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  • Question 1 - One of the functions of the spleen with regards to red blood cells...

    Correct

    • One of the functions of the spleen with regards to red blood cells is:

      Your Answer: To filter and remove aged and abnormal red blood cells

      Explanation:

      The spleen plays important roles in regard to red blood cells (also referred to as erythrocytes) and the immune system. It removes old red blood cells and holds a reserve of blood, which can be valuable in case of haemorrhagic shock, and also recycles iron. As a part of the mononuclear phagocyte system, it metabolizes haemoglobin removed from senescent erythrocytes. The globin portion of haemoglobin is degraded to its constitutive amino acids, and the haem portion is metabolized to bilirubin, which is removed in the liver.

    • This question is part of the following fields:

      • Haematology
      • Medicine
      15.7
      Seconds
  • Question 2 - Where is the most erythropoietin produced? ...

    Correct

    • Where is the most erythropoietin produced?

      Your Answer: Kidneys

      Explanation:

      Erythropoietin is produced by interstitial fibroblasts in the kidney in close association with peritubular capillary and proximal convoluted tubule. It is also produced in perisinusoidal cells in the liver. While liver production predominates in the fetal and perinatal period, renal production is predominant during adulthood.

    • This question is part of the following fields:

      • Haematology
      • Medicine
      2.4
      Seconds
  • Question 3 - In the normal adult, haematopoiesis is present ...

    Correct

    • In the normal adult, haematopoiesis is present

      Your Answer: Axial skeleton and proximal ends of long bones

      Explanation:

      In children, haematopoiesis occurs in the marrow of the long bones such as the femur and tibia. In adults, it occurs mainly in the pelvis, cranium, vertebrae, and sternum.

    • This question is part of the following fields:

      • Haematology
      • Medicine
      48.4
      Seconds
  • Question 4 - Which vitamin plays a major role in the metabolism of many amino acids?...

    Incorrect

    • Which vitamin plays a major role in the metabolism of many amino acids?

      Your Answer: Vitamin B12

      Correct Answer: Vitamin B6

      Explanation:

      Vitamin B6 is part of the vitamin B group, and its active form, pyridoxal 5′-phosphate (PLP) serves as a coenzyme in many enzyme reactions in amino acid, glucose, and lipid metabolism.

    • This question is part of the following fields:

      • Haematology
      • Medicine
      11.2
      Seconds
  • Question 5 - Which of the following vitamins are fat soluble? ...

    Correct

    • Which of the following vitamins are fat soluble?

      Your Answer: A, D, E, K

      Explanation:

      Vitamins are classified as either fat soluble (vitamins A, D, E and K) or water soluble (vitamins B and C).

    • This question is part of the following fields:

      • Haematology
      • Medicine
      4
      Seconds
  • Question 6 - Which of the following foods contain Vitamin B 12? ...

    Correct

    • Which of the following foods contain Vitamin B 12?

      Your Answer: Liver, meat

      Explanation:

      No fungi, plants, nor animals (including humans) are capable of producing vitamin B12. Only bacteria and archaea have the enzymes needed for its synthesis. Proved food sources of B12 are animal products (meat, fish, dairy products).

    • This question is part of the following fields:

      • Haematology
      • Medicine
      6.9
      Seconds
  • Question 7 - Which of the following is a function of Vitamin C? ...

    Correct

    • Which of the following is a function of Vitamin C?

      Your Answer: Hydroxylation of proline to hydroxyproline for collagen synthesis

      Explanation:

      Vitamin C acts as an electron donor for eight different enzymes: Three enzymes (prolyl-3-hydroxylase, prolyl-4-hydroxylase, and lysyl hydroxylase) that are required for the hydroxylation of proline and lysine in the synthesis of collagen.

    • This question is part of the following fields:

      • Haematology
      • Medicine
      13.2
      Seconds
  • Question 8 - The extrinsic coagulation pathway is initiated by activation of which clotting factor? ...

    Correct

    • The extrinsic coagulation pathway is initiated by activation of which clotting factor?

      Your Answer: Factor VII

      Explanation:

      The tissue factor pathway (extrinsic) begins following damage to the blood vessel. FVII leaves the circulation and comes into contact with tissue factor (TF) expressed on tissue-factor-bearing cells (stromal fibroblasts and leukocytes), forming an activated complex (TF-FVIIa).

    • This question is part of the following fields:

      • Haematology
      • Medicine
      8.2
      Seconds
  • Question 9 - Which of the following conditions is associated with eosinophilia? ...

    Correct

    • Which of the following conditions is associated with eosinophilia?

      Your Answer: Ascaris

      Explanation:

      Eosinophilia can be idiopathic (primary) or, more commonly, secondary to another disease. In the Western World, allergic or atopic diseases are the most common causes, especially those of the respiratory or integumentary systems. In the developing world, parasites are the most common cause e.g. Ascaris

    • This question is part of the following fields:

      • Haematology
      • Medicine
      7.5
      Seconds
  • Question 10 - The haemostatic plug formation in response to injured blood vessel wall is stimulated...

    Incorrect

    • The haemostatic plug formation in response to injured blood vessel wall is stimulated by exposure of which substance to platelets?

      Your Answer: von Willebrand factor (vWF)

      Correct Answer: Collagen

      Explanation:

      When the endothelium is damaged, the normally isolated, underlying collagen is exposed to circulating platelets, which bind directly to collagen with collagen-specific glycoprotein Ia/IIa surface receptors. This adhesion is strengthened further by von Willebrand factor (vWF), which is released from the endothelium and from platelets.

    • This question is part of the following fields:

      • Haematology
      • Medicine
      32.8
      Seconds
  • Question 11 - Which statement is correct about the clinical state of methemoglobinemia? ...

    Incorrect

    • Which statement is correct about the clinical state of methemoglobinemia?

      Your Answer: It is due to carbon monoxide reacting with haemoglobin.

      Correct Answer: May arise due to a hereditary deficiency of NADH.

      Explanation:

      Methaemoglobin is a form of haemoglobin that contains ferric [Fe3+] iron and has a decreased ability to bind oxygen. Spontaneously formed methaemoglobin is normally reduced by protective enzyme systems, e.g., NADH methaemoglobin reductase, hence a deficiency of NADH may result in increased levels of methaemoglobin

    • This question is part of the following fields:

      • Haematology
      • Medicine
      14.1
      Seconds
  • Question 12 - Which of the following is a granulocyte? ...

    Correct

    • Which of the following is a granulocyte?

      Your Answer: Eosinophil

      Explanation:

      Granulocytes are a category of white blood cells characterized by the presence of granules in their cytoplasm. There are three principal types of granulocytes, distinguished by their appearance under Wright’s stain:

      • Basophil granulocytes
      • Eosinophil granulocytes
      • Neutrophil granulocytes

    • This question is part of the following fields:

      • Haematology
      • Medicine
      4.2
      Seconds
  • Question 13 - Select one true statement about haemoglobin synthesis… ...

    Incorrect

    • Select one true statement about haemoglobin synthesis…

      Your Answer: Produces the tetramer α2ß2 as the end result.

      Correct Answer: Occurs in the cytosol of developing red cells.

      Explanation:

      Haemoglobin (Hb) is synthesized in a complex series of steps. The haem part is synthesized in a series of steps in the mitochondria and the cytosol of immature red blood cells, while the globin protein parts are synthesized by ribosomes in the cytosol. Production of Hb continues in the cell throughout its early development from the proerythroblast to the reticulocyte in the bone marrow.

    • This question is part of the following fields:

      • Haematology
      • Medicine
      26.8
      Seconds
  • Question 14 - In the clotting mechanism, activation of factor IX can occur through the direct...

    Incorrect

    • In the clotting mechanism, activation of factor IX can occur through the direct actions of:

      Your Answer: Factor XIa & XIIa

      Correct Answer: Factor VIIa & XIa

      Explanation:

      Factor IX is processed to remove the signal peptide, glycosylated and then cleaved by factor XIa (of the contact pathway) or factor VIIa (of the tissue factor pathway). When activated into factor IXa, in the presence of Ca2+, membrane phospholipids, and a Factor VIII cofactor, it hydrolyses one arginine-isoleucine bond in factor X to form factor Xa. Factor IX is inhibited by antithrombin.

    • This question is part of the following fields:

      • Haematology
      • Medicine
      30.3
      Seconds
  • Question 15 - What is the average life span of neutrophils? ...

    Incorrect

    • What is the average life span of neutrophils?

      Your Answer: 7 days

      Correct Answer: 24 hours

      Explanation:

      The average lifespan of inactivated human neutrophils in the circulation has been reported by different approaches to be between 5 and 90 hours.

    • This question is part of the following fields:

      • Haematology
      • Medicine
      49.4
      Seconds
  • Question 16 - The process in which tissue thromboplastin activates factor VII is best known as:...

    Correct

    • The process in which tissue thromboplastin activates factor VII is best known as:

      Your Answer: The extrinsic pathway

      Explanation:

      In the tissue factor pathway (extrinsic), following damage to the blood vessel, FVII leaves the circulation and comes into contact with tissue factor (TF) expressed on tissue-factor-bearing cells (stromal fibroblasts and leukocytes), forming an activated complex (TF-FVIIa).

    • This question is part of the following fields:

      • Haematology
      • Medicine
      7.9
      Seconds
  • Question 17 - Which enzyme deficiency causes Beriberi? ...

    Correct

    • Which enzyme deficiency causes Beriberi?

      Your Answer: Thiamine

      Explanation:

      Beriberi refers to a cluster of symptoms caused primarily by thiamine (vitamin B1) deficiency. Symptoms of beriberi include weight loss, emotional disturbances, impaired sensory perception, weakness and pain in the limbs, and periods of irregular heart rate.

    • This question is part of the following fields:

      • Haematology
      • Medicine
      22.4
      Seconds
  • Question 18 - All of the following are Vitamin K-dependent clotting factors except: ...

    Correct

    • All of the following are Vitamin K-dependent clotting factors except:

      Your Answer: Factor XI

      Explanation:

      Activated Vitamin K is used to gamma carboxylate (and thus activate) certain enzymes involved in coagulation: Factors II, VII, IX, X, and protein C and protein S. Inability to activate the clotting cascade via these factors leads to the bleeding symptoms

    • This question is part of the following fields:

      • Haematology
      • Medicine
      14.7
      Seconds
  • Question 19 - Where is retinol mainly stored? ...

    Correct

    • Where is retinol mainly stored?

      Your Answer: Liver

      Explanation:

      Vitamin A is a group of unsaturated nutritional organic compounds that includes retinol, retinal, retinoic acid, and several provitamin A carotenoids (most notably beta-carotene). The liver stores a multitude of substances, including glucose (in the form of glycogen), vitamin A (1–2 years’ supply), vitamin D (1–4 months’ supply), vitamin B12 (3–5 years’ supply), vitamin K, iron, and copper.

    • This question is part of the following fields:

      • Haematology
      • Medicine
      20.8
      Seconds
  • Question 20 - Which of the following vitamin deficiencies is associated with xerophthalmia? ...

    Correct

    • Which of the following vitamin deficiencies is associated with xerophthalmia?

      Your Answer: Vitamin A

      Explanation:

      Xerophthalmia caused by a severe vitamin A deficiency is described by pathologic dryness of the conjunctiva and cornea. The conjunctiva becomes dry, thick and wrinkled. If untreated, it can lead to corneal ulceration and ultimately to blindness as a result of corneal damage.

    • This question is part of the following fields:

      • Haematology
      • Medicine
      2.9
      Seconds
  • Question 21 - Lymphoid stem cells give rise to the following cells: ...

    Correct

    • Lymphoid stem cells give rise to the following cells:

      Your Answer: T cells, b cells and natural killer cells

      Explanation:

      T Cells, B Cells and NK Cells (and all other Innate lymphoid cells) are unique to the lymphocyte family, but dendritic cells are not. Dendritic cells of identical appearance but different markers are spread throughout the body, and come from either lymphoid and myeloid lineages.

      Myeloid stem cells lead to myeloblasts, which evolve into macrophages, monocytes, neutrophils, basophils, and eosinophils.

    • This question is part of the following fields:

      • Haematology
      • Medicine
      6
      Seconds
  • Question 22 - Which of the following cells will degranulate and release histamine when binding to...

    Incorrect

    • Which of the following cells will degranulate and release histamine when binding to IgE?

      Your Answer: Monocytes

      Correct Answer: Basophils

      Explanation:

      Basophils have protein receptors on their cell surface that bind IgE, an immunoglobulin involved in microparasite defence and allergy. When activated, basophils degranulate to release histamine, proteoglycans (e.g. heparin and chondroitin), and proteolytic enzymes (e.g. elastase and lysophospholipase).

    • This question is part of the following fields:

      • Haematology
      • Medicine
      10.6
      Seconds
  • Question 23 - What is the average life span of platelets? ...

    Correct

    • What is the average life span of platelets?

      Your Answer: 8 days

      Explanation:

      The average life span of circulating platelets is 8 to 9 days.

    • This question is part of the following fields:

      • Haematology
      • Medicine
      21.5
      Seconds
  • Question 24 - In adults, the major site of haematopoiesis is? ...

    Correct

    • In adults, the major site of haematopoiesis is?

      Your Answer: The axial skeleton

      Explanation:

      Bone marrow is the flexible tissue in the interior of bones. In humans, red blood cells are produced by cores of bone marrow in the heads of long bones.

    • This question is part of the following fields:

      • Haematology
      • Medicine
      4.3
      Seconds
  • Question 25 - Stem cell characteristics include the following except ...

    Incorrect

    • Stem cell characteristics include the following except

      Your Answer: Ability to proliferate / differentiate outside the bone marrow in an adult during times of stress/disease of the bone marrow

      Correct Answer: Differentiation and proliferation into progenitor cells committed to multiple cell lines

      Explanation:

      The classical definition of a stem cell requires that it possess two properties:Self-renewal: the ability to go through numerous cycles of cell division while maintaining the undifferentiated state.Potency: the capacity to differentiate into specialized cell types. In the strictest sense, this requires stem cells to be either totipotent or pluripotent to be able to give rise to any mature cell type

    • This question is part of the following fields:

      • Haematology
      • Medicine
      5.7
      Seconds
  • Question 26 - Transport of Iron into enterocytes occurs via which membrane transporter? ...

    Incorrect

    • Transport of Iron into enterocytes occurs via which membrane transporter?

      Your Answer: Fe2+ / h+ pump

      Correct Answer: Divalent metal transporter 1(dmt1)

      Explanation:

      To be absorbed, dietary iron can be absorbed as part of a protein such as haem protein or iron must be in its ferrous Fe2+ form. A ferric reductase enzyme on the enterocytes’ brush border, duodenal cytochrome B (Dcytb), reduces ferric Fe3+ to Fe2+. A protein called divalent metal transporter 1 (DMT1), which can transport several divalent metals across the plasma membrane, then transports iron across the enterocyte’s cell membrane into the cell.

    • This question is part of the following fields:

      • Haematology
      • Medicine
      17.7
      Seconds
  • Question 27 - The following occurs as a result of 2,3 Bisphosphoglycerate binding to deoxyhaemoglobin ...

    Incorrect

    • The following occurs as a result of 2,3 Bisphosphoglycerate binding to deoxyhaemoglobin

      Your Answer: Destabilization of the taut conformation of deoxyhaemoglobin

      Correct Answer: A reduction in deoxyhaemoglobin's affinity for oxygen

      Explanation:

      2,3-BPG acts as a heteroallosteric effector of haemoglobin, lowering haemoglobin’s affinity for oxygen by binding preferentially to deoxyhaemoglobin. An increased concentration of BPG in red blood cells favours formation of the T, low-affinity state of haemoglobin and so the oxygen-binding curve will shift to the right.

    • This question is part of the following fields:

      • Haematology
      • Medicine
      7.1
      Seconds
  • Question 28 - Which of the following factors is directly responsible for the breakdown of fibrinogen...

    Incorrect

    • Which of the following factors is directly responsible for the breakdown of fibrinogen to fibrin?

      Your Answer: Fibrinogen degradation products (FDPS)

      Correct Answer: Thrombin

      Explanation:

      Prothrombin (coagulation factor II) is proteolytically cleaved to form thrombin in the coagulation cascade, the clotting process. Thrombin in turn acts as a serine protease that converts soluble fibrinogen into insoluble strands of fibrin, as well as catalysing many other coagulation-related reactions.

    • This question is part of the following fields:

      • Haematology
      • Medicine
      79.2
      Seconds
  • Question 29 - With regard to the spleen which of the following has the correct match?...

    Incorrect

    • With regard to the spleen which of the following has the correct match?

      Your Answer: Marginal zone - B lymphocytes

      Correct Answer: Periarteriolar lymphoid sheets - T lymphocytes

      Explanation:

      The spleen consists of:Red pulp – responsible for mechanical filtration of red blood cells. Red pulp contains sinusoids, which are filled with blood, splenic cords of reticular fibers and a marginal zoneWhite pulp – responsible for active immune response through humoral and cell-mediated pathways. Composed of nodules, called Malpighian corpuscles. These are composed of: lymphoid follicles, rich in B-lymphocytes and periarteriolar lymphoid sheaths, rich in T-lymphocytes

    • This question is part of the following fields:

      • Haematology
      • Medicine
      30.5
      Seconds
  • Question 30 - Choose the correct statement regarding the protein C/S system? ...

    Incorrect

    • Choose the correct statement regarding the protein C/S system?

      Your Answer:

      Correct Answer: The protein C/S complex inactivates factor Va and VIIIa

      Explanation:

      The best characterized function of Protein S is its role in the anti coagulation pathway, where it functions as a cofactor to Protein C in the inactivation of Factors Va and VIIIa.

    • This question is part of the following fields:

      • Haematology
      • Medicine
      0
      Seconds

SESSION STATS - PERFORMANCE PER SPECIALTY

Haematology (22/29) 76%
Medicine (22/29) 76%
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