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1.
Korean Journal of Dermatology ; : 73-75, 2012.
Artículo en Coreano | WPRIM | ID: wpr-110230

RESUMEN

Disseminated superficial porokeratosis (DSP) is an autosomal dominant specific disorder of keratinization. Clinically, the lesions show a sharply demarcated and hyperkeratotic plaque with central atrophy, with a predilection for the extensor surface of the extremities. Unusual cases of DSP accompanied by severe pruritus have been reported as "eruptive pruritic papular porokeratosis" or "inflammatory DSP." Histopathologically, inflammatory DSP is characterized by the presence of cornoid lamella with a dense infiltration of lymphocytes in the perivascular area of the upper dermis. Here we report a case of inflammatory DSP in an 80-year-old man with choledocholithiasis.


Asunto(s)
Anciano de 80 o más Años , Humanos , Atrofia , Coledocolitiasis , Dermis , Extremidades , Queratinas , Linfocitos , Poroqueratosis , Prurito
2.
Korean Journal of Dermatology ; : 1053-1055, 2011.
Artículo en Coreano | WPRIM | ID: wpr-121198

RESUMEN

Disseminated superficial porokeratosis (DSP) is a keratinization disorder characterized by multiple small lesions with a slightly elevated, sharply defined ridge over the whole body. Inflammatory DSP has common clinical features, which involve a several-year history of asymptomatic DSP and the sudden appearance of intensively pruritic erythematous papules over the entire body. These lesions subside within several months, leaving a brownish atrophic lesion. We report on a 64-year-old man who displayed an atypical clinical feature of inflammatory DSP.


Asunto(s)
Humanos , Persona de Mediana Edad , Queratinas , Poroqueratosis
3.
Annals of Dermatology ; : 150-153, 2009.
Artículo en Inglés | WPRIM | ID: wpr-136563

RESUMEN

Disseminated superficial porokeratosis (DSP) is a specific disorder of keratinization. Genetic studies show that DSP is an autosomal dominant trait. Clinically, the lesions show a sharply demarcated and hyperkeratotic plaque with central atrophy. The lesions appear mainly in the extremities and generally develop with bilateral symmetry. Unusual cases of DSP accompanied by severe pruritus have been reported as "eruptive pruritic papular porokeratosis" or "inflammatory DSP." Histopathologically, inflammatory DSP is characterized by the presence of cornoid lamella with a dense infiltration of eosinophils and lymphocytes in the perivascular area of the upper dermis. Here we report a case of inflammatory DSP in a 84-year-old man with colon cancer who presented with multiple hyperpigmented atrophic macules.


Asunto(s)
Anciano de 80 o más Años , Humanos , Atrofia , Colon , Neoplasias del Colon , Dermis , Eosinófilos , Extremidades , Queratinas , Linfocitos , Poroqueratosis , Prurito
4.
Annals of Dermatology ; : 150-153, 2009.
Artículo en Inglés | WPRIM | ID: wpr-136562

RESUMEN

Disseminated superficial porokeratosis (DSP) is a specific disorder of keratinization. Genetic studies show that DSP is an autosomal dominant trait. Clinically, the lesions show a sharply demarcated and hyperkeratotic plaque with central atrophy. The lesions appear mainly in the extremities and generally develop with bilateral symmetry. Unusual cases of DSP accompanied by severe pruritus have been reported as "eruptive pruritic papular porokeratosis" or "inflammatory DSP." Histopathologically, inflammatory DSP is characterized by the presence of cornoid lamella with a dense infiltration of eosinophils and lymphocytes in the perivascular area of the upper dermis. Here we report a case of inflammatory DSP in a 84-year-old man with colon cancer who presented with multiple hyperpigmented atrophic macules.


Asunto(s)
Anciano de 80 o más Años , Humanos , Atrofia , Colon , Neoplasias del Colon , Dermis , Eosinófilos , Extremidades , Queratinas , Linfocitos , Poroqueratosis , Prurito
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