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Published on: February 9, 2011
Meckel's diverticulum manifested by a subcutaneous abscess
Oguzhan Karatepe1, Gokhan Adas, Merih Altiok
1Department of General Surgery, Okmeydani Training and Research Hospital, Istanbul 34715, Turkey. drkaratepe@yahoo.com
Abstract:
This case report describes an extremely rare complication of a Meckel's diverticulum: enterocutaneous fistula of the diverticulum. The presence of Meckel's diverticulum is a well known entity, but subcutaneous perforation of the diverticulum is very rare. Here we report the case of a patient with the complaint of a right lower quadrant abscess, preoperatively diagnosed as enterocutaneous fistula, which was determined intraoperatively to be a fistula resulting from Meckel's diverticulum.
Insights
This case report details a rare complication of Meckel's diverticulum: an enterocutaneous fistula. The study highlights a patient diagnosed with a right lower quadrant abscess, ultimately identified as a Meckel's diverticulum fistula.
Area of Science:
- Gastroenterology
- Surgical Case Reports
Background:
- Meckel's diverticulum is a common congenital anomaly of the small intestine.
- Complications of Meckel's diverticulum are well-documented, but subcutaneous perforation leading to fistula formation is exceptionally rare.
Observation:
- A patient presented with a right lower quadrant abscess.
- Preoperative diagnosis suggested an enterocutaneous fistula.
- Intraoperative findings confirmed the fistula originated from a Meckel's diverticulum.
Findings:
- The case report documents an extremely rare instance of enterocutaneous fistula secondary to Meckel's diverticulum.
- Subcutaneous perforation of the diverticulum was the underlying cause.
Implications:
- This case underscores the importance of considering Meckel's diverticulum in the differential diagnosis of unexplained abdominal abscesses and fistulas.
- Highlights the rarity and diagnostic challenges associated with Meckel's diverticulum complications.
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