Publication:
Graham-Little-Piccardi-Lassueur Syndrome: Two Case Reports

creativeworkseries.issnISSN 2091-0231 eISSN 2091-167X
dc.contributor.authorPiya, Smriti
dc.contributor.authorBhusal, Mohan
dc.contributor.authorThapa, Deeptara Pathak
dc.contributor.authorShrestha, Joshana
dc.date.accessioned2025-10-09T09:37:41Z
dc.date.available2025-10-09T09:37:41Z
dc.date.issued2024
dc.descriptionAuthor Biographies Smriti Piya, Nepal Medical College and Teaching Hospital, Attarkhel, Kathmandu, Nepal Resident, Department of Dermatology,Nepal Medical College and Teaching Hospital, Attarkhel, Kathmandu, Nepal Mohan Bhusal, Nepal Medical College and Teaching Hospital, Attarkhel, Kathmandu, Nepal Lecturer, Department of dermatology,Nepal Medical College and Teaching Hospital, Attarkhel, Kathmandu, Nepal Deeptara Pathak Thapa, Nepal Medical College and Teaching Hospital, Attarkhel, Kathmandu, Nepal Professor & HOD, Department of Dermatology, Nepal Medical College and Teaching Hospital, Attarkhel, Kathmandu, Nepal Joshana Shrestha, Nepal Medical College and Teaching Hospital, Attarkhel, Kathmandu, Nepal Resident, Department of Dermatology, Nepal Medical College and Teaching Hospital, Attarkhel, Kathmandu, Nepal
dc.description.abstractAbstract: Graham-Little-Piccardi-Lassueur Syndrome (GLPLS) is a rare lichen planopilaris (LPP) subtype associated with scarring alopecia. It is thought to be an immune-mediated cause of alopecia. It is characterized by a triad of multifocal cicatricial alopecia of the scalp, noncicatricial alopecia of the axilla, and groin and a follicular lichen planus (LP) eruption. Herein, we present 2 cases of GLPLS. The first case is of a 33-year-old female presented with classical lichen planopilaris (LPP) of the scalp, follicular hyperkeratosis of bilateral arms, and noncicatricial alopecia of armpits. In the second case, a 17-year-old female presents with frontal fibrosing alopecia (FFA) of the scalp, follicular hyperkeratotic papules of the scalp, and noncicatricial alopecia of the bilateral armpits and genitalia. The physician can miss GLPLS due to the rarity of the condition.
dc.identifierhttps://doi.org/10.3126/njdvl.v22i2.68412
dc.identifier.urihttps://hdl.handle.net/20.500.14572/2546
dc.language.isoen_US
dc.publisherSociety of Dermatologists, Venereologists and Leprologists of Nepal (SODVELON)
dc.subjectFrontal fibrosing alopecia
dc.subjectGraham-Little-Piccardi-Lassueur Syndrome
dc.subjectLichen planopilaris
dc.titleGraham-Little-Piccardi-Lassueur Syndrome: Two Case Reports
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage31
oaire.citation.startPage28
relation.isJournalIssueOfPublicationcad24931-fc67-4ba8-9434-1063bb22b3e2
relation.isJournalIssueOfPublication.latestForDiscoverycad24931-fc67-4ba8-9434-1063bb22b3e2
relation.isJournalOfPublicationb2ab7aab-75b0-4bd1-9ed0-b8a91c68201a

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