Lecture 7 AML (select topics) Flashcards

1
Q

What AML subtypes have pseudo pelger huet and hypo granulation as a lab finding?

A

M0, M1, M2

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2
Q

What AML subtype features numerous abnormal promyelocytes? Describe some of their key features.

A

M3 and M3m (microgranular variant of M3)

Key features:
M3 - promyelocytes with heavy granulation, aurer rods may be seen, and kidney or bilobed shape nucleus.
M3m - nucleus is usually deeply notched or folded, butterfly, bi-lobed or kidney shaped. Cells appear devoid of granules or display a few. Auer rods occasioally. Note: Need Electron Mic to see.

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3
Q

What complication of M3 and M3m is frequently encountered?

A

DIC

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4
Q

What symtpoms are specific to M4, M4e, M5a&b? What other specific symptoms does M4 affect?

A

M4 & M4e: Soft tissue infiltrates due to monocytic component resulting in gum hypertrophy and infiltration, rectal ulcers, and skin involvement.

M5a&b: Skin and gum involvement.

M4: Meningeal symptoms: Headache, nausea, vomiting, blurring of vision and occasional intracranial hemorrhage.

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5
Q

What systems are affected by the large monocytic involvement in M5a and M5b?

A

Extramedullary tissue masses and central nervous involvement.

High incidence of organ involvement of the AML subtypes!

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6
Q

What can be measured in chemistry that supports the AML diagnosis for subtypes with a large monocytic component and why?

A

Serum and urine lysozyme are high because of monocytes.

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7
Q

What AML subtype can be show positive with a PAS stain?

A

AML - M6 Erythroleukemia.

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8
Q

What functional issue is common for all AML subtypes?

A

Functional abnormalities of granulocytes in phagocytosis, microbial killing, and chemotaxis resulting in increased
risk of infection.

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9
Q

What other conditions can AML-M6 be confused with when looking at the morphology under the light microscope?

A

M6 can be confused with B12, folate deficiencies and
Myelodysplastic syndromes when diagnosing.

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10
Q

What separates M2 from M1 subtypes of AML?

A

M2 has Type I, II, and III blasts where as M1 only has Type I and II. Both have Auer rods but M1 will only present in 50% of cases and in M2 they are often present. Also, M2 has > 10% granulocytes beyond the promyelocytes stage and <20% monocytic cells.

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11
Q

What is the key difference between M4 and M2 subtypes of AML?

A

M4 has >20% of non-erythroid cells are monocytic whereas M2 it is <20%.

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12
Q

What AML subtype has both abnormal granulocytic and monocytic differentiation observed in the peripheral blood and bone marrow? What is it called?

A

M4 - Acute Myelomonocytic Leukemia

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13
Q

What AML subtype is associated with Eosinophilia and its criteria?

A

M4e

Eosinophils >5% of non-erythroid cells in marrow, separates it from M4.

Eosinophils are abnormal - immature, single lobed, unsegmented and may have large basophilic granules. Generaly these cells only seen in the marrow.

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14
Q

What is another name for AML-M5?

A

Schilling Leukemia (with 2 types M5a and M5b).

It has the highest incidence of organ and soft tissue involvement due to monocytic component

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15
Q

In what AML subtype could you find >80% of non-erythroid cells as monoblasts? Auer rods?

A

AML-M5a (poorly differentiated)

Auer rods may be present but less common than as with M1, M2, and M3.

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16
Q

What AML subtype would you find the most predominate cell in the marrow promonocytes? What’s the predominant cell than in the blood?

A

AML-M5b (well differentiated).

Blood - monocyte.

Auer rods may be present. Less common than M1, M2, and M3.

17
Q

What are some of the RBC morphology that one can expect to find in a case of AML-M6 (Acute Erythroleukemia)?

A

RBC morphology (peripheral blood) displays large variety: anisocytosis,
poikilocytosis, macrocytosis with oval forms, schistocytes, dimorphic population. Numerous NRBCs.

18
Q

Can AML-M6 include myeloblasts in the bone marrow, if so what %? What about the erythrocytic component i the bone marrow?

A

Yes, >30% of non-erythroid cells are Type I and Type II Myeloblasts which may contain auer rods.

Over 50% of nucleated cells in the bone marrow are erthrocytic, i.e. erythroid hyperplasia.

19
Q

Describe the abnormal morphology associated with AML-M7 that one can find in the peripheral blood? PLT counts?

A

Megakaryocytic fragments and abnormal giant platelets.

Micromegakaryocytes, some with naked nuclei and groups of platelets surrounding them may be seen.

Platelet counts normal or increased

20
Q

What can be found in the bone marrow of AML-M7?

A

Acute Megakaryocytic Leukemia:

Bone marrow -
a) Frequent diffuse fibrosis.
b) Aggregates of Meagakaryoctyes.
c) Sheets of Megakaryoblasts.

21
Q

What AML subtype is associated with a poor prognosis and pancytopenia? How high can the blasts get in the bone marrow?

A

AML-M0

Blasts in the bone marrow may be as high as 90%. Although blasts generally present in the peripheral in most cases, but also may be absent.

Poor prognosis - Higher incidence of refractory to chemotherapy adn relaspe than other AML’s.

22
Q

What are typical symptoms of almost all AML’s?

A

AML rapidly fatal if untreated. Death due to pancytopenia such as anemia, bleeding and infection.