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Light chain nephropathy

Authors :
Hafedh Hedri
Raja Aouadia
Rym Goucha
Ezzeddine Abderrahim
Sihem Darouich
Ilhem Bettaieb
Adel Khedher
Source :
Saudi Journal of Kidney Diseases and Transplantation, Vol 26, Iss 3, Pp 437-442 (2015)
Publication Year :
2015
Publisher :
Wolters Kluwer Medknow Publications, 2015.

Abstract

Light chain deposition disease (LCDD) is characterized by the tissue deposition of monotypic immunoglobulin light chains of either kappa or lambda isotype. It is the archetypal systemic disease that is most frequently diagnosed on a kidney biopsy, although the deposits may involve several other organs. This brief review focuses on the clinicopathological features of LCDD-associated nephropathy with an emphasis on the diagnostic and therapeutic difficulties related to this elusive condition.

Details

Language :
English
ISSN :
13192442
Volume :
26
Issue :
3
Database :
OpenAIRE
Journal :
Saudi Journal of Kidney Diseases and Transplantation
Accession number :
edsair.doi.dedup.....de140fd94eba4f32ce69bfffb5f80918