| Literature DB >> 10992726 |
Y B Oh1, S C Bae, J H Jung, T H Kim, J B Jun, S S Jung, I H Lee, D H Yoo, M H Park, S Y Kim.
Abstract
We report a 25-year-old Korean woman with Adult onset Still's disease (AOSD) presented with renal amyloidosis, which had developed four years after disease onset. We successfully treated her with prednisolone, colchicine and cyclophosphamide. A review of the literature uncovered about 10 cases, most of which were treated by various regimens that resulted in poor outcomes. Renal amyloidosis should be suspected in patients with AOSD who have unexplained proteinuria. Although the mechanism of renal amyloid deposition is not well known, earlier histopathologic diagnosis and choice of regimen may affect prognosis.Entities:
Mesh:
Year: 2000 PMID: 10992726 PMCID: PMC4531753 DOI: 10.3904/kjim.2000.15.2.131
Source DB: PubMed Journal: Korean J Intern Med ISSN: 1226-3303 Impact factor: 2.884