MYELOMA LECTURE Flashcards

1
Q

front

A

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2
Q

What are the stereotypical findings on histology of multiple myeloma?

A

Bright purple/pink cytoplasmLarge Golgi from producing lots of proteinsNon-symmetrical nucleigreater than 1:20 ratio of plasma cells

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3
Q

Where does multiple myeloma begin?What are plasma cells?Where are they found?

A

Bone marrowPlasma cells are mature B lymphocytes that produce antibodies
~5% in the bone marrow and throughout lymphoid tissue

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4
Q

Is the disease patchy or continuous?Where does it mostly effect?

A

Patchy throughoutEffects pelvis, spine, rib cage, skull, shoulders, hips, humerus, femur

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5
Q

What is the most frequent feature of multiple myeloma?

A

Bone disease is the most common feature of multiple myeloma, approximately 2/3 of patients at diagnosis and in nearly all patients during the course of the disease.Evidence of bone disease is an indication to srat treatment (occasionally solitary plasmacytoma)

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6
Q

What is the best imaging tool for multiple myeloma?

A

Core whole body MRI protocol

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7
Q

Clonal plasma cells produce a single immunoglobulin. Monoclonal proteins are termed M-protein or paraprotein. This is an essential cancer marker. What is the difference with a light chain myeloma?

A

Some myelomas may only produce lambda light chains and not the full immunoglobulin molecule. These light chains are expressed in the urine and in the serum as Bence Jones protein.

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8
Q

How many new cases per year?What is the median age?Which race has the highest preponderance?

A

300065-70Afro-caribbean

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9
Q

What are the clinical features of myeloma? (CRABI)

A

C= HypercalcaemiaR= Renal impairmentA= AnaemiaB= Bone pain and destruction (fractures, cord compression)I= Recurrent infections

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10
Q

What are the diagnostic criteria for multiple myeloma?

A

M-protein serum >30g/L+/- bone marrow plasma cells >10% (excess plasma cells)Related organ damage

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11
Q

What is MGUS?

A

Monoclonal gammopathy of uncertain significanceIs a benign condition that does not cause symptoms or damage. Pre-malignant forerunner of myeloma, tiny clone of plasma cells.1% risk of progression each year, this does not increase or decrease over time.90% of MGUS’ do not progress to myeloma but 90% of myelomas have had an MGUS stage

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12
Q

{{10 1 0.png}}What is this?How would it be described?

A

This is a multiple myeloma lytic lesion.Most often when bone is destroyed through cancer there is a white rim around the lesion due to new bone formation (sclerotic), myeloma inhibits new bone formation and so it is referred to as lytic.

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13
Q

WHat causes renal damage in multiple myeloma?

A

Light chain deposition in renal tubules leading to cast nephropathy. In healthy people the light chain is filtered back via the proximal tubule. In myeloma the light chain precipitates out

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14
Q

What is a plasmocytoma?

A

A localised deposit of plasma cells. Can be in bony or soft tissue. May be associated with a small monoclonal paraprotein.Treat with radiotherapyRisk of recurrence into myeloma

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15
Q

How is myeloma diagnosed?

A

Serum electrophoresisBone marrow biopsySkeletal surveyFBCBlood chemistry

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16
Q

What is immunoparesis?

A

When normal immunoglobulins are suppressed

17
Q

What is the characteristic progression of the disease?

A

Relapsing remitting pattern of paraprotein production, with cancer evolving to make treatment less effective

18
Q

Half of translocations involve which chromosome?

A

14

19
Q

Which cells are activated in myeloma and how?

A

RANKL activates osteoclasts and so increases bone resorbtion.

20
Q

How should you manage hypercalcaemia in multiple myeloma?

A

Intraveneous fluid replacement- ideally 3 litres/24 hoursThen prescribe bisphosphonates such as pamidronate or zoledronate IV

21
Q

Which drugs should be avoided in myeloma for pain management?

A

NSAIDs because they are nephrotoxic

22
Q

What does VTD intensive treatment stand for?

A

Velcade, thalidomide, dexamethasone

23
Q

What is the mechanism of action for velcade?What are some of its main side-effects?

A

Blocks the proteasome and prevents recycling of proteins into aminto acids.N+V and peripheral neuropathy

24
Q

What does G CSF do?

A

Activates the white cells to leave the bone marrow in preparation for transplant.

25
Q

What is daratumumab?

A

Anti-CD38 monoclonal antibody