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Lung Tumours
Lung Tumours
Lung Tumours
Nodules
( )
Focal Abnormalities
Spiculated Calcified
Scar Nodule
Nodule
Benign SPN
• Infectious: Granulomatous Infections, Fungal Infections, Parasites
• Inflammatory: Rheumatoid Arthritis, Granulomatosis With
Polyangiitis
• Congenital Nodules
• Scars as a Sequela of Previous Infections
• Bronchogenic Cysts
• Arteriovenous Malformation
• Mucus Plugging, Rounded Atelectasis, Pulmonary Infarction
• Fibromas, Hamartomas
Malignant SPN
• Bronchogenic Carcinoma (Both Small Cell And Non-small Cell
Carcinomas)
• Metastatic Cancers
• Carcinoids
• Lymphomas
• Sarcomas
INVESTIGATIONS
• SPN (>8 mm)or high risk patient Positron emission tomography scan
• Tumor markers CEA, FR positive circulating tumor cells, LG3BP, and
C163A
• Biopsies – FNAC, liquid biopsy, or excisional biopsy
• CT-guided transthoracic needle aspiration
• Bronchoscopy
• Radial probe endobronchial ultrasound (RP-EBUS)
• Thin/ultrathin bronchoscopes
• Virtual navigation bronchoscopy (VBN)
• Robotic bronchoscopy
• Electromagnetic navigation bronchoscopy (ENB)
Lung imaging reporting and data system (Lung-RADS)
Classification tool to evaluate findings on a low dose CT scan when
screening for lung cancer
• Category 0 (incomplete)
• Category 1 (negative) less than 1% chance of malignancy
• Category 2 (benign appearance) <1% chance of malignancy
• Category 3 (probably benign) 1% to 2% chance of malignancy
• Category 4A (probably suspicious) 5 to 15% chance of malignancy
4B (suspicious) >15% chance of malignancy.
4X (suspicious) is either category 3 or 4 with other features
suspicious for malignancy
Mayo Clinic Calculator (1997)
• Increased age
• Upper lobe location of the nodule
• Nodule diameter in mm
• Spiculation
• Smoking
• Extra-thoracic cancer >5 years
Brock University calculator (2013)
Also adds
• Emphysema
• Ground-glass opacity
• Subsolid nodule
• Female sex
• Number of nodules
• Family history of lung cancer
• Adenocarcinoma
• - bronchial derived
• - bronchioloalveolar ca
Peripheral
tumors • Large cell carcinoma
2021 WHO Classification system
• Precursor glandular lesions • Salivary gland-type tumors
• Adenocarcinomas • Neuroendocrine tumors
• Adenosquamous carcinomas • Neuroendocrine carcinomas
• Squamous precursor lesions • And other epithelial tumors
• Squamous cell carcinomas
• Large cell carcinomas
• Sarcomatoid carcinomas
• Lung neuroendocrine neoplasms
Classification of bronchogenic
carcinoma
1. Squamous Epithelial
cell 2- Pulmonary
carcinoma blastoma
Fibrous
2. (spindle cell)
3- Melanoma
Adenocarcinoma
5- Others
-Adenocarcinomas is now the most frequent histologic subtype of bronchogenic
carcinoma
-More common in patients under the age of 40, women and non-smokers
-Peripheral adenocarcinomas are sometimes associated with pulmonary scars and
therefore are also referred to as scar carcinomas.
-Tend to metastasize widely at early stage
-They are classically peripheral tumors arising from the peripheral airways and alveoli.
-The hallmark of adenocarcinomas is the tendency to form glands that may or may not
produce mucin.
-Rarely cavitate
-Associated with hypertrophic pulmonary osteoarthropathy “Clubbing of the fingers”
-20% of adenocarcinoma of the lung are associated with mutations of epidermal
growth factor receptor (EGFR) and respond to its anti therapy
Large Cell Carcinoma
• Frequency: 10 %
• strongly associated with smoking
• usually located peripherally.
• This group of carcinomas is undifferentiated.
• They are made up of large and anaplastic cells.
• They may exhibit neuroendocrine or glandular differentiation markers when
studied by immunohistochemistry or electron microscopy.
• Poor prognosis.
Small cell carcinomas
SCLC are a type neuroendocrine tumors arising from neuroendocrine cells + more common in men.
Centrally located perihilar mass with early metastases (Early involvement of the hilar and
mediastinal nodes)
- Chemotherapy responsive
- least likely form to be cured by surgery; usually already metastatic at diagnosis
Able to secrete a host of polypeptide hormones like ACTH, antidiuretic hormone (ADH), calcitonin,
gastrin-releasing peptide and chromogranin.
• Paraneoplastic syndrome
• Chemotherapy
• Immunotherapy
• Radiation
• Primary Management