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American Journal of Respiratory and Critical Care Medicine logoLink to American Journal of Respiratory and Critical Care Medicine
. 2012 Dec 1;186(11):1191. doi: 10.1164/rccm.201206-1016IM

Dieulafoy’s Disease of the Bronchus

Todd Kolb 1, Christopher Gilbert 1, Elliot Fishman 2, Peter Terry 1, David Pearse 1, David Feller-Kopman 1, Lonny Yarmus 1
PMCID: PMC7051586  PMID: 23204378

A 44-year-old woman without significant medical history underwent bronchoscopy for recurrent hemoptysis. A tortuous, nonpulsatile vessel was prominent beneath the bronchial mucosa (Figure 1A, wide arrow). Computed tomography angiography (Figure 1B) and thoracic aortogram (Figure 1C) identified the tortuous vessel (arrows) as a hypertrophied bronchial artery arising from the distal aortic arch. Clinical evaluation showed no bronchiectasis, parenchymal lung disease, vascular malformation, mitral valve disease, or portal hypertension. Angiography revealed anastomosis between the hypertrophied bronchial artery and a pulmonary artery. The abnormal bronchial artery was embolized (Figure 1D), and the patient has had no further hemoptysis.

Figure 1.

Figure 1.

ML = middle lobe.

Dieulafoy initially described a tortuous, hypertrophied, submucosal artery as a gastrointestinal bleeding source in 1898 (1). Reports of similar lesions in the bronchial mucosa are rare, though endoscopic recognition is critical to prevent biopsy and iatrogenic hemorrhage, which may be life threatening.

Footnotes

Author disclosures are available with the text of this article at www.atsjournals.org.

Reference

  • 1.Dieulafoy G. Exulceratio simplex: l’intervention chirurgicale dans les hématémèsis foudroyantes consécutives à l’exulceration simple de l’estomac. Bull Acad Méd 1898;49:49–84. [Google Scholar]

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