Interstitial Lung Disease Flashcards

1
Q

What are diffuse parenchymal lung diseases?

A

DPLD is a heterogenous group of clinical entities that share the following features :
1. Dyspnoea
2. Hypoxia
3. Restrictive ventilatory defect
4. Presence of bilateral infiltrates on CXR
Note: affects the interstitium, alveolar space and sometimes the airways

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2
Q

Known causes of DPLD?

A
  1. infections
  2. occupational/environmental
  3. drugs
  4. neoplasia
  5. systemic disease
  6. radiation
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3
Q

Infectious causes of DPLD?

A
  1. Viral : Measles, HSV, VZV
  2. Bacterial : Mycoplasma, Legionella
  3. Miliary TB
  4. Fungal : Aspergillosis, PCP, Histoplasmosis
  5. Parasites : Toxo, Schistosomiasis
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4
Q

Occupational/environmental causes of DPLD?

A
  1. Inorganic dusts : Silica, Asbestos, Carbon
  2. Organic dusts : Pigeon, Budgie  HP/EAA
  3. Fumes : SO2, CL2, NO2
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5
Q

Drug causes of DPLD?

A
  1. Antibiotics : Sulphas, Nitrofurantoin
  2. Cytotoxics : Bleomycin, MTX
  3. Amiodarone, phenytion, gold
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6
Q

Neoplasia causes of DPLD?

A

1˚ - broncho alveolar carcinoma
2˚ - lymphangitis carcinomatosa

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7
Q

Systemic disease causes of DPLD?

A
  1. Cardiac : LVF, MS
  2. Renal : Uraemia and fluid overload
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8
Q

Idiopathic interstitial pneumonias?

A
  1. idiopathic pulmonary fibrosis
  2. desquamative interstitial pneumonia
  3. acute interstitial pneumonia
  4. non-specific interstitial pneumonia
  5. respiratory bronchiolitis interstitial lung disease
  6. cryptogenic organizing pneumonia
  7. lymphocytic interstitial pneumonia
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9
Q

Causes of Granulomatous DPLD?

A
  1. Sarcoidosis
  2. Berryliosis
  3. Lymphoma
  4. EAA
  5. TB
  6. Fungal infection
  7. Histiocytosis X
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10
Q

Causes of other forms of DPLD?

A
  1. Pulmonary Eiosinophilia(AEP, CEP)
  2. Collagen Vas Diseases (Scl, SLE, RA)
  3. Idiopathic Pulmonary Haemosiderosis
  4. Vasculitides : WG, Churg-Strauss
  5. Goodpasture’s syndrome
  6. Histiocytosis X / Langerhans cell granulomatosis / EG
  7. Lymphangioleiomyomatosis(LAM)
  8. Congenital : Neurofibromatosis, Tuberous sclerosis
  9. Amyloidosis
  10. Ankylosing spondylitis
  11. Liver disease
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11
Q

Approach to DPLD?

A
  1. Thorough History
  2. Thorough Physical Examination
  3. Lung Function Test
  4. CXR
  5. Bloods, Sputum, Urine, ECG, Echo
  6. HRCT
  7. Bronchoscopy (BAL/Transbronchial biopsy)
  8. OLB / VATS
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12
Q

History taking in DPLD?

A

Detailed medical, occupational ,hobby, drug & family histories

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13
Q

Symptoms of DPLD?

A

SOB and cough (dry in most cases)

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14
Q

Social history?

A

Rural background + indoor fossil fuel cooking in unventilated hut and maize-grinding > “Hut Lung”

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15
Q

Environmental/occupational history?

A
  1. Exposure to inorganic dusts > pneumoconioses
  2. Exposure to organic dusts(eg. birds) > EAA
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16
Q

Intoxication history and what it could mean?

A

Smoking
> EG, Goodpasture, Resp bronchiolitis, Alveolar proteinosis, Amiodarone induced DPLD

17
Q

Acute presentation of DPLD?

A