Bronchiectasis
Destruction & dilatation of proximal & medium sized bronchi > 2mm
Dry Bronchiectasis seen in
tb
Area involved in Bronchiectasis
Lower lobes
Right middle lobe
Lingula
Allergic Bronchopulmonary Aspergilloma
Hypersensitivity reaction against Aspergillus fumigatus
IgE elevated
Sputum : Fungal hyphae
HRCT : Central bronchiectasis
Tx : steroid
Colonisation of airway in cystic fibrosis by
P. aeruginosa
Kartagener syndrome triad
Recurrent sinusitis
Bronchiectasis
Sinus inversus
Kartagener syndrome vs cystic fibrosis
in KS : Male fertility
in CS : both Female & Male fertility
Upper lobe Bronchiectasis
Cystic fibrosis
TB
Post radiation fibrosis
ABPA
Middle lobe Bronchiectasis
Non TB mycobacterium mycobacteria
Kartagener Syndrome
William Campbell syndrome
Lower lobe Bronchiectasis
Scleroderma
Hypo gammaglobulinemia
ILD-IPF
-Productive cough
-Bronchorrhea, increase purulence with exacerbation
-Dyspnea on exertion
-Crept > ronchi
-CLUBBING
-weakness, weight loss
-cor pulmonale
cynosis -+
Bronchiectasis
-Smoker
-bronchorrhea
-repeated exacerbation
-ronchi
NO CLUBBING
-BLUE BLOATER
Chronic Bronchitis
Ix of Bronchiectasis
X-ray : Normal / Tram track appearance
IOC : HRCT - Tram track appearance
- Signet Ring ( d of airway > 1.5* Blood vessel)
Pulmonary Function test : obstructive
FEV1/FVC < 0.7
no improvement with bronchodilator
Sputum culture : DITTRICH PLUGS
ABLS - M/E - fungal hyphae
Quantitative Ig level
Genetic testing : Alpha 1 AT quantitative assay
Pilocarpine iontophoresis for cystic fibrosis
Nasal / lung biopsy / video microscopic analysis : Kartagener syndrome
Tx of Bronchiectasis
-Non-TB Mycobacterium : Macrolide + Rifampicin + Ethambutol
-Mucolytic for purulent bronchorrhea : DORNase / DNase CF
I-nspissated secretion : 3% saline nebulization with bronchodilator
-Percussion device : dislodgment of mucus
-Romsons Respirometer
-Vaccines
-Gamma globulins in hypogammaglobulinemia
-ABPA : Steroid or Itraconazole
-Antibiotics : Ciprofloxacin BD - 2 week on, 2 week off
Macrolide : OD
Tobramycin nebulization in Cystic Fibrosis