Objective: To assess the effectiveness of alternative treatments for p
atients with refractory neurosarcoidosis. Design: Nonrandomized, retro
spective patient survey. Setting: Multicenter, involving patients care
d for by their primary physicians and neurologists, and referred for m
anagement advice to a neurology consultant. Interventions: Patients we
re treated with corticosteroids and alternative treatments, including
azathioprine, cyclosporine, cyclophosphamide, chlorambucil, methotrexa
te, and radiation therapy. Results: Prednisone dosage was successfully
tapered to 10 to 20 mg/d without worsening symptoms in 10 (38%) of th
e 26 patients studied. Six (23%) patients had improved conditions whil
e receiving alternative medication and nine (35%) patients' conditions
remained stable with no further progression of their symptoms. Radiot
herapy was beneficial for one of three patients. Four (15%) patients d
id not respond to alternative treatment and died of worsening symptoms
or infection. Adverse effects of the alternate medications resolved o
n discontinuing treatment with the offending agent. Conclusion: Altern
ative treatment is an effective adjunct to corticosteroid therapy for
some patients with refractory neurosarcoidosis. Clinical deterioration
may occur despite combined therapy. Choice of alternative therapy sho
uld be determined, in part, by its potential adverse effects.