Weekly Pathology Exam - July 17, 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, leading to feelings of euphoria and pain reduction, commonly described as 'runner's high'.

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

    Answer: GABA

    Explanation: GABA (gamma-aminobutyric acid) is the primary inhibitory neurotransmitter in the central nervous system. Reduced GABAergic activity is strongly implicated in the pathophysiology of 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: The nucleus of a neuron contains the cell's DNA, which carries the genetic code for all proteins. This information is transcribed into RNA and then translated into proteins in the cytoplasm.

  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 principal inhibitory neurotransmitters in the mammalian central nervous system, mediating IPSPs.

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

    Answer: The importance of sodium channels in action potential propagation.

    Explanation: Tetrodotoxin blocks voltage-gated sodium channels. Its inhibitory effect on nerve impulse conduction highlights the critical role of sodium ions in the generation and propagation of action potentials along axons.

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

    Answer: Serotonin

    Explanation: Serotonin is a key neurotransmitter involved in mood regulation. Dysregulation of serotonin pathways is a major factor in the development of mood disorders like depression and anxiety.

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

    Answer: All neurotransmitters are excitatory.

    Explanation: Neurotransmitters can be either excitatory or inhibitory, depending on the type of receptor they bind to and the ion channels they affect.

  8. Q8. What neurotransmitter is associated with insomnia?

    Answer: Melatonin

    Explanation: While several neurotransmitters are involved in sleep regulation, melatonin is a hormone that plays a crucial role in the circadian rhythm and sleep-wake cycles. Dysregulation or deficiency of melatonin can contribute to insomnia.

  9. Q9. What neurotransmitter is associated with seizures?

    Answer: Glutamate

    Explanation: Glutamate is the primary excitatory neurotransmitter in the brain. Excessive glutamatergic activity can lead to neuronal hyperexcitability and seizures.

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

    Answer: Control of voluntary movement and reward pathways

    Explanation: Dopamine plays a crucial role in motor control, motivation, reward, and pleasure. Its deficiency is characteristic of Parkinson's disease, and its dysregulation is involved in addiction and schizophrenia.

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

    Answer: Blocking pain signals and inducing euphoria

    Explanation: Endorphins are endogenous opioid peptides that act as natural painkillers and mood elevators, producing 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 degeneration of dopaminergic neurons in the substantia nigra, leading to a deficiency in dopamine. This results in motor symptoms such as tremors, rigidity, and bradykinesia.

  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 a classic finding in iron deficiency anemia, which is often caused by insufficient iron intake or increased blood loss, leading to fatigue and pallor.

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

    Answer: Bone marrow

    Explanation: In adults, the bone marrow is the primary site where all blood cells (red blood cells, white blood cells, and platelets) are produced through the process of hematopoiesis.

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

    Answer: Eosinophils

    Explanation: Eosinophils play a key role in the immune response against helminthic (parasitic worm) infections and are also involved in allergic reactions.

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

    Answer: Factor VIII

    Explanation: Hemophilia A is an X-linked recessive disorder caused by a deficiency in clotting Factor VIII.

  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 (indicated by recurrent infections, petechiae, and anemia), is characteristic of aplastic anemia, a condition where the bone marrow fails to produce enough blood cells.

  18. Q18. Haemopoiesis is the process of:

    Answer: Production of blood cells

    Explanation: Hematopoiesis is the complex process by which all the cellular components of blood are formed from hematopoietic stem cells within the bone marrow.

  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 aspiration and biopsy with cytochemical staining and immunophenotyping

    Explanation: While a peripheral blood smear shows blasts, a definitive diagnosis of acute myeloid leukemia (AML) requires examination of the bone marrow, including cytochemical stains (e.g., MPO) and immunophenotyping to confirm the myeloid lineage of the blasts and assess the percentage.

  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 is commonly used in the diagnosis of acute lymphoblastic leukemia (ALL) as it stains the granules within lymphoblasts, appearing as diffuse or block-like cytoplasmic positivity.

  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 an abnormally low number of neutrophils, a type of white blood cell. Chemotherapy often suppresses bone marrow production, leading to neutropenia and an increased risk of infection.

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

    Answer: t(9;22)

    Explanation: The Philadelphia chromosome, a reciprocal translocation between chromosomes 9 and 22, t(9;22), is the hallmark genetic abnormality found in almost all cases of chronic myeloid leukemia (CML).

  23. Q23. Thrombopoietin primarily regulates the production of:

    Answer: Platelets

    Explanation: Thrombopoietin is a cytokine that plays a critical role in the regulation of megakaryopoiesis and platelet production. It stimulates the proliferation and differentiation of megakaryocyte progenitors.

  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 and progenitor cells. It is a widely used marker for identifying and isolating these cells for transplantation and research.

  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, leading to feelings of euphoria and pain reduction, commonly described as 'runner's high'.

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

    Answer: GABA

    Explanation: GABA (gamma-aminobutyric acid) is the primary inhibitory neurotransmitter in the central nervous system. Reduced GABAergic activity is strongly implicated in the pathophysiology of 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: The nucleus of a neuron contains the cell's DNA, which carries the genetic code for all proteins. This information is transcribed into RNA and then translated into proteins in the cytoplasm.

  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 principal inhibitory neurotransmitters in the mammalian central nervous system, mediating IPSPs.

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

    Answer: The importance of sodium channels in action potential propagation.

    Explanation: Tetrodotoxin blocks voltage-gated sodium channels. Its inhibitory effect on nerve impulse conduction highlights the critical role of sodium ions in the generation and propagation of action potentials along axons.

  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 is a key neurotransmitter involved in mood regulation. Dysregulation of serotonin pathways is a major factor in the development of mood disorders like depression and anxiety.

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

    Answer: All neurotransmitters are excitatory.

    Explanation: Neurotransmitters can be either excitatory or inhibitory, depending on the type of receptor they bind to and the ion channels they affect.

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

    Answer: Melatonin

    Explanation: While several neurotransmitters are involved in sleep regulation, melatonin is a hormone that plays a crucial role in the circadian rhythm and sleep-wake cycles. Dysregulation or deficiency of melatonin 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 is the primary excitatory neurotransmitter in the brain. Excessive glutamatergic activity can lead to neuronal hyperexcitability and seizures.

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

    Answer: Control of voluntary movement and reward pathways

    Explanation: Dopamine plays a crucial role in motor control, motivation, reward, and pleasure. Its deficiency is characteristic of Parkinson's disease, and its dysregulation is involved in addiction and schizophrenia.

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

    Answer: Blocking pain signals and inducing euphoria

    Explanation: Endorphins are endogenous opioid peptides that act as natural painkillers and mood elevators, producing 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 degeneration of dopaminergic neurons in the substantia nigra, leading to a deficiency in dopamine. This results in motor symptoms such as tremors, rigidity, and bradykinesia.

  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, 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 normal PT and prolonged PTT, in the absence of bleeding, suggests a deficiency in an intrinsic pathway clotting factor. Factor VIII deficiency (Hemophilia A) is a common cause of isolated prolonged PTT.

  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

    Explanation: This patient has evidence of coagulopathy (prolonged PT and PTT) and thrombocytopenia, along with significant anemia. Fresh frozen plasma (FFP) contains all clotting factors and can help correct the coagulopathy. Packed red blood cells would address the anemia, and platelets would address thrombocytopenia, but FFP is the most comprehensive choice for generalized bleeding due to coagulopathy and can also provide some volume expansion.

  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: Immune thrombocytopenic purpura (ITP)

    Explanation: Post-transfusion purpura (PTP) is a rare but serious complication characterized by a precipitous drop in platelet count 1-2 weeks after transfusion, typically due to an antibody against the HPA-1a platelet antigen. While the timing here is immediate, rapid destruction of transfused platelets suggests an immune-mediated process, and PTP fits this severe, non-response scenario.

  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: A normal PT, prolonged PTT, normal platelet count, and a history of hemarthroses strongly suggest a deficiency in an intrinsic pathway clotting factor. The fact that mixing with normal plasma corrects the PTT points towards a factor deficiency rather than an inhibitor. Hemophilia A (Factor VIII deficiency) is the most common inherited disorder causing these symptoms.

  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: Chronic obstructive pulmonary disease

    Explanation: The presence of gram-positive diplococci in sputum suggests bacterial pneumonia, commonly caused by Streptococcus pneumoniae. Patients with COPD are at increased risk for pneumonia due to impaired mucociliary clearance and weakened respiratory defenses. The elevated total protein and normal albumin might be related to the inflammatory response or underlying conditions, but the combination strongly points towards a complication of COPD.

  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 elevated Hgb F (90%) along with low MCV (69 fL) and severe anemia in a patient with chronic heart failure and elevated ferritin is highly suggestive of beta-thalassemia major. The elevated ferritin is due to increased iron absorption, common in thalassemia, and potential iron overload from repeated transfusions (though not explicitly mentioned, it's a consideration in severe cases). The low Hgb A2 is also consistent with beta-thalassemia.

  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 (typically 5 days at room temperature with agitation) and are stored at room temperature, which increases the risk of bacterial contamination and subsequent infection compared to refrigerated blood products.

  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: Paget's disease of bone

    Explanation: A markedly elevated alkaline phosphatase (200 U/L) in an asymptomatic elderly woman, especially with potential for bone involvement, is highly suggestive of Paget's disease of bone. Weight loss could be incidental or related to other subtle issues, but the alkaline phosphatase is the key finding pointing to increased bone turnover.

  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 fever, sore throat, generalized lymphadenopathy, and a CD4 count of 375/microliter is highly suggestive of an acute viral infection. Epstein-Barr virus (EBV) is the most common cause of infectious mononucleosis, which presents with these symptoms and can cause a transient decrease in CD4 count.

  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: Normal diurnal variation in glucose levels

    Explanation: A fasting glucose of 120 mg/dL is considered impaired fasting glucose. However, the subsequent measurement of 124 mg/dL, four hours later, without any specified reason for the test, likely reflects normal physiological variation and potentially a slight postprandial rise or diurnal fluctuation in blood glucose levels in a person who is not diabetic.

  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: West Nile virus

    Explanation: While screening for bloodborne pathogens is crucial, routine testing for West Nile virus in donated blood is not a standard practice in all regions or at all times, unlike HIV, HCV, and syphilis which are universally screened for.

  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: Recurrent venous and arterial thrombosis (DVT and TIA) in a young woman, coupled with prolonged PT and PTT that do not correct with mixing studies, is highly suggestive of antiphospholipid syndrome. This syndrome is characterized by the presence of antiphospholipid antibodies that interfere with coagulation testing and increase the risk of thrombosis.

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

    Answer: Chylomicrons

    Explanation: Chylomicrons are large lipoprotein particles that are synthesized in the small intestine and transport dietary fats (triglycerides and cholesterol) to various tissues in the body.

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

    Answer: Transport of cholesterol from peripheral tissues back to the liver.

    Explanation: HDL cholesterol, often referred to as 'good cholesterol,' plays a crucial role in reverse cholesterol transport by picking up excess cholesterol from peripheral tissues and transporting it back to the liver for excretion or reprocessing.

  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 responsible for the breakdown of stored triglycerides in adipocytes, releasing fatty acids and glycerol into the circulation during periods of fasting or increased energy demand.

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

    Answer: It is converted into LDL.

    Explanation: As VLDL particles in the circulation lose their triglyceride content through the action of lipoprotein lipase, they undergo a transformation and become progressively richer in cholesterol, eventually being converted into intermediate-density lipoprotein (IDL) and then 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 synthesis of fat (lipogenesis) by facilitating glucose uptake and conversion to fatty acids, and it also inhibits the breakdown of fat (lipolysis) by suppressing hormone-sensitive lipase.

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

    Answer: Defects in the LDL receptor or ApoB-100

    Explanation: Familial hypercholesterolemia (FH) is a genetic disorder characterized by very high levels of LDL cholesterol. The most common genetic defects involve mutations in the gene for the LDL receptor, which impairs the uptake of LDL from the circulation, or mutations in the gene for apolipoprotein B-100 (ApoB-100), the ligand for the LDL receptor.

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

    Answer: Xanthoma tuberosum

    Explanation: Xanthoma tuberosum refers to the deposition of cholesterol-rich material in the skin and subcutaneous tissues, often forming yellowish nodules. The Achilles tendon is a common site for these xanthomas in individuals with severe hypercholesterolemia, particularly familial hypercholesterolemia.

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

    Answer: Pancreatitis

    Explanation: Very high levels of triglycerides (typically above 1000 mg/dL) can lead to acute pancreatitis due to the formation of chylomicrons that obstruct pancreatic capillaries and trigger an inflammatory response.

  57. Q57. What is lipemia retinalis?

    Answer: White or creamy appearance of retinal blood vessels due to high triglyceride levels.

    Explanation: Lipemia retinalis is a clinical sign characterized by a milky or creamy appearance of the retinal blood vessels, which occurs when serum triglyceride levels are extremely high, typically above 2000 mg/dL.

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

    Answer: Atorvastatin

    Explanation: Atorvastatin is a potent statin medication widely prescribed to lower LDL cholesterol levels by inhibiting HMG-CoA reductase, a key enzyme in cholesterol synthesis.

  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 sequentially broken down into acetyl-CoA molecules, which then enter the citric acid cycle for ATP production.

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

    Answer: ApoE

    Explanation: Familial dysbetalipoproteinemia (Type III hyperlipoproteinemia) is caused by genetic defects in apolipoprotein E (ApoE). Specific variants of ApoE, such as ApoE2/E2 homozygosity, lead to impaired catabolism of chylomicron remnants and VLDL remnants, resulting in elevated cholesterol and triglyceride levels.

  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 chromosome 13 at band q14 (13q14).

  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 proposes that for a tumor suppressor gene, two separate inactivating mutations (hits) in both alleles are required for the development of cancer. In retinoblastoma, this means both copies of the RB1 gene must be inactivated.

  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' is a germline mutation in one allele of the RB1 gene, which is inherited by the individual. This means that all cells in the individual's body carry this predisposition.

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

    Answer: G1/S transition

    Explanation: The retinoblastoma protein (pRB) is a key regulator of the cell cycle, particularly at the G1/S transition. It acts as a brake on cell proliferation by binding to E2F transcription factors, preventing the expression of genes required for DNA synthesis and progression into the S phase.

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

    Answer: Hypophosphorylated

    Explanation: The active, tumor-suppressing form of pRB is hypophosphorylated. In this state, it can effectively bind to E2F transcription factors and inhibit cell cycle progression. Hyperphosphorylation inactivates pRB, allowing the cell cycle to advance.

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

    Answer: E2F

    Explanation: Hypophosphorylated retinoblastoma protein (pRB) binds to the E2F family of transcription factors. This binding prevents E2F from activating the transcription of genes necessary for DNA synthesis and cell cycle progression into the S phase.

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

    Answer: Approximately 50%

    Explanation: Mutations in the TP53 tumor suppressor gene are found in approximately 50% of all human cancers. In many of these cases, there is biallelic inactivation, meaning both copies of the gene are mutated or lost.

  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 disorder characterized by a germline mutation in one allele of the TP53 tumor suppressor gene. Individuals with Li-Fraumeni syndrome have a significantly increased lifetime risk of developing a wide range of cancers.

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

    Answer: The guardian of the genome

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

  70. Q70. Which stresses can activate p53 protein?

    Answer: All of the above

    Explanation: p53 is a stress-response protein that is activated by a variety of cellular insults, including DNA damage (e.g., from radiation or chemotherapy), hypoxia, oncogene activation, and other forms of cellular stress. Upon activation, p53 initiates a program to maintain genomic stability or eliminate damaged cells.

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

    Answer: Phosphorylation and acetylation

    Explanation: In response to DNA damage, p53 protein is stabilized and activated through post-translational modifications, primarily phosphorylation and acetylation. These modifications alter p53's conformation, increase its binding to DNA, and enhance its transcriptional activity.

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

    Answer: p21

    Explanation: Activated p53 induces the transcription of the CDKN1A gene, which encodes the cyclin-dependent kinase inhibitor p21. p21 then binds to and inhibits cyclin-CDK complexes, particularly cyclin E/CDK2, thereby blocking the G1-S transition and causing cell cycle arrest.

  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: Goblet cell hyperplasia and mucous gland hypertrophy

    Explanation: Chronic irritation from smoking leads to adaptive changes in the large airways. The hallmark histologic features of chronic bronchitis, as described by the clinical presentation, include hyperplasia of goblet cells and hypertrophy of mucous glands, resulting in increased mucus production.

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

    Answer: Parainfluenza virus type 1

    Explanation: The classic presentation of croup (laryngotracheobronchitis) in children, characterized by inspiratory stridor and a harsh barking cough, is most commonly caused by parainfluenza virus type 1.

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

    Answer: Paraseptal emphysema

    Explanation: Spontaneous pneumothorax is often associated with paraseptal emphysema (also known as distal acinar emphysema). This type of emphysema involves the distal airways and alveoli, leading to the formation of bullae and blebs, which are prone to rupture and cause pneumothorax.

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

    Answer: Interleukin-8 (IL-8)

    Explanation: Interleukin-8 (IL-8), also known as CXCL8, is a potent chemokine that is rapidly released in response to acute lung injury. It is a key chemoattractant for neutrophils, promoting their migration from the vasculature into the lung tissue, which is a critical early event in the pathogenesis of ARDS.

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

    Answer: Obstructive lung disease

    Explanation: In obstructive lung diseases, such as asthma, COPD, and emphysema, there is increased resistance to airflow, particularly during exhalation. This leads to a disproportionate decrease in FEV1 (forced expiratory volume in 1 second) compared to FVC (forced vital capacity), resulting in a reduced FEV1/FVC ratio.

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

    Answer: Panacinar emphysema, lower lobe predominance

    Explanation: Alpha-1-antitrypsin deficiency leads to unopposed elastase activity, primarily affecting the lower lobes of the lungs. This results in panacinar emphysema, characterized by the uniform destruction of alveolar walls throughout the acinus, with a predilection for the lower lung zones.

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

    Answer: Hyaline membranes

    Explanation: The hallmark microscopic finding in Acute Respiratory Distress Syndrome (ARDS) is the presence of diffuse hyaline membranes lining the alveoli. These membranes are composed of proteinaceous fluid, cellular debris, and surfactant, and they represent severe damage to the alveolar-capillary barrier.

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

    Answer: Scarlet fever

    Explanation: Scarlet fever is a rash that accompanies some streptococcal infections, but it is not considered a complication of untreated streptococcal tonsillitis in the same way that acute rheumatic fever and post-streptococcal glomerulonephritis are. Peritonsillar abscess is a local complication.

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