Hereditary palmoplantar keratoderma. Two clinical cases
- Authors: Rodin A.Y.1
-
Affiliations:
- Volgograd State Medical University
- Issue: Vol 32, No 4 (2025)
- Pages: 134-138
- Section: Dermatology/allergology
- URL: https://journals.rcsi.science/2073-4034/article/view/314348
- DOI: https://doi.org/10.18565/pharmateca.2025.4.134-138
- ID: 314348
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Abstract
A literature review of the pathogenesis, classification, clinical manifestations, diagnostics and treatment principles of hereditary palmoplantar keratoderma is conducted. Two clinical cases are presented. The first case is a 3-year-old girl and her mother with diffuse palmoplantar keratoderma type Unna-Thost (according to the patients words, similar lesions were found in the eldest daughter and grandfather). The second case is a 67-year-old patient with punctate palmoplantar keratoderma (Buschke-Fischer syndrome) in combination with bilateral cataracts and moderate neuropsychiatric disorders.
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##article.viewOnOriginalSite##About the authors
Aleksey Yu. Rodin
Volgograd State Medical University
Author for correspondence.
Email: dermavolgmu@yandex.ru
ORCID iD: 0000-0003-1630-5880
SPIN-code: 7963-3380
Dr. Sci. (Med.), Professor, Professor at the Department of Dermatovenereology
Russian Federation, VolgogradReferences
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Figure 1. Skin lesions of the palms of a 3-year-old patient
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Figure 2. Skin lesions of the soles of a 3-year-old patient
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Figure 3. Skin lesions of the palms of a mother and a 3-year-old patient
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Figure. 4. Focal skin lesions of the soles of a 67-year-old patient
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Figure. 5. Focal skin lesions of the palms of a 67-year-old patient
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