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Updated: Oct 18, 2025

Analyses of Proteinuria, Renal Infiltration of Leukocytes, and Renal Deposition of Proteins in Lupus-prone MRL/lpr Mice
Published on: June 8, 2022
Multiple myeloma presenting as acute tubulointerstitial nephritis
Ying Long1, Abed A Aljamal1, Hisham F Bahmad2
1Mount Sinai Medical Center, Department of Internal Medicine, Miami Beach, FL, USA.
Acute tubulointerstitial nephritis (ATIN) is a rare complication of multiple myeloma (MM). Early diagnosis requires considering ATIN in patients with acute kidney injury and testing for light chains.
Area of Science:
- Nephrology
- Oncology
- Pathology
Background:
- Acute tubulointerstitial nephritis (ATIN) is a rare paraneoplastic manifestation in multiple myeloma (MM).
- Renal involvement in MM typically presents differently than ATIN.
Observation:
- An 82-year-old male presented with acute kidney injury without typical MM symptoms.
- Renal biopsy revealed light chain-associated ATIN with interstitial inflammation and tubulitis.
- Immunoassays confirmed a significant lambda light chain burden and Bence Jones protein.
Findings:
- Immunofluorescence showed lambda light chain deposition along tubular basement membranes.
- Electron microscopy indicated interstitial edema and inflammation.
- The findings supported a diagnosis of MM presenting as ATIN.
Implications:
- Light chain-associated ATIN should be considered in the differential diagnosis of acute interstitial nephritis.
- Serum free light chains and protein electrophoresis are crucial for diagnosing MM-associated ATIN.
- This case highlights the importance of comprehensive renal workup in suspected paraneoplastic syndromes.
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