Atrophoderma of Pasini and Pierini (APP) is an uncommon form of localized m
orphoea that occurs as superficial, hyperpigmented plaques distributed main
ly on the trunk and proximal part of the limbs. There is little information
about the influence of genetic and environmental factors on disease suscep
tibility and expression for localized scleroderma, although APP familial ca
ses have been reported.(1) We report three siblings without a family histor
y of autoimmune disease presenting cutaneous lesions suggesting morphoea (A
PP variant).