ILD Flashcards

1
Q

Pulmonary acinus (singuler)

A

Functional unit of lung where gas exchange takes place
ducts
sacs
alveoli

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2
Q

definition of lobule (important anatomic unit of lung)

A

lung parenchyma bounded by pleura and interlobular spetae (venules and lymphatics)
5-8 acini per lobule
in the center of a lobule the bronchioles are found associated with arterioles and lymphatics

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3
Q

where are they ?
artery
veins

A

arteries close to bronchioles, in center of lobule

veins are around lobules

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4
Q

The interstitial tissue of the lung provides a supporting framework for the airways, vessels and alveolar airspaces. It can be considered in two interconnecting “compartments”:

A

parenchyml and non parenchymal

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5
Q

parenchymal

A

in the alveolar wall and surrounding small vessels and lymphatics where gas exchange occurs

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6
Q

non parenchymal

A

in the pleura, interlobular septa and surrounding the large vessels and airways (center of lobule). No gas exchange

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7
Q

T or F : ILD patterns a disease specific

A

false

The patterns often overlap and are a mixed. The final diagnosis is a clinico-radiologic and pathological correlation

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8
Q

AIP
what is pathological pattern ?
time course?
zonal predominance ?
Etiology ?

Acute interstitial pneomonitis

A

DAD
acute
everywhere
unknown

Diffuse alveolar damage

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9
Q

IPF
what is pathological pattern ?
time course?
zonal predominance ?
Etiology ?

Idiopathic pulmonary fibrosis

A

UIP
Years to dev
Lower lobes
Unknown

Usual interstitial pneumonitis

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10
Q

Asbestosis
what is pathological pattern ?
time course?
zonal predominance ?
Etiology ?

A

often UIP
Years to dev
lower lobes
exposure to asbestos fibers

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11
Q

CTD associated
what is pathological pattern ?
time course?
zonal predominance ?
Etiology ?

CTD = connective tissue disease

A

NSIP, UIP, or OP
acute to chronic
anywhere, more often lower lobes
associated with CTD

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12
Q

Idiopathic NSIP
what is pathological pattern ?
time course?
zonal predominance ?
Etiology ?

A

NSIP
subacute to chronic
lower lobe
unknown

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13
Q

Sarcoidosis
what is pathological pattern ?
time course?
zonal predominance ?
Etiology ?

A

granulomatous
years to dev
typically upper lobes
unclear

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14
Q

Hypersensitivity pneumonitis
what is pathological pattern ?
time course?
zonal predominance ?
Etiology ?

A

granulomatous
acute to chronic
typically upper lobes
exposure to antigens

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15
Q

COP
what is pathological pattern ?
time course?
zonal predominance ?
Etiology ?

cryptogenic organizing pneumonitis

A

OP
Subacute
Patchy distribution
Unknown

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16
Q

Treatment related (medications, radiation therapy)
what is pathological pattern ?
time course?
zonal predominance ?
Etiology ?

A

mixed patterns
acute to chronic
anywhere
exposure to drugs, chemotherapy, radiation therapy

17
Q

UIP pattern : 2 main features

A
  1. spatial heterogeneity
  2. Temporal heterogeneity
18
Q

NSIP pattern : 2 main features

A
  1. Diffuse (spatial homo)
  2. uniform (temporal homo) inflammation and/or fibrosis
19
Q

sarcoidosis characterized by

A

Non-necrotizing granulomas that follow bronchovascular bundles and lymphatics

20
Q

UIP pattern histo
1. spatial hetero
2. temporal hetero

A

Patchy fibrosis that is found in the subpleural and paraseptal compartments
Unaffected (“spared”) areas (centrilobular)

End-stage remodeling: loss of lung architecture due to dense fibrosis, bronchiolar metaplasia and smooth muscle hyperplasia (microscopic “honeycombing”)
Early-stage remodeling: loose fibroblastic bodies in the interstium

Very little inflammation outside areas of honeycombing
No granulomas, no hyaline membranes

21
Q

asbestosis CT scan
(comment différencier de IPF?)

A

calcified plaque on pleura
en plus du early honeycombing

22
Q

OP pattern
histo

A

Active fibroblastic tissue (fibroblasts and loose connective tissue) inside the alveolar spaces
Usually bronchiolocentric
Inflammatory cells in interstitium

23
Q

DAD pattern
histo

A

edema, epithelial necrosis, hyaline membranes in alveoli

24
Q

NSIP pattern

A
  • Diffuse (pan-lobular), uniform widening of interstitium with usually just focal intra-alveolar component
  • Lung architecture is preserved
25
Q

3 main pattern of NSIP

A

Cellular NSIP: interstium infiltrated by chronic inflammatory cells (lymphocytes and plasma cells)
Fibrotic NSIP: uniform interstitial fibrosis of alveolar walls
Mixed NSIP

26
Q

Granulomatous disease (2)

A

sarcoidosis
hypersensitivity penomonitis

27
Q
A