Heme Test Flashcards

1
Q

Malignant disease of normal bone marrow. Replacement of normal bone marrow with abnormal (neoplastic) blood cells.

A

Leukemia

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2
Q

2 Most common adult leukemias

A

acute myeloid leukemia and chronic lymphoid leukemia

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3
Q

Ratio of adult to child with leukemia

A

10:1

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4
Q

Most common leukemia in children

A

acute lymphoblastic leukemia

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5
Q

WBC is generally increased in this type of leukemia

A

Chronic leukemia

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6
Q

This gene regulates cell proliferation and tumor suppressor genes and its mutation is related to leukemia.

A

Oncogene

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7
Q

Leukemia is classified according to?

A

Cell type, its maturity and cell lineage.

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8
Q

Smudge cells are seen in what leukemia?

A

chronic lymphoid leukemia

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9
Q

Auer rod is indicative of this leukemia?

A

acute myeloid leukemia

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10
Q

According to WHO For acute leukemias __% of blasts must be found in peripheral blood for diagnosis confirmation.

A

20%

FAB requires 30%

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11
Q

Blasts are larger in AML or ALL?

A

AML

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12
Q

This test is useful in differentiating AML(+ blasts) from ALL(- blasts) and is more specific than the Sudan black B stain.

A

Myeloperoxidase stain

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13
Q

Phospholipids, neutral fats, and sterols are stained by this. Differentiates AML from ALL, used when specimen is not fresh.

A

Sudan black B stain (SBB)

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14
Q

This stain, not as sensitive as others, tests positive in neutrophils, basophils, mast cells and their precursors only. Main use is demonstrating myeloid differentiation in paraffin-embeded tissue.

A

Specific esterase stain

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15
Q

Stain used to identify monocytic cells. Positive in these cells while negative in granulocytic cells. Seperates mono (+) from myelo(-) blasts.

A

Nonspecific esterase test

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16
Q

Stains for glycogen and related compounds. Strong positivity may be present in eryhtroblasts in erythroleukemia. Helps differentiate from pernicious anemia.

A

Periodic Acid-Schiff

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17
Q

A unique nuclear enzyme found in the majority of lymphoblastic leukemias, allowing the distinction of ALL from AML.

A

TDT terminal deoxynucleotidyl transferase

18
Q

What stain is used to identify Hairy Cell Leukemia?

A

TRAP- Tartrate Resistant Acid Phosphatase Stain

19
Q

Myeloid CD markers

A

CD 14
CD33
CD13
CD 117

20
Q

Lymphoid CD markers

A
CD 19
CD 10
Common ALL antigen (CALLA)
CD 20
HLA-DR
21
Q

CD markers used to identify AML

A
CD 33
CD13
CD14
CD11b
CD 117
22
Q

Most common translocation in precursor B-cell ALL in children with peak incidence 2-5 years

A

ALL with t(12;21): TEL-AML1

23
Q

ALL with Results in the formation of an abnormal fusion protein

A

t(1:19): PBX1-E2A

24
Q

Seen in the most common form of ALL infancy

A

t(4;11): AF4-MLL

25
most useful marker for distinguishing HCL from other B-cell leukemias
CD103
26
``` System widely in use to predict prognosis of CML Criteria is based upon: Age Splenomegaly Platelet count (platelets > 700,000) Blast count ```
Sokol Score
27
Trisomy 12 | Deletions/translocations 13q14
B-CLL
28
In DNA, Each nucleotide is composed of one of four different types of nitrogenous bases
Adenine Guanine Thymine Cytosine
29
is a chromosome abnormality caused by rearrangement of parts between nonhomologous chromosomes
translocation
30
Purpose to detect and localize specific DNA sequences in G-banded metaphase chromosomes using a labeled probe Advantages Permits visualization of target DNA in the (karyotypic visualization of metaphase chromosomes Aids in the diagnosis of DiGeorge Syndrome Disadvantages Metaphase analysis requires live cells capable of entering mitosis Visualization of fluorochromes requires an input light source (fluorochromes fades with time)
Fluorescent In-situ Hybridization (FISH)
31
Purpose is to localize DNA or RNA to particular cells in a tissue section Clinical Applications Localize foreign organisms in relation to lesion cells Important for pathogens that might also exist as normal flora Detect and localize gene expression by targeting RNA transcripts Advantages Permits visualization of target nucleic acid in the context of cytologic and morphological features Sensitive to low numbers of affected cells Disadvantage Difficult to obtain adequate sensitivity for detecting single copy targets.
In-Situ Hybridization
32
Used to amplify target DNA a billion fold so that it may be easily detected Works by enzymatically replicating one particular segment of DNA in a patient’s sample 1st amplification method be introduced into clinical laboratories Clinical Applications Measure tumor burden to monitor efficacy of anticancer therapy Measure the viral load to monitor the efficacy of antiviral therapy Selectively amplify DNA that has a particular disease associated defect such as JAK2 point mutation or PML/RARA translocation Advantages Extremely sensitive to low numbers of target sequences Small sample size requirement Relatively fast and inexpensive unless extensive post-amplification is required Disadvantages Extreme precautions are require to avoid cross contamination of samples or reagents by extraneous DNA
Polymerase Chain Reaction (PCR)
33
Purpose is to detect RNA: Advantages Sensitive to low numbers of target sequences Small sample size requirement Disadvantages RNA is labile, RNA-based testing requires meticulous care to avoid degradation by RNases Avoiding cross contamination of samples or reagents
RT-PCR
34
Analyzes the molecular structure of DNA to identify disease specific genetic alterations Most accurate method of detecting clonal gene rearrangement in lymphoid neoplasms Advantages Most accurate method of detecting clonal gene rearrangement in lymphoid neoplasms Disadvantages Sensitivity is relatively low Labor-intensive and costly Relatively long turnaround time Requires fresh or frozen tissue and not amenable to formalin-fixed tissue
Southern Blot
35
Determine the nucleotide order in a given gene and compare it to that of health individuals Screen for mutations (deletions or insertion events) associated with disease Clinical Applications Detect mutation of the HBB(beta globin)gene in a patient with beta thal Predict drug responsiveness or resistance in patients with CML treated with tyrosine kinase inhibitors Perform HIV genotyping to predict which drugs will be effective Advantages Sequencing considered the gold standard assay for detecting mutations Disadvantages Expensive and relatively insensitive to acquired mutations affecting fewer than 20% of cells in the sample
DNA Sequencing
36
Trisomy 8 AML-
Acute Myelocytic Leukemia
37
t(15;17)
AML-M3
38
inv(16)
AML-M4
39
t(9:22)
CML (or ALL)- acquired mutation
40
del(5q)
MDS