Literature DB >> 7922184

Renal involvement in plasma cell dyscrasias.

P W Sanders1.   

Abstract

Monoclonal light chain-related renal diseases represent a unique collection of renal disorders with monoclonal light chain deposition underlying the pathogenesis of these disorders. Yet, despite this common pathogenic mechanism, each renal lesion is unique. In addition, these syndromes are unusual in that, unlike many other renal disorders, they are potentially reversible causes of renal failure. This review focuses on the pathogenesis of three light chain-related renal diseases: AL amyloidosis, granular light chain deposition disease, and cast nephropathy ("myeloma kidney"). Management of these renal lesions in relation to the different pathophysiologic mechanisms is also discussed. Treatment should be designed to decrease production of nephrotoxic light chains and to prevent the binding interaction between these light chains and the various structures of the nephron.

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Year:  1993        PMID: 7922184     DOI: 10.1097/00041552-199303000-00011

Source DB:  PubMed          Journal:  Curr Opin Nephrol Hypertens        ISSN: 1062-4821            Impact factor:   2.894


  3 in total

1.  Paraprotein-Related Kidney Disease: Attack of the Killer M Proteins.

Authors:  Mark A Perazella; Kevin W Finkel
Journal:  Clin J Am Soc Nephrol       Date:  2016-12-07       Impact factor: 8.237

Review 2.  Protein reabsorption in renal proximal tubule-function and dysfunction in kidney pathophysiology.

Authors:  Erik I Christensen; Jakub Gburek
Journal:  Pediatr Nephrol       Date:  2004-05-14       Impact factor: 3.714

3.  [Renal lesions of paraproteinemias and fibrillary glomerulopathies].

Authors:  K Amann; C S Haas
Journal:  Pathologe       Date:  2003-10       Impact factor: 1.011

  3 in total

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