Histo - resp Flashcards
Type 1 vs 2 Pneumocytes?
Type 1 : Flat - for gas exchange
Type 2 : Produce Surfactant
What cell types are airways lined by?
Ciliated cells - waft mucus and act as part of mucosal defence
Define Asthma and how does it present?
Widespread narrowing of the airways that changes in severity
- S/S include wheezing, Acute SOB, status asthmaticus
Causes and associations of Asthma?
- Allergens and atopy (including house dust mites)
- Pollution
- Drugs (esp NSAIDs)
- Occupational Exposure (inhaled gases and fumes)
- Diet
- cold/exertion
+ Underlying genetic factors
Pathogenesis of asthma?
- Sensitisation to allergen
- absorbed by APC in airway, presented to T cell
- Th2 / type 2 response - triggers IgE class switch on B cell
- IgE bind to mast cells and eosinophils
IL3/5 - Immediate phase
- mast cells degranulate : increased vascular permeability, brochochspasm, mucus production and inflammatory cell infiltration - Late phase
- tissue damage, muscle hypertrophy and hyperinflation/mucus plugs
Histology findings for asthma
- Hyperemia
- Eosinophilic inflammation and goblet cell hyperplasia
- hypertrophic constricted muscle
- mucus plugging and inflammation
COPD- Chronic bronchitis - define
Chronic cough, productive of sputum for mist days for at least 3 months over at least 2 consecutive years
COPD/Bronchitis causes?
Smoking
Air pollution
Occupational exposure
COPD/Bronchitis : Macroscopic histology
- Dilation of the airways
- Hypertrophy mucous glands
- goblet Cell hyperplasia
Complications of COPD
- Repeated infections
- Chronic hypoxia and reduced exercise tolerance
- Pulmonary HTN and RHF
-increased risk of lung damage independant to smoking
Bronchiectasis - define
Permanent abnormal dilation of bronchi
Causes of bronchiectasis
- congenital
- Inflamatory
- post infections (++CF in kids)
- Ciliary dyskinesia (1y kartnegers or 2y)
- Obstruction
- post-inflammatory/aspiration
- secondary to bronchiolar disease and interstitial fibrosis
- systemic disorders (CTD)
-asthma
Compliations fo bronchiectasis
- Recurrent infection
-haemoptysis - Pul HTN/RHF
- amyloidosis from recurrent inflammation
Macroscopic histology of bronchiectasis
Massively dilated airway with mucus
CF - Genetics
AR Ch7q3 mutation
- CFTR gene mutation leads to constant Cl- ion channel open = thick sticky mucous
CF - s/s
Define pulmonary oedema?
Accumulation of fluid in alveolar spaces as a consequence of “leaky capillaries” or back pressure from LVF
Causes of pulmonary oedema?
LHF
Alveolar injury
neurogenic
high altitude
Pathology of acute and chronic pulmonary oedema?
Acute : heavy water lungs, intra-alveolar fluid
Chronic : Iron laden macrophages and fibrosis