Respiratory JC013: Abnormal Lung Shadow On Chest Radiograph: CXR, CT Flashcards

1
Q

Focal lung lesions

A
  1. Solitary pulmonary nodule (SPN: <3 cm) / mass (>3 cm)
    - Benign / Malignant
    - DDx: Lung cancer etc.
  2. Lung cancer
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2
Q

How to investigate SPN

A

**Previous CXR (2 years)?
1. Yes
—> Been there before (2 years) + No growth —> Benign
—> Interval growth —> Suscipious —> **
CT scan

  1. No
    —> **Bronchoscopy + Sputum analysis / **CT scan
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3
Q

CT thorax

A

Aim:

  1. Characterise lesion (benign / malignant)
  2. Solitary / Multiplicity
  3. ***Staging in malignant lesion

CT measures **density / **attenuation value of structures

***Hounsfield units (HU)
- Air: -1000 (i.e. very dark)
- Water: 0 (grey shade)
- Fat: -20
- Soft tissue: 30-50
- Calcification: >150
—> Compare the HU of the lesion to these standards —> Determine nature of lesion (E.g. Hamartoma: Fat containing nodule)

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4
Q

***Nodule characteristics

A
  1. Shape
    - Round / Lobulated
  2. Margins
    - Smooth / ***Spiculated (尖刺growing from mass, malignant, ∵ irregular + rapid growth)
  3. Calcification
    - Uniform, Central
    - Speckled (一點點), ***Eccentric (係埋一邊, non-homogenous, malignant)
    - Dense, homogenous
  4. Fat
  5. Cavitation
    - mostly contain air (others: fluid, fungus)
    - history and clinical presentation are important to narrow DDx
    - Abscess: pyrexia, cough, drug abuse history
    - Infarction (e.g. PE): haemoptysis, pleuritic chest pain, SOB
    - Tumour: weight loss, haemoptysis
  6. Air bronchograms
    - phenomenon of air-filled bronchi (dark) being made visible by the opacification of surrounding alveoli (i.e. consolidated lung, grey/white)
    - alveoli can be filled with **fluid, **pus, ***tumours
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5
Q

Contrast CT

A
  • 2.5-5 mm sections through thorax (can best achieve 0.625mm)
  • ***Volumetric (spiral) scans with IV contrast
    —> overlapping of tissue
    —> whole volume of tissue acquired (i.e. no gap)
    —> will not miss small things in between slices

Use:
- Enhance characteristics of nodules

Anxillary findings:

  • Other nodules
  • LN
  • etc.
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6
Q

***CT of nodule

A
Enhancement
—> ***>25 HU (↑ density ∵ vascularity of tumour, take up contrast) —> Malignant
—> ***15-25 HU —> Indeterminate
—> <15 HU —> Benign
—> No enhancement —> Benign
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7
Q

Features of Benign nodule

A
  1. Well circumscribed
  2. Central + Uniform calcifications
  3. Fat-containing
  4. ***Minimal / No enhancement

DDx:

  1. ***Granulomata (∵ TB)
    - small
  2. ***Inflammatory / Infectious lesions —> go away with treatment
  3. AV malformations, Pulmonary sequestration
  4. ***Harmatoma (fat)
  5. Adenoma

(***: common)

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8
Q

Features of Malignant nodules

A
  1. Ill-defined, ***spiculated margins
  2. ***Eccentric calcification
  3. ***Pleural retraction (nodules pulling on pleura causing fibrotic changes)
  4. Enhancement (esp. ***heterogenous enhancement)
  5. Heterogeneous
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9
Q

Management of Indeterminate nodules

A
  1. Close follow-up with CXR / CT (3-6 months) (most)
  2. Biopsy (if suspicion index high enough)
    - Percutaneous
    - Transbronchial
    - Surgical
  3. Resection
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10
Q

Investigations of Lung cancer

A
  1. CXR
    - lung mass
    - mediastinal widening

Further evaluation

  1. Contrast CT scan
    - staging +/- biopsy (percutaneous)
  2. **Bronchoscopy
    - **
    biopsy + ***BAL
  3. ***Post-bronchoscopy sputum analysis
    - higher yield than pre-bronchoscopy
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11
Q

Staging of Lung cancer

A

TNM staging (Universally accepted)

  1. T: primary tumour
  2. N: nodal involvement (malignant LN: round)
  3. M: metastasis
    - Liver
    - Adrenal
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12
Q

***Pancoast tumour

A

Aka Apical tumour

Clinical features:

  1. Invade into **brachial plexus
    - Hard to be assessed by CT —> require **
    MRI (only scenario when MRI is used for lung cancer)
  2. ***Horner’s syndrome
  3. ***SVC syndrome
  4. **Thoracic outlet syndrome
    - compression at the superior thoracic outlet involving compression of a neurovascular bundle passing between the anterior scalene and middle scalene. It can affect the **
    brachial plexus (nerves that pass into the arms from the neck), and/or ***subclavian artery or rarely the vein which does not normally pass through the scalene hiatus (blood vessels as they pass between the chest and upper extremity)
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13
Q

CT evaluation of Lung cancer

A

Remains ***modality of choice for lung cancer staging

  • Favourable cost
  • Speed of examination
  • Simultaneous evaluation of intrathoracic and ***abdominal organs
  1. Stage disease
    - assess ***operability (inoperable if invaded to mediastinum)
  2. ***Radiation planning
    - anatomic relationship
    - disease extent
    - surrounding tissue thickness
  3. Assess treatment response

Pitfalls of CT:

  1. Mediastinal LN
    - now can only rely on ***size criteria
    - inflammation (i.e. reactive LN) vs metastasis
    - microscopic metastasis
  2. Indeterminate chest wall / mediastinal invasion
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14
Q

Ancillary investigation

A

Flexible bronchoscope
- thin enough for direct visualisation of up to 6th generation bronchi (21 generations before alveoli reached)

  • good for **Proximal lesion (central, close to hilum / main bronchi)
    —> **
    Saline washing and brushing: Microbiology + Cytology
    —> ***Biopsy under direct vision: Histology
  • Peripheral lesion relatively difficult
    —> not visualised directly
    —> **BAL: Microbiology + Cytology
    —> **
    Percutaneous / ***Transbronchial biopsy: Histology
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15
Q

Other staging techniques of Lung cancer

A
  1. ***Mediastinoscopy + Biopsy
    - can assess chest wall / mediastinal invasion
  2. Transesophageal USG + Biopsy
  3. ***Thoracotomy + Nodal sampling
  4. ***PET
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16
Q

MRI of Lung cancer

A

Good for looking at ***soft tissues (esp. in Pancoast tumour)

  1. Similar limitations to CT
    - ***Signal in lung is poor on MRI
  2. Expensive
  3. ***Pancoast / Superior sulcus tumours
  4. Chest wall, ***Brachial plexus
17
Q

PET/CT of Lung cancer

A
  • 18-FDG
  • Make use of glucose metabolism —> ↑ metabolic activity (hot) —> identify Neoplasms
  • False positive: **Inflammatory lesions, **TB

Advantages:

  • Whole body scan —> detect ***occult metastases elsewhere (very sensitive)
  • High sensitivity (90-95%)

Disadvantages:
- ***Lower specificity (false +ve)

18
Q

Diffuse lesions (vs Focal lesions e.g. Nodules)

A

Disease affecting:

  1. Interstitium
  2. Airspace
  3. Small airways

Lesions:

  1. ***Interstitial lung disease
    - Interstitial pulmonary fibrosis
    - Occupational lung disease
  2. Infections
    - Pneumocystis pneumonia (PCP) / Pneumocystis carinii
    - TB
  3. ***Bronchiectasis and Bronchiolitis
  4. ***Emphysema
19
Q

Interstitial lung disease

A
  • ***Reticular shadowing
  • ***Volume loss (Fibrotic lungs)
  • ***Shaggy heart borders
  • Associated with Rheumatoid Arthritis
20
Q

High resolution CT

A
  • Thin 1mm sections at 10mm interval (∵ looking at diffuse lesions, ∴ does not matter to miss small lesions vs Spiral CT)
  • ***No need to give contrast (∵ not looking at focal nodules)
  • ***High spatial resolution algorithm
  • ***Reduce radiation
  • ***Excellent for studying:
    1. Lung parenchyma
    2. Interstitium
    3. Airways

Aim in diffuse lesions:

  1. Characterise disease
  2. Determine ***extent of disease
    - upper / mid / lower
    - central / peripheral
  3. ***Localise site for biopsy
  4. Post-treatment evaluation
21
Q

Pneumocystis pneumonia

A

Ground glass appearance around hilum on HRCT

22
Q

Lymphangioleiomyomatosis

A

Associated with Tuberous sclerosis

  • Cystic changes in lungs
  • ↑ Lung volume
23
Q

Summary

A

Focal:

  • Thin section / Contrast CT
  • MR / PET

Diffuse: HRCT

If Biopsy required:
- Localise lesion with CT +/- Biopsy

Other ancillary investigations
- ***Bronchoscopy
- ***BAL
- ***Sputum analysis
- Mediastinoscopy
- ***Thoracotomy
- Biopsy:
—> Percutaneous
—> Transbronchial
—> Surgical