monoclonal immunoglobulin deposition disease (MIDD)
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Etiology
Pathology
- disorganized glomerular monoclonal immunoglobulin deposits
- no beta-pleated sheets,
- Congo-red negative staining
- immunoglobulin light chain or immunoglobulin heavy chain deposits
- deposits granular rather than fibrillary on histopathology
Clinical manifestations
- renal failure, proteinuria +/- nephrotic syndrome
- renal tubular dysfunction
- hypertension
- hepatomegaly (rare)
- cardiomyopathy (rare)
Laboratory
- urine protein -> proteinuria +/- nephrotic range
- renal biopsy
More general terms
References
- ↑ Medical Knowledge Self Assessment Program (MKSAP) 17, American College of Physicians, Philadelphia 2015
Medical Knowledge Self Assessment Program (MKSAP) 19 Board Basics. An Enhancement to MKSAP19. American College of Physicians, Philadelphia 2022