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.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 398-401 |
| Number of pages | 4 |
| Journal | American Surgeon |
| Volume | 71 |
| Issue number | 5 |
| DOIs | |
| State | Published - 2005 |
ASJC Scopus subject areas
- Surgery
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