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Ustekinumab as an Effective Therapeutic Option in Papillon-Lefèvre Syndrome: Long-Term Follow-Up

dc.contributor.authorSengkioun, Ozlem Apti
dc.contributor.authorYucelten, Deniz
dc.contributor.authorErgun, Tulin
dc.date.accessioned2026-11-05T11:00:53Z
dc.date.issued2026
dc.description.abstractPapillon-Lef & egrave;vre syndrome (PLS) is a rare autosomal recessive genodermatosis characterized by palmoplantar hyperkeratosis and severe periodontitis, leading to premature loss of both primary and permanent teeth, and treatment responses are often unsatisfactory. We report a 20-year-old female patient with PLS who presented with extensive palmoplantar hyperkeratosis and widespread psoriasiform plaques refractory to multiple conventional therapies. Treatment with ustekinumab resulted in marked clinical improvement by the sixth month after three subcutaneous injections. The patient has remained in sustained clinical remission during 6 years of continuous therapy, with only mild and intermittent recurrent plaques on the knees, suggesting that biologic therapy may represent a sustainable option in selected cases of PLS.
dc.identifier.doi10.1111/pde.70351
dc.identifier.issn0736-8046
dc.identifier.issn1525-1470
dc.identifier.urihttps://doi.org/10.1111/pde.70351
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/10585
dc.identifier.wosWOS:001865868100001
dc.language.isoen
dc.publisherWILEY
dc.relation.hasversion10.1111/pde.70351
dc.relation.ispartofPEDIATRIC DERMATOLOGY
dc.subjectbiologic therapy
dc.subjectpalmoplantar keratoderma
dc.subjectPapillon-Lef & egrave
dc.subjectvre syndrome
dc.subjectustekinumab
dc.subjectDermatology
dc.subjectPediatrics
dc.titleUstekinumab as an Effective Therapeutic Option in Papillon-Lefèvre Syndrome: Long-Term Follow-Up
dc.typeArticle
oaire.citation.editionScience Citation Index Expanded (SCI-EXPANDED)
person.identifier.ridHLH-8046-2023
person.identifier.ridAAB-6553-2020

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