ArticleInternational journal of trichology
Graham-Little-Piccardi-Lassueur Syndrome with Mucosal Involvement: A Rare Case.
Article in International journal of trichology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Graham-Little-Piccardi-Lassueur syndrome (GLPLS) is a type of lichen planopilaris. It mainly affects females aged 40-60 years. It is characterized by the triad of patchy cicatricial alopecia of the scalp, noncicatricial alopecia of the axilla and groin and a follicular spinous papule on the body, scalp, or both. The diagnosis is based on clinicopathological correlation. Different modalities of treatment are available with unsatisfactory responses, so early diagnosis is necessary to prevent progression and scarring alopecia. A case of GLPLS with classical features on clinical, dermoscopic, and histopathological examination is presented in a 73-year-old female.
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