Atrophoderma vermiculatum: clinical presentation features, differential diagnosis and treatment
- Authors: Vishnevskaya O.A.1, Shnakhova L.M.2
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Affiliations:
- Ramenskoye Central City Clinical Hospital
- First Moscow State Medical University (Sechenov University)
- Issue: Vol 23, No 2 (2020)
- Pages: 115-118
- Section: CLINICAL PICTURE, DIAGNOSIS, AND THERAPY OF DERMATOSES
- URL: https://rjsvd.com/1560-9588/article/view/41934
- DOI: https://doi.org/10.17816/dv41934
- ID: 41934
Cite item
Abstract
Atrophoderma vermiculata is a rare, benign, follicular dermatosis localized in an esthetically important facial skin zone, which results in superficial scars formation. The disease usually occurs at the age of 5–12 years and may be autosomal-dominantly inherited. This type of dermatosis may be associated with other congenital abnormalities and some hereditary diseases, such as Marfan syndrome, neurofibromatosis, congenital heart defects, and mental retardation similar to Down’s syndrome. The authors also analyze the typical clinical presentations of atrophoderma vermiculata, from their own clinical experience, conduct a detailed analysis of differential diagnosis with other dermatoses, and provide contemporary therapeutic methods and approaches to this skin disorder.
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About the authors
O. A. Vishnevskaya
Ramenskoye Central City Clinical Hospital
Email: lika-slm@mail.ru
ORCID iD: 0000-0001-8036-1380
Department of Dermatology
Russian Federation, Moscow region, Ramenskoye, 140100L. M. Shnakhova
First Moscow State Medical University (Sechenov University)
Author for correspondence.
Email: lika-slm@mail.ru
ORCID iD: 0000-0003-3000-0987
Department of Dermatology and Venerology of I.M. Sechenov
Russian Federation, Moscow, 119991References
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