Piccardi-Lassueur-Graham-Little syndrome associated with frontal fibrosing alopecia*

نویسندگان

  • Andrea Alejandra Catalán Griffiths
  • Maribel Iglesias Sancho
  • Ana Iglesias Plaza
چکیده

Piccardi-Lassueur-Graham-Little syndrome is a rare entity characterized by progressive scarring alopecia of the scalp and keratotic papules on hairless skin, associated with non-scarring alopecia in the axilla and pubic area or lichen planus lesions. We describe the case of a 70-year-old woman who presented a Piccardi-Lasseur-Graham-Little syndrome, along with frontal fibrosing alopecia.

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Lichen planopilaris epidemiology: a retrospective study of 80 cases*

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Graham-Little Piccardi Lassueur syndrome: case report.

A 33-year-old woman presented with a 3-year history of progressive alopecia of the scalp. Past treatment with hydroxicloroquine did not show improvement. Physical examination revealed multiple areas of alopecia with atrophic aspect of the scalp, and axillary and pubic hypotrichosis. Dermoscopy showed hyperkeratosis and accentuation of follicular ostia. Anatomopathological examination revealed d...

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BACKGROUND Graham Little - Piccardi - Lassueur (GLPL) syndrome is a rare dermatosis characterized by scarring alopecia, loss of pubic and axillary hair, and progressive development of variously located follicular papules. We report a first case ever of an autoimmune response in a patient suffering from GLPL syndrome. METHODS Immunofluorescence and immunoblot analysis were used in a variety of...

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عنوان ژورنال:

دوره 92  شماره 

صفحات  -

تاریخ انتشار 2017