“…Two patients developed their SAH 3 and 36 months following the diag nosis of WG, and cerebral angiograms were negative in both cases [6], The other two SAHs were diagnosed at autopsy [5,7]. The last 3 patients presented with cerebral vasculitis, seizures, and a cerebrovascular accident, re spectively [10][11][12], CNS involvement in WG is caused primarily by three mechanisms: (l) Contiguous extension of granulomatous inflammation from primary sites outside the CNS.…”