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Congenital diffuse melanosis in a father and two Sons
Iranian Journal of Dermatology. 2005; 8 (3): 237-241
en Persa | IMEMR | ID: emr-71287
ABSTRACT
Congenital diffuse melanosis is one of the rarest clinical manifestations of hereditary universal melanosis and only few cases have been reported all over the world. The presented case is a 54-year-old man who presented to us complaining of erythematous annular lesions on his face and neck 8 months ago. Diffuse pigmentation of his skin took our attention. According to the patient, diffuse hyperpigmentation was present at birth and there was no obvious changes up to now. His mother and sister had similar hyperpigmentation. He had two sons with a similar hyperpigmentaion, but his daughter had normal skin pigmentation. All laboratory investigation for the causes of hyperpigmentaion were reported normal and investigation for causes of secondary hyperpigmentation did not reveal any abnormality. In histopathologic assay, the erythematous lesion was reported to be discoid lupus erythematosus and the diagnosis of hyperpigmented lesion reported as congenital diffuse melanosis
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Índice: IMEMR (Mediterraneo Oriental) Asunto principal: Hiperpigmentación / Melanosis Tipo de estudio: Informe de Casos Límite: Humanos / Masculino Idioma: Persa Revista: Iran. J. Dermatol. Año: 2005

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Índice: IMEMR (Mediterraneo Oriental) Asunto principal: Hiperpigmentación / Melanosis Tipo de estudio: Informe de Casos Límite: Humanos / Masculino Idioma: Persa Revista: Iran. J. Dermatol. Año: 2005