ArticleRespiratory medicine case reports2019
Massive hemoptysis due to recurrence of bronchial to pulmonary vascular malformation: A case report.
Article in Respiratory medicine case reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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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.
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Who cites it
4 citing papers in PubMed, 5 citations in OpenAlex.
- Dieulafoy's disease of the bronchus: rare but potentially fatal: a case report and a review of literature.Journal of cardiothoracic surgery · 2023Review
- A case of bronchial Dieulafoy disease and literature review.Journal of cardiothoracic surgery · 2023Review
- Pediatric bronchial Dieulafoy's disease with bronchial artery embolization: two case reports.Translational pediatrics · 2023Article
- Research advances in Dieulafoy's disease of the bronchus (Review).Experimental and therapeutic medicine · 2022Review
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Authors and funding
5 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Bronchial dieulafoy lesions are quite rare with relatively few case reports in the literature. Symptoms may vary but the lesion is often associated with hemoptysis and may present as massive hemoptysis. We present a case of a 69-year-old male with a recurrent episode of hemoptysis three years after treatment for a bronchial dieulafoy lesion. The bronchoscopy done three years prior during an initial episode of hemoptysis showed a visible dieulafoy deep within a subsegmental branch of the right lower lobe. This case is unique because there are no other reports within the literature of a delayed recurrence several years after previous treatment of a bronchial dieulafoy lesion, which in our case was due to bronchial to pulmonary vascular malformation. Bronchial arteriography revealed a bronchial artery to pulmonary artery vascular malformation, which was successfully treated with coil embolization.
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