Evidence map›Paper›PMID 41837091›Full record

ArticleInternational journal of surgery case reports2026

Type III abdominal cocoon syndrome presenting as mechanical small bowel obstruction: a rare pediatric case report.

Abdishakur Mohamed Abdi, Abdisalam Ismail Hassan, Abdullahi Yusuf Ali, Abdirahman Ahmed Mohamud, Abdinasir Mohamed Elmi, Ahmed Muhammad Bashir

Abstract readCase Reports
In one paragraph

Article in International journal of surgery case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Abdishakur Mohamed AbdiPediatric Surgery Department, Mogadishu Somali-Türkiye Recep Tayyip Erdoğan Training and Research Hospital, Mogadishu, Somalia.
Abdisalam Ismail HassanFaculty of Medicine and Health Sciences, Jamhuriya University of Science and Technology, Mogadishu, Somalia.ORCID https://orcid.org/0009-0008-0596-1106
Abdullahi Yusuf AliPediatric Surgery Department, Mogadishu Somali-Türkiye Recep Tayyip Erdoğan Training and Research Hospital, Mogadishu, Somalia.
Abdirahman Ahmed MohamudGeneral Surgery Department, Mogadishu Somali-Türkiye Recep Tayyip Erdoğan Training and Research Hospital, Mogadishu, Somalia.
Abdinasir Mohamed ElmiRadiology Department, Mogadishu Somali-Türkiye Recep Tayyip Erdoğan Training and Research Hospital, Mogadishu, Somalia.
Ahmed Muhammad BashirInternal Medicine Department, Somali Sudanese Specialized Hospital, Mogadishu, Somalia.ORCID https://orcid.org/0000-0002-7992-506X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction and importance: Abdominal cocoon syndrome, or sclerosing encapsulating peritonitis (SEP), is a rare cause of intestinal obstruction characterized by encasement of the bowel within a fibrous membrane. Its nonspecific presentation often delays diagnosis, with most cases identified intraoperatively. Type III SEP, involving the small bowel and additional abdominal organs, is especially uncommon. Case presentation: A 14-year-old Somali female presented with a 5-month history of intermittent abdominal pain and greenish vomiting, with acute worsening in the preceding 5 days. Examination and imaging indicated small bowel obstruction. Contrast-enhanced CT revealed clustered dilated small bowel loops with collapsed distal segments. Exploratory laparotomy demonstrated a thick fibrous membrane encasing the entire small bowel, cecum, and left colon, confirming Type III abdominal cocoon syndrome. The membrane was completely excised, and a prophylactic appendectomy was performed. The patient had an uneventful postoperative recovery and remained asymptomatic at her 2-month follow-up. Clinical discussion: Abdominal cocoon syndrome is difficult to diagnose preoperatively due to its rarity and vague clinical features. Type III disease is extremely rare and poses additional diagnostic and surgical challenges. Although imaging may suggest the condition, definitive diagnosis is typically made during surgery. Membrane excision is the standard treatment and generally results in excellent outcomes when performed promptly. Conclusion: Abdominal cocoon syndrome should be considered in patients with unexplained intestinal obstruction. Early surgical intervention leads to favorable outcomes. This case represents a rare instance of Type III abdominal cocoon syndrome in Somalia, underscoring the need for heightened clinical suspicion and timely management in low-resource settings, underscoring the need for heightened clinical suspicion and timely management in low-resource settings.

Indexed as

abdominal cocoon syndromecase reportintestinal encapsulationsclerosing encapsulating peritonitissmall bowel obstructiontype III abdominal cocoon

Identifiers

PMID41837091
PMCPMC12981865

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