AML Flashcards

(34 cards)

1
Q

Undifferentiated blasts, AML- -not otherwise categorized

A

M0 myeloid

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2
Q

Blasts and promyelocytes predominate without further maturation of myeloid cells

A

M1 myeloid

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3
Q

Myeloid cells demonstrate maturation beyond the blast and promyelocyte stage

A

M2 myeloid

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4
Q

Promvelocytes predominate in the bone marrow

A
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5
Q

Promvelocytes predominate in the bone marrow

A

M3 promyelocytic

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6
Q

Both myeloid and monocytic cells are present to the extent of at least 20% of the total leukocytes

A

M4 myelomonocytic

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7
Q

Most cells are monocytic; two subtypes (a and b) are recognized, one characterized by large blasts in bone marrow and peripheral blood, the other (differentiated type) by monoblasts, promonocytes, and monocytes

A

M5 monocytic

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8
Q

Also known as Di Guglielmo syndrome; abnormal proliferation of both erythroid and granulocytic precursors; may include abnormal megakaryocytic and monocytic proliferations

A

M6 erythroleukemia

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9
Q

Large and small megakaryoblasts with a high nuclear-cytoplasmic ratio; pale, agranular cytoplasm

A

M7 megakaryocytic

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10
Q

is characterized by either a rapid or gradual onset that may resemble an acute infection. The patient may have a history of fever, infections, fatigue, and bleeding episodes. Physical examination may reveal tenderness of the bones, particularly the ribs and sternum; ulcerated mucous membranes; petechiae; and purpura. Additional physical findings may include hepatomegaly, splenomegaly, and lymphadenopathy.

A

FAB M1

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11
Q

 The outstanding feature of the peripheral blood smear and bone marrow is the predominance of myeloblasts. These blasts usually have a regular cytoplasmic outline and may contain slender, red- staining Auer rods in the cytoplasm. The nuclear chromatin is very fine and homogeneous

A

M1

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12
Q

Associated with CHLOROMA = localized tumor masses consisting of myeloblasts. In these tumors, the presence of large quantities of the enzyme MPO produces a green appearance if the tissue is cut

A

M1

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13
Q

Hemorrhagic manifestations such as easy bruising, epistaxis, gingival bleeding, and petechiae are common initial symptoms. Hepatomegaly, splenomegaly, and lymphadenopathy are seen infrequentl

A

M2

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14
Q

Myeloblasts predominate on peripheral blood smears. The nuclei are usually round or oval with one or more prominent nucleoli and fi ne reticular chromatin. The cytoplasm is basophilic with a variable number of azurophilic granules. Auer rods are commonly seen

A

M2

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15
Q
A
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16
Q

Fatigue and symptoms of bleeding such as bruising, hematuria, and petechiae are common. Hepatomegaly, splenomegaly, and lymphadenopathy are seen infrequently.

18
Q

Appears to be the most aggressive of acute leukemia with a severe bleeding tendency and a fatal course
 Promyelocytes are the predominating cell type

19
Q

The promyelocytes may be hypergranular, microgranular, or hypogranular variations. Coarsely granular
promyelocytes with dumbbell-shaped or bilobed nuclei may be seen. The nuclear chromatin is finely reticular and
the cells often lack nucleoli

20
Q

is characterized by a balanced reciprocal translocation between chromosomes 15 and 17, which results in
the fusion between PML gene and retinoic acid receptor a (RARA)
 It is associated with DIC

22
Q

This form of leukemia may also be referred to as Naegeli type monocytic leukemia. Occurrence of this form of leukemia is uncommon in children and young adults. The highest frequency of occurrence is in adults older than 50 years of age

23
Q

Symptoms of this form of leukemia are similar to those of other forms of acute leukemia. Pharyngitis may be observed. Gingival hyperplasia due to leukemic infiltration may be noted
 Associated with leukostasis together with M5

24
Q

Leukostasis refers to a pathological finding of slightly dilated, thin-walled vessels filled with leukemic cells. The brain
and lungs are the most commonly involved organs. Symptoms of leukostasis are headache, visual impairment, and
shortness of breath
proliferation of granulocytes and monocytes is characteristic.

25
26
Also known as Schilling type
M5
27
28
The onset of this form of leukemia is dramatic, with headaches and fevers being the chief complaints. Typical symptoms of monocytic leukemia additionally include fatigue, weight loss, and bleeding from the mouth or nose. Physical examination frequently reveals gingival (mouth and gums) hyperplasia, as in myelomonocytic leukemia; pallor; and skin lesions
M5
29
Monocytes and promonocytes constitute 25% to 75% of the nucleated cells. Blasts frequently have a muddy or smoggy gray-blue cytoplasm containing tiny granules, and pseudopods are common. The nucleus has a reticular granular chromatin pattern and may contain from one to five large nucleoli
M5
30
Acute erythroid leukemia. This form of leukemia, also referred to as erythemic myelosis or Di Guglielmo syndrome represents a proliferation of both immature granulocytic and erythrocytic cells.
M6
31
Erythroblasts on blood smears typically have an irregular outline with a high nuclear-cytoplasmic ratio  Blasts of myeloid origin may have Auer rods  Promyelocytes may also be present as well as monocytes and promonocytes
M6
32
In this form of acute leukemia, 50% or more of the blasts are of megakaryocyte lineage.  Organomegaly is infrequent except in children. Radiographic evidence of bone lytic lesions has been observed in children
M7
33
Immunophenotyping reveals that megakaryoblasts express one or more of the platelet glycoprotein: CD41 or CD61. Blasts are negative with anti-MPO antibody.
M7
34