Acute Leukemias, Lymphoid & Plasma Cell Neoplasms, MPN Flashcards

1
Q

Tumor suppressor gene cause cancers such as leukemia when mutations result in:

A

Failure to prevent malignant process

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2
Q

In what age group does acute lymphoblastic leukemia occur with the highest frequency?

A

1-15 years old

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3
Q

The WHO classification requires what percentage for the blast count in the blood or bone marrow for the diagnosis of AML?

A

At least 20%

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4
Q

In addition to morphology, cytochemistry, and immunophenotyping, the WHO classification of myelo- and lymphoproliferative disorders is based upon which characteristic?

A

Cytogenetic abnormalities

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5
Q

In the FAB classification, myelomonocytic leukemia would be?

A

M4

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6
Q

The M:E ratio in myelocytic leukemia is usually:

A

High

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7
Q

Chloromas are associated with:

A

High

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8
Q

What is the most common presentation of acute erythroid leukemia?

A

> 50% of nucleated marrow cells are erythroid precursors & >20% are myeloblasts

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9
Q

The M:E ratio in erythroleukemia is usually

A

Low

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10
Q

Auer rods are most commonly seen in what type of leukemia?

A

Promyelocytic leukemia

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11
Q

What cytochemical stain can be used to differentiate AML from ALL?

A

MPO

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12
Q

Naphthol AS-D chloroacetate esterase is usually positive in ____ cells, and alpha-naphthyl acetate esterase is useful for identifying blast cells of ____ lineage.

A

Granulocytic; monocytic

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13
Q

A peripheral smear shows 75% blasts. These stain positive for both Sudan Black B and peroxidase. Given these values, which of the following is the most likely leukemia diagnosis?

A

Acute myelocytic

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14
Q

What is the gene translocation in FAB M2?

A

t(8;21)

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15
Q

What is the gene translocation in FAB M3?

A

t(15;17)

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16
Q

What AML cytogenetic abnormality is associated with acute myelomonocytic leukemia with marrow eosinophilia under the WHO classification of AML with recurrent genetic abnormalities?

17
Q

What leukemia is characterized by an increase in monoblasts and monocytes?

18
Q

What is the WHO classification of FAB M7?

A

Acute myeloid leukemia not otherwise specified

19
Q

Based on the WHO classification system, B cell ALL (FAB L3) and ____ represent different clinical presentations of the same disease identity.

A

Burkitt lymphoma

20
Q

Terminal deoxyribonucleotidyl transferase is present in:

A

Precursor B and precursor T lymphoid cell

21
Q

What is the translocation most commonly associated with Burkitt lymphoma?

22
Q

The (8;14) translocation brings which 2 genes in close proximitu?

A

c-myc and Ig heavy chain

23
Q

What genetic alterations is associated with favorable diagnosis in pre-B ALL?

24
Q

Chronic lymphocytic leukemia is defined as:

A

An accumulation of B lymphocytes

25
TRUE or FALSE: Hairy cells contain tartrate-resistant acid phosphatase (TRAP).
True
26
What are characteristic findings in multiple myeloma?
Increased IgG and hyperclacemia
27
Multiple myeloma is characterized by the presence in urine of large amounts of:
IgG light chains
28
What is the initial laboratory technique for the diagnosis of monoclonal gammopathies?
Serum and urine electrophoresis
29
What are characteristic findings in Waldenstrom's disease?
Increased IgM and blood hyperviscoscity
30
Presence of giant binucleated Reed-Sternberg cells with prominent nucleoli
Hodgkin's dsisease
31
What is the key diagnostic test for Hodgkin lymphoma?
Lymph node biopsy
32
What cells are identified in lesions of mycosis fungoides?
T lymphocytes
33
In what disorder is significant basophilia seen?
Chronic myelogenous leukemia
34
What would be the LAP score in CML?
10
35
Chromosome most closely associated with CML
Philadelphia chromosome
36
The ____ of Philadelphia chromosome in granulocytic leukemia suggests a rapid progression of the disease.
Absence
37
The hemorrhagic problems associated with scurvy are due to a deficiency of ____, which is a cofactor required for collagen synthesis.
Vitamin C