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.