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pubmed-article:19828585pubmed:abstractTextNeurofibromatosis type 1 (NF-1) is an autosomal dominant disease primarily characterized by cutaneous café au lait macules, benign neurofibromas, and iris hamartomas. A spectrum of vascular abnormalities is associated with NF-1. We present a case of a 49-year-old female with NF-1 and spontaneous rupture of the infrarenal aorta caused by invasion of a neurofibroma and treated with endovascular stent grafting.lld:pubmed
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pubmed-article:19828585pubmed:authorpubmed-author:MakarounMiche...lld:pubmed
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pubmed-article:19828585pubmed:articleTitleVascular wall invasion in neurofibromatosis-induced aortic rupture.lld:pubmed
pubmed-article:19828585pubmed:affiliationDivision of Vascular Surgery, Department of Pathology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania 15213, USA.lld:pubmed
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