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

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.

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Publication Details

Journal
Respirology Case Reports
Published
2026-01-01
DOI
https://doi.org/10.1002/rcr2.70450
Primary Topic
Vascular Anomalies and Treatments
Type
article
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article

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

Masayoshi Higashiguchi, Satoshi Tetsumoto, Yu Yamaguchi, Hideo Ishikawa
Respirology Case Reports
Vascular Anomalies and Treatments
article

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

Masayoshi Higashiguchi, Satoshi Tetsumoto, Yu Yamaguchi, Hideo Ishikawa
article en

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.

Respirology Case ReportsVol. 14(1)
Kishiwada City Hospital (JP), Suita Municipal Hospital (JP)
Good health and well-being
Openalex Percentile: Top 96%
Vascular Anomalies and Treatments
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