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Graham-Little Piccardi Lassueur syndrome: case report.

作者信息

Steglich Raquel Bissacotti, Tonoli Renata Elise, Pinto Giselle Martins, Müller Fernanda Melo, Guarenti Isabelle Maffei, Duvelius Ernani Siegmann

机构信息

Dermatology Service, Charity Hospital of Porto Alegre, RS, Brazil.

出版信息

An Bras Dermatol. 2012 Sep-Oct;87(5):775-7. doi: 10.1590/s0365-05962012000500019.

DOI:10.1590/s0365-05962012000500019
PMID:23044575
Abstract

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 decrease in the number of hair follicles, upper perifollicular infiltrate and areas with fibrosis. The Piccardi-Lassueur-Graham-Little syndrome is a rare disorder, characterized by the triad of multifocal scarring alopecia of the scalp, keratotic follicular eruption and hypotrichosis of axillary and pubic regions. Management is a challenge and many medications tried have controversial results. We report a case of this rare syndrome which improved with corticoids.

摘要

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