Benign Resp Path Flashcards

1
Q

what is the definition of asthma

A

chronic inflammatory disorder of airways - paroxysmal bronchospasm causing wheeze and cough - partially reversible

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2
Q

what is the pathogenesis of asthma

A

mucosal inflammation and oedema, hypertrophic mucous glands and mucus plugs in bronchi - hyperinflated lungs

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3
Q

what are the different types of asthma

A

atopic (extrinsic) non-atopic (intrinsic) allergic bronchopulmonary aspergillosis (ABPA)

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4
Q

describe an atopic asthma attack

A

type 1 hypersensitivity reaction
dust and pollen or animal products
exacerbated by cold, exercise, infection
bronchiolar smooth wall hypertrophy and mucous gland hyperplasia

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5
Q

what is the most common occupational lung disease

A

asthma

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6
Q

what are the two distinct pathological entities of COPD

A
chronic bronchitis (cough with sputum for 3 months in 2 years) 
emphysema - caused by chronic bronchitis, large alveolar spaces
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7
Q

what is the pathogenesis of COPD

A

bronchitis - cell damage - inflammation, scar and mucous infection - wall thickening
emphysema - increased elastase - alveolar wall loss - deceased gas exchange

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8
Q

what are the three classes of emphysema

A

centrilobular (centiacinar) - most associated with smoking and coal dust

pan lobular (panacinar) - severest lower lobe bases

paraseptal (distal acing) - can rupture and lead to pneumothorax

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9
Q

what are the clinical features of COPD

A
dyspnoea 
cough 
sputum 
infection 
right heart signs - increased work load - pulmonary hypertension and right ventricular hypertension
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10
Q

define bronchiectasis

A

permanent dilation of bronchi and bronchioles caused by destruction of the muscle and elastic tissue

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11
Q

what is the pathogenesis of bronchiectasis

A

bronchiole damage due to infection or autoimmune condition which lead to inflammation and scarring

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12
Q

what is a major complication of bronchiectasis

A

abscess formation

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13
Q

which syndromes and diseases are associated with bronchiectasis

A

CF, primary colliery dyskinesia, kartagener syndrome, RA

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14
Q

what are the clinical features of bronciectaiss

A

cough, fever, foul smelling sputum, abscesses

pneumonia, septicaemia

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15
Q

what is the definition of ILD (interstitial lung disease)

A

group and diffuse and chronic conditions of pulmonary connective tissue such as alveolar walls or bronchioles

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16
Q

what is the pathogenesis of ILD

A

idiopathic trigger causes inflammation and fibrosis in bronchioles and or alveolar walls = thickening and deceased lung compliance and reduced gas diffusion

17
Q

what are the two types of clinical features of ILD

A

acute - damage to lung parenchyma (type 1 pneumocytes) causing ARDS - repsiarory alkalosis

chronic - clubbing, fine crackles, dry cough, honey comb lung

18
Q

what is another name for idiopathic pulmonary fibrosis

A

cryptogenic fibbing alveolitis

19
Q

what is the pathogenesis of idiopathic lung fibrosis

A

interstitial chronic inflammation - fibrous tissue with normal alveolar walls - cobblestone pleural surface

20
Q

what is the pathogenesis of sarcoidosis

A

red, swollen, granulomas in lymph nodes of the lung usually hilariously nodes - can infect other organs

21
Q

what are the key clinical features of sarcoidosis

A

hypercalcaemia and elevated serum ACE

22
Q

what is pneumoconiosis

A

dust diseases which is occupational - inflation of fibrogenis mineral dust sin the workplace or vapours

23
Q

what is coal worker pneumoconiosis

A

black lung disease
inhalation of coal dust - biros and necrosis - restrictive disease
simple - macular or nodular lesion
complication - progressive massive fibrosis

24
Q

what is silicosis and the key clinical features

A

inhalation of silicotic noduli which leads to granulomatous chronic inflammation
possible reactivation of TB
increased risk of lung carcinoma
mixed dust pneumoconiosis

25
what is hypersensitivity pneumonitis and what is the pathogenesis
extrinsic alergic alveolitis - framer slung, pigeon fanciers lung inhaled allergy - hypersensitivity 3 - peribroncioalr inflammation - interstitial fibrosis
26
what is the definition of cystic fibrosis
inherited multiorgan disorder or epithelial cells affecting fluid secretion in exocrine glands and epithelial lining of repository, GI and reproductive organs
27
what is the causes and pathoegeniss of CF
AR inheritence, CFTR mutation chromosome 7 lack of chloride ion transport out of cells so w water can't follow and bronchioles or tubes become sticky and blocked - recurrent infection severe respiratory diseases and hyperplasia of secreting glands
28
what are the key clinical features of CF
pancreatic problems, atrophy and fibrosis impaired fat absorption and meconium ileum cirrhosis salivary problems infertility in males