Long-term dupilumab therapy in Netherton syndrome with severe atopic manifestations: Case report and review of the literature

Yükleniyor...
Küçük Resim

Tarih

2023

Dergi Başlığı

Dergi ISSN

Cilt Başlığı

Yayıncı

John Wiley and Sons Inc

Erişim Hakkı

info:eu-repo/semantics/closedAccess

Özet

We herein present a unique patient of Netherton syndrome (NS) with ichthyosis linearis circumflexa (ILC) lesions associated with severe atopic manifestations since infancy, showing different responses of atopic and ILC lesions to a 2-year dupilumab therapy. The atopic eczematous lesions and pruritus healed remarkably, dramatically improving the patient's quality of life, whilst the scalp hair showed a clinical and light microscopic improvement. The additional recovery in axillary/pubic/extremity hair growth, sweating and nail growth in the presented case was not previously reported in NS patients treated with dupilumab. However, dupilumab had no therapeutic effect on ILC lesions which were not pruritic and showed a treatment-independent wax and waned course.

Açıklama

Anahtar Kelimeler

Atopic dermatitis, Hypohidrosis, Hypotrichosis, Ichthyosis, Netherton syndrome, Pruritus, Therapy-systemic

Kaynak

Australasian Journal of Dermatology

WoS Q Değeri

Q3

Scopus Q Değeri

Cilt

64

Sayı

2

Künye

Özkaya, E, Günay, MB, Babuna Kobaner, G, Keskinkaya, Z, & Gökalp, MO. (2023) Long-term dupilumab therapy in Netherton syndrome with severe atopic manifestations: Case report and review of the literature. Australas J Dermatol, 64(2), 272–277. https://doi.org/10.1111/ajd.13986