ArticleCureus2026
A Rare Case of Recurrent Intestinal Obstruction in a Young Female: Abdominal Cocoon.
Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Abdominal cocoon syndrome (ACS), also known as sclerosing encapsulating peritonitis (SEP), is an uncommon cause of intestinal obstruction characterized by partial or total encapsulation of the small intestine by a fibrous membrane. It typically presents with recurrent or subacute episodes of bowel obstruction and is often diagnosed intraoperatively due to the non-specific nature of clinical and radiologic findings. A 17-year-old girl presented with symptoms of acute intestinal obstruction, including abdominal pain, vomiting, and obstipation. She had experienced similar episodes over the past year. Initial investigations were inconclusive, and though emergency laparotomy was considered, her symptoms transiently improved. Thus, an elective diagnostic laparoscopy was later performed, revealing the presence of an encapsulating fibrous membrane consistent with ACS. The membrane was dissected and removed. Histopathology showed fibrocollagenous tissue with inflammation but no granuloma or malignancy. The patient recovered well postoperatively, with a one-month follow-up uneventful. ACS remains a diagnostic challenge due to its rarity and non-specific presentation. Laparoscopic intervention serves as both a diagnostic and therapeutic tool, particularly in young patients with recurrent, unexplained episodes of obstruction.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.