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Light and heavy chain deposition disease associated with CH1 deletion.

Authors :
Cohen, Camille
El-Karoui, Khalil
Alyanakian, Marie-Alexandra
Noel, Laure-Hélène
Bridoux, Franck
Knebelmann, Bertrand
Source :
Clinical Kidney Journal; Apr2015, Vol. 8 Issue 2, p237-239, 3p
Publication Year :
2015

Abstract

Light and heavy chain deposition disease (LHCDD) is a rare complication of monoclonal gammopathy. In all documented cases, LHCDD is the association of deposits of a monoclonal light chain with a normal heavy chain, especially in the kidneys. We describe here a 78-year-old woman whose renal biopsy showed nodular glomerulosclerosis, initially diagnosed as diabetic nephropathy. Detailed kidney biopsy immunofluorescence study corrected the diagnosis to γ1-ĸ-LHCDD. Advanced immunoblot analysis showed deletion of CH1 in the both blood and kidney heavy chain.We report here, to our knowledge, the first case of γ1 LHCDD associated with a deletion of CH1. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20488505
Volume :
8
Issue :
2
Database :
Complementary Index
Journal :
Clinical Kidney Journal
Publication Type :
Academic Journal
Accession number :
102556925
Full Text :
https://doi.org/10.1093/ckj/sfv002