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Cite this article:
Hassan Mottaghi, Mahdi Kahrom, Mohammad Hassan Nezafati, Hadi Kahrom. Congenital pulmonary arteriovenous malformation: a rare cause of cyanosis in childhood. The Pan African Medical Journal. 2009;3:12 Key words: Pulmonary arteriovenous malformation, Cyanosis, Right to left shunting Permanent link: http://www.panafrican-med-journal.com/content/article/3/12/full Received: 17/09/2009 - Accepted: 21/10/2009 - Published: 08/11/2009 © Hassan Mottaghi et al. The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
Congenital pulmonary arteriovenous malformation: a rare cause of cyanosis in childhood
Hassan Mottaghi 1, Mahdi Kahrom 2,& , Mohammad Hassan Nezafati 2, Hadi Kahrom2
1Division of Cardiology, Department of Pediatrics, Imam Reza Hospital, 2 Department of Cardiac Surgery, Imam Reza Hospital, Mashhad University of Medical Sciences, Mashhad, Iran
&Corresponding author
Department of Cardiac Surgery, Imam Reza Hospital, Mashhad University of Medical Sciences, Mashhad, Iran
Abstract
Pulmonary arteriovenous malformation (PAVM) is a rare condition in which there is abnormal connection between pulmonary arteries and veins. The disorder usually appears in late childhood or early adult life, with dyspnea on exertion, clubbing or cyanosis. We present two patients with severe cyanosis and their work-up to diagnosis of PAVM, as a rare cause of cyanosis in childhood.

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