ArticleBJR case reports2022
Unusual case of small bowel intussusception in adult revealing a Peutz-Jeghers syndrome.
Article in BJR case reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
What it found
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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.
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Who cites it
4 citing papers in PubMed, 2 citations in OpenAlex.
- A case of multiple small bowel intussusceptions revealing a PEUTZ-JEGHERS syndrome.Radiology case reports · 2025Article
- Peutz-Jeghers syndrome revealed by CT finding of acute small bowel intussusception: A case report.Radiology case reports · 2025Article
- Poorly differentiated adenocarcinoma of the jejunum in a patient with Peutz-Jeghers syndrome: A case report.International journal of surgery case reports · 2024Article
- Peutz-Jeghers syndrome with polyps in the stomach, duodenum, and small and large intestine: a case report.Journal of medical case reports · 2024Article
Corrections and comments
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Authors and funding
5 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Peutz-Jeghers syndrome is a rare genetic disorder characterized by hyperpigmented mucocutaneous macules, hamartomatous polyps of the small intestine, and family history. These hamartomatous polyps can cause intermittent abdominal pain, chronic anemia, or even intussusception. Imaging has an important role in the diagnosis of this syndrome but also in the identification of complications and periodic surveillance. Here, we present a demonstrative case of a Peutz-Jeghers syndrome associated with intussusception in a 16-year-old patient.
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Registered trials
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