Pulmonary arteriovenous malformation revealing Osler-Weber-Rendu disease: A case report
- PMID: 35070308
- PMCID: PMC8762538
- DOI: 10.1002/ccr3.5294
Pulmonary arteriovenous malformation revealing Osler-Weber-Rendu disease: A case report
Abstract
Osler-Weber-Rendu disease is a genetic disease characterized by mucocutaneous and visceral telangiectasias. Pulmonary arteriovenous malformation is one of the main visceral complications revealing Osler-Weber-Rendu disease. The present case was a 34-year-old woman with exertional dyspnea and severe hypoxemia revealing pulmonary arteriovenous malformations on chest CT scan.
Keywords: Madagascar; Osler‐Weber‐Rendu disease; arteriovenous malformations; telangiectasias.
© 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.
Conflict of interest statement
None declared.
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References
-
- Shovlin CL, Guttmacher AE, Buscarini E, Faughnan ME, Hyland RH, Westermann CJ. Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu‐Osler‐Weber syndrome). Am J Med Genet. 2000;91:66‐67. - PubMed
-
- Dupuis‐Girod S, Ginon I, Saurin JC, Marion D, Guillot E, Decullier E. Bevacizumab in patients with hereditary hemorrhagic telangiectasia and severe hepatic vascular malformations and high cardiac output. JAMA. 2012;307:948‐955. - PubMed
-
- Cottin V, Blanchet AS, Cordier JF. Manifestations vasculaires pulmonaires de la maladie de Rendu‐Osler. Presse Med. 2005;34:1487‐1495. - PubMed
-
- Rendu M. Épistaxis répétées chez un sujet porteur de petits angiomes cutanés et muqueux. Gaz Hop Paris. 1886;135:1322‐1326.
-
- Plauchu H, Chadarevian JP, Bideau A, Robert JM. Age‐related clinical profi le of hereditary hemorrhagic telangiectasia in an epidemiologically recruited population. Am J Med Genet. 1989;32:291‐297. - PubMed
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