Evidence map›Paper›PMID 40026945›Full record

ArticleCureus2025

A Rare Case of Cystic Hemolymphangioma Associated With Intestine Duplication.

Nana Morishima, Rina Fujiwara-Tani, Ruiko Ogata, Shodo Sakai, Hiroki Kuniyasu

Abstract readCase Reports
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

5 authors.

Nana MorishimaMolecular Pathology, Nara Medical University, Kashihara, JPN.
Rina Fujiwara-TaniMolecular Pathology, Nara Medical University, Kashihara, JPN.
Ruiko OgataMolecular Pathology, Nara Medical University, Kashihara, JPN.
Shodo SakaiSurgery, Nozaki Tokushukai Hospital, Daito, JPN.
Hiroki KuniyasuMolecular Pathology, Nara Medical University, Kashihara, JPN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cystic hemolymphangioma and jejunal duplication are both typically congenital conditions and primarily identified in childhood, making adult diagnoses exceedingly uncommon. Cystic hemolymphangioma and intestinal duplication together are particularly rare. In this report, we present the case of an adult female patient with both. A pedunculated mass was identified outside the jejunal wall, with duplicated intestine on the stalk and cystic hemolymphangioma within the mass. Both lesions were surgically excised, and the patient has remained recurrence-free for five years postoperatively.

Indexed as

abdominal cystic tumordevelopmental disorderhemolymphangiomajejunal duplicationlymphangioma

Identifiers

PMID40026945
PMCPMC11870300

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.