Weekly Pathology Exam - July 24, 2026 (Section A: MCQs)

80 clinical MCQs in Weekly Exam: Pathology. What neurotransmitter is associated with runner's high?. Kenya, Africa and global revision.

Questions, Answers & Explanations

  1. Q1. What neurotransmitter is associated with runner's high?

    Answer: Endorphins

    Explanation: Endorphins are endogenous opioid peptides that are released during strenuous exercise and are responsible for the euphoric feeling known as 'runner's high'.

  2. Q2. What neurotransmitter is associated with anxiety disorders?

    Answer: GABA

    Explanation: Gamma-aminobutyric acid (GABA) is the primary inhibitory neurotransmitter in the central nervous system. Reduced GABAergic activity is linked to increased neuronal excitability and is implicated in anxiety disorders.

  3. Q3. Where do neurons store the genetic information they use to code and build all the proteins required for their functions?

    Answer: Nucleus

    Explanation: Neurons, like all eukaryotic cells, store their genetic information in the form of DNA within the nucleus. This DNA is transcribed into RNA, which is then translated into proteins.

  4. Q4. Which of the following are major inhibitory neurotransmitters, causing inhibitory postsynaptic potentials (IPSPs)?

    Answer: GABA and Glycine

    Explanation: GABA (gamma-aminobutyric acid) and Glycine are the primary inhibitory neurotransmitters in the central nervous system. Their binding to receptors on the postsynaptic neuron leads to an influx of negative ions or efflux of positive ions, hyperpolarizing the membrane and making it less likely to fire an action potential (IPSP).

  5. Q5. The effect of tetrodotoxin (puffer fish poison) on axons demonstrates

    Answer: The importance of ion channels in action potential generation

    Explanation: Tetrodotoxin blocks voltage-gated sodium channels, which are crucial for the rapid depolarization phase of the action potential. Its ability to block nerve conduction highlights the essential role of these ion channels in generating action potentials.

  6. Q6. What neurotransmitter is associated with mood disorders?

    Answer: Serotonin

    Explanation: Serotonin plays a significant role in regulating mood, appetite, and sleep. Dysregulation of serotonin levels and signaling is strongly implicated in the pathophysiology of mood disorders like depression and anxiety.

  7. Q7. Which of the following is not true?

    Answer: All neurotransmitters bind to the same type of receptor.

    Explanation: Neurotransmitters bind to specific receptors, and there are many different types of neurotransmitter receptors, each with unique signaling properties.

  8. Q8. What neurotransmitter is associated with insomnia?

    Answer: Melatonin

    Explanation: While GABAergic systems are involved in promoting sleep, Melatonin is a hormone that plays a crucial role in regulating the sleep-wake cycle. Disruptions in melatonin production or signaling can contribute to insomnia.

  9. Q9. What neurotransmitter is associated with seizures?

    Answer: Glutamate

    Explanation: Seizures are characterized by excessive and synchronous neuronal firing. Glutamate, the primary excitatory neurotransmitter, is involved in this hyperexcitability. Imbalances between excitatory (glutamate) and inhibitory (GABA) neurotransmission can lead to seizures.

  10. Q10. What is one of the functions of Dopamine?

    Answer: Control of motor movement and reward pathways

    Explanation: Dopamine is a key neurotransmitter involved in motor control (its deficiency is linked to Parkinson's disease), motivation, reward, pleasure, and reinforcement.

  11. Q11. What is one of the functions of Endorphins?

    Answer: Inhibition of pain perception

    Explanation: Endorphins are endogenous opioid peptides that act as natural painkillers and are involved in the body's response to stress and pain, as well as contributing to feelings of pleasure and well-being.

  12. Q12. What neurotransmitter is associated with Parkinson's disease?

    Answer: Dopamine

    Explanation: Parkinson's disease is characterized by the progressive loss of dopaminergic neurons in the substantia nigra, leading to a deficiency in dopamine. This deficiency results in the motor symptoms of the disease.

  13. Q13. A 28-year-old woman presents with fatigue and pallor. Complete blood count shows low haemoglobin level and peripheral blood film shows microcytic hypochromic red blood cells. What is the most likely diagnosis?

    Answer: Iron deficiency anemia

    Explanation: Microcytic hypochromic red blood cells are characteristic of iron deficiency anemia, where there is insufficient iron to synthesize hemoglobin, leading to small (microcytic) and pale (hypochromic) red blood cells. Fatigue and pallor are common symptoms of anemia.

  14. Q14. The primary site of haematopoiesis in adults is:

    Answer: Bone marrow

    Explanation: In healthy adults, the bone marrow, particularly the red marrow within flat and long bones, is the primary site for the production of all blood cell lineages (hematopoiesis).

  15. Q15. Which blood cell type is primarily responsible for defence against parasitic infections?

    Answer: Eosinophils

    Explanation: Eosinophils are granulocytes that play a significant role in the immune response against parasitic infections and in allergic reactions. They release cytotoxic proteins and enzymes that are effective against larger pathogens like parasites.

  16. Q16. Which clotting factor is deficient in Haemophilia A?

    Answer: Factor VIII

    Explanation: Hemophilia A is an inherited bleeding disorder caused by a deficiency in Factor VIII, a crucial protein in the coagulation cascade that helps blood to clot.

  17. Q17. A patient presents with recurrent infections, petechiae, and anaemia. A bone marrow biopsy shows reduced cellularity. What is the most likely diagnosis?

    Answer: Aplastic anemia

    Explanation: Reduced cellularity in the bone marrow, along with pancytopenia (leading to recurrent infections from low white cells, petechiae from low platelets, and anemia from low red cells), is characteristic of aplastic anemia, a condition where the bone marrow fails to produce sufficient blood cells.

  18. Q18. Haemopoiesis is the process of:

    Answer: Formation and development of blood cells

    Explanation: Hematopoiesis is the complex process by which all types of blood cells, including white blood cells, red blood cells, and platelets, are produced and developed from hematopoietic stem cells.

  19. Q19. A 62-year-old man presents with fatigue, fever and bruising. His full blood count shows WCC 40 × 10⁹/L with 25% circulating blasts, Hb 90 g/L and platelets 50 × 10⁹/L. Which investigation is required to definitively diagnose acute myeloid leukaemia?

    Answer: Bone marrow biopsy with cytochemistry and immunophenotyping

    Explanation: While a peripheral blood smear can show blasts, a definitive diagnosis of Acute Myeloid Leukemia (AML) requires a bone marrow biopsy. Cytochemical stains (like MPO) and immunophenotyping are essential to confirm the myeloid lineage of the blasts and classify the AML subtype.

  20. Q20. Which cytochemical stain is most useful to confirm lymphoblasts in suspected ALL?

    Answer: Periodic Acid-Schiff (PAS)

    Explanation: The Periodic Acid-Schiff (PAS) stain demonstrates glycogen granules, which are often present in lymphoblasts of Acute Lymphoblastic Leukemia (ALL). Myeloperoxidase, esterase, and lysozyme stains are more characteristic of myeloid blasts.

  21. Q21. A patient receiving chemotherapy shows a drop in neutrophil count. This condition is termed:

    Answer: Neutropenia

    Explanation: Neutropenia is a condition characterized by a lower-than-normal number of neutrophils, a type of white blood cell. Chemotherapy often causes myelosuppression, leading to neutropenia and an increased risk of infection.

  22. Q22. Which chromosomal translocation is pathognomonic of chronic myeloid leukaemia?

    Answer: t(9;22) - Philadelphia chromosome

    Explanation: The t(9;22) translocation, resulting in the Philadelphia chromosome (BCR-ABL fusion gene), is the hallmark genetic abnormality found in over 95% of patients with Chronic Myeloid Leukemia (CML).

  23. Q23. Thrombopoietin primarily regulates the production of:

    Answer: Platelets

    Explanation: Thrombopoietin (TPO) is the main hormone that stimulates the production of platelets (thrombocytes) from megakaryocytes in the bone marrow.

  24. Q24. Which of the following is a stem cell marker used to identify haematopoietic stem cells?

    Answer: CD34

    Explanation: CD34 is a transmembrane glycoprotein that is expressed on hematopoietic stem cells, progenitor cells, and endothelial cells. It is widely used as a marker for identifying and isolating hematopoietic stem cells.

  25. Q25. What neurotransmitter is primarily associated with the euphoric feeling experienced during a 'runner's high'?

    Answer: Endorphins

    Explanation: Endorphins are endogenous opioid peptides that are released during strenuous exercise and are responsible for the euphoric feeling known as 'runner's high'.

  26. Q26. Which neurotransmitter system is most implicated in the pathophysiology of anxiety disorders?

    Answer: GABA

    Explanation: Gamma-aminobutyric acid (GABA) is the primary inhibitory neurotransmitter in the central nervous system. Reduced GABAergic activity is linked to increased neuronal excitability and is implicated in anxiety disorders.

  27. Q27. Where do neurons store the genetic information they use to code and build all the proteins required for their functions?

    Answer: Nucleus

    Explanation: Neurons, like all eukaryotic cells, store their genetic information in the form of DNA within the nucleus. This DNA is transcribed into RNA, which is then translated into proteins.

  28. Q28. Which of the following are major inhibitory neurotransmitters, causing inhibitory postsynaptic potentials (IPSPs)?

    Answer: GABA and Glycine

    Explanation: GABA (gamma-aminobutyric acid) and Glycine are the primary inhibitory neurotransmitters in the central nervous system. Their binding to receptors on the postsynaptic neuron leads to an influx of negative ions or efflux of positive ions, hyperpolarizing the membrane and making it less likely to fire an action potential (IPSP).

  29. Q29. The effect of tetrodotoxin (puffer fish poison) on axons demonstrates:

    Answer: The importance of ion channels in action potential generation

    Explanation: Tetrodotoxin blocks voltage-gated sodium channels, which are crucial for the rapid depolarization phase of the action potential. Its ability to block nerve conduction highlights the essential role of these ion channels in generating action potentials.

  30. Q30. Which neurotransmitter is most commonly associated with the regulation of mood, and its dysregulation is implicated in mood disorders like depression?

    Answer: Serotonin

    Explanation: Serotonin plays a significant role in regulating mood, appetite, and sleep. Dysregulation of serotonin levels and signaling is strongly implicated in the pathophysiology of mood disorders like depression and anxiety.

  31. Q31. Which of the following statements is NOT true regarding neurotransmitters?

    Answer: All neurotransmitters bind to the same type of receptor.

    Explanation: Neurotransmitters bind to specific receptors, and there are many different types of neurotransmitter receptors, each with unique signaling properties.

  32. Q32. Which neurotransmitter system is heavily involved in regulating sleep-wake cycles and is often implicated in insomnia?

    Answer: Melatonin

    Explanation: While GABAergic systems are involved in promoting sleep, Melatonin is a hormone that plays a crucial role in regulating the sleep-wake cycle. Disruptions in melatonin production or signaling can contribute to insomnia.

  33. Q33. Which neurotransmitter plays a critical role in mediating excitatory neurotransmission and is implicated in the hyperexcitability seen in certain seizure disorders?

    Answer: Glutamate

    Explanation: Glutamate, the primary excitatory neurotransmitter, is involved in the hyperexcitability seen in certain seizure disorders. Imbalances between excitatory (glutamate) and inhibitory (GABA) neurotransmission can lead to seizures.

  34. Q34. What is one of the primary functions of Dopamine in the brain?

    Answer: Control of motor movement and reward pathways

    Explanation: Dopamine is a key neurotransmitter involved in motor control (its deficiency is linked to Parkinson's disease), motivation, reward, pleasure, and reinforcement.

  35. Q35. What is one of the primary functions of Endorphins?

    Answer: Inhibition of pain perception

    Explanation: Endorphins are endogenous opioid peptides that act as natural painkillers and are involved in the body's response to stress and pain, as well as contributing to feelings of pleasure and well-being.

  36. Q36. Which neurotransmitter deficiency is strongly associated with Parkinson's disease?

    Answer: Dopamine

    Explanation: Parkinson's disease is characterized by the progressive loss of dopaminergic neurons in the substantia nigra, leading to a deficiency in dopamine. This deficiency results in the motor symptoms of the disease.

  37. Q37. A 35-year-old man has no clinical evidence for bleeding and he feels fine. As part of a pre-operative workup for a hernia repair, laboratory studies show Hgb 14.8 g/dL, Hct 45%, MCV 96 fL, and WBC count 8500/microliter, and platelet count 275,000/microliter. His prothrombin time is normal, but the partial thromboplastin time is prolonged. A deficiency of which of the following coagulation factors is most likely be associated with these findings?

    Answer: Factor VIII

    Explanation: A prolonged PTT with a normal PT suggests a defect in the intrinsic or common pathway of coagulation. Factor VIII deficiency (Hemophilia A) is a common inherited disorder that causes a prolonged PTT but a normal PT. Factors VII and X are involved in the extrinsic and common pathways, respectively, and would affect PT. Factor XIII is involved in clot stabilization.

  38. Q38. A 20-year-old man is actively bleeding from multiple sites during surgery. He has a CBC that shows a WBC count of 4500/microliter, Hgb 7.6 g/dL, Hct 23.9%, MCV 98 fL, and platelet count 75,000/microliter. His prothrombin time is 30 seconds and partial thromboplastin time 63 seconds. What is the best blood product to use for him in this situation?

    Answer: Fresh frozen plasma (FFP)

    Explanation: This patient has evidence of significant coagulopathy (prolonged PT and PTT) and potentially thrombocytopenia (platelet count 75,000/microliter, which is low in the context of active bleeding), along with anemia. Fresh frozen plasma (FFP) contains all clotting factors and is the best choice to rapidly correct coagulopathy. Packed red blood cells would address anemia, cryoprecipitate would provide fibrinogen and Factor VIII (useful in specific coagulopathies but not the primary choice here), and platelets would address thrombocytopenia, but FFP addresses the systemic clotting factor deficiency indicated by the prolonged PT and PTT.

  39. Q39. A 31-year-old woman has oozing of blood from mucous membranes over the past 3 days. Laboratory studies show a platelet count of 10,000/microliter. She receives 6 units of platelets. An hour following this transfusion, her platelet count is 2,000/microliter. What is the most probable explanation for the change in pre- to post-transfusion platelet count?

    Answer: Rapid platelet consumption

    Explanation: A poor response to platelet transfusion (less than 20% increase in platelet count) with a very low post-transfusion count despite adequate infusion strongly suggests rapid platelet consumption or destruction. While splenomegaly can trap platelets, and DIC is a possibility, alloimmune destruction is a specific cause of refractoriness to transfusion. However, 'rapid platelet consumption' is a broader, yet highly probable explanation, especially if there's an underlying condition causing high platelet turnover or activation, such as severe infection, trauma, or thrombotic microangiopathy (which can be a cause of DIC). Given the options, rapid consumption is the most direct explanation for the rapid drop, suggesting the transfused platelets are being used up or destroyed quickly.

  40. Q40. A 12-year-old boy has had multiple episodes of bleeding since infancy. It is characterized by hemarthroses and decreased joint mobility. His prothrombin time (PT) is normal, but the partial thromboplastin time (PTT) is elevated. When his plasma is mixed with normal plasma, the PTT is not elevated. His platelet count is normal. Which of the following is the most likely cause for his illness?

    Answer: Hemophilia A

    Explanation: The presentation of bleeding since infancy, hemarthroses, normal PT, elevated PTT, and normal platelet count are classic signs of Hemophilia A (Factor VIII deficiency). The mixing study normalization suggests an intrinsic factor deficiency rather than an inhibitor (autoantibody).

  41. Q41. A 64-year-old nursing home patient receiving tube feedings is admitted with fever of two days' duration accompanied by a cough productive of yellowish sputum. On admission his temperature is 37.4°C. A sputum gram stain shows 4+ gram positive diplococci. He is also found to have a total serum protein of 9.4 g/dl with serum albumin of 3.8 g/dl. Which of the following underlying diseases do these findings most strongly suggest that he has?

    Answer: Pneumonia

    Explanation: The presence of fever, productive cough with gram-positive diplococci on sputum gram stain, and elevated total serum protein (likely due to inflammatory response) are highly suggestive of pneumonia. The patient's age and condition (nursing home, tube feedings) increase his risk. While COPD can predispose to pneumonia, the acute symptoms and gram stain findings point directly to an infectious process of the lung. Heart failure and diabetes mellitus are less directly supported by these acute findings.

  42. Q42. A 44-year-old man has had congestive heart failure for 2 years. His serum ferritin is markedly elevated. His CBC shows WBC count 6300/microliter, Hgb 7.8 g/dL, Hct 22.6%, MCV 69 fL, and platelet count 177,000/microliter. A hemoglobin electrophoresis reveals 2% Hgb A, 8% Hgb A2, and 90% Hgb F. Which of the following hematologic conditions is he most likely to have?

    Answer: Beta thalassemia major

    Explanation: The patient has microcytic anemia (low MCV), elevated ferritin (suggesting iron overload, common in chronic transfusions or ineffective erythropoiesis), and a high percentage of fetal hemoglobin (Hb F) with very little adult hemoglobin (Hb A). This pattern is highly characteristic of Beta thalassemia major, where the production of beta-globin chains is severely impaired, leading to ineffective erythropoiesis and a compensatory increase in Hb F. While congestive heart failure is present, the hematologic findings are the key.

  43. Q43. A study of blood product therapy is done. One product is identified that carries the greatest risk for infection. This blood product has the shortest shelf life, and it must be used as quickly as possible for transfusion. Which of the following products is best described by these findings?

    Answer: Platelets

    Explanation: Platelets have the shortest shelf life of blood products (typically 5-7 days under refrigeration and agitation) and are highly susceptible to bacterial contamination due to their storage conditions. While all blood products carry some risk of infection, platelets are considered to have a higher risk due to these factors.

  44. Q44. An 81-year-old previously healthy woman has had a 2 kg weight loss without dieting over the past 2 months. She reports no other problems. On examination there are no abnormal findings. Laboratory studies show a serum alkaline phosphatase of 200 U/L. Which of the following diseases is she most likely to have?

    Answer: Metastatic malignancy

    Explanation: Unexplained weight loss in an elderly individual, especially when accompanied by an elevated alkaline phosphatase (which can be elevated in various liver and bone conditions), is highly suspicious for malignancy. Metastatic disease to the liver or bone can cause elevated alkaline phosphatase and constitutional symptoms like weight loss. Acute viral hepatitis typically presents with jaundice and other signs of liver inflammation. Cholelithiasis might cause pain or jaundice but not typically weight loss and elevated ALP in this manner. Primary biliary cirrhosis is a chronic condition and the presentation doesn't fit as well as malignancy.

  45. Q45. A 17-year-old boy has developed a mild fever with sore throat over the past day. On physical examination he has generalized lymphadenopathy. Laboratory studies show a CD4 lymphocyte count of 375/microliter. He is most likely to be infected with which of the following agents?

    Answer: Epstein-Barr virus (EBV)

    Explanation: The constellation of symptoms: fever, sore throat, generalized lymphadenopathy, and a CD4 count that is moderately reduced (normal is 500-1500/microliter) is highly suggestive of infectious mononucleosis, which is typically caused by the Epstein-Barr virus (EBV). HTLV-1 is associated with adult T-cell leukemia/lymphoma. CMV can cause mononucleosis-like illness but is often less severe and lymphadenopathy may be less prominent. HSV causes pharyngitis but not typically generalized lymphadenopathy and reduced CD4 counts of this magnitude.

  46. Q46. A 62-year-old healthy woman has a pre-operative workup for an elective surgery. A serum glucose is ordered and is of 120 mg/dl. Four hours later that day, another glucose test is ordered unnecessarily, and the value is noted to be 124 mg/dl. Which of the following best explains the difference in these two values on this woman?

    Answer: Physiological diurnal variation

    Explanation: A fasting glucose of 120 mg/dL is considered pre-diabetic or borderline. However, glucose levels naturally fluctuate throughout the day. Without knowing when the first and second tests were taken relative to meals, and given the small increase, it is plausible that the second reading reflects a normal postprandial rise in blood glucose after a meal or snack consumed between the tests. Significant diabetes mellitus would typically present with higher fasting or random glucose levels and potentially larger fluctuations. Diurnal variation exists but usually within a narrower range, and laboratory error is possible but less likely to explain a small, consistent increase.

  47. Q47. A healthy 27 year old male donates blood. He completes the questionnaire and interview with no exclusions noted. The presence of which of the following infectious agents will not routinely tested for on his blood collected for transfusion?

    Answer: Human T-lymphotropic virus type 1

    Explanation: Routine screening of donated blood in most countries includes tests for HIV-1, Hepatitis C virus (HCV), and West Nile virus (WNV). While HTLV-1 can cause disease, it is not as commonly screened for routinely as the other agents listed, though it may be screened for in certain geographic regions or for specific blood products. Regulations for blood screening can vary, but HIV, HCV, and WNV are standard.

  48. Q48. A 33-year-old woman has had multiple episodes of deep venous thrombosis over the past year. Last week she had a transient ischemic attack. On examination there are no abnormal findings. Laboratory studies show a prolonged prothrombin and partial thromboplastin time. When her plasma is mixed in a ratio of 1:1 with normal plasma, neither the PT nor the PTT normalize. Which of the following conditions is she most likely to have?

    Answer: Antiphospholipid syndrome

    Explanation: Antiphospholipid syndrome (APS) is an autoimmune disorder characterized by the presence of antiphospholipid antibodies, which can lead to recurrent arterial and venous thrombosis, and pregnancy morbidity. The prolonged PT and PTT that do not correct upon mixing with normal plasma is a characteristic finding in some patients with APS due to the presence of lupus anticoagulants, which interfere with the clotting assays. While hemophilia A and Factor XI deficiency cause prolonged PTT, they would typically correct with mixing studies, and their thrombotic risk is lower than their bleeding risk. Von Willebrand disease primarily affects platelet function and the PTT may be normal or mildly prolonged.

  49. Q49. Which lipoprotein is responsible for transporting dietary triglycerides from the intestines to tissues?

    Answer: Chylomicrons

    Explanation: Chylomicrons are large lipoprotein particles synthesized in the intestinal cells. They are primarily composed of triglycerides and are responsible for the transport of dietary fats from the intestines to peripheral tissues, such as adipose tissue and muscle.

  50. Q50. What is the primary function of HDL cholesterol?

    Answer: Transporting cholesterol from peripheral tissues to the liver

    Explanation: High-density lipoprotein (HDL) cholesterol is often referred to as 'good cholesterol' because it plays a crucial role in reverse cholesterol transport. It picks up excess cholesterol from peripheral tissues and transports it back to the liver for excretion.

  51. Q51. Which enzyme is responsible for breaking down triglycerides in adipose tissue during lipolysis?

    Answer: Hormone-sensitive lipase

    Explanation: Hormone-sensitive lipase (HSL) is the key enzyme in adipose tissue that hydrolyzes stored triglycerides into free fatty acids and glycerol, releasing them into the bloodstream for energy. Lipoprotein lipase acts on circulating lipoproteins.

  52. Q52. What happens to VLDL as it loses triglycerides?

    Answer: It becomes LDL

    Explanation: Very-low-density lipoprotein (VLDL) is synthesized in the liver and secreted into the circulation to transport triglycerides. As VLDL particles lose triglycerides to peripheral tissues, they undergo structural changes and are progressively converted into intermediate-density lipoprotein (IDL), and then further transformed into low-density lipoprotein (LDL).

  53. Q53. Which hormone promotes lipogenesis and inhibits lipolysis?

    Answer: Insulin

    Explanation: Insulin is an anabolic hormone that promotes the storage of energy. It stimulates lipogenesis (synthesis of fatty acids and triglycerides) and inhibits lipolysis (breakdown of triglycerides) in adipose tissue.

  54. Q54. What is the genetic defect in familial hypercholesterolemia?

    Answer: Deficiency of LDL receptor

    Explanation: Familial hypercholesterolemia (FH) is a genetic disorder characterized by very high levels of low-density lipoprotein (LDL) cholesterol in the blood. The most common genetic defect in FH is mutations in the gene that codes for the LDL receptor, which impairs the liver's ability to remove LDL from the circulation.

  55. Q55. Which clinical sign consists of yellowish nodules commonly found on the Achilles tendon in hypercholesterolemia?

    Answer: Xanthomas

    Explanation: Xanthomas are collections of lipid-laden cells that appear as yellowish nodules or plaques in the skin and subcutaneous tissue. Tendinous xanthomas, particularly on the Achilles tendon, are a characteristic sign of familial hypercholesterolemia.

  56. Q56. What condition can severe hypertriglyceridemia lead to?

    Answer: Pancreatitis

    Explanation: Very high levels of triglycerides (severe hypertriglyceridemia, typically above 1000 mg/dL) can cause acute pancreatitis, a serious inflammation of the pancreas.

  57. Q57. What is lipemia retinalis?

    Answer: Creamy white appearance of retinal vessels due to high lipid content

    Explanation: Lipemia retinalis is a sign of severe hypertriglyceridemia, where the retinal blood vessels appear creamy white or yellowish due to the high concentration of lipids in the blood.

  58. Q58. Which statin is commonly used to lower LDL cholesterol?

    Answer: Atorvastatin

    Explanation: Statins are a class of drugs that inhibit HMG-CoA reductase, the rate-limiting enzyme in cholesterol synthesis. Atorvastatin is a potent statin commonly prescribed to lower LDL cholesterol levels.

  59. Q59. What is the primary metabolic pathway for fatty acid breakdown in mitochondria?

    Answer: Beta-oxidation

    Explanation: Beta-oxidation is the primary metabolic pathway that occurs in the mitochondrial matrix, where fatty acids are broken down into acetyl-CoA units, which then enter the Krebs cycle to generate ATP.

  60. Q60. Which apolipoprotein defect is responsible for familial dysbetalipoproteinemia?

    Answer: ApoE

    Explanation: Familial dysbetalipoproteinemia (also known as type III hyperlipoproteinemia) is caused by a defect in apolipoprotein E (ApoE). Specific isoforms of ApoE, particularly ApoE2/E2 homozygosity, lead to impaired clearance of chylomicron remnants and VLDL remnants.

  61. Q61. What is the chromosomal location of the RB gene?

    Answer: 13q14

    Explanation: The RB1 gene, which encodes the retinoblastoma protein (pRB), is located on the long arm of chromosome 13 at band q14.

  62. Q62. According to Knudson's two-hit hypothesis, how many mutations are required to develop retinoblastoma?

    Answer: Two

    Explanation: Knudson's two-hit hypothesis states that for a tumor suppressor gene like RB1 to cause cancer, both alleles must be inactivated. This typically involves an initial germline mutation (the first hit) in familial cases, and a second somatic mutation in the remaining functional allele in the target cell.

  63. Q63. In familial retinoblastoma, what is the origin of the first hit?

    Answer: Germline mutation inherited from a parent

    Explanation: In familial retinoblastoma, the first 'hit' (inactivation of one RB1 allele) is inherited as a germline mutation, meaning it is present in all cells of the individual, including their germ cells.

  64. Q64. What is the critical cell cycle checkpoint controlled by the RB gene?

    Answer: G1/S transition

    Explanation: The retinoblastoma protein (pRB) plays a crucial role in regulating the G1/S transition of the cell cycle. It binds to and inhibits transcription factors (like E2F) that are necessary for the expression of genes required for DNA synthesis and entry into S phase.

  65. Q65. In its active tumor suppressor form, what is the phosphorylation state of RB protein?

    Answer: Hypophosphorylated

    Explanation: Hypophosphorylated retinoblastoma protein (pRB) is the active tumor suppressor form. In this state, it can bind to transcription factors and inhibit cell cycle progression. Hyperphosphorylation inactivates pRB, allowing the cell cycle to proceed.

  66. Q66. What transcription factor does hypophosphorylated RB bind to?

    Answer: E2F

    Explanation: Hypophosphorylated RB binds to the E2F family of transcription factors. This binding sequesters E2F and prevents it from activating the transcription of genes necessary for DNA replication and cell cycle progression from G1 to S phase.

  67. Q67. What percentage of tumors demonstrate biallelic loss of TP53?

    Answer: Approximately 50-70%

    Explanation: TP53, the gene encoding the p53 protein, is the most frequently mutated gene in human cancers. Biallelic loss or mutation of TP53 is observed in approximately 50-70% of all tumors.

  68. Q68. Which syndrome is associated with germline mutation in one TP53 allele?

    Answer: Li-Fraumeni syndrome

    Explanation: Li-Fraumeni syndrome is a rare inherited cancer predisposition syndrome that results from germline mutations in one allele of the TP53 gene. Individuals with Li-Fraumeni syndrome have a significantly increased risk of developing various types of cancer at an early age.

  69. Q69. What is p53 commonly referred to as due to its critical role in genomic stability?

    Answer: The guardian of the genome

    Explanation: p53 is often called the 'guardian of the genome' because of its critical role in maintaining genomic integrity. It acts as a transcription factor that responds to cellular stress, such as DNA damage, by regulating genes involved in cell cycle arrest, DNA repair, and apoptosis, thereby preventing the propagation of mutations.

  70. Q70. Which stresses can activate p53 protein?

    Answer: All of the above

    Explanation: The p53 protein is a stress-response protein that is activated by a wide range of cellular stresses, including DNA damage, oncogene activation, hypoxia, nutrient deprivation, telomere shortening, and oxidative stress. Upon activation, p53 orchestrates a cellular response to either repair the damage or induce apoptosis.

  71. Q71. What mechanism activates p53 in response to DNA damage?

    Answer: Phosphorylation by ATM and ATR kinases

    Explanation: In response to DNA damage, upstream kinases like ATM (ataxia-telangiectasia mutated) and ATR (ataxia-telangiectasia and Rad3-related) are activated. These kinases then phosphorylate p53, leading to its stabilization and activation. MDM2 normally promotes p53 degradation, but its activity is inhibited upon DNA damage. Acetylation by p300 can further enhance p53 activity.

  72. Q72. What gene does activated p53 drive transcription of to cause G1-S cell cycle block?

    Answer: p21 (CDKN1A)

    Explanation: Activated p53 induces the transcription of the CDKN1A gene, which encodes the cyclin-dependent kinase inhibitor p21. p21 binds to and inhibits cyclin-CDK complexes (e.g., cyclin E-CDK2), thereby blocking the G1-S transition and preventing DNA replication until the damage is repaired.

  73. Q73. A 45-year-old male smoker presents with chronic productive cough for 4 months every year for the past 3 years. What is the histologic hallmark in the large airways?

    Answer: Bronchial gland hypertrophy

    Explanation: Chronic irritation from smoking leads to the characteristic changes of chronic bronchitis. In the large airways, the hallmark is hypertrophy and hyperplasia of the bronchial submucosal glands, which results in excessive mucus production. Squamous cell metaplasia and loss of cilia are also common, but gland hypertrophy is the most defining feature of the excessive mucus production.

  74. Q74. A child presents with inspiratory stridor and harsh barking cough. The most common causative agent is:

    Answer: Parainfluenza virus

    Explanation: The classic presentation of inspiratory stridor and a harsh barking cough in a child is indicative of croup (laryngotracheobronchitis). The most common viral cause of croup is the parainfluenza virus. Haemophilus influenzae type b is a cause of epiglottitis, which presents with drooling and inability to swallow, not typically a barking cough. Pneumococcus and staphylococcus are bacterial pathogens that can cause other respiratory infections but are not the primary cause of croup.

  75. Q75. A 30-year-old presents with spontaneous pneumothorax. The most likely underlying emphysema type is:

    Answer: Panacinar (panlobular)

    Explanation: Spontaneous pneumothorax, particularly in younger adults, is often associated with emphysema. Panacinar (panlobular) emphysema, which affects the entire alveolus and is often associated with alpha-1 antitrypsin deficiency, is more commonly linked to spontaneous pneumothorax. Centriacinar emphysema is more common in smokers and primarily affects the respiratory bronchioles.

  76. Q76. Which cytokine is released within 30 minutes of acute lung injury and drives neutrophil chemotaxis?

    Answer: IL-8

    Explanation: Interleukin-8 (IL-8), also known as CXCL8, is a potent chemokine that is rapidly released in response to lung injury. Its primary function is to attract and activate neutrophils, directing them to the site of inflammation. While IL-1, TNF-alpha, and IL-6 are also pro-inflammatory cytokines involved in lung injury, IL-8 is specifically known for its potent neutrophil chemotactic activity within this timeframe.

  77. Q77. The FEV1/FVC ratio is characteristically decreased in which condition?

    Answer: Obstructive lung disease

    Explanation: The forced expiratory volume in 1 second (FEV1) to forced vital capacity (FVC) ratio is a key spirometric parameter. In obstructive lung diseases (e.g., COPD, asthma), there is airflow limitation, meaning it takes longer to exhale. This leads to a proportionally greater decrease in FEV1 compared to FVC, resulting in a decreased FEV1/FVC ratio. In restrictive lung diseases, both FEV1 and FVC are reduced, but their ratio may be normal or even increased.

  78. Q78. A patient with α1-antitrypsin deficiency develops emphysema. Which type and distribution is expected?

    Answer: Panacinar, lower lobes

    Explanation: Alpha-1 antitrypsin deficiency is a genetic disorder that leads to the destruction of lung tissue, causing emphysema. The characteristic pattern is panacinar (or panlobular) emphysema, which affects the entire alveolus and is typically most severe in the lower lobes of the lungs due to the gravitational distribution of airflow and the protective effect of alpha-1 antitrypsin on lung proteases.

  79. Q79. Which morphologic finding is the HALLMARK of ARDS on microscopy?

    Answer: Hyaline membranes

    Explanation: Diffuse alveolar damage (DAD) is the pathological process underlying Acute Respiratory Distress Syndrome (ARDS). The hallmark microscopic finding of DAD is the presence of eosinophilic hyaline membranes lining the alveolar spaces, formed by edema fluid, cellular debris, and surfactant. Thickened alveolar septa and interstitial fibrosis are more characteristic of chronic lung diseases or later stages of ARDS.

  80. Q80. Streptococcal tonsillitis is important to recognize early because it can lead to all EXCEPT:

    Answer: Acute bacterial sinusitis

    Explanation: Streptococcal tonsillitis (strep throat) is a bacterial infection caused by Group A Streptococcus. Untreated or inadequately treated strep throat can lead to serious non-suppurative sequelae such as acute rheumatic fever and post-streptococcal glomerulonephritis. Peritonsillar abscess is a suppurative complication of tonsillitis. However, acute bacterial sinusitis is generally not considered a direct or common sequela of streptococcal tonsillitis itself, although both can occur in the same patient.

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