Evidence map›Paper›PMID 39726462›Full record

ArticleCureus2024

A Case Report of Rapunzel Syndrome in 14-Year-Old Girl.

Petar Stamov, Aleksandar Zlatarov, Stefan Mihaylov

Abstract readCase Reports
In one paragraph

Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

3 authors.

Petar StamovDepartment of General and Operative Surgery, Medical University "Prof. Dr. Paraskev Stoyanov", Varna, BGR.
Aleksandar ZlatarovDepartment of General and Operative Surgery, Medical University "Prof. Dr. Paraskev Stoyanov", Varna, BGR.
Stefan MihaylovDepartment of General and Operative Surgery, Medical University "Prof. Dr. Paraskev Stoyanov", Varna, BGR.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Trichobezoar or hairball in the proximal part of the gastrointestinal tract is a rare condition that occurs mainly in young and adolescent females. Since human hair is resistant to digestive enzymes and resistant to peristalsis, it easily accumulates between the folds of the mucosa. Over time, food and mucus accumulate within the hair, forming a compact mass that fills almost the entire lumen. When a trichobezoar passes through the pylorus and reaches the duodenum, and in some cases even the jejunum, it is referred to as Rapunzel syndrome. The treatment is surgical. Depending on the location and size of the trichobezoar, it can be removed endoscopically, laparoscopically, or by conventional laparotomy. Our report aims to present the surgical treatment of Rapunzel syndrome, as part of a comprehensive approach to this disease. We present a 14-year-old girl who was diagnosed and treated in our department. According to the world practice and our experience, conventional laparotomy as a method of treatment remains the first choice. The smaller gastrointestinal trichobezoars are asymptomatic or with unusual clinical manifestations. They grow undetected and combined with mental disorders can lead to significant gastrointestinal complications such as mainly intestinal obstruction and rarely erosions, ulcers, and perforation. The treatment is multimodal including surgeons, pediatricians, and psychiatrists.

Indexed as

abdominal painmental disorderspediatric surgeryrapunzel syndrometrichobezoartrichophagia

Identifiers

PMID39726462
PMCPMC11669606

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Registered trials

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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.