Acute Leukemias Flashcards

1
Q

ALL target population

A

Children

Male more than female s

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2
Q

ALL curability

A

Curable in 70% children

Bad in adults

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3
Q

AML Target

A

Adults

Male more than female

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4
Q

Curability AML

A

Low in adults

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5
Q

Causes of acute leukemia

A
Idiopathic 
Underlying hemato disorders
Chemical 
Drugs 
Ionizing radiation
 Viruses - HTLV1, EBV, HIV
Genetic conditions ( fanconi anemias, Down syndrome, ataxia telangiectasia)
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6
Q

What is a blast cell

A

Precursor cells arrested in an early stage of development

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7
Q

What is the pathophysiology of acute leukemia’s

A

Chromosomal translocation -> Abnormal expression of gene -> blast cells replace normal bone marrow -> anemia, neutropenia, thrombocytopenia

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8
Q

High amount of blast cells invade vital organs , what are the consequences

A

hyperleukocytosis
Increase in blood viscosity
Microthrombi, acute bleeding

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9
Q

Organs invaded by blast cells

A
Brain
Lungs
Eyes
Kidney 
Spleen
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10
Q

Metabolic manifestaction of acute leukemia

A

Hyponatremia due to vasopressin like element

Hypokalemia

Hyperuricemia

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11
Q

clinical manifestation of acute leukemia’s due to

A

Marrow failure
Leukostasis
Tissue infiltration

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12
Q

Clinical manifestation of acute leukemia

A
Fever
Weight loss
Gum hypertrophy
Dic 
Lymphadenopathy 
hepatosplenomegaly 
Petechiae
 confusion
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13
Q

Classification of acute lymphoblastic leukemia FAB

A

L-1 85%
L-2 14%
L-3 (Burkitt ) 1%

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14
Q

L1 characteristic

A

Small monomorphic type
Small homogeneous blasts
single and conspicuous nucleolus
Regular nuclear outline

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15
Q

L2 characteristics

A

Large heterogeneous typ
large blasts
more pleomorphic

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16
Q

L3 characteristics

A

Burkitt cell type

Blast cell with basophilic and vacuolated cytoplasm

17
Q

ALL classification WHO

A

Precursor B cell
Precursor T cell
Burkitt cell leukemia

18
Q

AML classification WHO

A

AML With recurrent genetic abnormalities
AML with multilineage dysplasia
AML therapy related
AML not otherwise categorized

19
Q

AML FAB classification

A
M0- minimally differentiated 
M1- without maturation 
M2- wirh maturation 
M4-myelomonocytic
M5- monoblastic / monocytic
M6- erythroid 
M7- megakaryoblastic

Basophilic
Acute oanmyelosis with myelofibrosis
Myeloid sarcoma

20
Q

Diagnosis

A
FBC 
Normocytic anemia 
High WBC 
Blast in peripheral blood 
Thrombocytopenia 
DIC 
BONE MARROW with more than 20% blasts
21
Q

How to distinguish AML FROM ALL

A

Light micro - AML-> auer rods, cytoplasmic , granules . ALL-> no auer rods, no granules
Flow cytometry in immunophenotyping
special stains - cytochemical staining peroxidase (+ AML ) , periodic acid Schiff (+ALL) , acid phosphatase (+ T-ALL)

ALL -> small basts , scant cytoplasm, dense chromatin, indistinct nucleoli, no auer rods

AML -> large blast, moderate cytoplasm , fine and lacy chromatin , prominent nucleoli, presence of auer rods

22
Q

Common antigens in AML

A

Cd13
Cd33
Cd117

23
Q

Common antigens in B- ALL

A

Cd10
Cd19
Cd22

24
Q

Common antigens T-ALL

A

Cd3

Cd7

25
Q

Type of chromosome type gives very poor prognosis in ALL

A

Philadelphia chromosome t(9:22)

26
Q

Common chromosome abnormalities

A
AML M2 - t(8:21)
AML m3 - t(15:17) 
AML M4 -  Inv16
T(9:22) ALL, CML
T(8:14) b-ALL