Literature DB >> 19450401

Four familial cases of epidermodysplasia verruciformis: mother and three sons.

Reza Mahmoud Robati1, Afsaneh Marefat, Marjan Saeedi, Mohammad Rahmati-Roodsari, Zahra Asadi-Kani.   

Abstract

Epidermodysplasia verruciformis (EV) is a rare genodermatosis associated with a high risk of skin cancer. In this report, we present three Iranian brothers and their mother with extensive seborrheic keratosis-like (SK-like) viral warts. Initial facial lesions developed in the first decade and disseminated with time. The patients showed SK-like viral warts characterized by dark brown or black pigmented proliferative lesions with hyperkeratotic surfaces. The histopathological findings were consistent with the diagnosis of EV. There are few reports of familial epidermodysplasia verruciformis especially in a mother and her three sons.

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Year:  2009        PMID: 19450401

Source DB:  PubMed          Journal:  Dermatol Online J        ISSN: 1087-2108


  1 in total

1.  Lewandowsky and lutz dysplasia: report of two cases in a family.

Authors:  Bhawna Bhutoria; Kaushik Shome; Sulekha Ghosh; Koushik Bose; Chhanda Datta; Subodh Bhattacharya
Journal:  Indian J Dermatol       Date:  2011-03       Impact factor: 1.494

  1 in total

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