Aml Flashcards

1
Q

AML usually occurs in the patients. Of age

A

15-40 years

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2
Q

Clinical presentation

A

Pallor and fatigue due to the hb decrease

Infections due to the tlc decrease

Purpurin , petechie
Hepatosplenomegaly

Gums are involved
Chloroma
Dic

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3
Q

Y Pallor and fatigue will occur

A

Hb decrease

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4
Q

Gums are involved in which AML

A

Gum hyperplasia and bleeding occurs more in M4 and M5

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5
Q

Which organs are not involved

A

Cns , testis , lymph node,

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6
Q

Chloroma is common I’m in which AML

A

M2 without maturation acc to fab

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7
Q

Dic is more common in

A

M4

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8
Q

What are the risk factors for the AML

A

Radiation
Down syndrome M7
Bloom’s syndrome
Franconia syndrome

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9
Q

Fab classification of AML

A
M0undifferentiated 
M1 without maturation 
M2 with maturation 
M3 acute promyelocytic leukaemia
M4 acutemyelomonocytic  leukaemia 
M5  acute monocytic leukaemia 
M6 acute erythroleulaemia
M7 acute megakaryocytic leukaemia
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10
Q

Describe about AML m2

A

More than 10 % matured cells will be there
It is associated with 8 21 translocation
Runx1 and runxt1

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11
Q

What is chorolma

A

Also known as granulocytic sarcoma and myeloblastoma

Soft tissue involvement
Mpo positive has greenish colour

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12
Q

Most common site for chloroma

A

Eye

Proptosisi occurs

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13
Q

Monocytes which are present in the chloroma are called as

A

Arbiskov cells

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14
Q

AML M3

A

Associated with t 15 and 17 translocations
PML gene on the 15 and RARA gena on the 17 fuse to form PML RARA Fusion

This leads to decrease in the vitamin A

Reduced conversion of the promyelocyte to myelocytes
Promyelocytes will be more

Acute promyelocytic leukaemia will be there

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15
Q

What are Auer rods

A

The granules in the promyelocytes fuse to form auer rods

Cross cross pattern is called faggot cell

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16
Q

What is the treatment of M3

A

All trans retinoic acid and arsenic trioxide

Best prognosis of all the aml

17
Q

AML M4 and M5 description

A

Tissue involvement gum bleeding and gum hyperplasia will be there
Non specific ester add postivity will be there

18
Q

Which chromosome abnormalities M4 is associated with

A

Chromosome 16

19
Q

AML m6 description

A

Diffuse positivity with pas

20
Q

Description about the AML 7 acute megakaryocytic syndrome

A

It is associated with Down’s syndrome
Least common syndrome
Megakaryocytes releases PDGF this is responsible for myelofibrosis

21
Q

What are the markers for megakaryocytes

A

CD41 and CD 61

22
Q

Lab diagnosis of AML

A

Hb decrease
TLC increase or decrease
Platelets decrease

Pheripheral smear more than 20 percent myeloblasts
Bone marrow more than 20 percent myeloblasts

23
Q

What are the stains used for myeloblasts

A

Mpo postindustrial
NSE
Sbb

24
Q

Marker of the myeloblasts

A

CD 13
CD33
CD117
Myeloperiosodase

25
Q

Blasts less than 20% can we make diagnosis of AML

A

Yes if 8 21 15 17 and inversion 16 is done

26
Q

B

A
27
Q

Definite treatment for AML

A

Stem cell Transplantation

28
Q

AML M3. Treatment

A

ATRA and arsenic trioxide

29
Q

Investigation of choice for AML

A

Flow cytometry assessment except for AML M 3 fish analysis is used

30
Q

What is bi phenotypic leukaemia

A

Both markers are present myeloblasts as well as lymphoblasts