Multiple Myeloma
Caused by malignant proliferation of plasma cells producing monoclonal immunoglobulin (M protein) that usually affects older adults (~60-70 years). This causes bone marrow infiltration and osteolytic bone lesions.
Clinical Features (CRAB)
- C: HyperCalcemia → confusion, constipation, polyuria
- R: Renal failure (due to light chain cast nephropathy)
- A: Anemia (normocytic, normochromic)
- B: Bone pain (especially back/ribs), lytic "punched-out" lesions, pathologic fractures
Other features: fatigue, infections (due to immunosuppression)
Diagnosis
- Serum/urine protein electrophoresis (SPEP/UPEP):
- Monoclonal spike (M protein), usually IgG or IgA
- Serum free light chain assay
- Bone marrow biopsy: >10% clonal plasma cells
- Skeletal survey: multiple punched-out lytic lesions
- Lab abnormalities:
- ↑ Calcium, ↑ Creatinine, anemia
- Rouleaux formation on peripheral smear
- When red blood cells (RBCs) stack together, resembling a pile of coins due to the increased fibrinogen and immunoglobulins, which coat the negatively charged RBCs, diminishing their surface charge. This allows the RBCs to adhere together.
- Urinalysis
- Proteinuria
- Bence Jones proteins
- Possible granular casts or light chain casts
- Nephrotic disease
- Oval fat bodies
- Proteinuria
Treatment
- Initial:
- Chemotherapy + corticosteroids (e.g. lenalidomide, bortezomib, dexamethasone)
- Stem cell transplant for eligible patients
- Supportive:
- Bisphosphonates for bone disease
- Hydration and avoid nephrotoxic drugs (protect kidneys)
- Treat hypercalcemia (IV fluids, bisphosphonates)
Complications
- Pathologic fractures, spinal cord compression
- Renal failure
- Infections (due to decreased normal immunoglobulins)
- Amyloidosis
- Older patient with bone pain, anemia, hypercalcemia, renal failure
- Labs show M spike and lytic bone lesions
- Rouleaux formation on blood smear