Rare clinical variant of palmoplantar keratoderma

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Abstract

The article presents a clinical case of an 18-year-old patient with aquagenic keratoderma. This is a rare variant of acquired palmoplantar keratoderma, which is characterized by the appearance of dense waxy foci of white-yellow hyperkeratosis with swelling of the skin, lichenification, as well as plaques with a surface in the form of a «cobblestone pavement» after contact with water. Aquagenic keratoderma occurs in 44–80% of cases in patients with cystic fibrosis who have a homo- or heterozygous mutation δF508 in the CFTR gene responsible for regulating electrolyte transport. This clinical case is of interest to practicing dermatologists.

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About the authors

Yu. A. Novikov

Omsk State Medical University

Email: zyk.alena@mail.ru
ORCID iD: 0000-0003-0391-5372

Department of Dermatovenereology and Cosmetology

Russian Federation, Omsk

O. V. Pravdina

Omsk State Medical University

Email: zyk.alena@mail.ru
ORCID iD: 0000-0002-1804-6248

Department of Dermatovenereology and Cosmetology

Russian Federation, Omsk

Elena A. Zykova

Omsk State Medical University

Author for correspondence.
Email: zyk.alena@mail.ru
ORCID iD: 0000-0002-8293-4127

Cand. Sci. (Med.), Teaching Assistant, Department of Dermatovenereology and Cosmetology

Russian Federation, Omsk

S. R. Gamza

Clinical Dermatovenerologic Dispensary

Email: zyk.alena@mail.ru
ORCID iD: 0009-0005-6066-3417
Russian Federation, Omsk

References

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Supplementary files

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2. Fig.1-2. Photo of the palms of patient M., born in 2004, suffering from aquagenic keratoderma (before treatment)

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3. Fig.3. Photo of the palms of patient M., born in 2004, suffering from aquagenic keratoderma (after treatment)

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