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 |
| State | Published - Dec 1 2005 |
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ASJC Scopus subject areas
- Surgery
Cite this
Single-stage reconstruction of perforated choledochal cyst : Case report and review of the literature. / Franga, Dion L.; Howell, Charles G.; Mellinger, John D.; Hatley, Robyn M.
In: American Surgeon, Vol. 71, No. 5, 01.12.2005, p. 398-401.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Single-stage reconstruction of perforated choledochal cyst
T2 - Case report and review of the literature
AU - Franga, Dion L.
AU - Howell, Charles G.
AU - Mellinger, John D.
AU - Hatley, Robyn M.
PY - 2005/12/1
Y1 - 2005/12/1
N2 - 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.
AB - 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.
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UR - http://www.scopus.com/inward/citedby.url?scp=22344442841&partnerID=8YFLogxK
M3 - Article
C2 - 15986969
AN - SCOPUS:22344442841
VL - 71
SP - 398
EP - 401
JO - Handbook of Behavioral Neuroscience
JF - Handbook of Behavioral Neuroscience
SN - 0003-1348
IS - 5
ER -