Plasma cell disorder- P Flashcards

1
Q

What is multiple myeloma?

A

Malignant proliferation of plasma cells in the BM

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2
Q

What is the significance of multiple myeloma?

A

IT is the most common primary malignancy of bone

- however most common malignancy lesion of bone overall is the Metastatic cancer

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3
Q

What would be high in the serum with someone who had multiple myeloma?

A

IL-6

- stimulates plasma cell growth and immunoglobulin production

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4
Q

What are the clinical features of multiple myeloma?

A
  1. bone pain with hypercalcemia
  2. elevated serum protein
  3. Increased risk of infection
  4. Rouleaux formation of RBC
  5. Primary AL amyloidosis
  6. Proteinuria
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5
Q

What is the cause of bone pain and hypercalcemia in multiple myeloma?

A

Neoplastic plasma cells secrete Osteoclast activating Factor which binds to RANK receptor on osteoclasts and stimulates them
- leading to lytic lesions (vertebra and skull)

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6
Q

Why would one have elevated serum protein in multiple myeloma?

A
  • Neoplastic plasma cell produce immunoglobulin
  • leads to an M spike on Serum protein electrophoresis
  • most commonly IgG and sometimes IgA
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7
Q

How does one with multiple myeloma have increased risk for infection?

A

Monoclonal proliferation lacks Antigenic diversity

- infection is the MOST common cause of death in multiple myeloma

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8
Q

What cause the RBC’s for form Rouleaux in multiple myeloma?

A

Increased serum protein decreases charge on RBC’s thus they start to stack on top of one another

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9
Q

What cause Primary AL amyloidosis in multiple myeloma?

A

Free light chains circulate in serum and deposit in tissue

-due to overproduction

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10
Q

What cause proteinuria in multiple myeloma?

A

Free light chains are excreted in the urine as Bence Jones proteins
- can lead to deposition in kidney tubules and leads to risk of renal failure

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11
Q

What is renal failure called in multiple myeloma?

A

Myeloma kidney

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12
Q

What is Monoclonal Gammopathy of Undetermined significance (MGUS)?

A
Increased serum protein with an M spike on SPEP
however lacks:
- lytic bone lesions
-hypercal 
-AL amyloid
-Bence jones proteinuria
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13
Q

Who commonly gets MGUS and what can it turn into?

A

Elderly - 5% of plp over 70

1% chance of multiple myeloma each year

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14
Q

What is Waldenstrom Macroglobulinemia?

A

B cell lymphoma with monoclonal IgM production

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15
Q

What are the clinical features of Waldenstrom macroglobulinemia?

A
  1. LAD no lytic bone lesions
  2. Increased Serum protein with M spike (IgM
  3. Visual and neuro deficits
  4. Bleeding
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16
Q

What cause the visual and neuro deficits in Waldenstrom macroglobulinemia?

A

Increased IgM leads to hyperviscosity of blood

- its a pentamer and rather large

17
Q

What is the treatment for Waldenstrom macroglobulinemia?

A

Plasmaphoresis

- removed the excess IgM