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Biomedical subjects

G B Gewirtzman

Publications and source records attributed to G B Gewirtzman.

4 recordsLinked to original sources

Naftifine cream 1% versus econazole cream 1% in the treatment of tinea cruris and tinea corporis.

Data from 104 subjects with tinea cruris or tinea corporis were evaluated in this double-blind, randomized study. The subjects applied naftifine cream 1% or econazole nitrate cream 1% to affected areas twice daily for 4 weeks. After 1 week of treatment naftifine had an overall cure rate of 19% compared with 4% for econazole (p = 0.03). A difference in favor of naftifine, although not statistically significant after the first week, persisted throughout treatment. Two weeks after the end of treatment both medications had overall cure rates of approximately 80%. Three percent of the naftifine-treated subjects had side effects compared with 13% of the econazole-treated subjects. In two subjects using econazole, the side effects were severe enough to warrant discontinuation of treatment.

Adolescent

Sweethearts' syndrome: purpura of a pleasant nature.

A common and a less common form of purpura seen in lovers are briefly reviewed. The diagnosis and course of a newly described syndrome of axillary purpura and paresthesia of the upper extremity in sweethearts is also discussed.

Adult

Erythrokeratodermia variabilis. A family study.

Erythrokeratodermia variabilis is a rare genodermatosis; American authors have reported only four previous cases. It had been a problem to obtain a large pedigree for clinical investigation. We studied a family with 12 involved members in five generations. Symmetrically distributed migratory patches and scaling plaques are characteristic and were found to involute with a combination of keratolytic agents and topical steroids. Exacerbations of these patches and plaques were noted in our female patients during such high estrogen states as pregnancy or oral contraceptive usage.

Adult

Nevus of Ota with ipsilateral congenital cataract.

A mongoloid woman had a nevus of Ota, an ipsilateral congenital cataract, and upper extremity hemiatrophy. To our knowledge, no similar patient has been previously reported. We review the literature concerning the nevus of Ota and cataracts in mongoloid indivuduals.

Adult