ICD·index Chapters ENESDE
8A45.44 category

Demyelination due to systemic vasculitis

Definition

Globally, cerebrospinal involvement is infrequent in small-medium size vessel vasculitis, including Wegener’s granulomatosis, microscopic polyangiitis, Churg-Strauss syndrome, polyarteritis nodosa, cryoglobulinemic vasculitis, and Behçet’s disease. CNS involvement occurs in less than 15% of patients. Transient ischaemic episodes or strokes can occur in a multifocal pattern in patients with a systemic vasculitis.Neurological involvement in polyarteritis nodosa, Churg-Strauss syndrome and Wegener's granulomatosis involves the peripheral nervous system with a rapidly involving and progressive mononeuritis multiplex or symmetrical polyneuopathy. Oculomotor palsies or visual impairment are seen with the orbital involvement that can occur in Wegener's granulomatosis [McAlpine, 2006, pg 404]. Patients with active polyarteritis will be systemically unwell and will have a raised erythrocyte sedimentations rate and the presence of anti-neutrophil cytoplasmic antobodies. This clinical picture, in addition to peripheral nerve and systemic non-neurologcial involvement, means that multiple sclerosis will rarely arise in the differential diagnosis of systemin vasulitis.

Also indexed as

Demyelination due to systemic vasculitis

Nearby in White matter disorders due to certain specified systemic disease