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혈청 보체 C3가 감소된 특발성 원섬유성 사구체신염 1예

Other Titles
 A Case of Idiopathic Fibrillary Glomerulonephritis with Hypocomplementemia 
Authors
 윤세희  ;  강구흠  ;  윤성로  ;  최낙원  ;  김윤미  ;  임범진 
Citation
 Korean Journal of Nephrology, Vol.27(3) : 364-368, 2008 
Journal Title
Korean Journal of Nephrology
ISSN
 1975-9460 
Issue Date
2008
Keywords
Microfibrils ; Glomerulonephritis ; Complement 3
Abstract
A 72-year-old woman presented with generalized edema and proteinuria. Renal biopsy disclosed highly organized fibrillary deposits in subendothelial area by electron microscopy. The microfibrils were 14 nm in diameter and randomly arranged. They did not have a microtubular appearance. These materials were negative for Congo red staining. Cryoglobulinemia or paraproteinemia including light chains was not found. So we can diagnose her as fibrillary glomerulonephritis (GN). In fibrillary GN serum complement levels are usually normal except in rare cases with systemic disease. Here we present a rare case of fibrillary GN with unusual hypocomplementemia.
Files in This Item:
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Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
Yonsei Authors
Lim, Beom Jin(임범진) ORCID logo https://orcid.org/0000-0003-2856-0133
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/108606
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