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Successful lung transplantation in a case with diffuse pulmonary arteriovenous malformations and hereditary hemorrhagic telangiectasia.
- Source :
-
American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons [Am J Transplant] 2013 Dec; Vol. 13 (12), pp. 3278-81. Date of Electronic Publication: 2013 Oct 24. - Publication Year :
- 2013
-
Abstract
- Diffuse pulmonary arteriovenous malformations (AVMs) are associated with a poor prognosis and the therapeutic strategy remains controversial. We describe a pediatric patient with diffuse pulmonary AVMs associated with hereditary hemorrhagic telangiectasia (HHT), who presented with two cerebral AVMs in the parietal and occipital lobes as well. Of note, successful bilateral lung transplantation not only improved the hypoxemia but also resulted in size reduction of the cerebral AVMs. Although it is essential to consider involvements other than pulmonary AVMs, especially brain AVMs, to decide the indication, lung transplantation can be a viable therapeutic option for patients with diffuse pulmonary AVMs and HHT.<br /> (© Copyright 2013 The American Society of Transplantation and the American Society of Transplant Surgeons.)
- Subjects :
- Adolescent
Arteriovenous Malformations therapy
Female
Humans
Intracranial Arteriovenous Malformations complications
Ischemic Attack, Transient complications
Lung Diseases therapy
Telangiectasia, Hereditary Hemorrhagic complications
Telangiectasia, Hereditary Hemorrhagic therapy
Treatment Outcome
Arteriovenous Malformations complications
Lung Diseases complications
Lung Transplantation
Subjects
Details
- Language :
- English
- ISSN :
- 1600-6143
- Volume :
- 13
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons
- Publication Type :
- Academic Journal
- Accession number :
- 24165284
- Full Text :
- https://doi.org/10.1111/ajt.12499