of Congenital Cystic Dilation of Common Bile Duct in Dakar (Senegal). Journal of Surgery, 7(6), 154-157. https://doi.org/10.11648/j.js.20190706.11
ACS Style
Toure Alpha Oumar; Seck Mamadou; Thiam Ousmane; Sylla Mohamed; Ka Ibrahima, et al. Management of Congenital Cystic Dilation of Common Bile Duct in Dakar (Senegal). J. Surg. 2019, 7(6), 154-157. doi: 10.11648/j.js.20190706.11
AMA Style
Toure Alpha Oumar, Seck Mamadou, Thiam Ousmane, Sylla Mohamed, Ka Ibrahima, et al. Management of Congenital Cystic Dilation of Common Bile Duct in Dakar (Senegal). J Surg. 2019;7(6):154-157. doi: 10.11648/j.js.20190706.11
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Download@article{10.11648/j.js.20190706.11,
author = {Toure Alpha Oumar and Seck Mamadou and Thiam Ousmane and Sylla Mohamed and Ka Ibrahima and Gueye Mohamadou Lamine and Seye Yacine and Sarr Ibrahima Sitor and Cisse Mamadou and Dieng Madieng},
title = {Management of Congenital Cystic Dilation of Common Bile Duct in Dakar (Senegal)},
journal = {Journal of Surgery},
volume = {7},
number = {6},
pages = {154-157},
doi = {10.11648/j.js.20190706.11},
url = {https://doi.org/10.11648/j.js.20190706.11},
eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.js.20190706.11},
abstract = {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 anse-en-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.},
year = {2019}
}
TY - JOUR T1 - Management of Congenital Cystic Dilation of Common Bile Duct in Dakar (Senegal) AU - Toure Alpha Oumar AU - Seck Mamadou AU - Thiam Ousmane AU - Sylla Mohamed AU - Ka Ibrahima AU - Gueye Mohamadou Lamine AU - Seye Yacine AU - Sarr Ibrahima Sitor AU - Cisse Mamadou AU - Dieng Madieng Y1 - 2019/10/10 PY - 2019 N1 - https://doi.org/10.11648/j.js.20190706.11 DO - 10.11648/j.js.20190706.11 T2 - Journal of Surgery JF - Journal of Surgery JO - Journal of Surgery SP - 154 EP - 157 PB - Science Publishing Group SN - 2330-0930 UR - https://doi.org/10.11648/j.js.20190706.11 AB - 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 anse-en-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. VL - 7 IS - 6 ER -
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