Infantile acropustulosis is a syndrome that is characterized by recurrent crops of 1- to 2-mm, intensely pruritic vesicopustules on the distal extremities. The eruption is unresponsive to topical steroids, and pruritus is relieved only by soporific doses of antihistamines.
(Arch Dermatol 115:834-836, 1979)
Jarratt M, Ramsdell W. Infantile Acropustulosis. Arch Dermatol. 1979;115(7):834-836. doi:10.1001/archderm.1979.04010070010010