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Key Questions on Hematology and Anemia

The document contains a series of medical questions and answers related to hematology, including topics such as anemia, leukemia, and coagulation disorders. Each question is structured with key terms, case scenarios, and specific answers, covering various conditions and diagnostic tests. The content serves as a study guide for understanding blood-related diseases and their management.

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0% found this document useful (0 votes)
8 views17 pages

Key Questions on Hematology and Anemia

The document contains a series of medical questions and answers related to hematology, including topics such as anemia, leukemia, and coagulation disorders. Each question is structured with key terms, case scenarios, and specific answers, covering various conditions and diagnostic tests. The content serves as a study guide for understanding blood-related diseases and their management.

Uploaded by

alya
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd

Keys:

• Key word of the Question

• Key word of the Answer

• Case Scenario

• Some Helpful Notes

Question No. 1

• Regarding red cell indices:

• Measurement of the amount of HB concentration per RBC is expressed by?

• ANSWER — MCHC test.

Question No. 2

• Bone marrow examination of aplastic anemia show?

• ANSWER — Loss of hematopoietic stem cells and replaced by fat cells.

Question No. 3

• Site of Vitamin B12 absorption?

• ANSWER — Ileum.

Question No. 4

• Test for pernicious anemia?

• ANSWER — Anti-parietal cell antibodies & anti-intrinsic factor antibodies.

Question No. 5

• HbF, characterized by?

• ANSWER — 2 alpha, 2 gamma.


Question No. 6

• Feature of AML:

• ANSWER — Splenomegaly.

Question No. 7

• B-ALL indication for allogenic stem cell transplantation:

• ANSWER — BCA-ABL gene positive (t9;22).

Question No. 8

• AML prognostic factor:

• ANSWER — Cytogenetics, >60 yr. WBCs >100x10, FLT3 mutation positive,

Secondary AML.

• NOTE — One of them will be in the choices.

Question No. 9

• Accelerated phase of CML?

• ANSWER —

• From lecture —

1. Signs and Symptoms — Worsening B-symptoms. Bleeding. Infections. Progressive

splenomegaly. Refractory leucocytosis, thrombocytosis.

2. Blasts PB and/or BM — 10-19%.

3. Basophils — ≥ 20%.

4. Karyotypes — Second Ph chromosome.

Question No. 10

• Hodgkin lymphoma present with?

• ANSWER — CD15, CD30.


Question No. 11 *

• Difference between hemophilia A and B?

• ANSWER —

Question No. 12

• Factor V Leiden mutation is hereditary thrombophilia due to?

• ANSWER — Protein C can’t cleave FVL.

Question No. 13

• Study of a thrombophilic state is appropriate when the patient has had one of the

following EXCEPT:

A. Idiopathic DVT and is younger than 50.

B. A family history of thrombosis.

C. Recurrent DVT

D. Pregnant woman.

E. Thrombosis in unusual sites

• NOTE —

Question No. 14

• Warfarin monitored by:

• ANSWER — INR.

Question No. 15

• Normocytic anemia?

• ANSWER — Sickle cells disease.


Question No. 16 *

• Short term complications of DVT:

• ANSWER —

Question No. 17

• Tumor lysis syndrome?

• ANSWER — Hyperkalemia, hypocalcaemia, hyperphosphatemia.

Question No. 18 *

• TTT of DLBCL:

• ANSWER —

Question No. 19 *

• Splenomegaly syndrome?? (Not complete question)

• ANSWER —

Question No. 20 *

• Investigation results of DIC:

• ANSWER —

Question No. 21 *

• Best prognosis of ALI?

• ANSWER —

Question No. 22 *

• Which medication cause neutrophilia?

• ANSWER —
Question No. 23 *

• Symptom of CML?

• ANSWER —

Question No. 24 *

• Which of the following suggests Intravascular hemolysis?

• ANSWER —

Question No. 25 *

• Finding of megaloblastic anemia?

• ANSWER —

Question No. 26

• Hepato-splenectomy occurs in:

• ANSWER — Sickle cell anemia.

Question No. 27 *

• Most common cause of acute limb ischaemia in our locality:

• ANSWER —

Question No. 28 *

• Direct Coombs test positive for IgG the first line treatment is:

• ANSWER —

Question No. 29 *

• Best management Aplastic anemia?

• ANSWER —
Question No. 30 *

• Best treatment for IDA? (iron deficiency anaemia)

• ANSWER —

Question No. 31 *

• Management of Dynamically unstable pulmonary embolism?

• ANSWER —

Question No. 32 *

• Philadelphia chromosome number?

• ANSWER —

Question No. 33 *

• All of the following are characters of primary Raynaud disease EXCEPT:

• ANSWER —

Question No. 34 *

• In sickle cell anemia the B globin chain gene formed by substitution of .... for......

in position

• ANSWER —

Question No. 35

• Investigations required multiple myeloma:

• ANSWER — CBC , renal function , protein electrophoresis.


Question No. 36

• Most common Plasmodium in Egypt?.

• ANSWER — P. falciparum.

Question No. 37

• CML

• ANSWER — imatinib

Question No. 38

• DVT long term complication

• ANSWER — ulcers

Question No. 39

• best prognosis

• ANSWER — thrombosis

Question No. 40

• CLL

• ANSWER — CD5/20/23/200

Question No. 41

• Myeloma:

• ANSWER — m proteins / plasma cells / osteolytic lesion

Question No. 42

• Major risk for PE:

• ANSWER — orthopaedic
Question No. 43

• Test in microcytic case:

• ANSWER — ferritin

Question No. 44

• Test for prolonged aPTT :

• ANSWER — mixing study

Question No. 45

• Schistocytes + dead fetus :

• ANSWER — DIC

Question No. 46

• Which of the following aggravate acute chest syndrome in sickle disease:

• ANSWER — diuretics

Question No. 47

• Normal HB:

• ANSWER — 4(fe+2) / 4protoporphyrin / 4 polypeptide chains

Question No. 48

• DIC ?

• ANSWER — increase d dimer , decrease platelet, increase aPTT , increase

INR.
Question No. 49

• AML will have:

• ANSWER — Gum hypertrophy + splenomegaly

Question No. 50

• Which of the following is NOT characteristic of critical limb injury :

• ANSWER — Rest pain relived by analgesics

Question No. 51 *

• Intravascular hemolysis has more hemoglobinuria than extravascular one

• ANSWER —

Question No. 52

• Mechanical valve replacement :

• ANSWER — warfarin

Question No. 53

• NOT characteristic pf falciparum:

• ANSWER — relapse due to hypotonized parasites in liver

Question No. 54

• Complicated falciparum malaria. 1st or best drug is?.

• ANSWER — Artesunate
Question No. 55

• Protein C removes what factors?

• ANSWER — 5 and 8

Question No. 56

• Best immediate management for patient just now diagnosed with acute

ischemia is thrombolysis or heparinization?.

• ANSWER — Heparinization

Case No. 1

• Patient CBC show microcytic anemia

• What is the next step?

• Assessments of iron status?

• ANSWER — S. ferritin

Case No. 2

• Patient with HLA, positive sister.

• What should you do next?

• ANSWER — Allogenic stem cell transplantation

Case No. 3

• Patient with bite cells (/Heinz bodies) in blood film.

• What type is his anemia?

• ANSWER — G6PD deficiency


Case No. 4

• Child hereditary spherocytosis requires blood transfusion more frequently and

missing out on school:

• What next?

• ANSWER — Splenectomy.

Case No. 5

• Patient with a healed ulcer.

• According to C.E.A.P he is considered which stage:

• ANSWER — C5

Case No. 6

• Patient with schistocytes in PB?

• ANSWER — DIC

Case No. 7

• Patient with acute leukaemia and has CNS symptom (intracranial tension).

• What to do next?

• ANSWER — MRI of brain

• NOTE — CT/MRI, before CSF exam.

Case No. 8

• Patient diagnosed with CML, (WBC = 80,000) with myeloid precursors

proliferation, (HB = 6 mg/L), (PLT = 260,000).

• What is the first line of treatment?

• ANSWER — Imatinib + interferon alpha (TKIs).


Case No. 9

• Lymphocytosis with lymphadenopathy , normal Hb and normal platelets.

• The stage is:

• ANSWER —

Case No. 10

• Patient with CLL, Binet b.

• What do think u will find in physical examination?

• ANSWER — More than 3 lymphoid sites are involved.

Case No. 11

• Patient with rheumatoid arthritis, has fatigue, decreased iron, normal

ferritin, normal bone marrow, decreased MCV/MCH.

• What is type of anemia?

• ANSWER —

Case No. 12

• Patient old age with symptoms of MM and 40% plasma cells in his BM.

• What is the diagnosis?

• ANSWER — MM

Case No. 13

• Patient with fever and weight loss, Diffuse large b-cell lymphoma, left cervical

lymph nodes and multiple axillary lymph nodes.

• What is stage and the management:

• ANSWER —
Case No. 14

• Woman 60 years 80% blasts cytochemistry positive for CD2, CD3, CD7.

• The clinical examination may reveal?

• ANSWER —

Case No. 15

• Patient with ITP , PLT is 30 x 10.

• What is best preoperative management?

• ANSWER —

Case No. 16

• Female with fracture underwent surgery then developed VTE.

• Administrate anticoagulant for ?

• ANSWER —

Case No. 17

• Minutes after transfusion present with 40 c, agitation, hypotension, urine

dipstick revealed HB presence.

• The cause is:

• ANSWER —

Case No. 18

• Patient with a Prolonged PT and prolonged aPTT with TT = 13.

• The deficiency is in factor:

• ANSWER —
Case No. 19

• Patient with high methylmalonic acid and homocysteine:

• ANSWER — Vitamin B12 Deficiency

Case No. 20

• Patient develop hypoxemia and hypotension after transfusion.

• Due to:

• ANSWER — anti leucocyte and anti-granulocytes in transfused blood.

Case No. 21

• Patient with pruritus and mediastinal mass:

• ANSWER — Hodgkin lymphoma

Case No. 22

• Patient chronic ischemia by occlusion at superficial femoral artery.

• Are his pulses decreased or increased in the femoral, popliteal, anterior tibial and

dorsalis pedis arteries?

• ANSWER — decreased in all of them EXCEPT for femoral pulse

Case No. 23

• Patient has anaemia haemolytic and has bite cells in blood film.

• What type is his anaemia?

• ANSWER — G6PD Deficiency


Case No. 24

• Patient with DM and renal failure and he has normocytic anemia with

reticulocytopenia while his WBCs and platelets are normal.

• Best investigation is sickle solubility, or Coombs test, or HB electrophoresis, or

ferritin or erythropoietin?

• ANSWER — Erythropoietin

Case No. 25

• Patient with heart problems and takes warfarin prophylaxis then he developed

intracranial hemorrhage.

• In addition to Vita. K, what else is suitable for urgent management?.

• ANSWER — Fresh Frozen Plasma

Case No. 26

• Patient with Multiple myeloma has?

• ANSWER — Hypercalcemia, anemia, bone lesion and renal insufficiency.

Case No. 27

• Patient CML, his BM biopsy shows granulocyte hyperplasia and BM blasts 1%.

• What phase is he?

• ANSWER — Chronic phase

Case No. 28

• Female patient bleeding with ecchymosis and purpura mucocutanous and she

has ITP (not directly said but easily concluded from the CBC and others)

• So, best choice is?

• ANSWER — Corticosteroid
Case No. 29

• Patient CLL asymptomatic then later came with severe infections, repetitive

pneumonia and cough.

• What is Best management now?

• ANSWER — Antibiotic with IV immunoglobulins

Case No. 30

• Patient warm AIHA and she came to you with Hb 4 and severely anemic.

• Best management now?.

• ANSWER — transfusion

Case No. 31

• Patient took two RBCS packs and came after 1 week by fever and hyper bilirubin.

• The reaction happened due to RBCS ABO incompatibility or RBCS minor groups

incompatibility?

• ANSWER — RBCS Minor Groups Incompatibility

Case No. 32

• Patient has leg edema increase by working during day with bursting pain in his

leg. Best investigation is?

• ANSWER — Doppler

Case No. 33

• Patient with massive Pulmonary Embolism and has shock.

• What type of shock is that?

• ANSWER — Obstructive shock


Case No. 34

• Patient with Hodgkin lymphoma.

• His treatment has a monoclonal antibody called?

• ANSWER — Brentuximab

Case No. 35

• Patient with toxemic manifestations and BM blasts 60% with gingiva

hyperplasia.

• His CD on flowcytometry is?

• ANSWER — CD 13, CD33 and CD117.

Case No. 36

• Patient bleeding and has normal APTT and prolonged PT.

• He could have deficiency in what of these factors?

• ANSWER — factor 7, as the rest were factors of intrinsic pathway.

Case No. 37

• Patient with megaloblastic anemia.

• His finding is.

• ANSWER — Low HB, Macrocytosis, and hyper bilirubin.

Common questions

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Megaloblastic anemia is characterized by low hemoglobin levels, macrocytosis (enlarged red blood cells), and hypersegmented neutrophils. These findings are due to impaired DNA synthesis caused by vitamin B12 or folate deficiency, leading to asynchronous maturation of the nucleus and cytoplasm in precursor cells .

During a hemolytic crisis in G6PD deficiency, the blood film typically shows "bite cells" and Heinz bodies due to oxidative damage to red blood cells. The G6PD enzyme deficiency leads to a decreased ability to handle oxidative stress, resulting in hemolysis .

CD15 and CD30 are cell surface markers expressed by Reed-Sternberg cells, which are characteristic of Hodgkin lymphoma. Their presence helps confirm the diagnosis since these markers are present on the large atypical cells seen in this type of lymphoma .

The presence of the BCR-ABL gene, resulting from the t(9;22) translocation known as the Philadelphia chromosome, is a poor prognostic indicator in B-ALL. It is associated with a higher risk of treatment failure and relapse, making aggressive treatment with allogenic stem cell transplantation advisable .

In tumor lysis syndrome, the rapid breakdown of malignant cells releases intracellular contents into the bloodstream, causing hyperkalemia due to leakage of potassium, hypocalcemia as phosphate combines with calcium, and hyperphosphatemia from the release of intracellular phosphates .

The International Normalized Ratio (INR) is used to monitor therapy with Warfarin because it standardizes prothrombin time results, regardless of the test method, to ensure consistent reporting of anticoagulation level .

Schistocytes, or fragmented red blood cells, in peripheral blood smears suggest microangiopathic hemolytic anemia, often seen in conditions such as Disseminated Intravascular Coagulation (DIC), Thrombotic Thrombocytopenic Purpura (TTP), or Hemolytic Uremic Syndrome (HUS), indicating significant hemolysis due to mechanical damage within small blood vessels .

Factor V Leiden thrombophilia arises from a mutation in the F5 gene that produces a Factor V variant resistant to inactivation by activated protein C, leading to an increased risk of thrombosis due to prolonged clotting activity as the regulatory pathway fails to effectively balance clot formation .

The accelerated phase of CML is marked by worsening B-symptoms, increasing splenomegaly, refractory leucocytosis, thrombocytosis, and a blast count in peripheral blood or bone marrow of 10-19%. Additionally, basophils are ≥ 20% and new chromosomal abnormalities may emerge, distinguishing it from the less severe chronic phase and the blast crisis phase where blasts are ≥ 20% .

Heparinization is favored for immediate management of acute limb ischemia to quickly prevent further clot propagation and stabilize the clot, reducing the risk of sudden limb loss or embolization. Thrombolysis can be considered later if initial therapy does not improve perfusion .

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