A Case of Interstitial Granulomatous Dermatitis / 대한피부과학회지
Korean Journal of Dermatology
;
: 548-551, 2016.
Article
Dans Coréen
| 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.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Polyarthrite rhumatoïde
/
Immunoglobuline D
/
Collagène
/
Derme
/
Maladies rares
/
Dermatite
/
Histiocytes
/
Lupus érythémateux disséminé
Limites du sujet:
Femelle
/
Humains
langue:
Coréen
Texte intégral:
Korean Journal of Dermatology
Année:
2016
Type:
Article
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