Graham‐Little Piccardi Lassueur syndrome and review of the literature
| Autor: | Hind M Almohanna, Fahad Alsudairy, Luluah Al Mubarak, Fares A Alkhayal |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2021 |
| Předmět: |
Medicine (General)
medicine.medical_specialty scaring alopecia Case Report Scarring alopecia Case Reports R5-920 medicine skin and connective tissue diseases Lichen planopilaris Groin integumentary system lichen planus business.industry Frontal fibrosing alopecia Graham‐Little Piccardi Lassueur syndrome Papule General Medicine medicine.disease Dermatology body regions Axilla stomatognathic diseases medicine.anatomical_structure Scalp Medicine medicine.symptom Graham Little Piccardi Lassueur syndrome business |
| Zdroj: | Clinical Case Reports Clinical Case Reports, Vol 9, Iss 9, Pp n/a-n/a (2021) |
| ISSN: | 2050-0904 |
| Popis: | Graham‐Little Piccardi Lassueur Syndrome (GLPLS) is a rare variant of lichen planopilaris (LPP) which characterized by triad of fibrosing alopecia of the scalp, non‐fibrosing alopecia of the axilla and groin, and a follicular spinous papule over the body. LPP is a rare follicular subtype of lichen planus which causes scarring alopecia of scalp, and there are three clinical subtypes of LPP including classic lichen planopilaris, frontal fibrosing alopecia, and GLPLS. Herein, we describe an adult dark‐skinned Saudi male with GLPLS who has numerous body follicular papules, complete loss of axillary hair, and partial loss of groin hair in addition to patchy fibrosing alopecia of the scalp. To the best of our knowledge, this is the first reported case of GLPLS in Saudi Arabia. Graham‐Little Piccardi Lassueur Syndrome (GLPLS) is a rare variant of Lichen planopilaris(LPP) which characterized by triad of fibrosing alopecia of the scalp, non‐fibrosing alopecia of the axilla and groin, and a follicular spinous papule over body. LPP is a rare follicular subtype of lichen planus. Which affects female most commonly. |
| Databáze: | OpenAIRE |
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