Evidence map›Paper›PMID 42130531›Full record

ArticleInternational journal of surgery case reports2026

Rapunzel Syndrome complicated by dual jejuno-jejunal intussusceptions: a case report.

Varag Abed, Marla Sacks, Sukaina B Alikhan, Christina Falcone, Hashmeet Kaur, Francisca T Velcek

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.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Varag AbedDepartment of General Surgery, Division of Pediatric Surgery, State University of New York, Downstate Health Sciences University, Brooklyn, NY, USA.ORCID https://orcid.org/0000-0001-8095-782X
Marla SacksDepartment of General Surgery, Division of Pediatric Surgery, State University of New York, Downstate Health Sciences University, Brooklyn, NY, USA.
Sukaina B AlikhanDepartment of General Surgery, Division of Pediatric Surgery, State University of New York, Downstate Health Sciences University, Brooklyn, NY, USA.
Christina FalconeDepartment of General Surgery, Division of Pediatric Surgery, State University of New York, Downstate Health Sciences University, Brooklyn, NY, USA.
Hashmeet KaurDepartment of General Surgery, Division of Pediatric Surgery, State University of New York, Downstate Health Sciences University, Brooklyn, NY, USA.
Francisca T VelcekDepartment of General Surgery, Division of Pediatric Surgery, State University of New York, Downstate Health Sciences University, Brooklyn, NY, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: A bezoar is a mass of indigestible material that accumulates in the gastrointestinal (GI) tract. Rapunzel Syndrome is a rare form of trichobezoar in which the hair mass extends beyond the pylorus into the small intestine, often leading to partial or complete GI obstruction. Presentation of case: A 9-year-old male with a significant medical history of non-verbal autism spectrum disorder and global developmental delay presented to the emergency department accompanied by his mother with a 1-week history of lethargy, abdominal pain, anorexia, and constipation. Computed tomography imaging demonstrated small bowel intussusception and a large, heterogeneous mass within the stomach. He was scheduled for urgent exploratory laparotomy with gastrotomy/enterotomy for foreign body removal. A longitudinal gastrotomy was performed, revealing a large gastrointestinal Rapunzel-type trichobezoar with foreign body components measuring 42 cm ×6 cm, extending from the stomach into the jejunum. The mass was successfully removed and sent for pathological evaluation. Intraoperative inspection of the bowel revealed two distinct points of intussusception: one located approximately 30 cm from the ligament of Treitz, and the other at 60 cm. Both were manually reduced, with the bowel appearing pink and well-perfused following the reduction. Discussion: The treatment of choice for Rapunzel Syndrome is surgical, often involving a gastrotomy and multiple enterotomies to thoroughly explore the stomach and small intestine for any retained bezoars. Conclusion: Rapunzel Syndrome is rare in children and has been linked to psychiatric disorders. Parental counseling, along with behavioral therapy and psychiatric follow-up plays an important role in the comprehensive management of these patients.

Indexed as

bezoarintussusceptionRapunzel Syndrometrichobezoar

Identifiers

PMID42130531
PMCPMC13166726

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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.