THORACIC Section 9: Interstitial Lung Disease Flashcards

1
Q

What two main questions should you ask when presented with Interstitial Lung Disease?

A
  1. Acute or chronic?
  2. What is the primary finding?
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2
Q

What is this density that obscures underlying vessels?

A

Consolidation

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3
Q

What is this density that does NOT obscure underlying vessels?

A

Ground Glass opacity

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4
Q

It is the smallest part of the lung that is surrounded by connective tissue.

A

Secondary Pulmonary lobule

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5
Q

What runs in the middle of the secondary pulmonary nodule?

A

Terminal bronchiol and and artery

Airway and Artery

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6
Q

What runs at the periphery of the secondary pulmonary nodule?

A

Veins and Lymphatics

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7
Q

Described the pleural nodule pattern.

A

Random

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8
Q

Described the pleural nodule pattern.

A

Perilymphatic

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9
Q

Described the pleural nodule pattern.

A

Centrilobular

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10
Q

Pleural nodules that Abut the pleura

A

Perilymphatic or Random

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11
Q

Pleural nodules that does not abut the pleura

A

Centrilobular

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12
Q

Nodule vocabulary
Subpleura + peribronchovascular

A

Perilymphatic

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13
Q

Nodule vocabulary:
Not subpleural or peribronchovascular predominant

A

Random

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14
Q

Key Differentials

Perilymphatic nodule pattern

A

Sarcoid (90%)
Lympahgitic Spread of CA
Silicosis

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15
Q

Key Differentials

Random nodule pattern

A

Miliary TB
Metastasis
Fungal

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16
Q

Key Differentials

Centrilobular nodule pattern

A

Infection
RB-ILD (Respiratory Bronchilitis ILD)
Hypersensitivity Pneumonitis

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17
Q

This reticulonodular abnormality outlines the lobules’ characteristic shape and size (About 2 cm).

A

Interlobular Septal Thickening

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18
Q

Symmetric and smooth interlobular septal thickening is usually seen in what condition?

A

Pulmonary edema

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19
Q

Aymmetric and nodule interlobular septal thickening is usually seen in what condition?

A

Lymphangitic spread of neoplasm

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20
Q

Cystic areas of lung destruction in a subpleural location

A

Honeycombing

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21
Q

Hallmark of UIP

A

Honeycombing

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22
Q

What condition mimics honeycombing?

A

Paraseptal emphysema

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23
Q

One row of bubbles of subpleural cystic areas

A

Paraseptal Emphysema

23
Q

2-3 rows of bubbles of subpleural cystic areas

A

Honeycombing

23
Causes of Interstitial Pneumonias
Idiopathic Collagen vascular disease medications inhilation
24
The MOST COMMON Interstitial Lung Disease (ILD)
Unutual Interstitial Pneumonia (UIP)
25
First finding of UIP in X ray
Reticular pattern in the posterior costophrenic angle
26
What is the definite UIP Criteria?
1. Honeycombing (must be present) +/- traction bronchiectasis 2. Reticular abnormalities 3. Subplerual basal predominant distribution 4. Absence of inconsistent features: Upper lobe GG>reticulations Air trapping involving 3 or more lobes
27
Definite UIP pattern = Biopsy?
Doesn't need a biopsy to prove diagnosis.
28
UIP Buzzwords!
Apical to basal gradient Traction bronchiectasis Honeycombing Heterogeneous on Histology
29
Chronic hypersensitivity Pneumonitis (HP) vs IUP Features favoring chronic HP?
Air Trapping involving 3 more lobes Mid-upper lobe predominant fibrosis
30
Pulmonariy fibrosis is a risk factor for?
Lung CA
31
Cancer in fibrotic Lung favors what lobe?
Lower lobes
32
Cancer in fibrotic Lung favors what interface?
Fibrotic cysts and normal lung
33
ILD that is a common pattern in collagen vascular disease, and drug reactions
Nonspecific Interstitial Pneumonia (NSIP)
34
ILD: Homogeneous inflammation or fibrosis
NSIP UIP - heterogeneous
35
Two FLAVORS of NSIP
Cellular or fibrotic
36
NSIP Groundglass alone
Cellular
37
NSIP GG+Reticulation
Cellular or fibrotic
38
NSIP Reticulation + Traction Bronchiectasis
Fibrotic NSIP
39
NSIP Honeycombing
Uncommon and minimal
40
The most common ILD in scleroderma
NSIP
41
ILD Immediate subpleural sparing
NSIP
42
NSIP vs UIP Presence of micronodules
NSIP
43
Apical Centrilobular ground glass nodules
Respiratory Bronchiolitis ILD (RB-ILD)
44
More diffuse GGO, with patchy or subpleural distribution
Desquamative interstitial pneumonia (DIP)
45
ILD showing Localized centrilobular ground glass nodules (due to macrophages filling up the terminal bronchioles).
RB-ILD
46
Thought as an end spectrum of RB-ILD
DIP
47
Filling of alveolar spaces with macrophages
DIP
48
Peripheral lower lobe predominant GG with small cystic spaces
DIP
49
This is a multi-system disease that creates “non-caseating granulomas.”
Sarcoid
50
Classic triad of Bilateral hilar lymph node enlargement Arthtitis Erythema nodosum
Acute Sarcoid
51
bilateral hila and right paratracheal
1-2-3 sign in sarcoid
52
Diagnosis?
NSIP
53
Diagnosis?
UIP