Lung Cancer Flashcards

1
Q

Types of Lung Cancers

A

Small Cell Lung Cancer
Non-small Cell Lung Cancer

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2
Q

Define small cell lung cancer

A
  • aggressive malignant epithelial cell tumour primarily in older smokers.
  • neuroendocrine carcinoma as the cells contain neurosecretory granules that release neuroendocrine hormones
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3
Q

Pathophysiology of small-cell lung cancer

A

accumulation of driver mutations causing benign progenitor cells to transform into neoplastic cells.
can cause paraneoplastic syndrome because the cells release neuroendocrine hormones
- i.e. if releasing ADH, can cause hyponatraemia.

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4
Q

where do SCLC typically arise from?

A

in central lung with mediastinal involvement, typically disseminated at time of diagnosis due to early metastasis

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5
Q

what percentage of Lung Cancers are SCLC?

A

15-20%

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6
Q

symptoms of lung cancer

A

cough
chest pain
haemoptysis
dyspnoea
weight loss
hoarseness
back pain

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7
Q

signs of lung cancer

A

lymphadenopathy
stridor, wheeze = obstruction
fever
clubbing
signs of pleural effusion
hypertrophic pulmonary osteoarthropathy
phrenic palsy -> hemidiaphragm paradoxical rise on sniffing

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8
Q

What is hypertrophic pulmonary osteoarthropathy?

A

refers to a fibrovascular proliferation that results in periostitis of the long bones, arthralgia and clubbing. It is almost always secondary to another condition and there are many causes aside from lung cancer.

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9
Q

Complications of SCLC (3)

A

paraneoplastic syndrome
obstruction and mucus -> giving wheeze
invasion and compression of mediastinal structures i.e., SVC obstruction; phrenic n. invasion; dysphagia; vertebral body erosion; pleural and pericardial effusions.

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10
Q

differentials for SCLC

A

non-small cell lung cancer
pneumonia/bronchitis
carcinoid tumour

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11
Q

Investigations for SCLC

A

first line: CXR
- central/peripheral mass
- lymphadenopathy in hilum or superior mediastinum
- pleural effusion
- broadening of mediastinum
- enlarged heart shadow

CT chest, liver, adrenal glands (mets)

CT for presence of lesion, staging, background changes (COPD)

Bronchoscopy

Biopsy

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12
Q

Management for SCLC

A

Chemotherapy

Radiotherapy

Immunotherapy

Radio-chemotherapy in limited stage disease

Responds well initially but relapses
Active treatment achieves around 6 month increase in overall survival time

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13
Q

Types of NSCLC

A

adenocarcinomas (most common - 40%)
squamous cell carcinomas (20%)
large cell carcinomas

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14
Q

features of lung adenocarcinoma

A
  • preceded by atypical adenomatous hyperplasia
  • commonly in peripheries
  • smaller than other types
  • EGFR mutations, increased frequency in non-smokers, suitable for TRK inhibitors
  • KRAS mutations
  • Gynaecomastia
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15
Q

features of lung squamous cell carcinoma

A
  • preceded by squamous metaplasia, dysplasia, SCC in situ
  • PTHrP -> hypercalcaemia
  • increasingly seen in periphery -> can cause cavitation (differential for TB, lung abscess): exophytic ulcerates, bleeds -> early presentation
    endophytic infiltrates airways -> presents late
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16
Q

what is bronchial carcinoids

A

5% of lung cancers
unrelated to smoking
in young adults
excellent prognosis

17
Q

Lung cancer on CXR

A

unilateral hilar enlargement
peripheral pulmonary opacities
lung, lobe, or segmental collapse
pleural effusion
broadening of mediastinum, enlarged cardiac shadow, elevation of hemidiaphragm
rib destruction

18
Q

targeted treatments for lung cancer

A

program death ligand 1 (PD-L1) inhibitor
tyrosine kinase inhibitors if EGFR mutated
cryzotininb for ALK and ROS translocations tumours