Lung pathology Flashcards

1
Q

asthma description

A

widespread reversible narrowing of airways that changes in severity over short periods of time

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2
Q

asthma sympto

A

episodic cough, SOB, wheeze

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3
Q

histo features of asthma

A

SM hypertrohy, goblet hyperplasia, eosinophilia, excess mucus, inflam

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4
Q

COPD

A

chrinoc bronchitis + emphysema -> chronic inj to airways

= chronic productive cough most days for > 3mo over > 2y

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5
Q

histo features of COPD

A

neutrophillic infiltration, loss of alveoli, elastic fib, lung perenchyma

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6
Q

cause of COPD in young non-smokers

A

alpha 1 antitrypsin def (will also have liver issues)

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7
Q

path of CF

A

auto rec mut to CFTR gene (Chr 7) -> def ion transport -> excess resorbtion of water from sec -> abn thick musouc sec

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8
Q

comp of CF

A

freq lung inj, panc insuff, malabs

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9
Q

histo of CF

A

mucous clogged airways, inflam cell infiltration

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10
Q

Path of bronchiectasis and major RF

A

patho airway dilation secondary to recurrent inf

CF = major RF

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11
Q

histo of bronchiectasis

A

dilated fibrotic airways w/ mucous plugging

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12
Q

comp of bronchiactasis

A

recurrent inf, haemoptysis, pulmo hyper, amyloidosis

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13
Q

causes of pulmo oedema

A

L heart failure, alv inj, neurogenic, inc altitude

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14
Q

acute and chornic presentation of pulmo oedema

A

acute = heavy, watery lungs, intra alv fluid

chronic = iron laden macrophages (due to HF), fibrosis

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15
Q

how will a pt with diffuse alveolar damage present

A

rapid onset resp F, req vent on ITU

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16
Q

what is the inv of choice for diffuse alv damage

A

CXR -> show white out all lung fields

17
Q

what causes bronchopneumonia, and in who

A

low virulence org (occurs in immunocomp)

staph, strep, pneumococcus

18
Q

what is lobar pneumonia and how will it present

A

acute bac inf of a lrg portion of a lobe/entire lobe

widespread fibrinosupportive consolidation

19
Q

what causes lobar pneumonia

A

high virulence org - s. pneumoniae

20
Q

idiopathic pulmo fibrosis

A

present in >50y male, chornic SOB + cough

inv = HR, CT + biopsy

21
Q

extrinsic allergic alveolus

A

chronic + progressive fibrosing lung disease in response or organic allergens (farmers lung)

22
Q

pneumoconiosis

A

chronic + progressive fibrosis disease in response to dusts in the workplace (industrial lung disease)

23
Q

what are the RFs for pulmonary thromboembolism

A

obesity, preg, malig, thrombotic FHx, older, surgery

24
Q

what is small cell LC asso with and where is it found

A

v asso with smoking

found centrally near bronchi

25
Q

what mutations are asso with SCLC

A

p53 and RB1

26
Q

what is the prognosis of SCLC

A

poor - mets to brain, ribs and spinal cord

27
Q

what syndrome is SCLC asso with

A

paraneoplastic syndrome

SIADH, lambert-eaton, cushings

28
Q

what can be seen on a blood fild of SCLC

A

small, poorly differentiated ‘oat cells’

29
Q

what mut is asso with adenocarcinoma

A

KRAS, EGFR

30
Q

what lung cancer is most common in non smokers and women

A

adenocarcinoma

31
Q

what lung cancer has the stronges asso with smoking

A

sq cell lung cancer

32
Q

what is sq cell LC asso with

A

hypercalcaemia of malig (PTHrP sec

33
Q

what lung cancer has no evidence of glandular or squamous differentiation

A

large cell carcinoma