Thalidomide,an oral drug introduced in Germany in 1953 as a mild sedative,
was withdrawn from the world market when its teratogenic effect was discove
red some years later. It has since been selectively reintroduced to treat a
variety of autoimmune or inflammatory diseases such as erythema nodosum le
prosum, prurigo nodularis, graft-versus-host disease, and discoid lupus ery
thematosus (DLE). We report on three patients with long-standing,severe DLE
showing no response to systemic first-, second- and third-line treatments.
After four weeks of therapy with thalidomide the skin lesions had improved
dramatically and after three to six months all three patients responded wi
th an almost complete remission. The side effects of thalidomide, especiall
y somnolence and paresthesias, were minor and well tolerated by the patient
s. Our data confirm that thalidomide provides one of the most useful therap
eutic alternatives for chronic refractory DLE, despite the risks of teratog
enicity and polyneuropathy.