Evidence map›Paper›PMID 41281098›Full record

ArticleCureus2025

A Case of Peutz-Jeghers Syndrome Complicated With Hirschsprung Disease.

Saori Murakawa, Masato Ogawa, Aoi Taku, Genshiro Esumi, Masanori Hisaoka, Takayuki Hoshina

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Cureus, 2025. 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.

Saori MurakawaDepartment of Pediatrics, University of Occupational and Environmental Health, Fukuoka, JPN.
Masato OgawaDepartment of Pediatrics, University of Occupational and Environmental Health, Fukuoka, JPN.
Aoi TakuDepartment of Pediatrics, Kyushu Rosai Hospital, Fukuoka, JPN.
Genshiro EsumiDepartment of Pediatric Surgery, University of Occupational and Environmental Health, Fukuoka, JPN.
Masanori HisaokaDepartment of Pathology and Oncology, University of Occupational and Environmental Health, Kitakyushu, JPN.
Takayuki HoshinaDepartment of Pediatrics, University of Occupational and Environmental Health, Fukuoka, JPN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report the first documented case of Peutz-Jeghers syndrome (PJS) complicated by Hirschsprung disease (HD). Despite the patient having intractable constipation since the neonatal period, the diagnosis of HD was significantly delayed due to the earlier diagnosis of PJS in infancy, which masked the presence of HD. This case highlights the importance of considering the possibility of an additional hereditary disease when a patient with a known hereditary gastrointestinal disease develops gastrointestinal symptoms that are atypical for that disease.

Indexed as

chronic constipationgastrointestinal diseasegenetic disorderhirschsprung diseasepeutz-jeghers syndrome

Identifiers

PMID41281098
PMCPMC12634138

What OpenQuestion holds

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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.