TY  - JOUR
T1  - DIsseminated superficial actinic porokeratosis in a black patient
AU  - Filho J, Cutin S, Cucé L
Y1  - 1986/08/01
N1  - 10.1001/archderm.1986.01660200020003
JO  - Archives of Dermatology
SP  - 852
EP  - 853
VL  - 122
IS  - 8
N2  - To the Editor.— 
    Since 1966, when Chernosky and Freeman1 first described disseminated superficial actinic porokeratosis (DSAP), almost all reported cases have been in white patients. Few cases have been reported in dark-skinned patients.2-5 In 1981, Mensch and Hazen6 published the first case of DSAP occurring in a black patient.Prior to Chernosky and Freeman's report, cases of DSAP were probably classified in the disseminated superficial form of porokeratosis of Mibelli.7Disseminated superficial actinic porokeratosis is considered a distinct and well-defined entity with the following clinical features: evident actinic influence, no predominance in either sex, constant symmetry, and the presence of small slightly keratotic and sometimes pruritic lesions varying from 1 to 10 mm in diameter. It differs from the other forms of porokeratosis as it does not appear before the age of 15 years, and the Koebner phenomenon or associated neurologic diseases are absent. Only one case has
SN  - 0003-987X
M3  - doi: 10.1001/archderm.1986.01660200020003
UR  - http://dx.doi.org/10.1001/archderm.1986.01660200020003
ER  -