Rare clinical variant of palmoplantar keratoderma
- Авторлар: Novikov Y.A.1, Pravdina O.V.1, Zykova E.A.1, Gamza S.R.2
-
Мекемелер:
- Omsk State Medical University
- Clinical Dermatovenerologic Dispensary
- Шығарылым: Том 30, № 8 (2023)
- Беттер: 126-128
- Бөлім: Clinical case
- URL: https://journals.eco-vector.com/2073-4034/article/view/623146
- DOI: https://doi.org/10.18565/pharmateca.2023.8.126-128
- ID: 623146
Дәйексөз келтіру
Ашық рұқсат
Рұқсат берілді
Аннотация
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.
Негізгі сөздер
Толық мәтін
Авторлар туралы
Yu. Novikov
Omsk State Medical University
Email: zyk.alena@mail.ru
ORCID iD: 0000-0003-0391-5372
Department of Dermatovenereology and Cosmetology
Ресей, OmskO. Pravdina
Omsk State Medical University
Email: zyk.alena@mail.ru
ORCID iD: 0000-0002-1804-6248
Department of Dermatovenereology and Cosmetology
Ресей, OmskElena Zykova
Omsk State Medical University
Хат алмасуға жауапты Автор.
Email: zyk.alena@mail.ru
ORCID iD: 0000-0002-8293-4127
Cand. Sci. (Med.), Teaching Assistant, Department of Dermatovenereology and Cosmetology
Ресей, OmskS. Gamza
Clinical Dermatovenerologic Dispensary
Email: zyk.alena@mail.ru
ORCID iD: 0009-0005-6066-3417
Ресей, Omsk
Әдебиет тізімі
- Бутов Ю.С., Потекаев Н.Н. Руководство для врачей по дерматовенерологии. Москва: Издательство ГЭОТАР-Медиа; 2017. [Butov Yu.S., Potekaev N.N. A guide for doctors in dermatology and venereology. Moscow: GEOTAR-Media Publishing, 2017. (In Russ.)].
- Потекаев Н.Н., Львов А.Н. Дерматология Фицпатрика в клинической практике. Москва: Издательство Панфилова; 2015. [Potekaev N.N., Lvov A.N. Fitzpatrick dermatology in clinical practice. Moscow: Panfilov Publishing House, 2015. (In Russ.)].
- Шнайдерман П., Гроссман М. Диф-ференциальная диагностика в дерматологии. Москва: Бином; 2017. [Schneiderman P., Grossman M. Differential diagnosis in dermato-logy. Moscow: Binom Publishing, 2017. (In Russ.)].
- Хэбиф Т.П. Кожные болезни. Диагностика и лечение. Москва: Медпресс-информ; 2016. [Нebif T.P. Skin diseases. Diagnosis and treatment. Moscow: Medpress-Inform Publishing House, 2016. (In Russ.)].
- Bragg J., Rizzo C., Mengden S. Striate palmoplantar keratoderma (Brunau- er–Fohs–Siemens syndrome). Dermatol Online J. 2008;14(5):26.
- Erkek E., Kocak M., Bozdogan O., et al. Focal acral hyper- keratosis: a rare cutaneous disorder within the spectrum of Costa acrokera- toelastoidosis. Pediatr Dermatol. 2004;21(2):128. doi: 10.1111/j.0736-8046.2004.21208.x.
- Itin P.H., Fistarol S.K. Palmoplantar keratodermas. Clin Dermatol. 2005;23(1):15–22. doi: 10.1016/j.clindermatol.2004.09.005.
- Kuster W., Reis A., Hennies H.C. Epidermolytic palmoplantar keratoderma of Vorner: re-evaluation of Vorner’s original family and identification of a novel keratin 9 mutation. Arch Dermatol Res. 2002;294(6):268–72. doi: 10.1007/s00403-002-0328-9.
- Sakiyama T., Kubo A. Hereditary palmoplantar keratoderma “clinical and genetic differential diagnosis”. J Dermatol. 2016;43(3):264–74. doi: 10.1111/1346-8138.13219.
- Stypczynska E., Placek W., Zegarska B., Czajkowski R. Keratinization dis- orders and genetic aspects in palmar and plantar keratodermas. Acta Der- matovenerol. Croat. 2016;24(2):116–23.
Қосымша файлдар
