Interstitial Lung Disease Flashcards

1
Q

Interstitial Lung Disease

A

Umbrella term for a number of conditions which cause scarring and inflammation of alveolar wall

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2
Q

ILD examples

A

Idiopathic Pulmonary Fibrosis
Drug Induced Pulmonary Fibrosis

Sarcoidosis

Extrinsic Allergic Alveolitis (EAA)

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3
Q

Connective Tissue Diseases

A

SLE and RA patients can develop ILD

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4
Q

Acute Presentation of Sarcoidosis (= Lofgren’s Syndrome)

A

Triad:

  1. Fever
  2. Arthralgia
  3. Erythema Nodosum
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5
Q

Lofgren’s Syndrome management

A

CXR - bilateral hilar lymphadenopathy

Should settle with NSAIDs
Repeat CXR in 3 months

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6
Q

Erythema Nodosum

A

Rash on ankles and around legs

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7
Q

Sarcoidosis bloods

A

Hypercalcaemia
Raised ACE
Raised ESR

Sarcoidosis = non-caseating granulomas.

Macrophages increase conversion of Vitamin D to active form.

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8
Q

Acute Sarcoidosis (Lofgren’s) common among

A

More common in:

Women
Afro Caribbean, Irish, Scandinavian

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9
Q

Sarcoidosis CXR

A

A chest x-ray may show the following changes:

Stage 0 = normal

Stage 1 = bilateral hilar lymphadenopathy (BHL)

Stage 2 = BHL + interstitial infiltrates

Stage 3 = diffuse interstitial infiltrates only

Stage 4 = diffuse fibrosis

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10
Q

Sarcoidosis Spirometry

A

Shows restrictive pattern

FEV1:FVC preserved

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11
Q

Sarcoidosis CT

A

Shows fissural nodularities

TB shows miliary nodules

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12
Q

Insidious Sarcoidosis Presentation

A

Difficult breathing
Dry Cough
Weight loss
Malaise

Differentials - TB, Lymphoma

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13
Q

Other Sarcoidosis presentations

A
Lungs 
Eyes (Uveitis Iritis) 
Erythema Nodosum 
Hepatomegaly 
VT
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14
Q

Sarcoidosis Steroids Indications

A

CXR Stage 2 or 3 Disease with symptoms

Hypercalcaemia

Eye, heart, lung involvement

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15
Q

Upper Zone Pulmonary Fibrosis - CHARTS

A

Coal Worker’s Pneumoconiosis

Hypersensitivity Pneumoconiosis (aka EAA)

Ankylosing Spondylitis

Radiation

TB

Sarcoidosis/Silicosis

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16
Q

Lower Zone Pulmonary Fibrosis

A

Lower Zone - DIAL

Drugs (Amiodarone)

Idiopathic

Asbestosis

Lupus

17
Q

Idiopathic Pulmonary Fibrosis - features

A

SOB
Dry cough

Clubbing
Fine crackles
Hypoxia

18
Q

Idiopathic Pulmonary Fibrosis - presentation

A

Common in:

Men
60-70 years old
Median survival is 3 years

19
Q

Idiopathic Pulmonary Fibrosis - initial treatment on admission

A

Oxygen alone!!

20
Q

Drug which slows disease progression of idiopathic pulmonary fibrosis

A

Pirfenidone

21
Q

Idiopathic pulmonary fibrosis - CT scan

A

Honeycombing