U 2 P 4 Flashcards

1
Q

CML is classified as what kind of disease?

A

Myleoproliferative

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2
Q

What mutation causes CML?

A

t(9:22)

Philadelphia chromosome

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3
Q

How common is CML and when does it usually appear in life?

A

Fairly common, around 45 years of age

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4
Q

How do we diagnose CML?

A

Philadelphia chromosome, absent LAP

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5
Q

What are the three phases of CML?

A

Chronic, accelerated, blast

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6
Q

What are some CML laboratory data?

A

Pro fusion of normal appearing granulocytes in all stages of development
WBC 50-500 MAY NEED TO dilute
N/N anemia
Peripheral blood resembles bone marrow aspirate
NRBCS increase as disease progresses
Bone marrow’s smear shows increased megakaryocytes

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7
Q

What are some ways to treat CML?

A

Gleevec, tyrosine kinase inhibitor, my Leo suppressive therapy leukapheresis

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8
Q

CLL is what kind of disease?

A

Lymphoproliferative disease

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9
Q

What is the most common form of leukemia in adults?

A

CLL

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10
Q

What is a symptom of CLL exclusive to CLL?

A

Lymphadenopathy Small lymphocytes that accumulate in bone marrow and spill into peripheral blood

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11
Q

What are some laboratory results of CLL?

A
WBC 20-200
     Peripheral smear
N/N
Lymphocytosis 70 to 95% of lymphocytes
Smudge cells maybe 100 to 200 per 100 white blood cells
CD 5, 19, 20, 23
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12
Q

When smudge cells exceed what percent of white blood cells present, and one drop of what to 8drops of blood?

A

When 15% smudge cells or more at one drop of 22% albumin

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13
Q

What are some other forms of CLL?

A

Hairy cell leukemia, pro lymphocytic leukemia, Waldenström’s macroglobulinemia, lymphosarcoma cell leukemia

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