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Acute exacerbation of idiopathic pulmonary fibrosis — SCE Acute Medicine MCQ

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HardAcute Respiratory PresentationsAcute exacerbation of idiopathic pulmonary fibrosisSCE Acute Medicine

A 63-year-old man with known idiopathic pulmonary fibrosis presents with four days of worsening breathlessness and dry cough. He is afebrile, CRP is 18 mg/L, BNP is normal and CT pulmonary angiography shows no embolus but new bilateral ground-glass change superimposed on basal honeycombing. He has no sputum production and blood cultures are negative at 24 hours. What is the most likely diagnosis?

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Correct answer: CAcute exacerbation of idiopathic pulmonary fibrosis

New bilateral ground-glass opacities on a background of established usual interstitial pneumonia, without PE, cardiac failure or clear infection, support acute exacerbation of IPF. Pulmonary oedema is less likely with a normal BNP and absent volume overload. Lobar pneumonia would usually produce focal consolidation and stronger inflammatory features. This is a high-mortality presentation where early respiratory and palliative discussions are often needed.

Reference: BTS interstitial lung disease guideline, NICE CKS idiopathic pulmonary fibrosis