1.
Ned Tijdschr Geneeskd
; 156(37): A3451, 2012.
Artigo
em Holandês
| MEDLINE
| ID: mdl-22971426
RESUMO
A 21-year-old patient suffering from neurofibromatosis type 1 had received radiotherapy for a chiasm glioma 17 years ago. Fourteen years later, there was progressive deterioration of several neurological functions. MRI scans showed a progressively increasing volume loss of the left hemisphere and stenoses around the circle of Willis with secondary parenchymal effects. Based on conventional cerebral angiography, the diagnosis 'moyamoya syndrome' was made.