Intersticium, Pleura and Chest disease Flashcards

1
Q

What is the interstitial space

A

Potential space between alveolar cells and capillary basement membrane

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2
Q

Functions of the interstitial space

A

Structural support
Immune function
Controls alveolar growth

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3
Q

What structural changes occur in the lungs in interstitial disease

A

Intersticium becomes apparent as it contains collagen, cells and fluid
Also affects acini, alveoli lumen, bronchioles, epithelia, endothelia, mesenchyme and macrophages
Inflammatory cells are recruited

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4
Q

How does interstitial disease affect lung function

A

Fibrosis decreases lung compliance, decreases perfusion and increases diffusion distance
It is a restrictive airflow disorder that causes type 2 respiratory failure

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5
Q

Symptoms and signs of interstitial disease

A

Symptoms: chronic dyspnoea, chronic cough
Signs: tachypnoea, tachycardia, bilateral reduce chest expansion, cyanosis, signs of right sided heart failure and clubbing in idiopathic pulmonary fibrosis

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6
Q

Broad causes of interstitial lung disease

A
Occupational
Treatment related
Connective tissue disorders
Immunological
Idiopathic
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7
Q

What are the occupational causes of interstitial lung disease

A

Asbestos
Silicosis
Coal workers pneumoconiosis

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8
Q

What can asbestos cause and what look like on a CXR

A

Mesothelioma
Bronchogenic cancers
Asbestosis
On a CXR - asbestos plaques (benign irregular mass of calcified asbestos)

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9
Q

What drugs can cause interstitial lung disease and what do each treat

A
Methotrexate - RA
Bleomycin - lymphoma
Amiadarone - arrhythmias 
Nitrofurantoin - UTIs 
Chemotherapy and radiation - cancer
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10
Q

What connective tissue disorders can cause interstitial lung disease

A
RA
Scleroderma 
Sjogren's syndrome  
Polymyositis 
Systemic lupus erythrematosis
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11
Q

What immunological disorders can cause interstitial lung disease

A

Sarcoidosis

Extrinsic allergic alveolitis

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12
Q

What is sarcoidosis

A

Non caseating granulomas, usually in the lungs

Alveoli contain macrophages and lymphocytes

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13
Q

What demographics does sarcoidosis occur in

A

Female

Afro-Caribbean and Asians

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14
Q

How do you confirm sarcoidosis

A

Biopsy lymph nodes to distinguish sarcoidosis (non caseating) and TB (caseating)

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15
Q

Treatment for sarcoidosis

A

No treatment

Steroids

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16
Q

What are the types of extrinsic allergic alveolitis

A

Acute - farmer’s lung

Chronic - bird fancier’s lung

17
Q

Cause and symptoms of farmer’s lung

A

Inhalation of actinomycetes in mouldy hay

Symptoms - dry cough, breathlessness on exertion, wheeze, inspiratory crackles

18
Q

Cause and symptoms of bird fancier’s lung

A

Long term pigeon exposure

Symptoms - extreme malaise, dry cough, chronic breathlessness, inspiratory crackles

19
Q

Describe idiopathic pulmonary fibrosis

A

Increased activation of alveolar macrophages which attracts neutrophils and eosinophils, leading to tissue damage (release of ROS and hydrolytic enzymes)
Fibrosis occurs to repair damage

20
Q

Symptoms and prognosis of idiopathic pulmonary fibrosis

A

Progressive SOB
Cough
Clubbing
Poor prognosis - 3 years

21
Q

Treatment of idiopathic pulmonary fibrosis

A

High dose oral steroids

Antifibrotics

22
Q

CXR appearance in idiopathic pulmonary fibrosis

A

Small lungs
Micro nodular shadowing in lower lobes
Ragged heart borders

23
Q

CXR appearance in acute extrinsic allergic alveolitis

A

Diffuse micro nodular infiltrate (denser towards hila)

24
Q

CXR appearance in chronic extrinsic allergic alveolitis

A

Almost normal but progresses to fibrosis

25
Q

CXR appearance in sarcoidosis

A

Miliary and nodular shadowing

Diffuse fibrosis

26
Q

What signs and symptoms suggest pleural disease

A

Pleuritic chest pain
Referred shoulder pain (diaphragmatic pleural irritation)
Pleural rub - creaking noise on auscultation with Resp movements
Pain worse when coughing, sneezing or laughing

27
Q

How is pleural fluid produced and reabsorbed and how much per day

A

Starling forces at parietal pleura
Absorbed by lymphatics of the parietal pleura
15ml turnover

28
Q

What can cause increased pleural fluid

A

Increased production - increased interstitial fluid volume, high hydrostatic pressure, increased permeability, low oncotic pressure

Decreased absorption - lymphatic blockage, high systemic venous pressure

29
Q

Causes of haemothorax, chylothorax and empyema

A

Haemothorax - trauma or iatrogenic
Chylothorax - lymphoma or iatrogenic
Empyema - infection complication (higher risk if immunocompromised or alcoholic)

30
Q

Features of empyema on CT

A

Loculations - scar tissue dividing chest into smaller cavities

31
Q

Treatment for empyema

A

Antibiotics

Drainage

32
Q

Describe malignancies of the pleura

A

Mesothelioma - malignant cancer due to asbestos exposure (almost always pleuritic pain)
Metastasis - most commonly from lung or breast

33
Q

What are some congenital chest wall abnormalities

A

Kyphosis
Scoliosis
Muscular dystrophy
Pectus excavatum

34
Q

What are some acquired chest wall abnormalities

A
Trauma
Ankylosing spondylitis 
Motor neurone disease
Polio
Iatrogenic
35
Q

Why does chest muscle weakness increase susceptibility to infection

A

Poor clearance of secretions because of reduced ventilation