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Diagnosis and monitoring a case of light-chain deposition disease in the kidney using a new, sensitive immunoassay.

Abstract
A 59-year-old male was diagnosed with nephrotic syndrome secondary to light-chain deposition disease. There was no other evidence of a B cell clonal disorder or amyloidosis; circulating free light chains were identified using a new immunoassay (Freelite) and used to monitor disease progression. Improvement in renal function and proteinuria following VAMP chemotherapy correlated with a reduction in circulating light-chain levels. This case demonstrates a new tool in monitoring light-chain deposition disease in the kidney.
AuthorsIan Brockhurst, Kevin P G Harris, Claire S Chapman
JournalNephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association (Nephrol Dial Transplant) Vol. 20 Issue 6 Pg. 1251-3 (Jun 2005) ISSN: 0931-0509 [Print] England
PMID15784642 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Immunoglobulin kappa-Chains
  • Immunoglobulin lambda-Chains
  • Vincristine
  • Prednisolone
  • Azathioprine
  • Methotrexate
Topics
  • Antineoplastic Combined Chemotherapy Protocols (administration & dosage)
  • Azathioprine (administration & dosage)
  • Basement Membrane (metabolism, ultrastructure)
  • Disease Progression
  • Humans
  • Hypergammaglobulinemia (blood, diagnosis, drug therapy, pathology)
  • Immunoassay (methods)
  • Immunoglobulin kappa-Chains (blood)
  • Immunoglobulin lambda-Chains (blood)
  • Kidney (pathology)
  • Kidney Tubules (metabolism, ultrastructure)
  • Male
  • Methotrexate (administration & dosage)
  • Middle Aged
  • Nephrotic Syndrome (etiology)
  • Prednisolone (administration & dosage)
  • Vincristine (administration & dosage)

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