Weekly Pathology Exam - July 3, 2026 (Section A: MCQs)

80 clinical MCQs in Weekly Exam: Pathology. What neurotransmitter is primarily associated with the euphoric feeling experienced during. Kenya, Africa an...

Questions, Answers & Explanations

  1. Q1. 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 prolonged exercise, leading to feelings of pleasure and pain reduction, often described as 'runner's high'.

  2. Q2. Which neurotransmitter system is most implicated in the pathophysiology of anxiety disorders?

    Answer: GABAergic system

    Explanation: Gamma-aminobutyric acid (GABA) is the primary inhibitory neurotransmitter in the central nervous system. Dysregulation of the GABAergic system is strongly linked to 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 holds the genetic blueprint for all proteins synthesized by the neuron.

  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 central nervous system, reducing neuronal excitability.

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

    Answer: The necessity of sodium channels for action potential propagation.

    Explanation: Tetrodotoxin blocks voltage-gated sodium channels, preventing the influx of sodium ions necessary for the depolarization phase of the action potential, thus demonstrating their crucial role in axon conduction.

  6. Q6. Which neurotransmitter is most commonly associated with the regulation of mood, and its dysregulation is implicated in mood disorders like depression?

    Answer: All of the above

    Explanation: Serotonin, dopamine, and norepinephrine are all neurotransmitters involved in mood regulation. Imbalances in any of these systems can contribute to mood disorders.

  7. Q7. Which of the following statements is NOT true regarding neurotransmitters?

    Answer: Neurotransmitters are always excitatory.

    Explanation: Neurotransmitters can be either excitatory or inhibitory, depending on the type of receptor they bind to on the postsynaptic neuron. Therefore, the statement that they are always excitatory is false.

  8. Q8. Which neurotransmitter system is heavily involved in regulating sleep-wake cycles and is often implicated in insomnia?

    Answer: Histaminergic system

    Explanation: Histamine acts as a wake-promoting neurotransmitter in the hypothalamus. Antihistamines, which block histamine receptors, can cause sedation and are often used to treat insomnia.

  9. Q9. 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 central nervous system. An excess of glutamatergic activity or a deficit in GABAergic inhibition can lead to seizures.

  10. Q10. What is one of the primary functions of Dopamine in the brain?

    Answer: Motivation, reward, and motor control

    Explanation: Dopamine is a key neurotransmitter in the brain's reward pathways, playing a significant role in motivation, pleasure, and motor control. It is also implicated in Parkinson's disease.

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

    Answer: Pain relief and pleasure

    Explanation: Endorphins are natural painkillers produced by the body and contribute to feelings of well-being and pleasure, similar to opioids.

  12. Q12. 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 of dopamine and resulting in motor symptoms.

  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, which is the most common cause of anemia in women of reproductive age due to blood loss (menstruation) and inadequate iron intake.

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

    Answer: Bone marrow

    Explanation: In healthy adults, the bone marrow is the primary site where all types of 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 and also plays a role in allergic reactions?

    Answer: Eosinophils

    Explanation: Eosinophils are granulocytes that are particularly effective against parasitic infections and release mediators that contribute to allergic inflammation.

  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 functional Factor VIII of the coagulation cascade, leading to impaired blood clotting.

  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 (implied by recurrent infections, petechiae, and anemia), 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 biological process by which all types of blood cells, including white blood cells, red blood cells, and platelets, are formed and mature.

  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 and aspirate with cytochemical staining

    Explanation: While peripheral blood findings are suggestive, a bone marrow biopsy and aspirate are essential for definitive diagnosis of AML, allowing for assessment of cellularity, morphology, immunophenotyping, cytochemistry, and cytogenetics.

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

    Answer: Periodic Acid-Schiff (PAS)

    Explanation: Periodic Acid-Schiff (PAS) staining typically shows cytoplasmic granules or diffuse positivity in lymphoblasts, helping to differentiate them from other myeloid blasts.

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

    Answer: Neutropenia

    Explanation: Neutropenia is a medical term for a lower-than-normal number of neutrophils, a type of white blood cell, in the blood. Chemotherapy often causes neutropenia.

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

    Answer: t(9;22)

    Explanation: The Philadelphia chromosome, resulting from the reciprocal translocation t(9;22), is the hallmark of chronic myeloid leukemia (CML).

  23. Q23. Thrombopoietin primarily regulates the production of:

    Answer: Platelets

    Explanation: Thrombopoietin (TPO) is the key 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 cell surface glycoprotein that is expressed on hematopoietic stem cells and progenitors, making it a widely used marker for their identification and isolation.

  25. Q25. 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 prolonged PTT with a normal PT suggests a defect in the intrinsic pathway of coagulation. Factor VIII deficiency (Hemophilia A) or Factor IX deficiency (Hemophilia B) are the most common causes of isolated prolonged PTT.

  26. Q26. 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: The patient has a prolonged PT and PTT, indicating a coagulopathy. Fresh frozen plasma (FFP) contains all clotting factors and is the most appropriate product to rapidly correct a broad range of clotting factor deficiencies in actively bleeding patients.

  27. Q27. 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: Thrombotic microangiopathy (e.g., TTP/HUS)

    Explanation: A rapid drop in platelet count after transfusion, despite receiving platelets, suggests ongoing destruction of platelets. Thrombotic microangiopathies like TTP or HUS involve platelet consumption and can lead to this scenario.

  28. Q28. 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: Congenital Factor VIII deficiency (Hemophilia A)

    Explanation: A normal PT, prolonged PTT, normal platelet count, and correction upon mixing with normal plasma are classic findings for a factor deficiency in the intrinsic pathway. Hemophilia A (Factor VIII deficiency) is the most common inherited disorder presenting with hemarthroses and is X-linked.

  29. Q29. 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: Aspiration pneumonia

    Explanation: The patient's presentation with fever, productive cough, and gram-positive diplococci on sputum gram stain is highly suggestive of pneumococcal pneumonia, a common bacterial infection, especially in elderly and debilitated individuals.

  30. Q30. 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 combination of microcytic anemia (low MCV), markedly elevated serum ferritin (indicating iron overload, not deficiency), and a high percentage of Hemoglobin F (HbF) with low HbA is characteristic of beta-thalassemia major or intermedia.

  31. Q31. 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 at a higher risk for bacterial contamination and growth compared to red blood cells or plasma products, which are stored at colder temperatures.

  32. Q32. 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 breast cancer

    Explanation: A mildly elevated alkaline phosphatase in an elderly patient with weight loss and bone lesions can be suggestive of metastatic disease to the bone. While other options can cause elevated alkaline phosphatase, metastatic breast cancer is a strong consideration given the general presentation.

  33. Q33. 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: Fever, sore throat, generalized lymphadenopathy, and atypical lymphocytes are classic symptoms of infectious mononucleosis, typically caused by Epstein-Barr virus (EBV). A CD4 count of 375 is not directly indicative of HIV without further context.

  34. Q34. 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 and laboratory variability

    Explanation: A fasting glucose of 120 mg/dl is slightly elevated, but the subsequent value of 124 mg/dl, especially if not taken in a strictly fasting state or if there was a slight delay, can be attributed to normal variations and laboratory imprecision. It does not definitively indicate diabetes.

  35. Q35. 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 routine screening for HIV, HCV, and HBV is standard for blood donations, testing for West Nile virus is not universally performed but may be implemented during outbreaks or in specific geographic regions.

  36. Q36. 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 thrombosis (DVT, TIA), prolonged PT and PTT that do not correct with normal plasma are highly suggestive of antiphospholipid syndrome, particularly the presence of lupus anticoagulant.

  37. Q37. Which lipoprotein is responsible for transporting dietary triglycerides from the intestines to tissues?

    Answer: Chylomicrons

    Explanation: Chylomicrons are large lipoprotein particles assembled in the intestinal cells that transport dietary fats (triglycerides and cholesterol) from the small intestine into the lymphatic system and then into the bloodstream for distribution to peripheral tissues.

  38. Q38. What is the primary function of HDL cholesterol?

    Answer: Reverse cholesterol transport (transport of cholesterol from peripheral tissues to the liver)

    Explanation: High-density lipoprotein (HDL) cholesterol, often referred to as 'good' cholesterol, plays a crucial role in reverse cholesterol transport, picking up excess cholesterol from peripheral tissues and transporting it back to the liver for elimination.

  39. Q39. 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 circulation during periods of fasting or increased energy demand.

  40. Q40. What happens to VLDL as it loses triglycerides?

    Answer: It is converted into LDL.

    Explanation: Very-low-density lipoprotein (VLDL) delivers triglycerides to peripheral tissues. As it loses triglycerides, it becomes denser and is progressively converted into intermediate-density lipoprotein (IDL) and then into low-density lipoprotein (LDL).

  41. Q41. Which hormone promotes lipogenesis (fat synthesis) and inhibits lipolysis (fat breakdown)?

    Answer: Insulin

    Explanation: Insulin is a key anabolic hormone that promotes glucose uptake and storage, and it also stimulates lipogenesis and inhibits lipolysis, thus promoting fat storage.

  42. Q42. What is the genetic defect in familial hypercholesterolemia?

    Answer: Deficiency in LDL receptor

    Explanation: Familial hypercholesterolemia is most commonly caused by mutations in the gene encoding the LDL receptor, leading to impaired clearance of LDL cholesterol from the bloodstream and consequently very high LDL levels.

  43. Q43. Which clinical sign consists of yellowish nodules commonly found on the Achilles tendon in hypercholesterolemia?

    Answer: Xanthomas (specifically Tuberous xanthomas)

    Explanation: Xanthomas, particularly tuberous xanthomas on the Achilles tendon, are characteristic cutaneous manifestations of severe hyperlipidemia, especially familial hypercholesterolemia.

  44. Q44. What condition can severe hypertriglyceridemia lead to?

    Answer: Acute pancreatitis

    Explanation: Severely elevated triglyceride levels (typically 1000 mg/dL) significantly increase the risk of acute pancreatitis due to the formation of chylomicron remnants that can obstruct pancreatic ducts.

  45. Q45. What is lipemia retinalis?

    Answer: Cloudy appearance of the retina due to high triglyceride levels

    Explanation: Lipemia retinalis is a clinical finding where the retinal blood vessels appear milky white or creamy due to extremely high levels of triglycerides in the blood, which causes the plasma to become opaque.

  46. Q46. Which statin is commonly used to lower LDL cholesterol?

    Answer: Atorvastatin

    Explanation: Atorvastatin is a potent statin medication widely prescribed for its efficacy in reducing low-density lipoprotein (LDL) cholesterol levels by inhibiting HMG-CoA reductase.

  47. Q47. What is the primary metabolic pathway for fatty acid breakdown in mitochondria?

    Answer: Beta-oxidation

    Explanation: Beta-oxidation is the catabolic process occurring in the mitochondrial matrix that breaks down fatty acid chains into acetyl-CoA units, which then enter the citric acid cycle for energy production.

  48. Q48. Which apolipoprotein defect is responsible for familial dysbetalipoproteinemia?

    Answer: ApoE

    Explanation: Familial dysbetalipoproteinemia (Type III hyperlipoproteinemia) is characterized by a defect in apolipoprotein E (ApoE), leading to impaired clearance of chylomicron remnants and very-low-density lipoprotein (VLDL) remnants.

  49. Q49. What is the chromosomal location of the RB gene?

    Answer: 13q14

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

  50. Q50. 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 tumor suppressor genes like RB, both alleles must be inactivated (mutated or lost) for the cancer to develop. In hereditary cases, one hit is inherited, and the second hit occurs somatically.

  51. Q51. In familial retinoblastoma, what is the origin of the first hit?

    Answer: Germline mutation inherited from a parent

    Explanation: In familial retinoblastoma, the first genetic 'hit' (inactivation of one RB allele) is present in all cells of the body, having been inherited in the germline from an affected parent.

  52. Q52. What is the critical cell cycle checkpoint controlled by the RB gene?

    Answer: G1/S transition

    Explanation: The retinoblastoma protein (RB) acts as a key regulator of the G1/S phase transition in the cell cycle. It prevents the cell from entering the S phase (DNA synthesis) until appropriate signals are received.

  53. Q53. In its active tumor suppressor form, what is the phosphorylation state of RB protein?

    Answer: Hypophosphorylated

    Explanation: The active, tumor-suppressor form of the RB protein is hypophosphorylated. When RB is hyperphosphorylated, it releases its bound transcription factors, allowing the cell cycle to progress.

  54. Q54. What transcription factor does hypophosphorylated RB bind to?

    Answer: E2F

    Explanation: Hypophosphorylated RB binds to the E2F family of transcription factors, preventing them from activating genes required for DNA replication and entry into S phase.

  55. Q55. 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. Biallelic inactivation (both alleles mutated or lost) is required for its tumor suppressor function to be abolished.

  56. Q56. 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 TP53 allele, significantly increasing the risk of developing a wide range of cancers at an early age.

  57. Q57. 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 it plays a crucial role in maintaining genomic stability by preventing DNA mutations and halting the cell cycle in response to cellular stress.

  58. Q58. Which stresses can activate p53 protein?

    Answer: All of the above

    Explanation: p53 can be activated by a variety of cellular stresses, including DNA damage, hypoxia, ribosomal dysfunction, and oncogene activation, triggering protective cellular responses.

  59. Q59. What mechanism activates p53 in response to DNA damage?

    Answer: Phosphorylation and stabilization by kinases like ATM

    Explanation: In response to DNA damage, kinases such as ATM phosphorylate p53 and its negative regulator MDM2. This phosphorylation event stabilizes p53 and prevents its degradation, allowing it to accumulate and function as a transcription factor.

  60. Q60. What gene does activated p53 drive transcription of to cause G1-S cell cycle block?

    Answer: CDKN1A (p21)

    Explanation: Activated p53 induces the transcription of CDKN1A (also known as p21), which encodes a protein that inhibits cyclin-dependent kinases (CDKs) responsible for cell cycle progression, thereby causing a G1-S cell cycle arrest.

  61. Q61. 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 squamous metaplasia

    Explanation: Chronic bronchitis, a component of COPD, is characterized histologically in the large airways by hypertrophy and hyperplasia of goblet cells (increasing mucus production) and squamous metaplasia of the respiratory epithelium, which is a defense mechanism against irritants like smoke.

  62. Q62. A child presents with inspiratory stridor and harsh barking cough. The most common causative agent is:

    Answer: Parainfluenza virus

    Explanation: Croup, characterized by inspiratory stridor and a barking cough, is most commonly caused by viral infections, with parainfluenza virus being the most frequent culprit. Haemophilus influenzae type b is a common cause of epiglottitis, a more severe airway obstruction.

  63. Q63. A 30-year-old presents with spontaneous pneumothorax. The most likely underlying emphysema type is:

    Answer: Panacinar (panlobular)

    Explanation: Panacinar emphysema is characterized by destruction of alveoli throughout the acinus and is typically associated with alpha-1-antitrypsin deficiency. This type of emphysema, particularly in the upper lobes, is strongly linked to spontaneous pneumothorax.

  64. Q64. Which cytokine is released within 30 minutes of acute lung injury and drives neutrophil chemotaxis?

    Answer: TNF-alpha

    Explanation: Tumor necrosis factor-alpha (TNF-alpha) is a pro-inflammatory cytokine that is rapidly released within minutes to hours of acute lung injury, promoting neutrophil recruitment and activation.

  65. Q65. The FEV1/FVC ratio is characteristically decreased in which condition?

    Answer: Obstructive lung disease

    Explanation: In obstructive lung diseases (like asthma, COPD), there is airflow limitation, leading to a decreased ratio of forced expiratory volume in 1 second (FEV1) to forced vital capacity (FVC) because the airways close prematurely during forced expiration.

  66. Q66. A patient with α1-antitrypsin deficiency develops emphysema. Which type and distribution is expected?

    Answer: Panacinar, upper lobes

    Explanation: Alpha-1-antitrypsin deficiency typically leads to panacinar emphysema, which predominantly affects the lower lobes of the lungs, although it can involve all zones.

  67. Q67. Which morphologic finding is the HALLMARK of ARDS on microscopy?

    Answer: Hyaline membranes lining the alveolar spaces

    Explanation: The pathognomonic microscopic feature of Acute Respiratory Distress Syndrome (ARDS) is the presence of diffuse hyaline membranes lining the alveolar spaces, which are composed of proteinaceous exudate and cellular debris.

  68. Q68. Streptococcal tonsillitis is important to recognize early because it can lead to all EXCEPT:

    Answer: Scarlet fever

    Explanation: Scarlet fever is a manifestation of streptococcal tonsillitis (a rash), not a complication that develops later. Rheumatic fever and post-streptococcal glomerulonephritis are autoimmune sequelae, and peritonsillar abscess is a local suppurative complication.

  69. Q69. A biopsy shows polypoid plugs of organizing connective tissue within alveolar ducts, all of the same age, with normal underlying lung architecture. The diagnosis is:

    Answer: Organizing pneumonia

    Explanation: Organizing pneumonia (formerly bronchiolitis obliterans organizing pneumonia or BOOP) is characterized by polypoid plugs of granulation tissue within alveolar ducts and alveoli, often of uniform age, and preservation of underlying lung architecture.

  70. Q70. Which of the following is TRUE about nasopharyngeal carcinoma?

    Answer: It is strongly associated with the Epstein-Barr virus (EBV).

    Explanation: Nasopharyngeal carcinoma has a high prevalence in Southeast Asia and is strongly associated with Epstein-Barr virus (EBV) infection. It often presents with cervical lymphadenopathy due to early metastasis.

  71. Q71. A farmer presents with fever, cough, and dyspnea 6 hours after entering a barn with moldy hay. Serum shows precipitating antibodies. BAL shows increased CD4+ and CD8+ T cells. What is the diagnosis?

    Answer: Farmer's lung (Hypersensitivity pneumonitis)

    Explanation: This clinical scenario is classic for acute hypersensitivity pneumonitis (farmer's lung). Exposure to moldy hay (antigens) leads to an immune response (precipitating antibodies, T cell infiltration) causing respiratory symptoms.

  72. Q72. A patient with asthma dies during status asthmaticus. Whorls of shed epithelium found within mucous plugs are called:

    Answer: Curschmann's spirals

    Explanation: Curschmann's spirals are microscopic findings in sputum of asthmatic patients, consisting of coiled, whitish, mucus-filled casts of the smaller bronchioles, often containing shed epithelial cells.

  73. Q73. A 62-year-old man has 3 months of dull back pain and develops a productive cough. CXR of the spine shows several 1–2 cm lytic vertebral lesions. Labs show BUN 49, creatinine 5, total protein 8.3, albumin 3.7. Sputum grows Streptococcus pneumoniae. Most likely bone marrow biopsy finding?

    Answer: Increased plasma cells with M-protein

    Explanation: The constellation of lytic bone lesions, elevated BUN and creatinine (suggesting renal involvement, potentially from amyloidosis or light chain deposition), and plasma cell dyscrasia is highly suggestive of multiple myeloma. Bone marrow biopsy would reveal a significant increase in plasma cells, often producing a monoclonal immunoglobulin (M-protein).

  74. Q74. A 33-year-old woman has 2 months of low-grade fever, night sweats, and malaise. She has non-tender cervical and supraclavicular lymphadenopathy. Lymph node biopsy shows CD15+ and CD30+ Reed-Sternberg cells, large and small lymphocytes, and bands of fibrosis. Most likely diagnosis?

    Answer: Hodgkin lymphoma, nodular sclerosis type

    Explanation: The presence of Reed-Sternberg cells (CD15+ and CD30+) in a lymph node biopsy, along with lymphocytes and fibrosis, is the hallmark of Hodgkin lymphoma. Nodular sclerosis is the most common subtype in this age group.

  75. Q75. A 17-year-old has 3 weeks of malaise, mild pharyngitis, tender axillary and inguinal lymphadenopathy, and a palpable spleen. CBC shows atypical lymphocytes on smear. Most likely acquisition mechanism?

    Answer: Sexual transmission

    Explanation: The symptoms described (malaise, pharyngitis, lymphadenopathy, splenomegaly, atypical lymphocytes) are highly suggestive of primary infection with Epstein-Barr virus (EBV), which causes infectious mononucleosis. The most common mode of transmission for EBV is through oral secretions, often via sexual contact or close personal contact like kissing.

  76. Q76. A 30-year-old woman has mild chronic fatigue. Exam shows a palpable spleen tip. CBC: Hgb 11.1, MCV 77, reticulocyte count 3.9%. Peripheral smear shows small RBCs lacking central pallor. Most likely pattern of inheritance?

    Answer: Autosomal recessive

    Explanation: The findings of mild anemia (Hgb 11.1), microcytosis (MCV 77), elevated reticulocyte count (3.9%), and small RBCs lacking central pallor are indicative of a thalassemia trait, most likely alpha or beta thalassemia. Thalassemia traits are typically inherited in an autosomal recessive pattern.

  77. Q77. A 3-year-old child has pinpoint hemorrhages on skin appearing over 3 days. CBC: Hgb 14.3, MCV 90, platelet count 19,300, WBC 9370. It resolves over a month without treatment. Most likely antecedent event?

    Answer: Recent viral infection

    Explanation: The patient has thrombocytopenia (platelet count 19,300) presenting as petechiae, which resolved spontaneously. This clinical picture in a child is highly suggestive of immune thrombocytopenic purpura (ITP), which is often triggered by a preceding viral infection.

  78. Q78. A 30-year-old man has 5 days of sore throat and fever. Exam shows mildly tender cervical lymphadenopathy and enlarged erythematous tonsils with exudate. WBC 12,670 with 75 segs, 10 bands, 15 lymphs. Most likely diagnosis?

    Answer: Bacterial pharyngitis (e.g., Streptococcus pyogenes)

    Explanation: The presence of fever, exudate on tonsils, cervical lymphadenopathy, and a leukocytosis with a significant number of neutrophils (segs + bands = 85%) suggests a bacterial cause, most commonly Group A Streptococcus (Streptococcus pyogenes).

  79. Q79. A 30-year-old man has a month of worsening productive cough. Exam shows a palpable spleen tip and small axillary lymph nodes. CBC: WBC 67,000, Hgb 10.2, platelets 36,000. Peripheral smear shows many blasts with Auer rods. Most likely diagnosis?

    Answer: Acute myeloid leukemia (AML)

    Explanation: The extremely high white blood cell count with a predominance of blasts and the presence of Auer rods are diagnostic features of acute myeloid leukemia (AML). The splenomegaly and lymphadenopathy can also be seen in AML.

  80. Q80. A 68-year-old man has a year of malaise. CBC: Hgb 10.5, MCV 88, platelet count 211,000, WBC 6980. Total iron 130, TIBC 230, soluble serum transferrin receptor normal. Bone marrow shows normal maturation in all cell lines with increased stainable iron. Most likely underlying disease?

    Answer: Anemia of chronic disease

    Explanation: The patient has anemia (Hgb 10.5) with normal MCV (88), normal iron studies (iron 130, TIBC 230), and a normal soluble transferrin receptor, which argues against iron deficiency. The bone marrow showing increased stainable iron and normal maturation is characteristic of anemia of chronic disease/inflammation, where iron is sequestered and unavailable for erythropoiesis.

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