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Comparative evaluation of skin atrophy in man induced by topical corticoids
Author(s) -
JABLONSKA S.,
GRONIOWSKA M.,
DABROSWKI J.
Publication year - 1979
Publication title -
british journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.304
H-Index - 179
eISSN - 1365-2133
pISSN - 0007-0963
DOI - 10.1111/j.1365-2133.1979.tb05561.x
Subject(s) - fluocinolone acetonide , triamcinolone acetonide , atrophy , corticosteroid , medicine , acetonide , dermatology , significant difference , surgery
SUMMARY In this in‐patient study, mild skin atrophy was observed clinically in 6 out of a total of 22 patieents after fluocinolone acetonide an in one patient after flumethasone pivalate ointment applications. ( P < 0·005) Investigations were discontinued prematurely on days 14 and 17 in 2 patients because they developed early atrophy due to fluocinolone acetonide applications. Histological findings indicating either moderate or marked skin atrophy were evident in 15 patients after flucinolone acetonide as against one patient after flumethasone pivalate ointment applications ( P < 0·001). In comparison with the controls the mean decrease in epidermal thickness was more marked after fluocinolone acetonide applications, namely 30·5% vs 21·3% after flumethasone pivalate applications. The ultrastructural tissue changes were less marked at the sites to which flumethasone pivalate was applied. In comparison with controls, the percentages of mean decrease in diameters of collagen fibrils measured in six volunteer patients ranged from 5.1% to 27·6% after fluocinolone acetonide and from 0% to 12.3% following flumethasone pivalate ointment applications. This difference was statistically significant (range P < 0·001 to < 0·001). The experimental study has demonstrated that flumethasone pivalate displays only a mild atrophogenic effect and it is clinically and histologically significantly less atrophogenic than fluocinolone acclonide. Flumethasone pivalate can therefore be reckoned as a suitable topical corticosteroid especially for the long‐term treatment of corticoid‐responsive dermatoses.