Síndrome Graham-Little-Piccardi-Lasseur: a propósito de un caso y revisión de la literatura / Graham-Little-Piccardi-Lasseur syndrome: about a case and review of the literature
Rev. chil. dermatol
;
32(1): 58-60, 2016. ilus
Article
in Spanish
| LILACS
| ID: biblio-946805
RESUMEN
El Síndrome Graham-Little-Piccardi-Lasseur (GLPLS) corresponde a una variante clínica del llamado Liquen plano pilar y se caracteriza por presentar alopecia cicatrizal progresiva de cuero cabelludo con las características del Liquen plano pilar, alopecia no cicatrizal que compromete axilas y pubis, y erupción folicular liquenoide en tronco, extremidades, cara y/o cejas. Presentamos el caso de una paciente de 19 años que ha sido diagnosticada con GLPLS y cuyo curso ha sido de difícil manejo.
ABSTRACT
The Graham-Little-Piccardi-Lasseur Syndrome (GLPLS) corresponds to a clinical variant of Lichen planopilaris and is characterized by progressive scarring scalp alopecia with features of flat lichen, non-scarring alopecia localized in the armpits and pubis, and lichenoid follicular eruption in trunk, extremities, face and / or eyebrows. We present the case of a 19-year-old female patient who has been diagnosed with GLPLS and whose course has been difficult to manage.
Full text:
Available
Index:
LILACS (Americas)
Main subject:
Cicatrix
/
Alopecia
/
Lichen Planus
Type of study:
Diagnostic study
Limits:
Adult
/
Female
/
Humans
Language:
Spanish
Journal:
Rev. chil. dermatol
Journal subject:
Dermatology
Year:
2016
Type:
Article
Affiliation country:
Chile
/
Spain
Institution/Affiliation country:
Hospital Universitario de Bellvitge/ES
/
Pontificia Universidad Católica de Chile/CL
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