| Literature DB >> 15986969 |
Dion L Franga1, Charles G Howell, John D Mellinger, Robyn M Hatley.
Abstract
Choledochal cysts represent a rare disease in the Western world. We reviewed our recent experience with a case of perforated choledochal cyst, define the currently accepted treatment options, and review the literature of this unusual disease. An 11-month-old girl presented with abdominal pain and distention as well as non-bilious vomiting. Subsequent workup included endoscopic retrograde cholangiopancreatography revealing a perforated type I choledochal cyst. She underwent single-stage excision and reconstruction with a Roux-en-Y hepaticojejunostomy. Perforated choledochal cyst is a rare event, and prompt surgical intervention is warranted. Single-stage cystectomy and Roux-en-Y reconstruction is possible in select patients. A thorough understanding of the pathophysiology, management, and follow-up is required.Entities:
Mesh:
Year: 2005 PMID: 15986969
Source DB: PubMed Journal: Am Surg ISSN: 0003-1348 Impact factor: 0.688