Graham Little-Piccardi-Lassueur syndrome (GLPLS) is a rare variant of lichen planopilaris, characterized by a triad of clinical signs including follicular spinous papules on the body area, scarring alopecia of the scalp and non-scarring alopecia of the groin and/or axilla. To date, fewer than 50 cases have been described in the literature. We first report a case of GLPLS investigated with non-invasive techniques such as dermoscopy and in vivo reflectance confocal microscopy (RCM) and successfully treated with narrowband-UVB (NB-UVB) phototherapy.

Clinical, Dermoscopic and In-Vivo Reflectance Confocal Microscopy Evaluation of a Case of Graham Little-Piccardi-Lassueur Syndrome Successfully Treated with Narrowband-UVB Phototherapy

Arisi M.
;
Gelmetti A.;Zanca A.;Rossi M.;Lorenzi L.;Calzavara-Pinton P.;Venturini M.
2020-01-01

Abstract

Graham Little-Piccardi-Lassueur syndrome (GLPLS) is a rare variant of lichen planopilaris, characterized by a triad of clinical signs including follicular spinous papules on the body area, scarring alopecia of the scalp and non-scarring alopecia of the groin and/or axilla. To date, fewer than 50 cases have been described in the literature. We first report a case of GLPLS investigated with non-invasive techniques such as dermoscopy and in vivo reflectance confocal microscopy (RCM) and successfully treated with narrowband-UVB (NB-UVB) phototherapy.
2020
2020
Ateneo di appartenenza
Inglese
10
4
887-892
892
Cicatricial alopecia; Graham Little-Piccardi-Lassueur syndrome; Lichen spinulosus; NB-UVB phototherapy
no
Not applicable
8
info:eu-repo/semantics/article
262
Arisi, M.; Gelmetti, A.; Zanca, A.; Rossi, M.; Lorenzi, L.; Incardona, P.; Calzavara-Pinton, P.; Venturini, M.
1 Contributo su Rivista::1.1 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11379/532164
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