A Case of Ankylosing Spondylitis in a Patient with Henoch-Schonlein Purpura.
10.4078/jkra.2008.15.3.268
- Author:
Su Jin KIM
1
;
Tae Kyung LIM
;
Yu Jin KIM
;
Suho KIM
;
Seong Gyun KIM
;
Young Il SEO
;
Hyun Ah KIM
Author Information
1. Department of Internal Medicine, Hallym University Sacred Heart Hospital, Anyang, Korea. being97@hallym.or.kr
- Publication Type:Case Report
- Keywords:
Ankylosing spondylitis;
Henoch-Schonlein purpura
- MeSH:
Male;
Humans
- From:The Journal of the Korean Rheumatism Association
2008;15(3):268-272
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Ankylosing spondylitis (AS) is a common inflammatory arthritis that affects the axial skeleton, causing characteristic inflammatory back pain, which can lead to structural and functional impairments and a decrease in quality of life. The disease can be accompanied by extraskeletal manifestations, such as acute anterior uveitis, inflammation in the colon or ileum, aortic insufficiency, cardiac conduction defects, fibrosis of the upper lobes of the lungs, neurologic involvement, or renal (secondary) amyloidosis. We report the case of a 19 year-old man who developed Henoch-Schonlein purpura (HSP) and subsequently AS. It has been recognized that AS may be associated with cutaneous vasculitis and IgA nephropathy, but the association of HSP with AS has not been reported. This association of IgA nephropathy or HSP with AS raises the possibility of a common or related pathogenesis.
