Diagnosis: Reticulate Acropigmentation of Dohi
Description: Reticulate acral hyperpigmentation and hypopigmentation.
Morphology: Hyperpigmentation
Site: Hands and Feet
Sex: F
Age: 10
Type: Clinical
Submitted By: Nameer Al-Sudany
Differential DiagnosisHistory: Acropigmentation of Dohi or also known as Dyschromatosis Symmetrica Hereditaria is inherlied most commonly as an autosomal-dominant trait. Patients develop progressive pigmented and depigmented macules, often mixed in a reticulate pattern, concentrated on the dorsal extremities. Lesions appear in infancy or early childhood and commonly stop spreading before adolescence. The pigmentary lesions last for life.