Alnazawi Faisal F, Bnqadim Aseel T, Chapra Sumayyah M
General Surgery, International Medical Center, Jeddah, SAU.
Surgery, King Abdulaziz University Hospital, Jeddah, SAU.
Cureus. 2025 May 13;17(5):e84065. doi: 10.7759/cureus.84065. eCollection 2025 May.
Encapsulating peritoneal sclerosis (EPS) is a rare condition characterized by a fibrocollagenous membrane encasing the small intestine, leading to bowel obstruction. We report a case of a 31-year-old healthy male presenting with chronic abdominal pain, distention, weight loss, and jejuno-ileal intussusception managed conservatively at another facility. Despite hydration and bowel rest, symptoms persisted, prompting surgical intervention. A thick fibrous capsule encased the small bowel intraoperatively, necessitating adhesiolysis and capsule excision. The appendix was also removed prophylactically. Postoperatively, the patient experienced prolonged paralytic ileus, managed successfully with total parenteral nutrition and supportive measures. Histopathology confirmed collagenous peritoneal thickening with inflammatory infiltrates. The patient recovered well and is regaining bowel function; follow-ups showed no recurrence. This case highlights the diagnostic challenges of EPS, emphasizing the role of computed tomography and the need for surgical intervention in advanced cases to prevent complications. Early recognition and management are crucial for favorable outcomes.
包裹性腹膜硬化症(EPS)是一种罕见疾病,其特征为纤维胶原膜包裹小肠,导致肠梗阻。我们报告一例31岁健康男性病例,该患者在另一机构接受保守治疗,最初表现为慢性腹痛、腹胀、体重减轻和空肠回肠套叠。尽管进行了补液和肠道休息,症状仍持续存在,促使进行手术干预。术中可见一层厚厚的纤维性包膜包裹着小肠,需要进行粘连松解和包膜切除。阑尾也预防性切除。术后,患者出现了长时间的麻痹性肠梗阻,通过全胃肠外营养和支持措施成功处理。组织病理学证实胶原性腹膜增厚伴炎症浸润。患者恢复良好,肠道功能正在恢复;随访显示无复发。该病例突出了EPS的诊断挑战,强调了计算机断层扫描的作用以及晚期病例手术干预以预防并发症的必要性。早期识别和处理对于取得良好预后至关重要。