AKI is relatively common in myeloma, occuring in 20-30% of affected individuals at the time of diagnosis, and is mainly due to the nephrotoxic effects of the abnormal immunoglobulins
Aetiology
- Age at presentation ~60 years, greater incidence in males
Pathophysiology
- Cancer of plasma cells involving excessive clonal production of immunoglobulins (proteins)
- Collections of abnormal plasma cells can accumulate in the bone marrow and/or soft tissue
- Impairment of production of normal blood cells leads to anaemia
- Monoclonal production of a paraprotein (abnormal antibody), which can potentially cause renal dysfunction

Renal manifestations
- 20-40% present with renal impairment
- Multi-factorial aetiology

Glomerular
- AL amyloidosis
- Monoclonal immunoglobulin deposition (light-heavy chains)
Tubular
- Light chain cast nephropathy
Miscellaneous
- Dehydration
- Hypercalcaemia
- Renotoxic exposure - contrast, bisphonates, NSAIDs
Clinical presentation
- Classic presentation - back pain and renal failure
Symptoms
- Bone pain
- Weakness
- Fatigue
- Weight loss
- Recurrent infections
Signs
- Anaemia
- Hypercalcaemia
- Renal failure
- Lytic bone lesions
Investigations
- Bloods - serum protein electrophoresis, serum free light chains
- Urine - Bence Jones Protein
- Bone marrow biopsy
- Skeletal survey - lytic bone lesions
- Renal biopsy - not generally needed for diagnosis, but may be needed in complex cases to confirm that myeloma is the cause of the renal dysfunction

Management
- General measures - stop nephrotoxics, manage hypercalcaemia (saline +/- bisphonates)
- Diseases specific - chemotherapy, stem cell transplant
- Supportive - dialysis