Evidence map›Paper›PMID 42465157›Full record

ArticleCureus2026

Aorto-Oesophageal Fistula Presenting With Massive Upper Gastrointestinal Haemorrhage in Early Childhood: A Case Report.

Rukhsana Kausar, Shahir Ulazam

Abstract readCase Reports
In one paragraph

Article in Cureus, 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

2 authors.

Rukhsana KausarPaediatrics, Cork University Hospital, Cork, IRL.
Shahir UlazamPaediatrics, Cork University Hospital, Cork, IRL.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aorto-oesophageal fistula is an exceptionally rare but life-threatening cause of upper gastrointestinal bleeding in children. Early diagnosis is challenging because of its nonspecific presentation and rapid clinical deterioration. We report the case of a previously healthy young child who presented with massive haematemesis following a short viral prodrome and rapidly developed haemorrhagic shock. Initial laboratory investigations demonstrated severe acute anaemia requiring activation of the massive haemorrhage protocol and blood product resuscitation. Computed tomography imaging revealed abnormal vascular communication between the thoracic aorta and oesophagus consistent with an aorto-oesophageal fistula associated with significant aortic malformation. The patient required urgent multidisciplinary management, including intubation, transfer to a tertiary paediatric intensive care unit, and endovascular repair with covered aortic stent placement. Extensive investigations excluded infectious, inflammatory, and connective tissue disorders. The child recovered well following intervention, was gradually reintroduced to enteral feeding, and was discharged with ongoing specialist follow-up. This case highlights the importance of considering vascular causes in unexplained massive paediatric haematemesis. Prompt cross-sectional imaging, early haemodynamic stabilization, and multidisciplinary intervention are essential for survival. Endovascular repair may provide a life-saving minimally invasive treatment option in selected paediatric patients.

Indexed as

aorto-oesophageal fistulahaemorrhagic shockmassive haematemesispaediatric gastrointestinal bleedingthoracic endovascular repair

Identifiers

PMID42465157
PMCPMC13373295

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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.