HEMATOLOGY - alterations in leukocyte function: leukemia Flashcards

EXAM 2 content

1
Q

what is leukemia? what does it do?

A

leukemia = clonal malignant disorder = hematopoietic cells makes new cells with the same genetic mutation
- different types BUT all types have – uncontrolled proliferation of malignant leukocytes –> bone marrow overcrowded & decreased production + function of normal hematopoietic cells

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2
Q

what haves if the same genetic mutation keeps happening?

A

cells of same genetic mutation –> prevents cells maturation + activities progrowth signaling pathways –> prevents apoptosis (programmed cell death)

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3
Q

what are the two types of leukemia?

A
  • myeloid leukemia = RBC, WBC, & plates
  • lymphoid leukemia = B & T cells
  • acute leukemia
  • chronic leukemia
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4
Q

what types of disorders are under myeloid leukemia?

A
  • myelodysplastic syndrome (MDS)
  • acute myeloid leukemia (AML)
  • chronic myeloid leukemia (CML)
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5
Q

what are the types of disorders under lymphoid leukemia?

A
  • acute lymphoblastic leukemia (ALL)
  • chronic lymphoblastic leukemia (CLL)
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6
Q

what is acute leukemia?

A

the predominant cells are – undifferentiated or immature cells (blasts cells)
- abrupt & rapid onset
- fatal without treatment

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7
Q

what is chronic leukemia?

A

the predominant cell is – more differentiated but does NOT function normally
- slow progressive
- insidious onset

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8
Q

what is the pathophysiology of leukemia?

A

abnormal immature WBCs (leukemic blasts) fill in bone marrow –> spills into blood –> leukemic blasts crowd out bone marrow –> proliferation of other cells to decrease (pancytopenia = reduced WBCs, RBCs, & plates) –> genetic translocations (mitotic errors) in leukemic blasts (??? asked a q to profs, fill in later) –>
1. immature cells increase proliferation, have decrease sensitivity to apoptosis, & its premature release in circulation
2. immature cells infiltrate & accumulate in liver, spleen, lymph nodes, & other organs

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9
Q

what are the risk factors of leukemia?

A

environmental
- radiation exposure
- exposure to cigarette smoke

genetic
- leukemia reappears in families

other diseases
- past chemotherapy: bc of suppressed bone marrow
- HIV
- hepatitis C

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10
Q

what are the general manifestations for leukemia?

A
  • anemia: decreased RBC, Hgb & Hct
  • bleeding: decreased plates (thrombocytopenia) –> purpura, petechiae, ecchymosis & hemmorhage
  • infection: opportunistic infections –> fever & chills
  • weight loss: due to anorexia & hypoalbuminemia
  • bone pain: if leukemic cells infiltrate bone or intramedullary infection
  • liver, spleen & lymph node enlargement: if leukemic cells infiltrate here
  • elevated uric acid level: due to increase catabolism of proteins & nucleic acids
  • neurologic: due to leukemic infiltration or cerebral bleeding –> headache, vomit, & blurred vision
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11
Q

what are the diagnostic procedures to determine if someone has leukemia? which one of the most definitive way to diagnose?

A
  • CBC with differential: specifically counts # of WBCs & detects abnormal cells
  • bone marrow biopsy: sample of bone under a microscope – THE MOST DEFINITIVE WAY TO DIAGNOSE CANCER
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12
Q

what is our end goal to treating leukemia?

A

REMISSION = disappearance of s/s of cancer
- if some have partial that is just decrease of s/s

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13
Q

since leukemia is a cancer, what is the primary treatment? how does it work?

A

chemotherapy – divided into two phases
1. induction = attain remission
2. post remission = retaining remission
- need higher doses of chemo

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14
Q

what are other forms of treating leukemia?

A
  • radiation therapy
  • chemo + stem cell transplant
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15
Q

even tho we are treating leukemia, what can it result into?

A

myelosuppression
- decrease production of myeloid cells –> PANCYTOPENIA

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16
Q

why would treatment be delayed if someone has chronic leukemia?

A

bc we want to observe first & if necessary then start treatment