Peripheral Distribution (Reverse Bat-Wing)
Robert B. Carr, MD
DIFFERENTIAL DIAGNOSIS
Common
Contusion
Less Common
Eosinophilic Lung Disease
Cryptogenic Organizing Pneumonia
Pulmonary Infarct
Acute Respiratory Distress Syndrome
Radiation Pneumonitis
Rare but Important
Collagen Vascular Disease
Fat Embolism Syndrome
ESSENTIAL INFORMATION
Key Differential Diagnosis Issues
Spares perihilar regions
Initially described on chest radiography
CT is more sensitive for detection of peripheral consolidation
Clinical history is essential
Helpful Clues for Common Diagnoses
Contusion
Interstitial and alveolar hemorrhage due to blunt thoracic injury
Occurs adjacent to site of chest wall trauma
Contrecoup contusions can occur, but rare
Not confined by fissural or segmental anatomic boundaries
Usually resolves within a few days
Persistence of opacities beyond a few days suggests alternate diagnosis, such as superimposed infection or aspiration
Helpful Clues for Less Common Diagnoses
Eosinophilic Lung Disease
Accumulation of eosinophils within distal airways and interstitium
Several forms of disease exist
Loeffler syndrome is most common form
Peripheral opacities are typical findings with these forms
Loeffler syndrome: Idiopathic peripheral consolidation that clears within 1 month (fleeting); also known as simple eosinophilic pneumonia
Chronic eosinophilic pneumonia: Peripheral consolidation associated with severe respiratory symptoms lasting at least 3 months, often with upper lobe predominance
Churg-Strauss syndrome: Middle-aged patient with allergies; lung disease resembles simple or chronic eosinophilic lung disease
Peripheral opacities are less commonly associated with these forms
Acute eosinophilic pneumonia: Acute respiratory failure with rapid response to steroids; appearance resembles more typical pulmonary edema
Hypereosinophilic syndrome: Multiorgan infiltration of eosinophils; usually presents with bilateral pulmonary nodules
Cryptogenic Organizing Pneumonia
Formerly known as idiopathic bronchiolitis obliterans organizing pneumonia (BOOP)
Accumulation of foamy macrophages and fibrosis in distal airways
Restrictive lung disease with chronic cough, shortness of breath, low-grade fever
Patchy areas of airspace consolidation or ground-glass opacities
Airspace disease is often in peripheral distribution
Tends to be peribronchovascular; can be unilateral or bilateral
More common in lower lungs
Other CT findings include
Peribronchial and centrilobular nodules
Atoll or reverse halo sign: Crescentic opacity with central ground-glass opacity
Pulmonary Infarct
Usually due to pulmonary artery emboli
Also associated with central bronchogenic carcinoma
More common in patients with poor cardiopulmonary reserve, impaired bronchial circulation
Subpleural pulmonary parenchymal consolidation, often wedge-shaped
Hampton hump: Wedge-shaped peripheral opacity with medial border oriented toward hilum
Central “bubbly” lucencies within peripheral consolidation is suggestive of diagnosis
Acute Respiratory Distress Syndrome
Damage to capillaries allows for loss of fluid into lung interstitium and alveolar spaces
Numerous causes: Trauma, infection, toxin exposure, emboli, DIC, drugs, pancreatitis, etc.
Idiopathic ARDS is known as acute interstitial pneumonia (AIP)
Often follows predictable time course
1st 12-24 hours: Normal radiographic appearance
Several days: Bilateral scattered areas of consolidation; begins peripherally and then becomes confluent
Weeks: Slow resolution of lung consolidation
Months: May progress to lung fibrosis, often with anterior predominance
Radiation Pneumonitis
Occurs 1-3 months after radiation therapy
Occurs in approximately 40% of patients
Associated with diffuse alveolar damage within irradiated tissue
Ground-glass opacity &/or consolidation within lung tissue corresponding to location of radiation port
Does not respect fissural and segmental boundaries
Often asymptomatic
May resolve or progress to radiation fibrosis
Persistence > 9 months post radiation suggests presence of radiation fibrosis
Helpful Clues for Rare Diagnoses
Collagen Vascular Disease
Heterogeneous group of diseases
Systemic lupus erythematosus
Dermatomyositis/polymyositis
Scleroderma
Rheumatoid arthritis
Interstitial lung disease is most common pulmonary complication
May see peripheral ground-glass opacity and reticulation
Fat Embolism Syndrome
Usually caused by trauma to long bone or pelvis
Fat droplets are deposited within small vascular spacesStay updated, free articles. Join our Telegram channel
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