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PA25.1-7 | Respiratory System — Practice Quiz

Practice 14 questions · Untimed · Unlimited attempts

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Q1 PA25.1 1 pt

On gross examination, a lobe of lung from a 55-year-old male who died of pneumonia appears grey, airless, and liver-like. Microscopically the alveoli are packed with neutrophils and fibrin strands, with no macrophages visible. Which stage of lobar pneumonia is this specimen in?

A Congestion
B Red hepatisation
C Grey hepatisation
D Resolution

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Q2 PA25.2 1 pt

A 70-year-old bedridden patient with aspiration pneumonia develops a foul-smelling, thick purulent cough over 3 weeks. Chest X-ray shows a 4 cm cavity with an air-fluid level in the right lower lobe. The most likely causative organisms are:

A Streptococcus pneumoniae and Haemophilus influenzae
B Klebsiella pneumoniae alone
C Mycobacterium tuberculosis
D Anaerobes (Bacteroides, Fusobacterium, peptostreptococci)

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Q3 PA25.3 1 pt

A 38-year-old with a history of chronic heavy smoking presents with progressive dyspnoea. PFTs reveal FEV1/FVC = 0.62, increased TLC, and reduced DLCO. HRCT shows bilateral basal-predominant emphysema involving the lower zones with destruction spanning the full acinus from respiratory bronchiole to alveolar sac. Which morphological type of emphysema is this?

A Panacinar emphysema
B Centriacinar (centrilobular) emphysema
C Paraseptal emphysema
D Irregular emphysema

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Q4 PA25.3 1 pt

Chronic bronchitis is defined clinically. Microscopically, the pathological hallmark used to quantify mucous gland hypertrophy in bronchial biopsies is the Reid index. The Reid index is the ratio of:

A Mucous gland thickness to bronchial wall thickness (cartilage to epithelium)
B Mucous gland layer thickness to total bronchial wall thickness (inner epithelium to outer perichondrium)
C Number of mucous glands per mm² of submucosa
D Goblet cell proportion to total epithelial cells

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Q5 PA25.3 1 pt

A 60-year-old male with COPD is described as a 'pink puffer': thin, using accessory muscles, PaO2 relatively preserved, minimal cyanosis, and prominent dyspnoea. The underlying predominant pathological finding in this phenotype is:

A Predominant emphysema with loss of alveolar walls and reduced gas exchange surface
B Predominant mucus hypersecretion with retained secretions and V/Q mismatch
C Pulmonary arterial hypertension with cor pulmonale
D Bronchospasm with eosinophilic airway inflammation

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Q6 PA25.3 1 pt

A 28-year-old medical student with asthma dies suddenly during an acute exacerbation. At autopsy, the bronchi show plugged mucoid casts. Microscopy of the plugs reveals spirals of shed epithelium and rhomboid crystalline structures derived from eosinophil granule proteins. These findings are:

A Hyaline membranes and type II pneumocyte hyperplasia
B Lamellar bodies and surfactant protein inclusions
C Ferruginous bodies and asbestos fibres
D Curschmann spirals and Charcot-Leyden crystals

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Q7 PA25.5 1 pt

A 10-year-old child presents with a 3-week history of cough and low-grade fever. Chest X-ray shows a 1.5 cm calcified nodule in the lower lobe periphery with ipsilateral calcified hilar lymph nodes. The combination of peripheral nodule + draining hilar lymph node calcification is called the:

A Simon focus
B Ghon complex (Ranke complex)
C Assmann focus
D Rokitansky lesion

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Q8 PA25.5 1 pt

Histology of a caseating granuloma in pulmonary TB would characteristically show:

A Central amorphous eosinophilic necrosis surrounded by epithelioid macrophages, Langhans giant cells, and a lymphocytic rim
B Central liquefactive (pus) necrosis surrounded by neutrophils and a fibrotic wall
C Coagulative necrosis with preserved nuclear outlines and surrounding granulation tissue
D Non-caseating granulomas with no necrosis and negative ZN stain

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Q9 PA25.6 1 pt

A 45-year-old sandstone quarry worker develops progressive exertional dyspnoea and radiological 'eggshell calcification' of hilar lymph nodes. His occupational history also puts him at significantly elevated risk for tuberculosis. The pathological pulmonary lesion is a:

A Asbestos body (ferruginous body)
B Caplan nodule
C Silicotic nodule
D Coal macule

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Q10 PA25.6 1 pt

A 55-year-old shipyard insulation worker presents with progressive dyspnoea and bilateral basal fine crackles over 10 years. HRCT shows bilateral basal sub-pleural reticulation and honeycombing. Bronchoalveolar lavage shows golden-brown dumbbell-shaped structures that stain with Prussian blue. These structures are best called:

A Silicotic nodules
B Charcot-Leyden crystals
C Hamazaki-Wesenberg bodies
D Ferruginous (asbestos) bodies

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Q11 PA25.7 1 pt

A 65-year-old male, ex-smoker with 40 pack-years, presents with a central hilar mass on CT, post-obstructive pneumonia, and haemoptysis. Bronchoscopic biopsy shows a tumour with intercellular bridges and keratin pearl formation. This tumour is most likely:

A Small cell lung carcinoma (SCLC)
B Squamous cell carcinoma of the lung
C Adenocarcinoma of the lung
D Large cell carcinoma

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Q12 PA25.7 1 pt

A 62-year-old woman, never-smoker, presents with a peripheral 2.8 cm lung nodule. EBUS-guided biopsy shows a tumour with glandular formation, lepidic growth pattern, and TTF-1 positivity. Molecular testing is requested to identify a targetable driver mutation for first-line tyrosine kinase inhibitor therapy. The most clinically relevant mutation to test for in this tumour type is:

A KRAS G12C mutation
B TP53 missense mutation
C EGFR exon 19 deletion or exon 21 L858R point mutation
D RB1 deletion

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Q13 PA25.7 1 pt

A 58-year-old male with a 30-year history of asbestos exposure presents with progressive unilateral chest pain, dyspnoea, and a pleural-based mass encasing the lung on CT. Pleural fluid cytology is inconclusive. Thoracoscopic biopsy shows elongated malignant cells growing along pleural surfaces. Immunohistochemistry is positive for calretinin, WT-1, and CK5/6, and negative for CEA and TTF-1. The diagnosis is:

A Pleural metastasis from peripheral adenocarcinoma
B Reactive mesothelial hyperplasia
C Malignant pleural mesothelioma (epithelioid subtype)
D Sarcomatoid carcinoma

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Q14 PA25.6 1 pt

A 52-year-old male coal miner with 25 years of underground work presents with progressive dyspnoea. Chest X-ray shows small round opacities (< 1 cm) predominantly in the upper and mid zones bilaterally. Histology of the lung shows carbon-laden macrophages aggregated around respiratory bronchioles with focal centrilobular emphysema. This is consistent with:

A Progressive massive fibrosis (complicated CWP)
B Silicosis with eggshell calcification
C Asbestosis with basal fibrosis
D Simple coal workers' pneumoconiosis (CWP) — coal macules and nodules

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