Pruritus Anesis in Dystrophic Epidermolysis Bullosa Pruriginosa with Dupilumab

2Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Dystrophic epidermolysis bullosa pruriginosa (DEB-Pr) is a rare subtype of dystrophic epidermolysis bullosa, and traditional treatments have limited efficacy. Dupilumab has demonstrated remarkable efficacy in relieving pruritus. In this case study, after traditional treatment failed, providers recommended the patient begin dupilumab to treat his pruritus. The patient was administrated a loading dose of 600 mg of dupilumab and a dose of 300 mg every 2 weeks. The Dermatology Life Quality Index and Pruritic Numeric Rating Scale were used to assess the patient's situation. After several months, the patient's DEB-Pr was considered in remission. Dupilumab may be a better choice than immunosuppressants for the treatment of pruritus in patients with DEB-Pr.

Cite

CITATION STYLE

APA

Yang, D. Y., Jing, W. W., Liu, X., Li, L., Lu, T., & Li, X. L. (2024). Pruritus Anesis in Dystrophic Epidermolysis Bullosa Pruriginosa with Dupilumab. Advances in Skin and Wound Care, 37(2). https://doi.org/10.1097/ASW.0000000000000096

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free