Abstract
A 46-year-old woman developed takotsubo cardiomyopathy and nephrotic syndrome. The first kidney biopsy suggested non-immune-complex-mediated membranoproliferative glomerulonephritis (MPGN), and she was diagnosed with glomerular endothelial injury associated with takotsubo cardiomyopathy. A second biopsy was performed two years later because of persistent proteinuria despite renin-angiotensin system inhibition. This biopsy indicated non-immune-complex-mediated MPGN, but a mesangial and subendothelial substance of a higher electron density than that in the first biopsy was detected, suggesting the possibility of glomerular disease with non-immune deposits rather than endothelial injury. Finally, she was diagnosed with fibronectin nephropathy. Although rare, fibronectin glomerulopathy should be considered in non-immune-complex-mediated MPGN.
Original language | English |
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Pages (from-to) | 2027-2032 |
Number of pages | 6 |
Journal | Internal Medicine |
Volume | 61 |
Issue number | 13 |
DOIs | |
Publication status | Published - 2022 |
Keywords
- endothelial injury
- fibronectin glomerulopathy
- nephrotic syndrome
- takotsubo cardiomyopathy
ASJC Scopus subject areas
- Internal Medicine