Zobrazeno 1 - 10
of 91
pro vyhledávání: '"porokeratosis of mibelli"'
Publikováno v:
Clinical Case Reports, Vol 12, Iss 9, Pp n/a-n/a (2024)
Key Clinical Message This case illustrates the clinical heterogeneity of porokeratosis (PK), with a patient presenting with both disseminated superficial actinic PK‐like facial lesions and PK of Mibelli‐like lesions on the buttocks and lower limb
Externí odkaz:
https://doaj.org/article/a836f6ff8c4f4898b5750c45f331d375
Publikováno v:
Indian Journal of Dermatology, Vol 69, Iss 4, Pp 365-365 (2024)
Porokeratosis (PK) is a chronic progressive disorder of keratinization characterized clinically by hyperkeratotic papules or plaques surrounded by a threadlike, elevated border that expands centrifugally. Pathogenesis involves heterozygous mutations
Externí odkaz:
https://doaj.org/article/ca44beaa7f8e4267839f7a6da3fe5f30
Publikováno v:
Indian Dermatology Online Journal, Vol 11, Iss 6, Pp 983-987 (2020)
Giant porokeratosis (PK) is a rare entity. Many consider it as a variant of PK of Mibelli, while others describe it as a separate variant. The diameter may range between 10 and 12 cm and the wall of hyperkeratotic ridge may be upto 1 cm. High tropica
Externí odkaz:
https://doaj.org/article/90e28ce8247348f4b0ec2c73147aefa6
Publikováno v:
Clinical Dermatology Review, Vol 5, Iss 2, Pp 223-225 (2021)
Porokeratosis (PK) is a rare group of heterogeneous disorders of keratinization representing diverse phenotypic expressions of the same genetic defect, which is mainly inherited in an autosomal dominant manner. This report describes the case of a 40-
Externí odkaz:
https://doaj.org/article/02bbb2571cf84f8696c0b5bffca69959
Akademický článek
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Autor:
Renata Brito Marinho Perpetuo, Maraya De Jesus Semblano Bittencourt, Fábio Henrique Dolzany Rosales, Natani Santos Leite, Patricia Fabiana Zampiva Noedel, Suzana Maria Klautau Ferreira, Thairine Herica Oliveira De Lima, Arival Cardoso de Brito
As poroceratoses são um grupo heterogêneo e pouco frequente de dermatoses adquiridas ou hereditárias de etiologia desconhecida, caracterizada por um distúrbio de queratinização. Apresentamos caso de paciente feminina, 61 anos, fototipo V, evolu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12c478abc3a9bf1fc5592b31002f7441
Publikováno v:
Indian Dermatology Online Journal
Indian Dermatology Online Journal, Vol 11, Iss 6, Pp 983-987 (2020)
Indian Dermatology Online Journal, Vol 11, Iss 6, Pp 983-987 (2020)
Giant porokeratosis (PK) is a rare entity. Many consider it as a variant of PK of Mibelli, while others describe it as a separate variant. The diameter may range between 10 and 12 cm and the wall of hyperkeratotic ridge may be upto 1 cm. High tropica
Publikováno v:
Clinical Dermatology Review, Vol 1, Iss 2, Pp 76-77 (2017)
Porokeratosis is a rare specific disorder of keratinization with distinct clinical and histopathological features with rare malignant degeneration. Clinically, it is characterized by papular lesions or annular plaques with central atrophy and periphe
Externí odkaz:
https://doaj.org/article/0a9a355079e740c697240d8530b53796
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Publikováno v:
JAAD Case Reports, Vol 9, Iss, Pp 54-56 (2021)
JAAD Case Reports
JAAD Case Reports
Porokeratoses are precancerous keratinocyte proliferations with distinct hyperkeratotic rims called cornoid lamellae. The most common porokeratosis is disseminated superficial actinic porokeratosis, characterized by multiple thin papules on the lower