Coexistence of Vulvar Dowling-Degos Disease and Seborrhoeic Keratosis
Dowling-Degos disease is a rare autosomal dominant inherited pigmentary disorder, mostly confined to the flexures. Diagnosis is established based on the clinical and histopathological correlation. The authors describe the clinical case of a female patient with vulvar involvement and multiple seborrh...
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2011-01-01
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Series: | Case Reports in Medicine |
Online Access: | http://dx.doi.org/10.1155/2011/605841 |
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doaj-a472d95e08cd4503a26f70d927169f062020-11-25T01:08:16ZengHindawi LimitedCase Reports in Medicine1687-96271687-96352011-01-01201110.1155/2011/605841605841Coexistence of Vulvar Dowling-Degos Disease and Seborrhoeic KeratosisR. Guedes0Luiz Leite1Serviço de Dermatología, Centro Hospitalar de Vila Nova de Gaia, Rua Conceição Fernandes, 4434-502 Vila Nova de Gaia, PortugalDepartamento de Dermatología, Clínica Laser Belém, Calçada da Ajuda 72, 1300 012 Lisboa, PortugalDowling-Degos disease is a rare autosomal dominant inherited pigmentary disorder, mostly confined to the flexures. Diagnosis is established based on the clinical and histopathological correlation. The authors describe the clinical case of a female patient with vulvar involvement and multiple seborrhoeic keratoses on her face, neck, and upper trunk. Major and minor clinical manifestations of Dowling-Degos disease are discussed, with particular emphasis on the genital location of the lesions, which is a rare finding. Also the presence of seborrhoeic keratosis is discussed as a coincidence or a true-associated phenomenon.http://dx.doi.org/10.1155/2011/605841 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
R. Guedes Luiz Leite |
spellingShingle |
R. Guedes Luiz Leite Coexistence of Vulvar Dowling-Degos Disease and Seborrhoeic Keratosis Case Reports in Medicine |
author_facet |
R. Guedes Luiz Leite |
author_sort |
R. Guedes |
title |
Coexistence of Vulvar Dowling-Degos Disease and Seborrhoeic Keratosis |
title_short |
Coexistence of Vulvar Dowling-Degos Disease and Seborrhoeic Keratosis |
title_full |
Coexistence of Vulvar Dowling-Degos Disease and Seborrhoeic Keratosis |
title_fullStr |
Coexistence of Vulvar Dowling-Degos Disease and Seborrhoeic Keratosis |
title_full_unstemmed |
Coexistence of Vulvar Dowling-Degos Disease and Seborrhoeic Keratosis |
title_sort |
coexistence of vulvar dowling-degos disease and seborrhoeic keratosis |
publisher |
Hindawi Limited |
series |
Case Reports in Medicine |
issn |
1687-9627 1687-9635 |
publishDate |
2011-01-01 |
description |
Dowling-Degos disease is a rare autosomal dominant inherited pigmentary disorder, mostly confined to the flexures. Diagnosis is established based on the clinical and histopathological correlation. The authors describe the clinical case of a female patient with vulvar involvement and multiple seborrhoeic keratoses on her face, neck, and upper trunk. Major and minor clinical manifestations of Dowling-Degos disease are discussed, with particular emphasis on the genital location of the lesions, which is a rare finding. Also the presence of seborrhoeic keratosis is discussed as a coincidence or a true-associated phenomenon. |
url |
http://dx.doi.org/10.1155/2011/605841 |
work_keys_str_mv |
AT rguedes coexistenceofvulvardowlingdegosdiseaseandseborrhoeickeratosis AT luizleite coexistenceofvulvardowlingdegosdiseaseandseborrhoeickeratosis |
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1725183439665102848 |