Migratory Distribution
Jonathan H. Chung, MD
DIFFERENTIAL DIAGNOSIS
Common
Asthma
Recurrent Aspiration
Atelectasis
Pulmonary Infarct
Less Common
Septic Emboli
Organizing Pneumonia
Cystic Fibrosis
Allergic Bronchopulmonary Aspergillosis
Eosinophilic Pneumonia
Rare but Important
Pulmonary Vasculitis
ESSENTIAL INFORMATION ˜
Key Differential Diagnosis Issues
Migratory pulmonary opacities more suggestive of infectious or inflammatory abnormalities rather than malignancy
Helpful Clues for Common Diagnoses
Asthma
Airway inflammation resulting in reversible airflow obstruction
Imaging for complications: Pneumomediastinum, pneumonia, pneumothorax
Patchy distribution
Bronchial wall thickening and bronchial dilation
Air-trapping or mosaic attenuation
Mucus plugging, subsegmental to lobar atelectasis
Occasional bronchiectasis
Recurrent Aspiration
Consolidation in gravity-dependent portions of lungs
Predisposed patients (i.e., those with alcoholism, epilepsy, hiatal hernia, esophageal dysmotility or obstruction, neuromuscular disorders)
Supine: Superior segments of lower lobes and posterior segments of upper lobes
Upright: Basilar segments of lower lobes
Centrilobular or tree in bud opacities common
May progress to necrotizing pneumonia or pulmonary abscess without treatment
Bland aspiration clears quickly (within hours)
Atelectasis
Recurrent mucus plugging can result in fleeting or migratory atelectasis
Subsegmental to lobar in distribution
Low-density material visible in airways
Recurrent atelectasis or pneumonitis due to incomplete obstruction of airway by aspirated foreign body or endobronchial lesion
Pulmonary Infarct
Lower lung predominant, peripheral/subpleural, wedge-shaped consolidation
Acute pulmonary arterial thromboembolism
CT: Reverse halo configuration common (central ground-glass opacity and peripheral rim of consolidation)
Also central lucencies and absence of air bronchograms
Often in setting of superimposed cardiac dysfunction (cardiomyopathy, congestive heart failure)
Both pulmonary and bronchial arterial supply to lung reduced
May be migratory: Recurrent emboli lead to new pulmonary infarcts as old infarcts resolve
Helpful Clues for Less Common Diagnoses
Septic Emboli
Multiple, peripheral, and basilar consolidation or nodules with early cavitation
Feeding artery sign: Pulmonary artery branches extend to nodules, implying hematogenous spread
Loculated pleural effusion common
Risk factors: Indwelling intravenous catheter or right heart endocarditis
Migratory appearance from recurrent septic embolic events
Organizing Pneumonia
Bilateral basal-predominant peripheral and peribronchovascular consolidation
Scattered areas of ground-glass opacities and nodules
Atoll sign (a.k.a. reverse halo sign): Central ground-glass opacity surrounded by rim of consolidation
Perilobular opacities: Ill-defined opacities outlining interlobular septa of secondary pulmonary lobule
Opacities may wax and wane
Waxing and waning pulmonary opacities in breast cancer following radiation therapy
Not isolated to irradiated portion of lungs
Cystic Fibrosis
Diffuse, upper lung preponderant bronchiectasis and bronchial wall thickening
Mucus plugging in airways: Centrilobular or tree in bud opacities
Air-trapping or mosaic lung attenuation
Hyperinflation
Recurrent areas of consolidation: Pneumonia or atelectasis distal to secretions in airways
Fatty atrophy of pancreas in combination with above findings highly suggestive
Allergic Bronchopulmonary Aspergillosis
Occurs in patients with cystic fibrosis and asthma
Central bronchiectasis in multiple lobes; often severe (cystic or varicoid)
Mucus-filled bronchi; may have gas-fluid levels
Centrilobular nodules
Fleeting pulmonary opacities and atelectasis
Eosinophilic Pneumonia
Simple eosinophilic pneumonia
Usually asymptomatic
Patchy mid and upper lung consolidation
Migratory; changes rapidly; spontaneous regression
Chronic eosinophilic pneumonia
Photographic negative of pulmonary edema: Upper and peripheral preponderant consolidation
May shift in distribution
Most peripheral portions resolve 1st in response to steroids
Tendency to recur in same locations
Helpful Clues for Rare Diagnoses
Pulmonary Vasculitis
Diffuse alveolar hemorrhage
Ground-glass opacities > consolidation; may be diffuse, patchy, lobular, or centrilobular
Tendency to spare peripheral, apical, and costophrenic aspects of lungs
Increased interlobular and intralobular septal thickening over 1-2 days
Resolution in days; not as rapid as in cardiogenic pulmonary edema or bland aspiration
Large, medium, and small vessel vasculitides
Takayasu arteritis, Behçet disease, Churg-Strauss syndrome, microscopic polyangiitis, Goodpasture disease, Wegener granulomatosisStay updated, free articles. Join our Telegram channel
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