| Literature DB >> 8751640 |
W I Schievink1, M R Puumala, F B Meyer, C Raffel, J A Katzmann, J E Parisi.
Abstract
Recent studies have suggested that a deficiency of alpha 1-antitrypsin may be a genetic risk factor for the development of intracranial aneurysms and arterial fibromuscular dysplasia. The authors report a 16-year-old girl with a history of lung disease who suffered a cerebral hemorrhage due to the rupture of a giant intracranial aneurysm arising from the middle cerebral artery. This fusiform aneurysm was associated with fibromuscular dysplasia of the intimal type. She was found to have an unusual alpha 1-antitrypsin deficiency (PiMP phenotype). This case provides further evidence of an underlying arteriopathy in alpha 1-antitrypsin deficiency.Entities:
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Year: 1996 PMID: 8751640 DOI: 10.3171/jns.1996.85.3.0503
Source DB: PubMed Journal: J Neurosurg ISSN: 0022-3085 Impact factor: 5.115