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. 2019 Jan 31;5(2):195–197. doi: 10.1016/j.jdcr.2018.10.026

Fig 1.

Fig 1

EV presenting in a patient with activated PI3Kδ syndrome. A to C, Physical examination notable for innumerous flat-topped, hypopigmented to gray, pinpoint papules that coalesce into larger plaques on the scalp, face, trunk, and bilateral upper and lower extremities. Koebnerization noted at some sites.