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Graham-Little syndrome.

B Zegarska, D Kallas, R A Schwartz,R Czajkowski, G Uchanska,W Placek

Acta dermatovenerologica Alpina, Pannonica, et Adriatica(2010)

Cited 32|Views1
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Abstract
Graham-Little syndrome, also know as Graham-Little-Piccardi-Lassueur syndrome, is an unusual form of lichen planopilaris, characterized by the presence of cicatricial alopecia on the scalp, keratosis pilaris of the trunk and extremities, and non-cicatricial hair loss of the pubis and axillae. We present the case of a 47-year-old woman whose condition was unusual in that there was a prominence of scalp findings. Her treatment included a topical steroid plus systemic prednisone beginning at 30 mg every morning, which rendered her skin smooth, but did not alter her scalp lopecia.
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Key words
lichen planus,lichen planopilaris,alo-pecia,keratosis pilaris,lichenoid dermatosis,Graham-Little syndrome,Graham-Little-Piccardi-Lasseur syndrome
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