| Literature DB >> 16516609 |
Arnaud Fotso1, Didier Aubert, Khalil Saltoun, Giacomo Galli, Jean François Bonneville, Serge Bracard.
Abstract
Congenital paraspinal arteriovenous fistulae are rare and usually diagnosed after neurologic or cardiovascular manifestations. They may be discovered unexpectedly in children during clinical examination, which reveals the presence of a vascular murmur. The association with multicystic kidney is exceptional. We report 1 case with thoracic localization of a congenital paraspinal arteriovenous fistula associated with a multicystic kidney in a 3-year-old boy who was treated by endovascular embolization.Entities:
Mesh：
Year: 2006 PMID： 16516609 DOI： 10.1016/j.jpedsurg.2005.12.031
Source DB: PubMed Journal: J Pediatr Surg ISSN： 0022-3468 Impact factor: 2.545