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Bronchiectasis
Dr / Hytham Nafady
Definition
• Irreversible dilatation of the cartilage containing airways.
Bronchial tree
Types of bronchiectasis
Cylindrical bronchiectasis
Varicose bronchiectasis
Cystic bronchiectasis
Mild Moderate Sever
Tram track appearance
String of beads Cluster of grapes
Cylindrical bronchiectasis
Varicose bronchiectasis
Cystic bronchiectasis
Plain radiographic signs of bronchiectasis
Mucoid impaction
Fluid filled bronchi
CTsigns of bronchiectasis
•Signet ring sign (broncho-arterial ratio > 1).•Lack of bronchial tapering.•Abnormal bronchial contour.•Visibility of peripheral air ways.
Signet ring signbroncho-arterial ratio > 1
Normal bronchus Lack of bronchial tapering
Abnormal bronchial contour
Visibility of peripheral air ways within 1cm from the costal pleura
• Peribronchial cuffing (thickened hazy bronchial wall).
• Finger in glove opacities (mucus filled bronchi).• Multiple air fluid levels (fluid filled bronchi).
Bronchial wall thickening
Mucoid impaction
Multiple air fluid levels
• Mosaic perfusion.• Air trapping.• Tree in bud opacities.
Mosaic perfusion
Air trapping
Tree in budd opacities
Pseudo-bronchiectasis
• Pitfalls in diagnosis of bronchiectasis.
• Motion artifact (respiratory or cardiac motion artifact).
Endobronchial tumor (carcinoid)
Broncholithiasis
Bronchial atresia
Bronchial stenosis
Post-irradiation fibrosis (traction bronchiectasis)
Diffuse bronchiectasiswith central predominance
• ABPA.
• Mounier Kuhn syndrome.
• William Campbell syndrome.
ABPA
Mounier Kuhn syndrometracheobronchomegaly
William Campbell syndrome
Congenital cystic bronchiectasis that results from a deficiency of cartilage in the 4th to 6th order bronchi
Diffuse bronchiectasis with upper lobe predominance
• Cystic fibrosis.
• Sarcoidosis.
Cystic fibrosis
Sarcoidosis
Diffuse bronchiectasis with middle lobe & lingula predominance
• Non tuberculous mycobacterial infection.
• Immobile cilia syndrome.
Mycobacterium avium intercellulare infection
Immotile cilia syndrome
Bronchiectasiswith lower lobe predominance
1. Idiopathic (40% of cases).
2. Recurrent childhood infection.
3. Repeated aspiration.
4. Interstitial lung disease.
Interstitial lung disease
Case
• 65-year-old man with a chronic productive cough and progressive dyspnea on exertion.
Atlas of bronchiectasis
Bronchietasis
Lack of bronchial tapering
+
Tree in bud opacities
LUL bronchiectasis
RML bronchiectasis