Published online Aug 6, 2025. doi: 10.12998/wjcc.v13.i22.106122
Revised: April 7, 2025
Accepted: April 21, 2025
Published online: August 6, 2025
Processing time: 77 Days and 16.1 Hours
Sclerosing encapsulating peritonitis (SEP), also known as abdominal cocoon syndrome, is rare in children. The etiology of primary SEP is believed to be associated with retrograde menstruation or viral peritonitis in young adolescent girls, whereas secondary SEP refers to SEP caused by other factors such as sur
We report the case of a 10-year-old girl with secondary SEP who was admitted to our center with acute bowel obstruction.
In this report, we emphasized the imaging manifestations, diagnosis, and operative management of the case. Although postoperative SEP in children is rare, the long-term prognosis is favorable when accompanied with accurate diagnosis, appropriate perioperative management, and timely follow-up.
Core Tip: Sclerosing encapsulating peritonitis (SEP) (abdominal cocoon syndrome), a rare etiology of pediatric intestinal obstruction, is predominantly secondary to prior abdominal surgery, peritoneal dialysis, or tuberculosis. Characterized by non-specific clinical presentations, it poses diagnostic challenges in children and frequently progresses to mechanical bowel obstruction. We present a 10-year-old female with postoperative SEP, highlighting its distinctive imaging features (including "cocoon-like" peritoneal encapsulation on computed tomography), intraoperative confirmation via adhesiolysis, and successful multi-disciplinary management. This case underscores the critical role of early radiological suspicion and surgical intervention in mitigating morbidity, while providing insights for differentiating SEP from other adhesive pathologies in pediatric populations.
