Topical administration of tretinoin has proved to be effective in trea
ting clinical signs of photodamaged skin. In large-scale, double-blind
, placebo-controlled, 6-month trials, 0.05% tretinoin emollient cream
(Renova, Retinova) reduced fine wrinkles and skin roughness, and it pr
oduced histologic changes such as epidermal thickening, increased gran
ular layer thickness, stratum corneum compaction, and decreased melani
n content. Smaller changes were also observed at lower tretinoin conce
ntrations. Continued for another 6 months, 0.05% tretinoin emollient c
ream produced some additional clinical improvement but the histologic
changes observed in the epidermis (with the exception of melanin conte
nt) regressed toward baseline, raising questions as to what was respon
sible for the clinical improvement. After 12 months of treatment, ther
e were additional signs of tissue normalization including deposition o
f new collagen in the papillary dermis and ultrastructural evidence of
dermal reconstruction with improvement in the dermoepidermal junction
and correction of keratinocyte degeneration, changes that presumably
relate directly to tretinoin's mechanism of action. There was no sugge
stion of cytologic atypia in these studies or in biopsy specimens obta
ined after up to 4 years of continued use. Mild to moderate dermatitis
was the only common adverse reaction to tretinoin use. Percutaneous t
retinoin absorption is low, raising plasma levels by amounts that are
negligible compared with the normally low endogenous tretinoin levels.
No teratogenic effects have been observed in retrospective studies of
topical tretinoin application during the first trimester of pregnancy
. Thus, topical tretinoin is safe and effective in the treatment of ph
otodamage.