A 65-year-old non-smoker woman presents with progressive dyspnea. HRCT shows bilateral basilar honeycombing with traction bronchiectasis. Biopsy shows temporal heterogeneity — areas of fibrosis and honeycombing adjacent to relatively normal parenchyma — with fibroblastic foci at the leading edge. This pattern is:
- A Nonspecific interstitial pneumonia (NSIP)
- B Desquamative interstitial pneumonia (DIP)
- C Usual interstitial pneumonia (UIP) — pattern of idiopathic pulmonary fibrosis ✓
- D Cryptogenic organizing pneumonia (COP)
Explanation
Usual interstitial pneumonia (UIP) is the histological pattern diagnostic of idiopathic pulmonary fibrosis (IPF), characterized by spatial and temporal heterogeneity — patchy fibrosis and honeycombing coexisting with normal lung — with fibroblastic foci at the advancing edge of fibrosis. NSIP shows temporally uniform fibrosis without fibroblastic foci and has a better prognosis. DIP shows macrophage accumulation in air spaces (related to smoking). COP (previously BOOP) shows intraluminal fibroblastic plugs in bronchioles and alveoli.
Reference: Robbins & Cotran Pathologic Basis of Disease, 10th ed.
High-yield for: NEET PGINI-CETNExTFMGEUSMLEPLABMRCP
Written and medically reviewed by the StethoPrep medical team.