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

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Abstract

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.

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About the authors

Alla O. Litovkina

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

Author for correspondence.
Email: dr.litovkina@gmail.com
ORCID iD: 0000-0002-5021-9276
SPIN-code: 2337-7930

MD

Russian Federation, Moscow; Moscow

Evgeniy V. 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-code: 4874-8100

MD

Russian Federation, Moscow; Moscow; Moscow

Olga G. 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-code: 9567-1894

MD, Dr. Sci. (Med.)

Russian Federation, Moscow; Moscow

Elena S. Fedenko

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

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

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

Russian Federation, Moscow

References

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Supplementary files

Supplementary Files
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1. JATS XML
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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