393 - Multiple Myeloma and Myelodysplastic Syndromes Flashcards

1
Q

What does multiple myeloma look like histologically?

A

numerous plasma cells with a fried egg appearance, “clock face” chromatin, and intracytoplasmic inclusions containing Ig (in bone marrow)

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2
Q

What types of antibodies are produced in MM?

A

IgG (55%) or IgA (25%)

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3
Q

What is the most common primary tumor arising within the bones of the elderly?

A

multiple myeloma

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4
Q

What is found in the urine of patients with MM?

A

Bence Jones protein - Ig light chain

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5
Q

What is seen on x-ray in MM?

A

punched-out lytic bone lesions

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6
Q

What is seen in the blood smear of MM patients?

A

Rouleaux formation

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7
Q

What is seen in electrophoresis in MM?

A

M spike

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8
Q

What type of amyloidosis is associated with MM?

A

primary amyloidosis

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9
Q

Does MM increase susceptibility to infection?

A

yes

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10
Q

Differentiate the causes of M spike found in MM vs. Waldenstrom macrogobulinemia.

A

MM: IgG and/or IgA
WM: IgM

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11
Q

What blood and bone findings differentiate Waldenstrom macroglobulinemia from MM?

A
  1. IgM –> hyperviscosity symptoms

2. NO lytic bone lesions

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12
Q

What are the two main characteristics of MGUS?

A
  1. serum monoclonal protein < 3g/dL (M spike)

2. bone marrow with < 10% monoclonal plasma cells

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13
Q

How does MGUS relate to MM?

A

it is an asymptomatic precursor to MM; patients with MGUS develop MM at a rate of 1-2% per year

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14
Q

What are myelodysplastic syndromes?

A

Stem cell disorders involving ineffective hematopoiesis –> defects in cell maturation of all non-lymphoid lineages.

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15
Q

What causes MDS?

A

De novo mutations or environmental exposure (e.g. radiation, benzene, chemotherapy)

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16
Q

What cancer might MDS progress to?

A

AML

17
Q

What is the Pseudo-Pelger-Huet anomaly?

A

Neutrophils with bilobed nuclei typically seen after chemotherapy