Multiple myeloma Flashcards

1
Q

what is the abnormal protein produced in multiple myeloma?

A

M protein

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2
Q

what is the most common heavy chain proliferation in multiple myeloma?

A

IgG

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3
Q

what are the symptoms of myeloma?

A
  1. lytic bone lesions

2. numbness / tingling in lower back / legs

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4
Q

what test is required to view the lytic bone lesions of multiple myeloma?

A

bone survey

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5
Q

what are the criteria for multiple myeloma diagnosis?

A
  1. serum / urine monoclonal protein
  2. clonal plasma cells in bone marrow
  3. end organ damage
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6
Q

how is smoldering myeloma different from multiple myeloma?

A

no end organ damage

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7
Q

how is smoldering myeloma different from MGUS?

A

for smoldering serum monoclonal protein is greater than 3 g/dL and 10-60% bone marrow clonal plasma cells

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8
Q

what is the mainstay therapy for myelomas?

A

steroids

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9
Q

what is the overall goal of stem cell transplant therapy?

A

remission

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10
Q

where are plasmacytomas located?

A

isolated myeloma mass in bone, most commonly humerus

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11
Q

what is the most common site for extramedullary plasmacytoma?

A

upper respiratory tract

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12
Q

what are the diagnostic criteria for plasmacytoma?

A
  1. biopsy proven solitary lesion of bone or soft tissue with evidence of clonal plasma cells
  2. bone survey
  3. absence of end organ damage
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13
Q

what is the treatment for plasmacytoma?

A
  1. radiation for bone or soft tissue

2. surgery and/or radiation for extramedullary

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14
Q

definition: amyloidosis

A

protein conformation disorder associated with clonal plasma cell dyscrasia

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15
Q

what is the clinical feature of amyloidosis?

A

extracellular deposition of light chain fragments in an abnormal insoluble fibril form

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16
Q

what % of patients with myeloma have concurrent amyloidosis?

A

10%

17
Q

what is the diagnosis for amyloidosis?

A

definitive - congo red stain

18
Q

what are the screening tests for amyloidosis?

A
  1. electrophoresis and urine IF

2. serum free light chains

19
Q

what is the most important factor for prognosis of amyloidosis?

A

cardiac involvement

20
Q

what is the treatment goal for amyloidosis?

A

retardation of further damage

21
Q

what are the clinical features of waldenstroms macroglobulinemia?

A
  1. excess IgM in blood

2. lymphoplasmacytic lymphoma in marrow

22
Q

what is the main symptom associated with waldenstroms macroglobulinemia?

A

hyperviscosity

23
Q

what is the diagnosis for waldenstroms?

A
  1. IgM monoclonal gammopathy (any size)

2. over 10% monoclonal lymphocytes and plasma cell differentiation in bone marrow

24
Q

what are the treatments for symptomatic waldenstroms?

A

chemo, plasmapheresis