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Congenital Peritoneal Encapsulation: A Review.

Alison M Schultz1, Paul E Creger2, Trey J Mathews2

  • 1Edward Via College of Osteopathic Medicine, Spartanburg, SC, USA.

The American Surgeon
|May 9, 2025
PubMed
Summary

Congenital peritoneal encapsulation (CPE) is a rare condition where the small intestine is encased in a sac, causing obstruction. Early consideration of CPE is vital for unexplained abdominal pain or bowel obstruction.

Keywords:
congenital peritoneal encapsulationsmall bowel obstruction

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Area of Science:

  • Gastroenterology
  • Surgical Pathology
  • Developmental Biology

Background:

  • Congenital peritoneal encapsulation (CPE) is a rare developmental anomaly.
  • It involves the small intestines being enclosed within an accessory peritoneal sac.
  • CPE is an uncommon cause of abdominal pain and small bowel obstruction.

Purpose of the Study:

  • To highlight the diagnostic challenges of CPE.
  • To present a case of CPE presenting as small bowel obstruction.
  • To review recent cases and emphasize CPE in differential diagnoses.

Main Methods:

  • Case report of a 34-year-old male with acute abdominal pain.
  • CT imaging indicating possible small bowel obstruction.
  • Explorative laparotomy revealing peritoneal encapsulation and subsequent membrane removal.

Main Results:

  • The patient's small bowel obstruction was caused by congenital peritoneal encapsulation.
  • Histopathology confirmed the diagnosis of CPE.
  • A review of 21 recent cases provided insights into demographics, presentation, and management.

Conclusions:

  • CPE diagnosis is challenging due to nonspecific symptoms and imaging.
  • Considering CPE is crucial for unexplained abdominal pain or bowel obstruction.
  • Modern analysis underscores the importance of including CPE in differential diagnoses when conventional methods fail.