TEST 1 Flashcards

PAST PAPER (66 cards)

1
Q

What virus causes lymphoid malignancies in humans

A

Epstein-Bar virus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Tumor suppresor genes causes cancers such as leukemia when mutations result in

A

Failure to prevent malignant process

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Oncogenes are said to act in a dominant fashion because

A

A mutation in a single allele is sufficient for malignancy to develop

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what is a cellular abnormality produced by oncogenes

A

Acceleration of DNA catabolism

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Compared with autologous bone marrow transplantation, allogeneic transplantation has

A

better long term succes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Chemotherapeutic agents are divided into which two major subgroups

A
  1. phase specific
  2. phase non specific
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Qualitative and quantitative neutrophil hanges noted in response to infection include

A
  1. neutropenia
  2. toxic granulation
  3. vacuolization
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

The WHO classification requires what percentage for the blast count in the blood or bone

A

At least 20%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

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

A

AML with inv

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

neutropenia is present in patients with which absolute count

A

<1.5*10^9/L

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

A m:e (myeloid:erythroid ration) of 10:1 is mostly seen in

A

Leukemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Which of the following leukemias are included in the 2008 World Health Organization
classification of myeloproliferative neoplasms?

A

Chronic myelogenous leukemia (CML)
Chronic neutrophilic leukemia (CNL)
Chronio eosinophilic leukemia (CEL)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Repeated phlebotomy in patients with polycythemia vera (PV) may lead to the
development of:

A

Iron deficiency anaemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

in essential thrombocytopenia the platelets are

A

increased in number and fuctionality abnormal

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Which of the following cells is considered pathognomonic for Hodgkin’s disease?

A

Reed- sternberg cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Which of the morphological findings are characteristics of reactive lymphocytes

A
  1. high nuclear: cytoplsmic ration
  2. prominent nucleoli
  3. basophilic cytoplasm
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Auer rods may be seen in all of the following

A
  1. acute myelomonocytic leukemia (M4)
  2. acute myeloid leukemia leukemia without maturation (M1)
  3. acute promyelocytic leukemia (M3)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Which type of anaemia is ussually present in a patient with acute leukemia

A

Normocytic, Normochromic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

In leukemia which term decribes a peripheral blood finding of leukocytosis with a shift to the left, accompanied by nucleated red cells

A

Leukoerythroblastosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

The basic pathophysiological mechanisms responsible for producing signs and symptoms in leukemia include all of the following except

A

Decreased erythropoietin production

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Which type of acute myeloid leukemia is called the true monocytic leukemia and follows an acute or sub acute course charcterized by monoblasts, promonocytes and monocytes

A

Acute monocytic anaemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

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

A

1-15 years

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Disseminated intravascular coagulation (DIC) is mostly often associated with which of the following types of acute leukemia

A

Acute promyelocytic leukemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
In Myelofibrosis, the characteristic abnormal red blood cell morphology is that of
Tear drop cell
18
PV is characterized by
Absolute increase in total red cell mass
19
Features of secondary polycynthemia incude all of the foloowing except
splenomegaly
20
The erythrocytosis seen in relative polycythemia occurs because of
Decreased plasma volume of circulating blood
21
In PV, what is characteristically seen in the peripheral blood?
Pancytosis
22
The leukocyte alkaline phosphatase (LAP) stain on a patient gives the following results: 10(0) 48(1+) 38(2+) 3(3+) 1(4+). Calculate the LAP score. The LAP score is calculated as: (the number of 1+ cells x 1) + (2+ cells x 2) + (3+ cells> 3) + (4+ cells x 4).
137
23
CML is distinguished from leukemoid reaction by which of the following?
CML: low LAP; leukemoid: high LAP
24
Which of the following occurs in idiopathic Myelofibrosis (IMF)?
All of these options
25
What influence does the Philadelphia (Ph1) chromosome have on the prognosis of patients with chronic myelogenous leukemia?
The prognosis is better if Ph1 is present
26
Which of the following is (are) commonly found in CML?
An increase in basophils
27
In which of the following conditions does LAP show the least activity?
In leukomoid reactions
28
A striking feature of the peripheral blood of a patient with CML is a:
Presence of granulocytes at different stages of development
29
Which of the following is often associated with CML but not with AML?
Splenomegaly
30
The JAK2(V617F) mutation may be positive in all of the following chronic myeloproliferative disorders Except
CML
31
All of the following are major criteria for the 2008 WHO diagnostic criteria for essential thrombocythemia Except:
Sustained platelet count >600 x 109/L
32
A patient in whom CML has previously been diagnosed has circulating blasts and promyelocytes that total 30% of leukocytes. The disease is considered to be in what phase?
Transformation to acute leukemia
33
Normal ranges of WBC
4.5 -11.5 X 10^9/L
34
Normal ranges of RBC
4 - 6 X 10^9/L
35
Normal ranges of Hgb
14 - 18 g/dL
36
Normal ranges of HCT
40 - 54 %
37
Normal ranges of HCT
40 - 54 %
38
Normal ranges of MCV
80 - 100 fL
39
Normal ranges of MCHC
32 - 36 g/dL
40
Normal ranges of MCH
26 - 32 pg
41
Normal ranges of platelet
150 - 450 x 10^9/L
42
Normal ranges of RDW
11.5 - 14.5 %
43
Normal ranges of reticulocyte
25 - 75 x 10^9/L
44
In a table differentiate CML and Leukomoid reaction
CML LEUKOMID REACTION 1. There is increase in 1. increase in all granules neutrophils and their immature forms 2. Precence of dyspoietic 2. Reactive morphology morphology is is present but no dyspoietic morphology 3. Platelet are involved; giant 3. No abnormal and hypogranular forms platelet morphology seen 4. Leukocyte alkaline 4. Leukocyte phosphatase score is markedly phosphatase decreased markedly increased
45
The neoplastic cells in Nodular sclerosis morphological subtype of classical Hodgkin lymphoma (3)
1. Reed sternberg cells 2. Lacular cells 3. Hodkin cells
46
The hallmark feature of Burkitt lymphoma is a high proliferation rate, a feature linked to constitutive expression of(1):
MYC gene
47
The cell of origin for chronic lymphocytic leukemia/small lymphocytic lymphoma (2)
1. Naive B cell 2. Memory B cell
48
WHO classification variant of Burkitt lymphoma common in Africa and its presentation(2)
endemic, presenting with jawbone
49
The genetic feature that interconnect ET, PV and PMF and suggests a continuum of diseases(1)
JAK2 gene mutation
50
Disintegrated lymphoid cells present on the PB film in CLL not seen in other types of malignant lymphoma (1)
smudge cells
51
one important difference between chronic lymphocytic leukemia and small lymphocytic lymphoma
Chronic lymphocycytic leukemia are present in a peripheral blood and bone marrow while small lymphocytic lymphoma is present in lymoh nodes and other lymphoid organs
52
one important difference between the Pre-germinal center CLL and post-germinal center CLL (2 marks)
Pregeminal center of CLL there is no mutation of VH gene and there is trisomy 12 while in post germinal center there is mutation of VH gene and deletion of chromosome 13q14
53
Whta is the important difference between Accelerated phase and Blastic phase of CML (2 marks)
Accelerated phase there is 10 - 19 of blast while in blastic phase there is greater than or equal to 20% of blast.
54
one important difference between Small lymphoblast and large lymphoblast (2 marks)
small lymphocytes are involved in antibody production while large lymphoblasts are involved in differentiation process to produce more specialized and functional cells such as mature lymphocytes
55
one important difference between Blast count in Blastic crisis and metamorphosis (acceleration) phase of CML (2 narks)
Blast count in blastic crisis os greater than or equal to 20% while in acceralation phase is 10-19
56
Write a scientific reason for the occurrence of the following: 1.12 Higher dosages of Imatinib will restore remission in most patients who acquire additional BCR/ABL during treatment of CML (4 marks).
Normal dosage of imatinib will restore remission in patient who have a single mutation of chromosome which has came due to translocation ofchromosome 9 and 22
57
Write a scientific reason for the occurrence of When performing differential counts and encountering a lymphocytic cell that looks like a blast is most likely a reactive lymphocyte if all other findings are normal.
1. Chemical Exposure: Exposure to certain chemicals, such as benzene, can elevate the risk of lymphocytosis. While this link is stronger for acute myeloid leukemia (AML), it can also apply to acute lymphocytic leukemia (ALL). 2. Viral Infections: Rarely, viral infections like the human T-cell lymphoma/leukemia virus-1 (HTLV-1) or Epstein-Barr virus (EBV) can lead to blast-like lymphocytes, especially in specific geographic regions 3. Infection: Reactive lymphocytes can resemble blasts due to an immune response triggered by infections. These activated lymphocytes undergo rapid proliferation, leading to their blast-like appearance
58
Write a scientific reason for the occurrence, Clinical symptoms mimic those of acute leukemia in the Blastic phase of CML .
Neutrophil Deficits: Patients with acute myeloid leukemia (AML) exhibit qualitative and quantitative deficits in granulocytes, which predispose them to bacterial and fungal infections. These deficits arise from the underlying malignancy and are compounded by periods of neutropenia induced by chemotherapeutic agents1.