Authors
Ozlem Apti Sengkioun, Deniz Yücelten, Tülin Ergun
Published in
Pediatric dermatology. Sep 02, 2026. Epub Sep 02, 2026.
Abstract
Papillon-Lefèvre 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.
PMID:
42683751
Bibliographic data and abstract were imported from PubMed on 02 Sep 2026.
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