ILD Oct11 M2 Flashcards

(44 cards)

1
Q

Idiopathic interstitial pneumonias, some diseases

A
  • Usual interstitial P
  • Nonspecific interstitial P
  • Acute interstitial P
  • Cryptogenic organizing P
  • Desquamative interstitial P
  • Lymphocytic interstitial P
  • Respiratory bronchiolotis interstitial lung disease (RBILD)
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2
Q

Why idiopathic interstitial pneumonias is a bad name (2)

A
  • We know RBILD for ex is caused by cigarette smoking

- COP is in alveolar airspace and lumen or resp bronchioles

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3
Q

Clinical counterpart of usual interstitial pneumonia (UIP)

A

idiopathic pulmonary fibrosis (IPF)

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4
Q

pathological counterpart of nonspecific interstitial pneumonia (NSIP)

A

NSIP

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5
Q

pathological counterpart of acute interstitial pneumonia (AIP)

A

diffuse alveolar damage

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6
Q

pathological counterpart of cryptogenic organizing pneumonia (COP)

A

organizing pneumonia

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7
Q

idiopathic pulmonary fibrosis (IPF) examples of symptoms

A

dyspnea, non productive cough, clubbing of fingers and toes

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8
Q

IPF CT findings

A

thickened linear lines, prominent along pleura. Holes in the lines

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9
Q

UIP macroscopic findings

A

honeycombing (wasp nest like spaces)

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10
Q

UIP location

A

peripheral, subpleural

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11
Q

what interstitium affected by UIP

A

parenchymal interstitium

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12
Q

Most important pathologic feature of fibrosis

A

something activates fibroblasts to produce collagen

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13
Q

UIP distribution and inflammation extent

A
patchy distribution (intra and interlobular severity)
Mild interstitial inflammation
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14
Q

UIP progression of fibrosis and structural changes

A
biphasic fibrosis (on and off)
Architectural remodelling (honeycombing)
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15
Q

how pleura and interlobular septa are affected in UIP

A

stay normal bc doesn’t affect non parenchymal IS

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16
Q

UIP what happens to alveolar wall and airspaces as it becomes more severe

A

alveolar septum IS thickened by lymphocytes and collagen.

airspaces contain macrophages

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17
Q

two phases of idiopathic pulmonary fibrosis (IPF) and which was easier to treat

A

Alveolitis (interstitial pneumonitis)
Fibrosis
Alveolitis easier to treat

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18
Q

IPF prognosis

A

mean survival from onset is 5 years. few respond to steroids

19
Q

ILDs: how affect

compliance

20
Q

ILDs: how affect

elasticity and elastic recoil (elastance)

21
Q

ILDs: how affect TLC, RV, VC

A

TLC decreased
RV same or little decreased
VC decreased

22
Q

ILDs: how affect diffusion capacity

23
Q

ILDs: how affect large airway caliber

A

unchanged or increased a little (scarring pulls them open in advanced disease)

24
Q

name for slight increase of large airway caliber in advanced ILD

A

bronchiectasis

25
ILDs: how affect small airway caliber
decreased
26
respiratory pattern of ILD (UIP included)
rapid and shallow breathing
27
auscultation findings in ILDs (UIP included)
crepitations
28
advanced ILD particular finding
cyanosis
29
acute interstitial pneumonia (AIP) examples of symptoms
fever, fatigue, muscle aches, headaches, dyspnea,
30
medical word for muscles aches
myalgia
31
AIP (diffuse alveolar damage) macroscopic appearance
diffuse small holes in the lung
32
Reason for small holes in the lung in AIP
branching bronchioles are empty and alveolar airspaces are filled with material and are consolidated. Same principle as air bronchogram
33
High magnif: what we see in AIP (2) + name of phenomenon
alveolar septum contains neutrophils (shows IS pneumonitis) | pink eosinophilic material (fluid and protein and dead cells)
34
UIP vs diffuse alveolar damage of AIP
UIP: lymphocytes and slow fibrosis AIP: toxic injury to endothelium and alveoli. leak of protein in airspace
35
name of what we see on airway lining in AIP + name for the IS inflam _ protein leak in alveolar airspace
Hyaline membrane | Diffuse alveolar damage
36
Cryptogenic organizing pneumonia (COP) examples of symptoms
productive cough, yellow sputum, low grade fever
37
COP CXR findings + name for that
fluffy disease, airspace pattern. : Patchy airspace disease
38
COP CT findings
fluffy disease, airspace pattern + AIR BRONCHOGRAM
39
Organizing pneumonia: distribution and inflammation how and where
Patchy and varies within and between lobes | Mild IS inflammation
40
Organizing pneumonia: where fibrosis happens (where fibroblasts are)
fibroblastic tissue in resp bronchioles, alveolar duct lumens and airspaces
41
Why COP classified in IS pneumonitises if shows consolidation on CT
Bc often see interstitial pneumonitis with the disease (mild-moderate IS inflammation)
42
Fibroblastic tissue similarity and difference in UIP vs COP
same fibroblastic tissue in both but is in alveolar airspace in COP
43
how alveolar septa appear in COP on microscopy
thickened with lymphocytes: IS pneumonitis
44
diffuse alveolar damage: what + seen in what disease
hyaline membrane lines airways, IS inflammation, alveolar airspace filled with protein and fluid