Adult Onset Still's Disesae: A Case Report.
- Author:
Byung Jik KIM
1
;
Si Yong KIM
;
Gyong Moon KIM
Author Information
1. Department of Dermatology, College of Medicine, The Catholic University of Korea, Seoul, Korea. gyongmoonkim@catholic.ac.kr
- Publication Type:Case Report
- Keywords:
Adult onset Still's disease
- MeSH:
Adrenal Cortex Hormones;
Adult;
Anti-Inflammatory Agents, Non-Steroidal;
Arthritis;
Aspirin;
Exanthema;
Female;
Fever;
Hepatomegaly;
Humans;
Immunosuppressive Agents;
Lymphatic Diseases;
Pharyngitis;
Serositis;
Splenomegaly;
Still's Disease, Adult-Onset
- From:Korean Journal of Dermatology
2009;47(10):1203-1205
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Adult-onset Still's disease (AOSD) is a systemic inflammatory disease of an unknown etiology, and AOSD is characterized by high fever, skin rash, arthritis, lymphadenopathy, hepatomegaly, sore throat and serositis. The typical skin rash of AOSD patients is an evanescent, erythematous maculopapular lesion. There is no single diagnostic test; therefore, the diagnosis is based upon the clinical criteria. Treatment consists of anti-inflammatory medications such as aspirin, NSAIDs, corticosteroids, anti-rheumatics and immunosuppressants. We report here on a case of AOSD in which a 53 year-old female patient presented with a high fever, a typical rash, arthritis, a sore thoat and mild splenomegaly.
