Light chain deposition disease without glomerular proteinuria: a diagnostic challenge for the nephrologist
Renal involvement in light chain (LC) deposition disease (LCDD) is typically characterized by nodular glomerulosclerosis and nephrotic range proteinuria. Rare cases of LCDD without glomerular symptoms have been reported, but clinical and pathological characteristics of this entity remain poorly desc...
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Veröffentlicht in: | Nephrology, dialysis, transplantation dialysis, transplantation, 2014-10, Vol.29 (10), p.1894-1902 |
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Hauptverfasser: | , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Renal involvement in light chain (LC) deposition disease (LCDD) is typically characterized by nodular glomerulosclerosis and nephrotic range proteinuria. Rare cases of LCDD without glomerular symptoms have been reported, but clinical and pathological characteristics of this entity remain poorly described.
This multi-centre retrospective study included 14 patients with biopsy-proven renal LCDD and proteinuria |
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ISSN: | 0931-0509 1460-2385 |
DOI: | 10.1093/ndt/gfu045 |