Four familial cases of epidermodysplasia verruciformis: mother and three sons
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 dissem...
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| Veröffentlicht in: | Dermatology online journal 2009-04, Vol.15 (4), p.8-8 |
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| container_title | Dermatology online journal |
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| creator | Robati, Reza Mahmoud Marefat, Afsaneh Saeedi, Marjan Rahmati-Roodsari, Mohammad Asadi-Kani, Zahra |
| description | 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. |
| doi_str_mv | 10.5070/D37069T3V9 |
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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. 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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. 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| subjects | Adolescent Adult Carcinoma, Squamous Cell - epidemiology Child Diagnosis, Differential Disease Susceptibility Epidermodysplasia Verruciformis - diagnosis Epidermodysplasia Verruciformis - genetics Facial Dermatoses - diagnosis Facial Dermatoses - genetics Female Hand Dermatoses - diagnosis Hand Dermatoses - genetics Humans Male Middle Aged Tinea Versicolor - diagnosis |
| title | Four familial cases of epidermodysplasia verruciformis: mother and three sons |
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