A Study of Granulomatous Pigmented Purpuric Dermatosis / 대한피부과학회지
Korean Journal of Dermatology
;
: 501-504, 2014.
Artículo
en Coreano
| WPRIM
| ID: wpr-122326
ABSTRACT
Pigmented purpuric dermatoses (PPD) are a group of diseases characterized by petechiae and bronze discoloration of the skin on the lower extremities. Histopathologically, superficial perivascular lymphocytic infiltration and hemosiderin deposition are seen. PPD can be subdivided into progressive pigmentary dermatosis of Schamberg, purpura annularis telangiectoides of Majocchi, pigmented purpuric dermatitis of Gougerot and Blum, eczematid-like purpura of Doucas and Kapetanakis, itching purpura, and lichen aureus. The granulomatous variant of PPD was described in 1996. Granulomatous PPD share common histopathologic features of PPD with granulomatous inflammation. We present the findings of a patient who presented with a clinical picture of PPD and histologic patterns of granulomatous inflammation.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Prurito
/
Púrpura
/
Piel
/
Enfermedades de la Piel
/
Extremidad Inferior
/
Dermatitis
/
Hemosiderina
/
Inflamación
/
Líquenes
Límite:
Humanos
Idioma:
Coreano
Revista:
Korean Journal of Dermatology
Año:
2014
Tipo del documento:
Artículo
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