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pubmed-article:6320398pubmed:abstractTextThalidomide (alpha-N-phtalimido-glutarimide) was withdrawn from sale in 1961 since it was held responsible for the birth of hundreds of phocomelus children. Despite this teratogenic potential, thalidomide remains a useful tool in the treatment of erythema nodosum leprosum, as well as in discoid lupus erythematosus when antimalarial drugs are ineffective or contraindicated. In addition, good results have been reported in several diseases such as actinic prurigo, polymorphous light eruption, Behçet syndrome, Weber-Christian disease, prurigo nodularis, pyoderma gangrenosum and ulcerative colitis. The mechanism of action is under debate but it is likely that thalidomide has immunomodulating properties by controlling T-suppressor lymphocytes, and anti-inflammatory effects, particularly an inhibition of neutrophil chemotaxis. Several attempts at synthesis of effective thalidomide derivatives devoid of teratogenic effects are ongoing.lld:pubmed
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pubmed-article:6320398pubmed:dateRevised2008-11-21lld:pubmed
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pubmed-article:6320398pubmed:year1983lld:pubmed
pubmed-article:6320398pubmed:articleTitle[Should thalidomide be rehabilitated?].lld:pubmed
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pubmed-article:6320398pubmed:publicationTypeEnglish Abstractlld:pubmed