Literature DB >> 8270338

Epidermodysplasia verruciformis in Africans.

W K Jacyk1, E M De Villiers.   

Abstract

BACKGROUND: Epidermodysplasia verruciformis (EV) is a rare cutaneous disorder characterised by persistent, refractory infection with human papillomaviruses (HPV). Although EV does not seem to have racial or geographic preference, there is a scarcity of reports on its occurrence in Africans.
METHODS: Twenty Africans with EV were studied, and the literature on this condition in Africans was reviewed. Virologic studies were performed on 10 patients.
RESULTS: Three types of lesions were observed: flat warts, pityriasis versicolor-like macules, and seborrheic keratosis-like changes. Malignant transformation occurred in only one patient. HPV-3 was isolated only from flat warts, HPV-5 and HPV-17 were isolated only from PV-like lesions, whereas an HPV-5-related type was found in all three types of changes. HPV-5-related type revealed DNA that was related but not identical to any of the viruses in the HPV-5 group. This particular type was isolated from all five South African patients with EV in whom virologic studies were performed.
CONCLUSIONS: The benign nature of EV in dark-skinned Africans has been confirmed. Four HPV types have been isolated, of which HPV-related type was found in all South African patients with EV and in all types of skin changes, regardless of their morphology. African patients with EV frequently present seborrheic keratosis-like changes.

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Year:  1993        PMID: 8270338     DOI: 10.1111/j.1365-4362.1993.tb02768.x

Source DB:  PubMed          Journal:  Int J Dermatol        ISSN: 0011-9059            Impact factor:   2.736


  2 in total

1.  Human papillomavirus infection and ultraviolet light exposure as epidermoid inclusion cyst risk factors in a patient with epidermodysplasia verruciformis?

Authors:  Ryan Ramagosa; Ethel-Michele de Villiers; James E Fitzpatrick; Robert P Dellavalle
Journal:  J Am Acad Dermatol       Date:  2008-05       Impact factor: 11.527

2.  A distinct variant of Epidermodysplasia verruciformis in a Turkish family lacking EVER1 and EVER2 mutations.

Authors:  Baki Akgül; Osman Köse; Mükerrem Safali; Karin Purdie; Rino Cerio; Charlotte Proby; Alan Storey
Journal:  J Dermatol Sci       Date:  2007-02-16       Impact factor: 4.563

  2 in total

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