Multiple Myeloma & Polycthemia Vera Flashcards
What is a multiple myeloma?
Neoplastic monoclonal proliferation of a plasma cell
What happens in MM?
Typically excess production of 1 x Ig (‘monoclonal paraprotein’)
55% Ig G
20% Ig A
Typical patient?
70 y/o afro carribean
Symptoms of MM
Old CRAB
Old = 70+
C=hypercalaemia
R= Renal failure
A=Anemia (BM failure)
B=Bone lesions (BM failure = painful, new onset back pain in elderly)
Why is there hypercalcemia?
increased osteoclast bone resorption
Bones (weak bones)
Stones (kidney stones)
Abdo moans
Psychedelic groans
Why is there renal failure?
hypercalcemia = calcium oxalate renal stones
Immunoglobulin light chain kappa deposition; Bence Jones protein in Pee!!! - nephrotoxic)
Diagnosis of MM
Tests?
FBC + Blood film = normocytic normochromic + high ESR, rouleaux formation (aggregation of RBCs together, abnormal)
Urine dipstick - Bence Jones protein
U&Es = Renal failure; consider XR KUB (Kidney stone)
Bone profile = hypocalemia + high ALP
Serum electrophoresis = IgM paraprotein spike; hypergammaglobulin for that specific Ig
X Ray = skull; pepper pot skull, osteolytic lesions, punched out holes
Special test = BM Biopsy >10% plasma cells
Treatment for MM
Chemotherapy
Bisphosphonates (eg. alendronate) - bone protection
Dialysis
(consider BM stem cell transplant)
What is NICE recommendation for MM?
Full body MRI to ID BM infiltration systemically
What is polycthemia vera?
Increased blood cell level - overproduction by BM (Especially RBC)
What is PV caused by?
Mutation in JAK2 gene (JAK2V617) - 95%
Activation of gene means haematopoetic stem cells divide & produce RBCs even without EPO
Symptoms of PV?
Itchy (especially after a bath) - due to increased basophil & mast cells = histamine release
Burning in fingers & toes (erythromegalia)
Reddish plethoric complexion (pulpy face like cushings)
Blurry vison/headache
Hepatosplenomegaly (helps remove excel cells)
*features non specifically related to hyperviscosity = high RBC = High haematocrit = more solid mass of blood
Diagnosis of PV?
FBC = High WCW, Platelets and RBC
High Hb
Genetic test = JAK2V617
Complication of PV?
high risk of thromboemboli
Treatment for PV?
Non curative; maintain normal blood count
1. Venesection (often used solely) - take blood out like blood test
+ aspirin
*consider chemotherapy - hydroxycarbamide aka hydroxyurea (only in high risk patients)