Korean J Nephrol.
2009 May;28(3):243-247.
A Case of Anti-Glomerular Basement Membrane Disease Improved
by Early Plasmapheresis and Immunosuppression Therapy
- Affiliations
-
- 1Department of Internal Medicine, Hanyang University College of Medicine, Seoul, Korea.
- 2Department of Pathology, Konkuk University School of Medicine, Seoul, Korea.
- 3Department of Internal Medicine, Konkuk University School of Medicine, Seoul, Korea. nephlee@kuh.ac.kr
Abstract
- Anti-glomerular basement membrane disease is a rare autoimmune disease characterized by rapidly progressive renal failure and/or pulmonary hemorrhage. The presence of severe crescentic glomerular inflammation with linear deposition of immunoglobulin G along the glomerular basement membrane is pathognomonic. Because renal function is rapidly and often irretrievably destroyed, many patients require hemodialysis all through their lifetime. We report a case of 33 year(s)-old man who was diagnosed as anti-glomerular basement membrane disease without pulmonary hemorrhage. The patient was treated with pulse methylprednisolone and plasmapheresis followed by oral corticosteroid and cyclophosphamide. His renal function was successfully recovered with early diagnosis and aggressive treatment.