So now make me an ultra-short, high-yield, concise, and point-to-point difference of lobar pneumonia, bronchopneumonia, and interstitial pneumonia. Lobe, one particular lobe is involved and consolidated can be seen on the chest X-ray. Bronchopneumonia is like small like patchy areas where the alveoli have, that is the bronchopneumonia. And then interstitial edema is like where the interstitium, explain me what lung interstitium actually means, and if it is inflamed, then we'll have the lung surface markings can be pronounced, can be seen, like in case of an interstitial pneumonia, like that.
| Compartment | Contents |
|---|---|
| Peribronchiovascular | Connective tissue surrounding airways + pulmonary vessels (the "bronchovascular bundles") |
| Interalveolar (alveolar walls) | Thin connective tissue + capillaries between adjacent alveoli |
| Subpleural | Connective tissue just beneath the visceral pleura |
| Feature | Lobar Pneumonia | Bronchopneumonia | Interstitial Pneumonia |
|---|---|---|---|
| Also called | β | Lobular pneumonia | Atypical pneumonia |
| Primary site of inflammation | Alveolar air spaces (distal airspaces/alveoli) | Bronchiolar walls + peribronchiolar alveoli | Interstitium (alveolar walls, peribronchial CT, subpleural CT) |
| Pattern of spread | Via pores of Kohn (collateral drift) β uniform spread across entire lobe | Peribronchiolar β patchy/segmental spread | Thickening of interstitial scaffold |
| Distribution | One whole lobe (or segment) | Patchy, multifocal, bilateral | Diffuse bilateral |
| CXR finding | Dense homogeneous consolidation of a lobe | Patchy, ill-defined opacities in multiple segments | Reticular / reticulonodular pattern β prominent/increased lung markings |
| Air bronchogram | β Characteristic (airway visible through fluid-filled alveoli) | β Usually absent | β Absent |
| Volume loss | Absent/minimal in acute phase | Variable | Absent |
| CT hallmarks | Lobar/sublobar consolidation, sharply demarcated by fissures | Centrilobular nodules, tree-in-bud, multifocal lobular consolidation | Ground-glass opacities (GGO), peribronchovascular thickening |
| Organisms | S. pneumoniae (most common), Klebsiella, Legionella | S. aureus, H. influenzae, P. aeruginosa, anaerobes | Viruses, Mycoplasma pneumoniae, Chlamydia |
| Classic presentation | Rusty sputum, sudden onset, lobar dullness | Post-viral, hospital-acquired, underlying COPD/bronchiectasis | "Walking pneumonia," insidious, dry cough, mild symptoms |
| Histology key point | Fibrinopurulent exudate fills alveoli uniformly | Epithelial ulceration of bronchial walls + exudate in surrounding peribronchiolar alveoli | Inflammatory cells in alveolar walls + interstitial edema; alveoli relatively spared |
| Type | Logic |
|---|---|
| Lobar | Alveoli are full of fluid/pus β solid white lobe β you can still see airways (air bronchogram) because airways are clear |
| Bronchopneumonia | Infection starts around bronchioles β patchy blobs β no single lobe, no clean air bronchogram |
| Interstitial | Walls thicken, not the air spaces β reticular (mesh/net) pattern β lung markings are accentuated/prominent, not consolidated |
"Lobe fills, lobule patches, interstitium thickens"
- Lobar = whole lobe white
- Bronchopneumonia = patchy white blobs
- Interstitial = prominent net-like markings, no white consolidation