Hemeonc 13 Flashcards

1
Q

Malignancies of hematopoietic stem cells, Characterized by the uncontrolled growth of abnormal white blood cells and deficiencies of normal hematopoietic cells
(Growth of the abnormal cells is clonal)

A

Leukemias

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2
Q

Primitive cells that can:

  • -make more primitive cells just like itself (self-renewal)
  • -make lots of mature cells of different types
  • -Source of all blood cells
  • -Resides in the bone marrow
  • -Normally quiescent (dormant)
A

Hematopoietic stem cells

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3
Q

What is the largest tissue in the body?

A

bone marrow

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4
Q

How would you expect an acute leukemia to present as far as lab values?

A

TYPICALLY, with low blood counts across the board (except WBC, which could be high or low)

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5
Q

True or False, hematopoietic stem cells produce hundreds of billions of cells every day in a healthy person

A

True

200B-RBC, 200B-PLT, 70B-WBC

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6
Q

When you think ACUTE leukemia, you should think?

A

Rapid proliferation, immature malignant WBC’s

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7
Q

When you think CHRONIC leukemia, you should think?

A

Slow proliferation, partially differentiated mature WBC’s

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8
Q

T-cells, B-cells, and natural killer cells come from what type of cell?

A

Lymphoid cell

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9
Q

RBC’s, PLT, granulocytes, come from what type of cell?

A

Myeloid cell

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10
Q

What cell is experiencing malignancy in an ALL?

A
ALL=acute lymphoid leukemia,
the Lymphoblast (acute is immature, therefore the blast cell)
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11
Q

What cell is experiencing malignancy in an AML

A

acute = blast

Myeloblast cell

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12
Q

Which leukemia is most common and highly curable in children?

A

ALL

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13
Q

If all blood counts in acute leukemia are low (except WBC, could be high or low), what types of symptoms would you expect?

A

anemia, infection(WBC malfunctioning), bleeding (along with fever, fatigue, wt loss common in all cancer)

Also lymphadenopathy, splenomegaly, bone pain, meningeal symptoms, metabolic derangement (electrolyte imbalance, etc)

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14
Q

what is the term for “thick blood” due to a white count >50,000?

A

Leukostasis

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15
Q

how can you definitively determine whether a leukemia is ALL or AML?

A

bone marrow bx

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16
Q

If you suspected an acute leukemia and your patient had gingival hyperplasia, which would you suspect?

A

AML

17
Q

Which leukemia has multiple classifications with many different genetic mutations?

A

AML

18
Q

What cytogenetic factor will cause AML patients to likely need a transplant even after remission?

A

high number of mutations, because recurrence is so likely

19
Q

What is the typical tx plan for AML?

A

Induction chemo-one round
consolidation chemo x 3-4 cycles
eval for transplant

20
Q

What is the typical tx plan for ALL?

A

Induction chemo x 6-12 months
Maintenance chemo x 2 years
eval for transplant

prophylactic intrathecal injections of chemo since these patients are more likely to have invasion of CSF

21
Q

your patient has Asymptomatic leukocytosis
Fatigue, weight loss, fever, night sweats
Splenomegaly (95%) and early satiety. What is her most likely leukemia classification?

A

Chronic stable phase CML or chronic stable phase CLL

22
Q

How do you treat a patient who has entered into the blast crisis of CML?

A

Just like an acute myeloid leukemia

23
Q

What is the name of a daily oral medication that can maintain remission for years?

A

Gleevec

24
Q

How do you manage asymptomatic CLL? When would you escalate treatment?

A

observation/watchful waiting.
Begin chemo for new symptoms or disease progression. May add Rituxan.

transplant rare and controversial