Evidence map›Paper›PMID 39629260›Full record

ArticleRespirology case reports2024

Hemoptysis caused by bronchial artery-pulmonary artery fistula complicated with Dieulafoy disease: A case report.

Chongqing Lv, Tao Feng, Shishou Wang, Chen Lin

Abstract read
In one paragraph

Article in Respirology case reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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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.

Chongqing LvDepartment of General Surgery Shengli Oilfield Central Hospital Dongying China.
Tao FengDepartment of Respiratory and Critical Care Medicine Shengli Oilfield Central Hospital Dongying China.
Shishou WangDepartment of Respiratory and Critical Care Medicine Shengli Oilfield Central Hospital Dongying China.
Chen LinDepartment of Respiratory and Critical Care Medicine Shengli Oilfield Central Hospital Dongying China.ORCID https://orcid.org/0009-0002-6826-1437

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bronchial artery-pulmonary artery fistula (BPF) is a rare vascular malformation of the bronchial arteries, associated with congenital heart disease, pulmonary hypertension, or pulmonary infections. It typically presents in adulthood and has a low incidence. Another rare vascular anomaly, bronchial Dieulafoy disease (BDD), is characterized by an abnormally developed artery within the submucosa of the bronchial tree. This condition is thought to arise from a combination of congenital dysplasia and chronic airway inflammation or injury. Both BPF and BDD are uncommon causes of hemoptysis, and their simultaneous occurrence is exceptionally rare. This report discusses a case of BPF complicated by BDD in a patient who presented with recurrent hemoptysis. The diagnosis was established through bronchial artery angiography, bronchoscopy, and surgical pathology. By examining the clinical features, imaging findings, and diagnostic criteria of these conditions, this case report aims to enhance clinicians' understanding of cryptogenic hemoptysis and provide valuable insights for clinical practice.

Indexed as

bronchial artery‐pulmonary artery fistulabronchial Dieulafoy diseasehemoptysis

Identifiers

PMID39629260
PMCPMC11613096

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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.