Lung Pathology Flashcards
Pathogenesis of asthma
Sensitisation to allergen; followed by…
Immediate phase = mast cell degranulation mediator release inc. vascular permeability, eosinophil and mast cell recruitment and bronchospasm
Late phase = tissue damage, increased mucous production, muscle hypertrophy
Histology of asthma
Hyperaemia
[Top right] Eosinophils and goblet cell hyperplasia
Hypertrophic constricted muscle
Mucus plugging and inflammation
Histology of COPD
Dilatation of airways
Hypertrophy of mucous glands
Goblet cell hyperplasia
Causes of bronchiectasis
Congenital (CF, ciliary dyskinesia
Inflammatory (post-infectious, obstruction, 2nd to bronchiolar disease and interstitial fibrosis, asthma)
Histoogy of pulmonary oedema
Intra-alveolar fluid on histology
“Heart failure cells” = iron-laden macrophages (right)
Pathology of ARDS
- Capillary congestion
- Exudative phase
- Hyaline membranes
- Organising phase
Bronchopneumonia pathology
Patchy bronchial and peribronchial distribution, lower lobes, inflammation surrounding the airways themselves and is within the alveoli
Lobar pneumonia pathology
- (1) Congestion Hyperaemia, Intra-alveolar fluid
- (2) Red hepatization Hyperaemia, Intra-alveolar neutrophils (non-atypical)
- (3) Grey hepatization (looks like liver) Intra-alveolar connective tissue
- (4) Resolution Restoration normal architecture
90-95% pneumococci (i.e. strep)
Inflammation in atypical pneumonias
Interstitial inflammation without the accumulation of intra-alveolar inflammatory cells
Pathogenesis of emphysema
Cigarette smoke inhibits A1AT- causes proteases to degrade the tissue causing permanent loss of alveolar parenchyma distal to terminal bronchiole
Causes of granuloma
TB, sarcoidosis, FB aspiration
Sarcoidosis lung involvement
discrete epithelioid and giant cell granulomas, preferential distribution in upper zones with a tendency to peri-lymphatic and peri-bronchial advanced disease becomes fibrocystic
Diagnosis of sarcoidosis
non-caseating granuloma, elevated serum ACE, hypercalcaemia (1a-hydroxylase)
Types of fibrosis interstitial lung disease
Idiopathathic pulmonary fibrosis
Extrinsic allergic alveolitis
Pneumoconiosis
IPF pathology
- Macro = basal and peripheral fibrosis and cyst formation
* Micro = interstitial fibrosis (varying stages)