MCQ: Respiratory System Pathology

38 clinical MCQs in Respiratory System Pathology. Adenocarcinoma has become the most common primary lung tumour. Which population is most ch. Kenya, Afr...

Questions, Answers & Explanations

  1. Q1. Adenocarcinoma has become the most common primary lung tumour. Which population is most characteristically affected?

    Answer: Women, non-smokers, and individuals under 45 years

    Explanation: Adenocarcinoma is now the most common lung cancer overall, particularly in women, non-smokers, and those under 45 — a demographic shift from squamous cell carcinoma. ---

  2. Q2. A 62-year-old male smoker presents with a central hilar mass and haemoptysis. Biopsy shows keratin pearls and intercellular bridges. Which paraneoplastic syndrome is most expected?

    Answer: Hypercalcaemia from PTH-related peptide secretion

    Explanation: Squamous cell carcinoma secretes PTH-related peptide causing humoral hypercalcaemia — the most characteristic paraneoplastic syndrome of squamous cell carcinoma. ---

  3. Q3. The overall 5-year survival for all stages of lung cancer combined is approximately

    Answer: 16%, largely unchanged over the past 35 years

    Explanation: The overall 5-year survival for all stages combined remains approximately 16%, reflecting the fact that most patients present with advanced metastatic disease. ---

  4. Q4. A non-smoking 40-year-old Asian woman is diagnosed with lung adenocarcinoma. Molecular testing reveals an EGFR mutation. KRAS testing is unnecessary because

    Answer: KRAS and EGFR mutations are mutually exclusive as KRAS lies downstream of EGFR

    Explanation: EGFR and KRAS mutations are mutually exclusive because KRAS lies downstream of EGFR — activating either produces overlapping oncogenic effects, making co-mutation redundant. ---

  5. Q5. A lung biopsy shows tumour cells growing in a monolayer along alveolar septa without stromal invasion, desmoplasia, or architectural destruction. The lesion measures 2.8 cm. What is the diagnosis?

    Answer: Adenocarcinoma in situ — lepidic growth under 3 cm without invasion

    Explanation: AIS is defined by lepidic growth ≤3 cm along pre-existing alveolar septa with absolutely no stromal invasion, desmoplasia, or alveolar architectural destruction. ---

  6. Q6. A patient with SCLC develops proximal limb weakness that paradoxically improves with repeated movement. Electromyography shows facilitation with repetitive stimulation. This paraneoplastic syndrome is

    Answer: Polymyositis from immune complex deposition within skeletal muscle

    Explanation: Lambert-Eaton myasthenic syndrome is most associated with SCLC. Unlike true myasthenia gravis, strength paradoxically improves with repetitive stimulation due to calcium accumulation. ---

  7. Q7. The "field effect" in lung carcinogenesis means

    Answer: Widespread mutagenesis of respiratory mucosa with 3p deletions even in benign epithelium

    Explanation: The field effect describes large areas of respiratory mucosa being mutagenised by carcinogens — loss of chromosome 3p is found even in benign bronchial epithelium of smokers without cancer. ---

  8. Q8. A 58-year-old male with a right apical lung mass develops right-sided ptosis, miosis, anhidrosis, enophthalmos, and severe pain radiating down the ulnar aspect of the right arm. CT shows rib destruction. The complete diagnosis is

    Answer: Pancoast tumour causing Pancoast syndrome including Horner syndrome

    Explanation: An apical lung tumour invading the brachial and cervical sympathetic plexus causes Pancoast syndrome — Horner syndrome plus ulnar nerve pain and rib destruction are collectively termed Pancoast syndrome. ---

  9. Q9. Which molecular profile is most characteristic of small cell lung carcinoma?

    Answer: RB mutation 90%, TP53 mutation 90%, rare KRAS mutation, absent EGFR mutation

    Explanation: SCLC is characterised by RB mutations (~90%), TP53 mutations ( 90%), rare KRAS mutations, and absent EGFR mutations — a profile distinctly different from NSCLC subtypes. ---

  10. Q10. A patient with ALK-rearranged adenocarcinoma responds brilliantly to crizotinib but relapses after 9 months with a new mutation at the ALK drug-binding domain. This mechanism of resistance is

    Answer: Alteration of the drug target itself through a secondary resistance mutation

    Explanation: The most common mechanism of kinase inhibitor resistance involves secondary mutations within the target kinase domain that directly prevent drug binding to the altered target. ---

  11. Q11. A 30-year-old non-smoking male develops spontaneous left pneumothorax. CT reveals a subpleural bulla. Which emphysema subtype is responsible?

    Answer: Distal acinar (paraseptal) emphysema producing subpleural bullae in young adults

    Explanation: Distal acinar emphysema affects the subpleural distal acinus in young adults without smoking history, producing subpleural bullae that rupture causing spontaneous pneumothorax. ---

  12. Q12. At the time of lung cancer diagnosis, what proportion already have distant metastases?

    Answer: More than 50%, with an additional 25% having regional lymph node disease

    Explanation: More than 50% of lung cancer patients already have distant metastases at diagnosis, with an additional 25% having regional lymph node involvement — only a minority have truly localised disease. ---

  13. Q13. The Azzopardi effect in SCLC refers specifically to

    Answer: Basophilic encrustation of vascular walls by DNA from necrotic tumour cells

    Explanation: The Azzopardi effect is the basophilic encrustation of vascular walls by DNA released from necrotic SCLC cells — a specific and diagnostically recognisable morphologic hallmark. ---

  14. Q14. Heavy smokers with asbestos exposure face approximately what level of increased lung carcinoma risk?

    Answer: Approximately 55-fold increased risk from synergistic interaction of both carcinogens

    Explanation: Asbestos alone increases lung carcinoma risk 5-fold in non-smokers; combined with heavy smoking the risk rises synergistically to approximately 55-fold due to carcinogen adsorption onto fibres. ---

  15. Q15. What is the correct precursor sequence leading to invasive squamous cell carcinoma of the lung?

    Answer: Basal cell hyperplasia → squamous metaplasia → dysplasia → carcinoma in situ → invasion

    Explanation: The squamous cell carcinoma precursor sequence is basal cell hyperplasia → squamous metaplasia → squamous dysplasia → carcinoma in situ → invasive squamous cell carcinoma. ---

  16. Q16. Typical carcinoid tumours fundamentally differ from SCLC in which way?

    Answer: Typical carcinoids are low-grade with greater than 85% 5-year survival versus SCLC median 1 year

    Explanation: Both are neuroendocrine tumours but typical carcinoids are low-grade with 85% 5-year survival, while SCLC is extremely aggressive with a median survival of approximately 1 year even with treatment. ---

  17. Q17. An atypical carcinoid differs from a typical carcinoid by which features?

    Answer: Higher mitotic rate, focal necrosis, greater metastatic potential, and TP53 mutations in 20–40%

    Explanation: Atypical carcinoids show higher mitotic rates, focal necrosis, increased metastatic potential, and TP53 mutations in 20–40% of cases — features absent in typical carcinoids. ---

  18. Q18. A patient with a central lung mass develops Cushing syndrome with high urinary cortisol that fails high-dose dexamethasone suppression. Which tumour is most responsible?

    Answer: Small cell carcinoma producing ectopic ACTH causing Cushing syndrome

    Explanation: SCLC produces ectopic ACTH causing Cushing syndrome that characteristically fails high-dose dexamethasone suppression — distinguishing it from pituitary-driven Cushing disease. ---

  19. Q19. Malignant mesothelioma most commonly arises from which location and with what asbestos exposure history?

    Answer: Parietal or visceral pleura with asbestos history in 80–90% of cases

    Explanation: Malignant mesothelioma arises from the parietal or visceral pleura (also peritoneum/pericardium rarely), with 80–90% of cases having a history of asbestos exposure. ---

  20. Q20. At autopsy a lung is ensheathed by thick yellow-white firm tumour obliterating the pleural space. Microscopy shows cuboidal cells with papillary buds lining tubular and microcystic spaces. This pattern is most likely confused with

    Answer: Pulmonary adenocarcinoma due to similar glandular architecture

    Explanation: The epithelial pattern of malignant mesothelioma — the most common pattern — is most frequently confused with pulmonary adenocarcinoma due to strikingly similar glandular morphology. ---

  21. Q21. After asbestos exposure ceases, what happens to the lifetime risk of mesothelioma?

    Answer: Lifetime risk does not diminish because asbestos fibres remain permanently in body tissues

    Explanation: Unlike smoking where risk decreases after cessation, inhaled asbestos fibres persist permanently in body tissues, meaning the lifetime risk of mesothelioma never diminishes after any exposure. ---

  22. Q22. Which gene is most commonly mutated in both sporadic and familial malignant mesothelioma?

    Answer: BAP1 — tumour suppressor involved in DNA repair affected in familial cases

    Explanation: BAP1 is the most commonly mutated gene in sporadic mesothelioma and is also affected by germline mutations in familial mesothelioma — asbestos generates reactive oxygen species causing DNA damage. ---

  23. Q23. A pleural effusion with protein 30 g/L and neutrophilic infiltrate develops following right lower lobe pneumonia. This is best classified as

    Answer: Exudate from microbial invasion — suppurative pleuritis progressing toward empyema

    Explanation: An exudate (protein 30 g/L with inflammatory cells) from pneumonia represents suppurative pleuritis from direct microbial extension — one of the four principal causes of pleural exudate formation. ---

  24. Q24. A young male develops sudden dyspnoea, absent right breath sounds, tracheal deviation to the left, and rapidly falling blood pressure. The immediately life-threatening mechanism is

    Answer: Tension pneumothorax — ball-valve air leak causing mediastinal shift and circulatory collapse

    Explanation: Tension pneumothorax occurs when a ball-valve leak allows air into but not out of the pleural space — the resulting mediastinal shift compresses the pulmonary circulation and can cause rapid death. ---

  25. Q25. Chylothorax is described as always clinically significant. The most important reason is

    Answer: It implies major lymph duct obstruction, most commonly by intrathoracic malignancy

    Explanation: Chylothorax (milky lymphatic fluid with lipid microglobules) is always significant because it implies obstruction of major lymph ducts, most commonly by an intrathoracic malignancy such as lymphoma. ---

  26. Q26. In approximately what percentage of common cold cases can no causative agent be identified?

    Answer: About 40%, possibly from undiscovered respiratory viral agents

    Explanation: In approximately 40% of common cold cases, no causative agent can be identified despite thorough investigation — possibly involving as-yet undiscovered respiratory viruses. ---

  27. Q27. A 4-year-old presents with sudden fever, drooling, refusal to swallow, and a muffled voice while sitting leaning forward with her neck extended. The most critical immediate management is

    Answer: Immediate airway maintenance and ENT consultation for acute epiglottitis

    Explanation: Acute bacterial epiglottitis (H. influenzae) can cause fatal airway obstruction — maintaining a patent airway is the absolute immediate priority before any other investigation or intervention. ---

  28. Q28. Streptococcal tonsillitis must be identified and treated early to prevent

    Answer: Peritonsillar abscess, acute rheumatic fever, and poststreptococcal glomerulonephritis

    Explanation: Untreated group A streptococcal tonsillitis risks peritonsillar abscess (quinsy), acute rheumatic fever, and poststreptococcal glomerulonephritis — all potentially serious non-suppurative complications. ---

  29. Q29. Diphtheritic laryngitis produces its classic dirty-grey pseudomembrane through which mechanism?

    Answer: Corynebacterium diphtheriae exotoxin causing mucosal necrosis and fibrinopurulent exudate

    Explanation: C. diphtheriae elaborates a powerful exotoxin causing necrosis of the mucosal epithelium with a dense fibrinopurulent exudate forming the characteristic dirty-grey pseudomembrane. ---

  30. Q30. A 3-year-old develops a barking cough, inspiratory stridor, and low-grade fever following a mild cold. Which statement is correct?

    Answer: Parainfluenza virus is the most common cause; occasionally airway narrowing causes respiratory failure

    Explanation: Parainfluenza virus causes most cases of croup. It is generally self-limited with barking cough and stridor, but occasional cases develop dangerous subglottic oedema causing respiratory failure. ---

  31. Q31. The undifferentiated variant of nasopharyngeal carcinoma is characterised by

    Answer: Large epithelial cells with syncytial growth, prominent eosinophilic nucleoli, and dense T cell infiltrate

    Explanation: The undifferentiated variant — most common and most EBV-linked — shows large cells with syncytial growth, prominent eosinophilic nucleoli, and dense T cell infiltration responding to viral antigens. ---

  32. Q32. Laryngeal papillomas in children (RRP) differ from those in adults because

    Answer: Children acquire HPV 6/11 vertically during delivery developing multiple recurrent lesions

    Explanation: Children acquire HPV 6/11 via vertical transmission during delivery developing recurrent respiratory papillomatosis — multiple lesions that recur after excision, unlike the typically single adult lesions. ---

  33. Q33. A 55-year-old male smoker has a pearly-grey plaque on the right true vocal cord confirmed as SCC confined to the glottis. What prognosis does this location confer?

    Answer: Favourable prognosis as approximately 90% of glottic tumours are confined to the larynx at diagnosis

    Explanation: Glottic tumours cause early symptoms (hoarseness), have sparse lymphatics limiting spread, and approximately 90% are larynx-confined at diagnosis — conferring the best prognosis among laryngeal locations. ---

  34. Q34. Which laryngeal tumour location carries the worst prognosis due to rich lymphatics causing early cervical nodal metastases?

    Answer: Supraglottic tumours — rich lymphatics cause nodal metastases in approximately one-third

    Explanation: Supraglottic tumours have rich lymphatic spaces causing approximately one-third to metastasise to cervical lymph nodes at diagnosis — worse nodal involvement than glottic but subglottic tumours present latest. ---

  35. Q35. A 2 cm incidental coin lesion on chest X-ray in a 50-year-old shows mature cartilage, fat, and fibrous tissue on biopsy. Cytogenetics reveals clonal chromosomal abnormalities. The correct statement is

    Answer: This is a pulmonary hamartoma — technically a benign neoplasm despite the developmental-sounding name

    Explanation: Clonal cytogenetic abnormalities confirm this is a true benign neoplasm. Despite being called a hamartoma, it is not a developmental anomaly — the name is technically a misnomer. ---

  36. Q36. The neuroendocrine spectrum of lung tumours ordered from lowest to highest malignant potential is

    Answer: Typical carcinoid → atypical carcinoid → large cell neuroendocrine carcinoma → SCLC

    Explanation: The correct spectrum of increasing aggressiveness is: typical carcinoid → atypical carcinoid → large cell neuroendocrine carcinoma → SCLC. ---

  37. Q37. A patient with lung cancer has adrenal glands nearly obliterated by metastases on CT but shows no clinical signs of adrenal insufficiency. This is explained by

    Answer: Residual islands of cortical cells being sufficient to maintain adequate adrenal function

    Explanation: Even when adrenal glands are nearly obliterated by metastatic tumour, residual islands of cortical cells persist and produce sufficient cortisol to prevent clinical Addison disease. ---

  38. Q38. A non-smoking woman with lung adenocarcinoma responds dramatically to gefitinib but relapses after 11 months. Rebiopsy shows a T790M secondary EGFR mutation. This represents

    Answer: Alteration of the drug target itself through a secondary resistance mutation preventing drug binding

    Explanation: T790M is a secondary EGFR mutation altering the drug-binding domain, directly preventing gefitinib from binding — the most common mechanism of acquired resistance to first-generation EGFR inhibitors.

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