The patient's COPD and aspiration history make bronchopneumonia the expected diagnosis.
| Feature | Bronchopneumonia | Lobar Pneumonia |
|---|---|---|
| Anatomical distribution | Patchy; peribronchial and peribronchiolar | Entire lobes; segmental |
| Airway involvement | Bronchi occluded by purulent exudate | Bronchi patent |
| Pathological stages | NO classic stages; suppuration → abscess | Red → Gray → Resolution (4 stages) |
| Exudate character | Purulent (neutrophil-rich) | Fibrinous (fibrin-rich) |
| Pleural involvement | Uncommon | Fibrinous pleuritis common |
| Common organisms | Staph aureus, H. influenzae, gram-negatives | Streptococcus pneumoniae |
| X-ray pattern | Patchy, ill-defined opacities around hilum | Dense, homogeneous consolidation |
Option 3 states: "Pathologically, the process progresses through well-defined stages of red hepatization followed by gray hepatization."
This is FALSE for bronchopneumonia. The classic four-stage progression (red hepatization → gray hepatization → resolution) is pathognomonic for lobar pneumonia, not bronchopneumonia.
Bronchopneumonia does NOT have these stages. Instead, it is characterized by:
There is no orderly progression through hepatization stages in bronchopneumonia.
Option 1: Correct. Bronchopneumonia is defined by peribronchial distribution with bronchial occlusion by purulent material.
Option 2: Correct. These are the classic causative organisms in bronchopneumonia, especially in aspiration and COPD contexts.
Option 4: Correct. COPD, aspiration, and immunosuppression are major predisposing factors for bronchopneumonia.
Robbins 10e Ch 15
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