CT 15 Lung Cancer Flashcards

1
Q

Common driver mutations in non smokers in adenocarcinomas of the lungs

A

EGFR
ALK
RET
ROS1

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2
Q

common driver mutations more common in smokers in adenocarcinomas

A

KRAS
BRAF

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3
Q

mutations common in Squamous cell carcinoma

A
  • Tp53
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4
Q

mutations associated with small cell carcinoma

A
  • TP53
  • RB1
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5
Q

examples of causes of lung cancer

A
  • smoking (90% of cases)
  • carcinogenic metals
  • carcinogenic chemicals like acetaldehyde
  • occupational exposure to radon etc
  • environmental radon accounts for 10% of cases
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6
Q

Symptoms of lung cancer

A
  • SOB
  • persistent cough
  • weight loss
  • chest pain
  • hoarseness
  • haemoptysis
    -paraneoplastic syndromes
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7
Q

classification of lung cancer

A
  • non small cell lung cancer (85%)
    includes adenocarcinoma, Squamous cell and large cell
  • small cell lung cancer (accounts for 10 -15% of cancer cases)
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8
Q

carcinoid syn drome

A

Carcinoid tumors produce hormones like:

Serotonin (causes diarrhea and flushing)

Histamine (contributes to skin reactions)

Bradykinins (cause low blood pressure)

over time causes RHF and valvular disease
- investigated with urinary 5HIAA or blood test chromogranin A

treated with surgery and ocreotide (somatostatin analogue)

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9
Q

histology of the lungs

A
  • pseudostratified columnar epithelium
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10
Q

the progression of squamous cell cancer

A
  • starts off as squamous cell metaplasia (replacement of normal bronchial histology to squamous epithelium triggered by chronic irritation)

next is squamous dysplasia

  • last step is malignancy
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11
Q

what type of lung cancer are non smokers likely to get

A

adenocarcinoma of the lung

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12
Q

what are some complications of lung cancer

A
  • pneumonia, pleural effusion, abscess (caused by tumour obstruction of the airway)
  • hoarseness(indicates invasion of recurrent laryngeal nerve)

-diaphragm paralysis (indicates invasion of phrenic nerve)

  • dysphagia (indicates oesophageal invasion)
  • SVC syndrome (SVC is compressed by tumour)
  • Horner’s syndrome (sympathetic ganglia is invaded by tumour)

-pericarditis, tamponade

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13
Q

how does SVC syndrome present

A
  • positive pemberton’s sign

rising arms above head causes facial congestion, cyanosis, neck swelling and respiratory distress

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14
Q

how does horner’s syndrome present

A

-ptosis (partial, drooping)
- anhidrosis
- miosis (pupil constriction)

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15
Q

how else may a pancoast tumour present

A
  • shoulder pain
  • upper limb neurological signs
  • horner’s syndrome
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16
Q

PNS associated with small CC

A
  • SIADH (ADH secretion)
  • ACTH secretion
  • Lambert eaton syndrome
  • PNS cerebellar degeneration (autoimmune) leads to ataxia
  • encephalomyelitis
17
Q

what is lambert eaton syndrome

A

reduction in Ach release from presynaptic nerve terminals, which arises from autoimmune antibodies targeting VGCCs within the presynaptic neuronal cell membrane. (influx of ca causes release of ACh)

  • muscle weakness
  • dry eyes and mouth
  • constipation
18
Q

which PNS are associated with squamous CC

A
  • PTH secretion: hypercalcaemia
    (bones, groans, stones and psychiatric overtones)
  • Ectopic TSH leading to hyperthyroid
  • hypertrophic pulmonary osteoarthropathy (Swollen joints and pain) + clubbing
19
Q

what is HPOA

A

The tumor secretes growth factors (VEGF, PDGF, and PGE2), leading to:

Increased blood vessel growth (vascular proliferation).

New bone formation in the periosteum (bone lining).

Fibrosis and swelling of connective tissue.

These changes cause pain, clubbing, and joint symptoms.

20
Q

PNS associated with adenocarcinoma of the lung

A
  • HPOA
  • trosseaus sign of malignancy
    Adenocarcinoma increases blood clotting factor production.

Symptoms:

Deep vein thrombosis (DVT) – Leg pain, swelling.

Pulmonary embolism (PE) – Chest pain, difficulty breathing.

Migratory thrombophlebitis – Recurrent blood clots in different locations.

  • gynaecomastia
21
Q

treatment for small CC

A

early stage disease is treated with radical chemo and RT

extensive disease: palliative chemo and RT

22
Q

treatment for NSCC

A

surgery or radical RT

tyrosine kinase inhibitors like erlotinib or gefitinb for EGFR mutations

ALK inhibitors like crizotinib

PDL1 inhibitors atexolizumab

PD1 inhibitors permbrolizumab

23
Q

Mesothelioma is associated with what

A

asbestos exposure

no current cure

24
Q

what are the central cancers

A

squamous and small cell

25
Investigations for lung cancer
- FBC - CXR - contrast enhanced CT - PET scan biopsies: - Bronchoscopy - sputum cytology - thoracentesis - endobronchial ultrasound
26
what diagnostic tests are used for mesothelioma
- CXR for pleural effusions, plaques - contrast CT (masses) - PET for staging - thoracentesis + Cytology - gold standard = pleural biopsy via CT guided core needle biopsy
27
Pleural effusions: how to decide between transudate or exudate
⚖️ The Core Difference: Transudate Exudate Cause Due to systemic factors (↑ hydrostatic pressure or ↓ oncotic pressure) Due to local factor (inflammation, infection, malignancy) Protein content: Low High LDH level: Low High Appearance: Clear, watery Cloudy, thick, sometimes bloody
28
Pleural effusion: transudate causes
due to systemic causes: Congestive heart failure (most common) Cirrhosis (hepatic hydrothorax) Nephrotic syndrome Hypoalbuminemia
29
Pleural effusion : exudate causes
(local inflammation/damage) Pneumonia (parapneumonic effusion) Tuberculosis Pulmonary embolism Malignancy (e.g., lung cancer, mesothelioma) Autoimmune diseases (e.g., lupus, rheumatoid arthritis)