PULMONARY Flashcards

1
Q

benign
lung tissue + cartilage
calcified on imaging

A

bronchial hamartoma

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2
Q

list subtypes (4) of non-small cell carcinoma

A

adenocardinoma
squamoud cell carcinoma
large cell neuroendocrine carcinoma
carcinoid tumour

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3
Q

seen in

A

small cell carcinoma
(lung)

mitotic activity
poorly differentiated small cells

smoking
sentral tumour (central)
syndromes - paraneoplastic (ADH, ACTH, LEMs) - lambert eaton
Tx with chemotherapy

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4
Q

what is a unique site of distant metastasis of primary lung carcinoma

A

adrenal gland

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5
Q

lung cancer causing horseness is likely affecting

A

recurrent laryngeal nerve

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6
Q

lung cancer at apex
ptosis
miosis
anhidrosis

A

pancost tumour
(apex of lung)

Horner syndrome - SNS chain involvement

affected by lung cancer

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7
Q

what mutations (2) may be present in adenocarcinoma of lung

A

EGFR
ALK translocation

common non-smoking asian females

EGFR = tyrosine kinase receptor

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8
Q

what lung cancer subtypes affect male smokers, are located centrally and posess paraneoplastic syndromes

A

SCLC
SCC (squamous)

SCLC - LEMs, ADH, ACTH
SCC - PTHrP

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9
Q

what group of persons is adenocarcinoma of lung most seen in

A

female non-smokers

EFGR mutation association - asian non-smoking females

cancer located peripherally

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10
Q

male
smoker
mitotic changes
necrosis
poorly differentiated small cells
chromogranin (+)
LEMs

A

SCLC

PNP syndrome - also ADH, ACTH

central location
male smokers
small cells

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11
Q

male
smoker
hypercalcaemia

A

SCC
(squamous cell carcinoma)

keratin pearls
intercellular bridges

central
male smoker
PNP syndrome - PTHrP

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12
Q

glands
mucin
nonsmoker
female
peripheral tumor
pneumonia-like consolidation

A

adenocarcinoma lung

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13
Q

lepidic pattern
columnar cells along preexisting brtonchioles/aveoli
peripheral
pneumonia-like consolidation
good prognosis

A

adenocarcinoma in situ = bronchioalveolar carcinoma

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14
Q

what lung cancer is determined by diagnosis of exclusion

A

large cell neuroendocrine carcinoma

smoking
central or perihpheral

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15
Q

well differentiated
neuroendocrine cell nests
chromogranin (+)
polyp like

A

carcinoid tumour

can cause carcinoid syndrome
central = polyp-like
peripheral

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16
Q

flushing
diarrhoea
abdominal pain
wheezing
tumour

A

carcinoid syndrome

serotonin secreting - can be from carcinoid tumour (rare)
Tx with so

but common on exam Q

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17
Q

2 causes of emphysema

A

smoking
a-1 antitrypsin deficiency
*
(imbalance proteases:antiproteases)*

centriacinar - smoking - UL
panacinar - a-1 AT - LL

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18
Q

centriacinar and panacinar emphysema affects which parts of the lung

A

centriacinar = UL (smoking)
panacinar = LL (a-1 AT)

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19
Q

cause of a1-AT deficiency

A

misfolding of mutated protein

ccumulates in endoplastic reticulum of hepatocytes –> liver damage

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20
Q

what marker is seen in a-1 AT

A

PAS (+)

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21
Q

what is the function of a-1 AT

A

neutralises proteases

deficiency a-1 AT = increased proteases (inflammation)

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22
Q

what is the PiM allele in a-1 AT

A

normal
(PiM or PiMM)

23
Q

what allele mutation is associated with low levels of a-1 AT

24
Q

what allele mutation is associated with increased risk of emphysema with smoking

25
Q

what allele mutation is associated with increased risk of panacinar emphysema and cirrhosis

26
Q

a Ried index of >50% is seen in

A

chronic bronchitis

27
Q

hypertrophy of bronchial mucous glands
smoking
productive cough
cyanosis

A

chronic bronchitis

produceive cough lasting >3 months over min of 2 years

28
Q

what induces fibrosis in idiopathic pulmonary fibrosis

A

TGF-B (tissue healing factor)

injured pneumocytes induce fibrosis

29
Q

what drugs induce pulmonary fibrosis

A

Methotrexate
nitrofurantoin
carmustine
bleomycin
busulfan
amiodarone

30
Q

progressive dyspnoea, cough
subpleural bilateral fibrosis
honey combing

A

interstitial pulmonary fibrosis

31
Q

what induces fibrosis in pneumoconioses

A

alveolar macrophages

engulf partciles and induce fibrosis
small particles

32
Q

AA female
non-caseating granulomas
hilar LN
uveitis
dry mough/eyes
erythema nodosum

A

sarcoidosis

increased serum ace
hypercalcaemia

DxDx - berylliosis (same s/s but JOB = aerospace, beryllium miner)

33
Q

how does hypercalcaemia in sarcoidosis or berylliosis occur

A

non-caseating granulomas posess 1-a hydroxylase activity of epithyloid histiocytes

convert vitamin D to active form -> calcium reabsorption

34
Q

type of granuloma in sarcoidosis

A

non-caseating

1-a hydroxylase activity –> hypercalcaemia

also occurs in berylliosis (non-caseating)

35
Q

caplan syndrome is what and related to what

A

rheumatoid arhtritis in coal workers pneumoconiosis

36
Q

anthracosis

A

carbon laden macrophages

coal workers pneumoconiosis

37
Q

silicosis occurs in what part of lung, and has increased risk for what condition

A

upper lung
TB

38
Q

how does silicosis affect the lung

A

impairs phagolysosome formation by macrophages

39
Q

asbestosis can be seen in

A

construction
plumbers
shipyard workers

40
Q

abestos causes fibrosis or carcinoma of

A

lung and pleura

carcinoma of pleura = mesothelioma

lung carcinoma MORE COMMON than mesothelioma

41
Q

seen in

A

(asbestos bodies)
ferruginous bodies

asbestosis
brown with iron deposits

42
Q

granulomatous reaction
pigeon breeder

A

hypersensitivity pneumonitis

43
Q

affects upper acinar
smokers, coal miners
___acinar

A

centriacinar

44
Q

affects entire acinus
lower zones
a1-AT deficiency
___acinar

45
Q

hypoxaemia
respiratory acidosis (from CO2 retention)
normal alveolar-arterial gradient

A

respiratory depression

(hypoventilation)
i.e. barbituates

normal A-a gradient = 10mmHg (physiologic shunt)
hypoventilation causing CO2 retention = normal A-a gradient as decreased gas exchange, butno disruption to diffusion or perfusion

46
Q

difuse wheeze
dry cough
dyspnoea
tachycardia, tachypnoea
prolonged expiration
decreased tactile fremitis
URTI common trigger in children

A

astha exacerbation

chest RADs normal
pulmonary function tests normal (between epsides)
obstructive (during episode)

decreased tactile fremitis - air trapping (obstructive)

47
Q

m/c cause pneumococcal pneumonia

A

strep pneumoniae

fever
dyspnoea
productive cough
pleuritic chest pain
consolidation;
increased tactiel fremitis

48
Q

how is COPD best evaluated (test)

A

spirometry

49
Q

decreased breath sounds
prolonged expiration
distant heart sounds
FEV1 65%
FVC 90%
FEV1/FVC 60%

A

COPD

FEV1/FVC <80%

50
Q

tachycardia
hypotension
JVD
pulsus paradoxus
muffled heart sounds
S3, S4 gallop

A

cardiac tamponade

51
Q

malaise
dyspnoea
nonproductive cough
pleuritic chest pain
tachypnoea
pulmonary crackles
pleural rub
recent radiation

A

radiation pneumonitis

late stges - contraction and fibrois (atelectasis)

52
Q

collapse and deflation of pulmonary alveoli

A

atelectasis

contraction

53
Q

ARDS is characterised by

A

pulmonary capillary leakage

i.e. caused by e coli –> sepsis –> ALI –> ARDS

sepsis most comon
Sepsis (most common), aspiration pneumonia, burns, trauma, pancreatitis, drowning injuries.

54
Q

best test to use for recurrent pneumonias in same location

A

bronchoscopy
(risk of obstructive pneumonia from i.e. tumour)