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
Q

what is hypersensitivity pneumonitis and what is the pathogenesis

A

extrinsic alergic alveolitis - framer slung, pigeon fanciers lung

inhaled allergy - hypersensitivity 3 - peribroncioalr inflammation - interstitial fibrosis

26
Q

what is the definition of cystic fibrosis

A

inherited multiorgan disorder or epithelial cells affecting fluid secretion in exocrine glands and epithelial lining of repository, GI and reproductive organs

27
Q

what is the causes and pathoegeniss of CF

A

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
Q

what are the key clinical features of CF

A

pancreatic problems, atrophy and fibrosis
impaired fat absorption and meconium ileum
cirrhosis
salivary problems
infertility in males