Activated zinc pyrithione in topical treatment of atopic dermatitis: a case report

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详细

Atopic dermatitis is a systemic multifactorial genetically determined inflammatory skin condition characterized by an impairment of the epidermal barrier and Type 2 inflammation. Atopic dermatitis is highly prevalent, especially among children. Many authors consider atopic dermatitis as the initial stage of the atopic march, which typically manifests in the first year of life. Topical agents such as topical glucocorticosteroids and topical calcineurin inhibitors are the first-line treatments for atopic dermatitis. In recent years, there has been an increasing use of modern systemic anti-inflammatory agents, such as monoclonal antibodies and Janus kinase inhibitors.

Therapy of patients with atopic dermatitis is aimed at relieving itching, improving skin barrier function, reducing inflammation, preventing skin infection and exacerbations. The effectiveness of treatment lies not only in improving the symptoms and quality of life of patients with atopic dermatitis, but also in preventing them from developing chronic or severe symptoms.

Modern topical glucocorticosteroids and their combinations, have a proven high safety profile. However, available data on adverse events associated with their use often lead patients and their parents to develop a negative, phobic attitude towards treatment with these drugs. Zinc pyrithione, an activated form of zinc, is a safe and highly effective medication with anti-inflammatory, antifungal, and antibacterial properties.

This article presents two clinical cases of moderate to severe atopic dermatitis in children, demonstrating the effectiveness of using activated zinc pyrithione in comprehensive therapy for this condition.

作者简介

Alla Litovkina

National Research Center-Institute of Immunology Federal Medical-Biological Agency of Russia; Peoples' Friendship University of Russia

编辑信件的主要联系方式.
Email: dr.litovkina@gmail.com
ORCID iD: 0000-0002-5021-9276
SPIN 代码: 2337-7930

MD

俄罗斯联邦, Moscow; Moscow

Evgeniy Smolnikov

National Research Center-Institute of Immunology Federal Medical-Biological Agency of Russia; Peoples' Friendship University of Russia; National Research Nuclear University MEPhI (Moscow Engineering Physics Institute)

Email: qwertil2010@yandex.ru
ORCID iD: 0000-0003-1302-4178
SPIN 代码: 4874-8100

MD

俄罗斯联邦, Moscow; Moscow; Moscow

Olga Elisyutina

National Research Center-Institute of Immunology Federal Medical-Biological Agency of Russia; Peoples' Friendship University of Russia

Email: el-olga@yandex.ru
ORCID iD: 0000-0002-4609-2591
SPIN 代码: 9567-1894

MD, Dr. Sci. (Med.)

俄罗斯联邦, Moscow; Moscow

Elena Fedenko

National Research Center-Institute of Immunology Federal Medical-Biological Agency of Russia

Email: efedks@gmail.com
ORCID iD: 0000-0003-3358-5087
SPIN 代码: 5012-7242

MD, Dr. Sci. (Med.), Professor

俄罗斯联邦, Moscow

参考

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2. Fig. 1. Patient А., 14 years: a ― erythematous-squamous plaques with infiltration and hypopigmentation areas over the face on the baseline; b ― skin on the 28th day of treatment. Hyperemia, infiltration, and scaling has significantly decreased, post-inflammatory hyperpigmentation is defined.

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3. Fig. 2. Patient M., 15 years: erythematous-squamous plaques with infiltration and pale skin areas, papular rashes with excoriation, lichenification over the face, trunk, back, upper extremities on the baseline (a, b); skin on the 28th day of treatment: hyperemia, infiltration, scaling, lichenification have decreased, the most part of excoriations has epithelized (c, d).

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