Objective:To assess the frequency and clinical characteristics of the increasingly recognised complication of cerebrovascular dysplasia in children with Neurofibromatosis type 1 (NF1).
Methods: A series of seven patients with NF1 and cerebrovascular dysplasias that were not secondary to radiotherapy were identified and prospectively assessed. An extensive review of the literature was also performed to identify associated features and the natural history of this potentially severe complication of NF1.
Results:The frequency of cerebrovascular dysplasia in NF1 is 2-5%, and vascular lesions are clearly visible on routine magnetic resonance imaging (MRI) of the brain. The majority of our patients were clinically asymptomatic, despite angiographic progression in some cases. Hypoplastic carotid canals and early appearance on MRI suggest that a proportion of cases of cerebrovascular dysplasia are congenital in origin.
Conclusion:These findings have implications for screening of asymptomatic patients with NF1, and highlight the difficult management decisions in those patients identified with cerebrovascular malformations.
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