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.
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Authors | H Fukushima, T Mitsuhashi, T Oto, Y Sano, K F Kusano, K Goto, M Okazaki, H Date, Y Kojima, H Yamagishi, T Takahashi |
Journal | American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons
(Am J Transplant)
Vol. 13
Issue 12
Pg. 3278-81
(Dec 2013)
ISSN: 1600-6143 [Electronic] United States |
PMID | 24165284
(Publication Type: Case Reports, Journal Article)
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Copyright | © Copyright 2013 The American Society of Transplantation and the American Society of Transplant Surgeons. |
Topics |
- Adolescent
- Arteriovenous Malformations
(complications, therapy)
- Female
- Humans
- Intracranial Arteriovenous Malformations
(complications)
- Ischemic Attack, Transient
(complications)
- Lung Diseases
(complications, therapy)
- Lung Transplantation
- Telangiectasia, Hereditary Hemorrhagic
(complications, therapy)
- Treatment Outcome
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