Hema (AML M0-M7) Flashcards

(56 cards)

1
Q

Undifferentiated blasts in BM and PBS, AML—not otherwise categorized

A

AML Undifferentiated/Minimally Differentiated (M0)

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2
Q

30% blast cells – indistinguishable

A

AML Undifferentiated/Minimally Differentiated (M0)

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3
Q

% blast cells in M0
as indistinguishable

A

30%

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4
Q

M0 constitutes ___ of AML

A

5%

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5
Q

Age group for M0

A

Adults

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6
Q

blasts show no myeloid differentiation
medium-sized, have an agranular basophilic cytoplasm, round or slightly indented nuclei with 1 or 2 nucleoli, and dispersed chromatin

A

AML Undifferentiated/Minimally Differentiated (M0)

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7
Q

<3% of blasts react to Sudan black, a-naphthyl acetate, or stains that
detects myeloperoxidase

A

AML Undifferentiated/Minimally Differentiated (M0)

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8
Q

M1 constitutes ___% of AML

A

10%

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9
Q

Age group for M1

A

Adults

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10
Q

Azurophilic granules and Auer rods in the cytoplasm of the blast may suggest their myeloid nature

A

AML Differentiated without maturation (M1)

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11
Q

In other cases, the blasts resemble lymphoblasts, from which they are differentiated by positivity to myeloperoxidase stains or Sudan black in at least 3% of blast cells

A

AML Differentiated without maturation (M1)

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12
Q

M2 constitutes ___% of AML

A

30-45%

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13
Q

Age group for M2

A

ALL ages

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14
Q

Blasts may show azurophilic granules and Auer rods, and evidence of maturation is present

A

AML with maturation (M2)

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15
Q

> 10% of marrow cells being promyelocytes, myelocytes, and mature neutrophils

A

AML with maturation (M2)

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16
Q

In M2, >10% of marrow cells are

A

promyelocytes,
myelocytes,
mature neutrophils

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17
Q

In M2, <20% of marrow cells are

A

monocytes

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18
Q

< 20% being monocytes

A

AML with maturation (M2)

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19
Q

Neutrophils may show abnormally increased or decreased segmentation and lobulation

Basophils, eosinophils, and mast cells may be increased

A

AML with maturation (M2)

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20
Q

Highest number of Auer rods, collectively named as Faggot cells/Firewood cells (bundles)

A

AML Promyelomonocytic (M3)

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21
Q

30% blasts, >10% granulocytic lineage and >10% Promyelocytes

A

AML Promyelomonocytic (M3)

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22
Q

% blasts in M3

A

30%

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23
Q

> 10% in M3 are

A

granulocytic lineage
promyelocytes

24
Q

Associated with chromosomal translocation of 15:17 (WHO)

A

AML Promyelomonocytic (M3)

25
Increased incidence of Disseminated Intravascular Coagulation (DIC)
AML Promyelomonocytic (M3)
26
aka Acute myelomonocytic leukemia/
Naegeli Biphasic M1 & M5
27
M4 constitutes ___% of AML
15-25%
28
Age group for M4
Elderly
29
Sometimes in patients preceding chronic myelomonocytic leukemia (CMML)
Acute myelomonocytic leukemia/ Naegeli Biphasic M1 & M5 (M4)
30
Indicator are monoblasts and promonocytes
Acute myelomonocytic leukemia/ Naegeli Biphasic M1 & M5 (M4)
31
In M4, these are large cells with round containing >1 prominent nuclei and abundant basophilic cytoplasm, sometimes with fine azurophilic granules, vacuoles, and pseudopods formation
Monoblasts
32
In M4, these are less basophilic and more granulated cytoplasm, containing occasional vacuoles, and azurophilic granules
Promonocytes
33
Irregular and indented nucleus
Acute myelomonocytic leukemia/ Naegeli Biphasic M1 & M5 (M4)
34
M5 constitutes ___% of AML
5% each type
35
M5 more common in children (<17 y/o)
M5a
36
M5 more common in adults (>18 y/o)
M5b
37
at least 80% of the leukemic cells are in the monocytic line
Acute monoblastic and acute monocytic leukemia (M5a, M5b)
38
at least 80% of the monocytic cells are monoblasts
acute monoblastic leukemia (M5a)
39
most of them are promonocytes
acute monocytic leukemia (M5b)
40
Acute erythroid leukemia subtypes
Erythroleukemia (erythroid/myeloid) – M6a Pure erythroid leukemia – M6b
41
M6a constitutes ___% of AML
5%
42
In M6a, 50% of the nucleated cells in the bone marrow is
ERYTHROID
43
In M6a, these are dysplastic, containing multiple and megaloblastoid nuclei, the cytoplasm often possessing poorly delineated, coalescing vacuoles
erythroid (50%)
44
In M6a, 20% of nonerythroid cells are
myeloblast
45
In M6a, these are similar to those in AML with and without maturation
myeloblast
46
Very rare type of M6
M6b
47
In M6b, >80% of the marrow cells are
erythroid
48
Erythroblast in this type have deeply basophilic, often agranular, cytoplasm that may contain poorly delineated vacuoles Round nuclei have fine chromatin and >1 nuclei
Pure erythroid leukemia – M6b
49
M7 constitutes ___% of AML
5%
50
Age group for M7
ALL ages
51
In M7, 50% of the blast are from
megakaryocyte lineage
52
Often pleomorphic and have a basophilic, often agranular cytoplasm, cytoplasm may demonstrate pseudopod and bleb formation, indicating budding platelets in M7; Nuclei have fine chromatin and 1-3 nucleoli
Megakaryoblasts
53
In M7, these may be visible in the blood, as may be circulating micromegakaryocytes and megakaryocyte fragments
Dysplastic platelets
54
aka Schilling type
M5
55
aka Erythemic myelosis or Di Guglielmo syndrome
M6
56
aka MDS with excess blasts
M6