Kikuchi-Fujimoto's Disease with Adult Onset Still's Disease / 대한류마티스학회지
The Journal of the Korean Rheumatism Association
;
: 58-62, 2008.
Article
in Korean
| WPRIM
| ID: wpr-22429
ABSTRACT
Kikuchi-Fujimoto's disease (KFD), or histiocytic necrotizing lymphadenitis, is a rare benign and self-limiting disease. KFD are confused with systemic autoimmune disease as they present with localized lymphadenopathy, fever, fatigue, arthritis, leukopenia. Furthermore as KFD can occur associated with other autoimmune disease, we need to diagnose carefully. Here, we describe a case of 27-year-old female patient, diagnosed as KFD, who subsequently developed adult onset Still's disesase (AOSD). As far as we know, this is the first case of KFD with AOSD in Korea.
Full text:
Available
Index:
WPRIM (Western Pacific)
Limits:
Adult
/
Female
/
Humans
/
Male
Language:
Korean
Journal:
The Journal of the Korean Rheumatism Association
Year:
2008
Type:
Article
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