1985
DOI: 10.1001/archderm.1985.01660070067017
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Etretinate Therapy for Psoriasis

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1986
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Cited by 25 publications
(30 citation statements)
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“…Retinoids promote differentiation, and inhibit PMN migration and clonal growth of leukemic cell lines in vitro [6][7][8][9][10]. However, toxicity and in particular teratogenicity have limited their use [11][12][13][14].…”
Section: Introductionmentioning
confidence: 99%
“…Retinoids promote differentiation, and inhibit PMN migration and clonal growth of leukemic cell lines in vitro [6][7][8][9][10]. However, toxicity and in particular teratogenicity have limited their use [11][12][13][14].…”
Section: Introductionmentioning
confidence: 99%
“…One of our 2 patients in fact received a total dose of etretinate of about 15 g, which is comparable to the dose administered to the patients studied by Gilbert et al [1]. Since OPLL is a rare condition which has main ly been studied in Japan [5] it is possible that this con dition has until now been overlooked in patients treat ed with retinoids.…”
Section: Discussionmentioning
confidence: 56%
“…[1] regarding the lack of skeletal radiographic changes during short term etretinate therapy for psoriasis prompt us to report a peculiar skeletal involvement that we have ob served in 2 patients treated with etretinate for keratinization disorders.…”
mentioning
confidence: 89%
“…Acitretin has the major advantage of a much shorter half-life (50 h us 120 days) but can be partially metaboIized to etretinate, particularly when ingested with ethanol (39) and so pregnancy is not considered safe for 2 years after treatment with either Results of retinoid therapy are u s d y noted within 6 weeks in plaque psoriasis and within 2 weeks in erythrodermic forms. Most patients show improvement; in one study over 90% of patients achieved at least a 50% clearance of their disease (40). Acitretin is expensive and, in view of the difficulties involved in its drug.…”
Section: Retinoidsmentioning
confidence: 99%