AML and ALL Flashcards

1
Q

causes of leukemia

A

genetic, occupational, environmental

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2
Q

FAB classifications

A

morphology
cytochemical stains
clinical findings

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3
Q

WHO classifications

A
morphology
cytochemical stains
clinical findings
flow cytometry
molecular genetic abnormalities
cytogenetics
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4
Q

AML is characterized by two fundamental features

A

ability to proliferate continuously

arrested development

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5
Q

When AML is suspected, the following lab evaluation must include

A

PB testing
BM testing
cytogenetic studies
immunophenotyping

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6
Q

AML with t(8;21)(q22;q22) RUNXI-RUNXIT1

A

abnormal protein causes irregulation of hematopoiesis

favorable outcome

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7
Q

AML with inv(16)(p13.1q22)

A

dysplastic eosinophils in bone marrow

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8
Q

AML with t(15;17)(qLeukemia (F22;q12) PML RARA

A
Acute Promyelocytic Leukemia M3
young adults
Differentiation block of promyelocyte stage
hypergranular, butterfly nucleus
can have a microgranular variant
causes DIC
treat with vitamin A (ATRA)
favorable outcome
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9
Q

AML (megakaryoblastic) with t(1;22)(p13,q13) RBM15-MKL1

A

associated with down syndrome
dry tap due to fibrosis
causes DIC

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10
Q

t(9;22)(q34:q11) BCR-ABL

A

B-ALL
poor prognosis
older adolescents

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11
Q

t(v;11)(v:23)

A

B-ALL
infants, older adults
poor prognosis

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12
Q

t(12;21)(p13;q22)

A

most common

good prognosis

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13
Q

three stages of chemotherapy for ALL

A

Induction therapy phase
CNS prophylaxis phase
Maintenance therapy phase

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14
Q

four ways to differentiate AML from ALL

A

morphology and cytochemistry
immunophenotyping
cytogenetic analysis
molecular analysis

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