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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1
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pubmed:dateCreated |
2010-1-21
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pubmed:abstractText |
Neurofibromatosis 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.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
1938-9116
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
44
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
52-5
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pubmed:meshHeading |
pubmed-meshheading:19828585-Aorta, Abdominal,
pubmed-meshheading:19828585-Aortic Rupture,
pubmed-meshheading:19828585-Aortography,
pubmed-meshheading:19828585-Autopsy,
pubmed-meshheading:19828585-Blood Vessel Prosthesis,
pubmed-meshheading:19828585-Blood Vessel Prosthesis Implantation,
pubmed-meshheading:19828585-Fatal Outcome,
pubmed-meshheading:19828585-Female,
pubmed-meshheading:19828585-Hematoma,
pubmed-meshheading:19828585-Humans,
pubmed-meshheading:19828585-Hypoxia, Brain,
pubmed-meshheading:19828585-Middle Aged,
pubmed-meshheading:19828585-Neurofibromatosis 1,
pubmed-meshheading:19828585-Stents,
pubmed-meshheading:19828585-Tomography, X-Ray Computed,
pubmed-meshheading:19828585-Treatment Outcome
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pubmed:year |
2010
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pubmed:articleTitle |
Vascular wall invasion in neurofibromatosis-induced aortic rupture.
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pubmed:affiliation |
Division of Vascular Surgery, Department of Pathology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania 15213, USA.
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pubmed:publicationType |
Journal Article,
Case Reports
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