Evidence map›Paper›PMID 41503238›Full record

ArticleRespirology case reports2026

A Case of Bronchial Dieulafoy's Disease Presenting as an Endobronchial Polypoid Lesion That Regressed After Bronchial Artery Embolisation.

Masayoshi Higashiguchi, Yu Yamaguchi, Satoshi Tetsumoto, Hideo Ishikawa

Abstract read
In one paragraph

Article in Respirology case reports, 2026. 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

4 authors.

Masayoshi HigashiguchiDepartment of Respiratory Medicine and Clinical Immunology Suita Municipal Hospital Osaka Japan.ORCID https://orcid.org/0000-0002-0617-1244
Yu YamaguchiHemoptysis and Pulmonary-Circulation Center, Eishinkai Kishiwada Rehabilitation Hospital Osaka Japan.
Satoshi TetsumotoDepartment of Respiratory Medicine and Clinical Immunology Suita Municipal Hospital Osaka Japan.
Hideo IshikawaHemoptysis and Pulmonary-Circulation Center, Eishinkai Kishiwada Rehabilitation Hospital Osaka Japan.ORCID https://orcid.org/0000-0002-5906-5285

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A 37-year-old woman presented to the hospital with a history of a small amount of hemoptysis. Bronchoscopy revealed a polypoid lesion in the left main bronchus. Due to oozing bleeding from the lesion, biopsy was deferred to avoid fatal haemorrhage risk. Bronchial angiography revealed an abnormal tortuous branch with pulmonary artery shunting. Bronchial artery embolisation with coils was successfully performed without complications. Bronchial Dieulafoy's disease was diagnosed. Follow-up bronchoscopy approximately 4 months post-embolisation showed regression of the polypoid lesion, with residual scar formation. Subsequently, the hemoptysis resolved completely. Dieulafoy's disease is characterised by a large-calibre, submucosal artery lying just beneath the mucosa, predisposing to abrupt haemorrhage despite minimal or no mucosal defect. Although this disease has been classically described in the gastrointestinal tract, analogous lesions also occur in the bronchial tree. This case highlights the visual confirmation of lesion regression by bronchoscopy after bronchial artery embolisation.

Indexed as

bronchial artery embolisationbronchial Dieulafoy's diseasehemoptysis

Identifiers

PMID41503238
PMCPMC12771591

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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.