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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11290539PMC
http://dx.doi.org/10.3324/haematol.2024.285031DOI Listing

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Renal disease is a common cause of morbidity and mortality in patients with plasma cell dyscrasias. The serum-free light chain assay is used in patients, mostly older, with unexplained acute kidney injury to screen for potential myeloma cast nephropathy. This study consists of a systematic review of diagnostic features in myeloma cast nephropathy.

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Article Synopsis
  • The study investigates kidney biopsies with diffuse monoclonal light chain staining, highlighting the challenges in diagnosing MIg-associated kidney disease, as findings can vary significantly and lead to misdiagnosis or unnecessary treatment.* -
  • Out of 32 cases analyzed, nearly half (47%) had active myeloma requiring immediate treatment, while some patients showed no myeloma, illustrating the complexity of interpreting biopsy results.* -
  • The authors stress the need for detailed hematologic evaluations and recommend ongoing monitoring to identify any malignant changes while avoiding inappropriate treatments for patients without active myeloma.*
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Background: Acute kidney injury (AKI) is common in patients with multiple myeloma (MM). Whether serum free light chain (sFLC) measurements can distinguish between myeloma and other causes of AKI requires confirmation to guide early treatment. A rapid and portable sFLC test (Seralite®) is newly available and could reduce delays in obtaining sFLC results and accelerate diagnosis in patients with unexplained AKI.

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Mutational landscape reflects the biological continuum of plasma cell dyscrasias.

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We subjected 90 patients covering a biological spectrum of plasma cell dyscrasias (monoclonal gammopathy of undetermined significance (MGUS), amyloid light-chain (AL) amyloidosis and multiple myeloma) to next-generation sequencing (NGS) gene panel analysis on unsorted bone marrow. A total of 64 different mutations in 8 genes were identified in this cohort. NRAS (28.

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