Graham-little-piccardi-lasseur syndrome: Case report and review of the syndrome in men

摘要

Graham-Little-Piccardi-Lasseur syndrome (GLPLS) is a rare lichenoid dermatosis characterized by progressive cic-atricial alopecia of the scalp, the loss of pubic and axillary hair, and keratosis pilaris. The syndrome is considered a form of follicular lichen planus. Clinically, GLPLS is characterized by a triad of features that include scarring alopecia of the scalp, non-cicatricial alopecia of the axillae and pubis, and a lichenoid follicular eruption. It was initially described by Piccardi in 1913 and in 1915, Graham-Little published a similar case observed by Lassueur.