6-2: Acute Leukemia Flashcards

1
Q

General concept: Hallmark of acute leukemia?

A

The Myeloid and lymphoid stem cells cannot mature further into other cells and they pile up (PROLIFERATIONG OF -BLASTS!)

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2
Q

How much of an increase in blasts is defined as acute leukemia?

A

> 20% –> move into blood stream and inc WBC count

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3
Q

Blasts on blood smear?

A

large, immature cells with punched out nucleoli

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4
Q

Accumulation of myeloid stem cell term=

*KEY MARKER?

A

Acute MYELOBLASTIC leukemia (AML)

-Myeloperoxidase (MPO) –. MPO can crystallize into AUER RODS!

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5
Q

Accumulation of lymphoid stem cell term=

*KEY MARKER?

A

Acute LYMPHOBLASTIC leukemia (ALL)

Positive for “tDt”in nucleus (tDt is a DNA polymerase)

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6
Q

AUER ROD THINK…

What are auer rods?

A

Acute MYELOBLASTIC LEUKEMIA

-crystallized myeloperoxidase =auer rod

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7
Q

tDt positive nuclear stain think?

A

Acute LYMPHOBLASTIC LEUKEMIA (or lymphoma if T-ALL)!

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8
Q

What is tDt and associated with which type of cell?

A

-tDt is a DNA polymerase only in lymphoblasts!

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9
Q

After the age of 5, ALL is associated with?

A

Children with Down Syndrome

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10
Q

ALL most commonly arises in what age group?

A

CHILDREN

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11
Q

ALL can be subclassified into what groups?

A

B-cell ALL (B-ALL)

T-cell ALL (T-ALL)

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12
Q

What are the surface markers to distinguish B-ALL and T-ALL?

A

Both will have tdt…

B will have CD10, CD19, and CD20

T will have CD2 -CD8

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13
Q

B-ALL treatment prognosis?

A

Excelent response to chemotherapy but need prophylaxis to scrotum and CSF

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14
Q

Chromosomal translocation relationships to B-ALL, prognosis, and affected age group?

A
  • t(12, 21) - Good prognosis - common in kids

- t(9, 22) - poor prognosis - common in adults (PHILADELPHIA ALSO DEFINING FEATURE OF CML!)

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15
Q
  • when see T-ALL think…

- What does T-ALL stand for?

A
  • “T” for THYMIC (Mediastinal mass) and “T” for TEENAGER

- SINCE ITS A THYMIC MASS (AND NOT CELLS FLOATING AROUND IN THE BLOOD) THIS IS AN ACUTE LYMPHOBLASTIC LYMPHOMA

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16
Q

Punched out nucleolus think…

A

AML OR (T or B)-ALL

17
Q

AML most commonly seen in what age range?

A

50-60 years

18
Q

Subclassification of AML:

A

1) cytogenetic abnormalities - determine if there is something reoccuring such as a translocation
2) lineage of myeloblasts
3) surface markers

19
Q

*AML chromosomal translocations (or what cytogenetic abnormality)? *and what happens?

A
  • -t(15;17) = CALLED ACUTE PROMYELOCYTIC LEUKEMIA
  • -> causes disruption of RAR receptor = disrupted ability to mature
  • these immature cells have numerous auer rods ==> increased risk for DIC
20
Q

*Tx for Acute promyelocytic leukemia?

A

*ATRA (all transretinoic acid) - causes the blasts to mature

21
Q

t(15;17) is called?

A

Acute Promyelocytic Leukemia

22
Q

Acute monocytic leukemia -

  • proliferation of what cell?
  • where do these cells infiltrate?
A

-monoblasts proliferate
-infiltrate the gums
LACK MPO

23
Q

Acute megakaryoblastic leukemia-

  • proliferation of what cell?
  • associated with what disease?
A

-proliferation of megakaryocytes
-associated with Down syndrome (before age 5)
(DONT HAVE MPO - dont need it bc they dont kill things)

24
Q

Down Syndrome associated diseases…

  • before age of 5=
  • after age of 5 =
A
  • before = acute megakaryoblastic leukemia

- after = acute lymphocytic leukemia (ALL)

25
Q

History of exposure to alkylating agents of radiotherapy yields what disease?

A

AML (from predisposing dysplasia) –> AKA myelodysplastic syndrome

26
Q

myelodysplastic syndrome - presentation:

A
  • cytopenias
  • hypercellular bone marrow
  • abnormal maturation of cells
  • increased blasts
27
Q

outcomes for people with myelodysplastic syndrome

A

-die from infection or bleed

OR may progress to acute leukemia if the WBC > 20%