<abstract xmlns="http://www.w3.org/1999/xhtml">

<p>Graham-Little-Piccardi-Lassueur syndrome (GLPLS) is a rare syndrome characterized by the triad of cicatricial alopecia of the scalp, non-cicatricial alopecia of the axilla and groin and follicular lichen planus eruptions on the trunk and extremities. GLPLS is considered to be a variant of lichen planopilaris. We report two cases that have fulfilled all of the criteria for GLPLS. The first case was a 71-year-old woman, admitted to the Department of Dermatology for pruritic perifollicullar erythema and scaling of the scalp, cicatricial scalp alopecia and hair loss of the axilla and pubic region for five months. Subsequently, follicular hyperkeratotic eruptions and hyperpigmented macules on the skin of the chest and abdomen appeared. The second case was a 48-year-old man with pruritic follicular papules on the face, trunk and extremities for four months. All of the laboratory examinations in both patients were within normal limits. No alternation in the general condition of the patients was observed. Histological examinations in both patients confirmed the diagnosis GLPLS. The patients were treated with systemic and local corticosteroid resulting in marked improvement of the skin lesions; however, cicatricial scalp alopecia showed no response to the treatment.</p>
</abstract>

Graham-Little-Piccardi-Lassueur syndrome (GLPLS) is a rare syndrome characterized by the triad of cicatricial alopecia of the scalp, non-cicatricial alopecia of the axilla and groin and follicular lichen planus eruptions on the trunk and extremities. GLPLS is considered to be a variant of lichen planopilaris. We report two cases that have fulfilled all of the criteria for GLPLS. The first case was a 71-year-old woman, admitted to the Department of Dermatology for pruritic perifollicullar erythema and scaling of the scalp, cicatricial scalp alopecia and hair loss of the axilla and pubic region for five months. Subsequently, follicular hyperkeratotic eruptions and hyperpigmented macules on the skin of the chest and abdomen appeared. The second case was a 48-year-old man with pruritic follicular papules on the face, trunk and extremities for four months. All of the laboratory examinations in both patients were within normal limits. No alternation in the general condition of the patients was observed. Histological examinations in both patients confirmed the diagnosis GLPLS. The patients were treated with systemic and local corticosteroid resulting in marked improvement of the skin lesions; however, cicatricial scalp alopecia showed no response to the treatment.

Graham-Little-Piccardi-Lassueur Syndrome: Two Case Reports and Review of the Literature

Acta Medica Bulgarica

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

Graham-Little-Piccardi-Lassueur syndrome (GLPLS) is a rare syndrome characterized by the triad of cicatricial alopecia of the scalp, non-cicatricial alopecia...

Graham-Little-Piccardi-Lassueur Syndrome: Two Case Reports and Review of the Literature

Pubblicato online: 24 nov 2020

Pagine: 58 - 62

Ricevuto: 08 lug 2020

Accettato: 15 lug 2020

DOI: https://doi.org/10.2478/amb-2020-0047

Parole chiave
lichen planopilaris, cicatricial alopecia, Graham-Little-Piccardi-Lassueur syndrome

© 2020 L. Dourmishev et al., published by Sciendo

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

Graham-Little-Piccardi-Lassueur Syndrome: Two Case Reports and Review of the Literature

Pubblicato online: 24 nov 2020

Pagine: 58 - 62

Ricevuto: 08 lug 2020

Accettato: 15 lug 2020

DOI: https://doi.org/10.2478/amb-2020-0047

Parole chiavelichen planopilaris, cicatricial alopecia, Graham-Little-Piccardi-Lassueur syndrome

© 2020 L. Dourmishev et al., published by Sciendo

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

Parole chiave
lichen planopilaris, cicatricial alopecia, Graham-Little-Piccardi-Lassueur syndrome