Abstract
Keratosis follicularis squamosa (KFS), first described by Dohi and Momose in 1903, is known to be a keratinizing disorder [1]. It is clinically characterized by 3–10mm diameter scaly patches scattered on the trunk and thighs, with brownish follicular plugs in the centre. The margins were slightly detached from the underlying epidermis. Histological examination reveals a dilated hair follicle with a follicular plug surrounded by lamellar orthohyperkeratosis and absence of the characterized keratinizing cells (corps and grains) appeared in Darier's disease[2].
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