A Case of Interstitial Granulomatous Dermatitis / 대한피부과학회지
Korean Journal of Dermatology
;
: 548-551, 2016.
Artículo
en Coreano
| WPRIM
| ID: wpr-12168
ABSTRACT
Interstitial granulomatous dermatitis (IGD) is a rare disease that has been associated with multiple systemic diseases, particularly autoimmune conditions like rheumatoid arthritis and systemic lupus erythematosus. IGD has a variable clinical presentation and highly characteristic histological features of interstitial infiltrate of histiocytes between the degenerated collagen bundles. Here we report the case of a 63-year-old woman who presented with a 3-month history of multiple asymptomatic erythematous papules on the bilateral aspects of the trunk. A histopathological examination of the lesion showed an interstitial lymphohistiocytic infiltrate in the dermis. There were also foci of palisading histiocytes along with degenerating collagen bundles.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Artritis Reumatoide
/
Inmunoglobulina D
/
Colágeno
/
Dermis
/
Enfermedades Raras
/
Dermatitis
/
Histiocitos
/
Lupus Eritematoso Sistémico
Límite:
Femenino
/
Humanos
Idioma:
Coreano
Revista:
Korean Journal of Dermatology
Año:
2016
Tipo del documento:
Artículo
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