Interstitial lung diseases Flashcards

1
Q

What is the definition of ILD

A

Inflammatory process involving alveolar wall leading to irreversible fibrosis, distortion of lung architecture, and impaired gas exchange

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2
Q

What are the six general categories of interstitial lung disease

A
  1. ) Environmental lung disease
  2. ) ILD with granulomas
  3. ) Alveolar filling disease
  4. ) Hypersensitivity lung disease
  5. ) Drug induced - amiodarone, nitrofurantoin, bleomycin, phenytoin
  6. ) Miscellaneous
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3
Q

What are the causes of environmental lung disease

A
  1. ) Coal worker’s pneumoconiosis
  2. ) Silicosis
  3. ) Beryillosis
  4. ) Asbesosis
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4
Q

What are causes of ILD associated with granulomas

A
  1. ) Sarcoidosis
  2. ) Histiocytosis X
  3. ) Wegener’s granulomatosis
  4. ) Churg-Strauss syndrome
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5
Q

What are causes of ILD associated with alveolar filling disease

A
  1. ) Goodpasture syndrome
  2. ) Idiopathic pulmonary hemosiderosis
  3. ) Alveolar proteinosis
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6
Q

What are the two causes of hypersensitivity lung disease

A
  1. ) Hypersensitivity pneumonitis

2. ) Eosinophilic pneumonitis

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7
Q

What are other miscellaneous causes of ILD

A
  1. ) Idiopathic pulmonary fibrosis
  2. ) Bronchiolitis obliterans organizing pneumonia (BOOP)
  3. ) Connective tissue diseases: Rheumatoid arthritis, scleroderma, SLE, mixed connective tissue disease
  4. ) ARDS
  5. ) Radiation pneumonitis
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8
Q

What are symptoms and signs of ILD

A

Symptoms

  1. ) Dyspnea
  2. ) Cough that is nonproductive
  3. ) Fatigue

Signs

  1. ) Rales at the bases
  2. ) Digital clubbing: Increased convexity of the nail due to increase in soft tissue
  3. ) Pulmonary HTN and cyanosis in advanced disease
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9
Q

What is a honeycomb lung

A

Scarred shrunken lung as an end stage finding with poor prognosis with dilated air spaces, fibrous scars in interstitum

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10
Q

What is the only definitive way to find out if someone has ILD

A

Clinical findings and imaging studies are non-specific, tissue biopsy is the only way

Fiberoptic bronchoscopy with transbronchial biopsy: Limited amount of tissue obtained

  1. ) open lung biopsy
  2. ) video assisted thoracoscopic lung biopsy
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11
Q

What do you see on a CXR of interstitial lung diseases

A

Reticular, reticulonodular, ground glass, and honeycombing - remember these

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12
Q

What do you see on the PFT’s of someone with ILD

A

Restrictive pattern with low diffusing capacity

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13
Q

What is the definitive diagnosis for ILD

A
  1. ) Fiberoptic bronchoscopy with transbronchial biopsy - limited because can’t get big enough tissue sample
  2. ) Open lung biopsy
  3. ) Video assisted thoracoscopic lung biopsy

Urinalysis also assists with diagnosis such as with goodpasture’s syndrome and Wegener’s granulomatosis

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14
Q

What are the interstitial diseases associated with granulomas

A
  1. ) Sarcoidosis
  2. ) Histiocytosis X
  3. ) Wegener’s
  4. ) Churg Strauss syndrome
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15
Q

Sarcoidosis is a noncaseating granulomatous disease that has granulomas in almost every system. What are the constitutional, lung, skin, and eye symptoms

A
  1. ) Constitutional: Malaise, fever, anorexia, weight loss
  2. ) Lungs: Dry cough, dyspnea with exercise
  3. ) Skin: Erythema nodosum
  4. ) Anterior uveitis: 75%, posterior 25%
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16
Q

Sarcoidosis is a noncaseating granulomatous disease that has granulomas in almost every system. What are the heart, MSK, and nervous system findings

A
  1. ) Heart - arrhythmias
  2. ) MSK: Arthralgias and arthritis
  3. ) Nervous system: Bells palsy, peripheral neuropathy
17
Q

How do you diagnose sarcoidosis

A

Based on clinical, radiographic, and histological findings

  1. ) CXR: Bilateral hilar adenopathy
  2. ) ACE elevation - only 50-80% of patients
  3. ) Hypercalciuria and hypercalcemia
  4. ) PFTS

Definitive: Biopsy

18
Q

What are the stages of sarcoidosis

A

Stage 1: Bilateral hilar adenopathy without parenchymal infiltrates
Stage 2: Both
Stage 3: Parenchymal infiltrates without bilateral hilar adenopathy
Stage 4: Pulmonary fibrosis

19
Q

What are the treatment choices for sarcoidosis

A

Most cases resolve spontaneously within 2 years without treatment

First line: Systemicc steroids
Second line: Methotrexate

20
Q

What is histiocytosis

A

Abnormal proliferation of histiocytes in the lung (related to langerhan ells of the skin) - 90% are cigarette smokers

Can present with pneumothorax, lytic bone lesions, and diabetes insipidus

21
Q

What is Wegener’s disease

A

Necrotizing granulomatous vasculitis affecting vessels of lungs, kidneys, upper airways

They easily get upper and lower respiratory infections, glomerulonephritis, and pulmonary nodules

Associated with c-anca

22
Q

What is churg strauss syndrome

A

Another granulomatous vasculitis like Wegener’s but now seen in patients with asthma

These people have pulmonary infiltrates, rash, and eosinophilia (eosinophilia especially in the blood)

Associated with p-anca

23
Q

What are the four environmental pneumoconioses

A
  1. ) Coal worker’s
  2. ) Asbestosis
  3. ) Silicosis
  4. ) Berylliosis
24
Q

What is the pathophysiology of pneumoconioses

A

Accumulation of non-organic dust in the lungs and the tissue reacting to it

25
Q

What are some clinical pearls of asbestosis

A

Predilection for lower lobes with increased risk of bronchogenic carcinoma and malignant mesothelioma

CXR shows hazy infiltrates with bilateral linear opacities

No treatment

26
Q

What are some clinical pearls of silicosis

A

Localized and nodular peribronchial fibrosis that occurs more in upper lobes (asbestosis is widespread and in lower lobes)

Happens in mining, stone cutting, and glass manufacturing

Increased risk of TB

27
Q

What are some clinical pearls of berylliosis

A

Acute form: Diffuse pneumonitis
Chronic form: Like sarcoidosis with hypercalcemia too

Test: Beryllium lymphocyte proliferation test