Graham Little-Piccardi-Lasseur syndrome

    B. Kamoona, D. Serafimova, V. Broshtilova, K. Drenovska, O. Bello, J. Kazandjieva, S. Marina
    Department of Dermatology and Venereology, Medical Faculty, Medical University – Sofia

    Graham Little-Piccardi-Lasseur syndrome is a rare lichenoid dermatosis defined by the triad of multifocal cicatricial alopecia of the scalp, noncicatricial alopecia of the axillae and groin, and a follicular lichen planus eruption on the body and scalp. This disease has caused much argument with respect to etiology, pathogenesis and difficulty responses to treatment.
    We present a 66 years old female patient with progressive cicatricial alopecia of the scalp, hyperpigmented lichen planus macules and few papules of the body skin, axillary and pubic hypotrichosis without skin atrophy of ten months duration. The diagnosis had been made depending on the clinical picture, dermoscopical and histological examinations.

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