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BRONCHOGENIC CARCINOMA
DR. SOOKUN RAJEEV. K
(MD)
DEPT OF GENERAL MEDICINE
ANNA MEDICAL COLLEGE
INTRODUCTION
• Malignant proliferation of cells arising from the
bronchial epithelium or mucous glands.
• Although largely preventable, carcinoma of the lung
kills about 8.8 million people each year globally.
• It is the most common cause of cancer death in men
and the second most common cause in women, after
breast cancer.
ETIOLOGY
1. Cigarette smoking –
both active and passive
smoking
• White area shows lung
cancer.
• Blackish area shows
discolouration due to
tobacco smoke
ETIOLOGY
2. Radon gas – Colourless and odourless gas generated by
breakdown of radium which is a radioactive substance.
3. Asbestos – Has a synergistic effect with cigarette smoking in
causing lung cancer. Also causes mesothelioma(different from
lung cancer)
4. Air pollution – Fine particulates and sulphate aerosols.
5. Genetics - ~ 8%. Polymorphism on chromosomes 5, 6 and 15
6. Others – Ionisation radiation, arsenic and inorganic arsenic
compounds, hemalite, vincristine-prednisone-nitrogen
mustard-procarbazine mixture
CLASSIFICATION
1. Squamous (35%)
2. Adenosquamous (30%)
3. Small Cell (20%)
4. Large Cell (15%)
SPREAD
1. Direct
2. Lymphatics
3. Hematogenous
SPREAD
1. Direct
Invades pleura
Invades Chest wall
Invades Intercostal nerves
Invades Brachial plexus
SPREAD
2. Lymphatics
Mediastinal lymph nodes
Compressing:
•Pericardium
•Esophagus
•Superior vena cava
•Trachea
•Phrenic/ left recurrent laryngeal nerve
SPREAD
3. Hematogenous
Liver
Bone
Brain
Adrenal
Skin
TNM CLASSIFICATION
TNM CLASSIFICATION
• Tumour (T)
T1: <3 cm and not involving main bronchus or pleura
T2: >3 cm, or involving main bronchus and visceral pleura
T3: any size, invading chest wall, or within 2 cm of carina
T4: invading mediastinum, great vessels, trachea
• Node (N)
N0: no regional node metastases
N1: ipsilateral hilar node metastases
N2: ipsilateral mediastinal or subcarinal node metastases
N3: contralateral mediastinal or hilar nodes
• Metastases (M)
M0: no distant metastasis
M1: distant metastasis
CLINICAL FEATURES
• These may be due to:
1. Local tumour effects
2. Metastatic tumour effects
3. Paraneoplastic manifestations.
• Many patients have no specific signs.
• In some, the lung cancer may be an incidental finding
on CXR or CT performed for another reason.
CLINICAL FEATURES
• Local Tumour effects
Persistent cough or change in usual cough
Haemoptysis
Chest pain (suggests chest wall or pleural involvement)
Unresolving pneumonia or lobar collapse
Unexplained dyspnoea (due to bronchial narrowing or obstruction)
Wheeze or stridor
Shoulder pain (due to diaphragm involvement)
Pleural effusion (due to direct tumour extension or pleural
metastases)
CLINICAL FEATURES
• Local Tumour effects
Hoarse voice (tumour invasion of the left recurrent laryngeal nerve)
Dysphagia
Raised hemidiaphragm (phrenic nerve paralysis)
SVCO
Horner’s syndrome (miosis, ptosis, enophthalmos, anhydrosis) due
to apical or pancoast’s tumour damaging sympathetic chain
Pancoast’s tumours can also directly invade the rib and brachial
plexus, causing C8–T1 dermatome numbness, shoulder pain, and
weakness of small muscles of the hand.
CLINICAL FEATURES
• Metastatic Tumour effects
Cervical/supraclavicular lymphadenopathy (common, present in
30%, and may be an easy site for diagnostic biopsy)
Palpable liver edge
Bone pain/pathological fracture due to bone metastases
Neurological sequelae 2° to cerebral metastases
Hypercalcaemic effects (due to bony metastases or direct tumour
production of parathyroid hormone (PTH)-related peptide or PTH)
Dysphagia (compression from large mediastinal nodes).
CLINICAL FEATURES
•Paraneoplastic syndromes
• Endocrine syndromes are due to the ectopic production of
hormones or hormonally active peptides.
• Neurological syndromes are due to antibody-mediated CNS
damage.
Cachexia and wasting
Clubbing (up to 29% of patients; any cell type, more common
in squamous and adenocarcinoma)
Hypertrophic pulmonary osteoarthropathy
CLINICAL FEATURES
Gynaecomastia
Ectopic ACTH (Cushing’s syndrome)
Cerebellar syndrome (usually SCLC)
Limbic encephalitis (SCLC, also breast, testicular, other
cancers).
Dermatomyositis/polymyositis
Glomerulonephritis.
CLINICAL FEATURES
INVESTIGATIONS
• In outpatients
1. History and examination, including smoking and occupational histories
2. Spirometry pre-biopsy or surgery
3. CXR (PA and possibly lateral)—location of lesion, pleural involvement, pleural
effusion, rib destruction, intrathoracic metastases, mediastinal
lymphadenopathy. CXR can be normal
4. Blood tests, including sodium, calcium, and LFTs. Check clotting if biopsy
planned
5. Sputum cytology only indicated in patients who are unfit for bronchoscopy
or biopsy
6. Diagnostic pleural tap, if effusion present
7. FNA of enlarged supraclavicular or cervical lymph nodes.
INVESTIGATIONS
• Radiology
1. CT neck, chest, liver, adrenals (contrast-enhanced) to assess tumour site and
size
2. USG of neck or liver may provide information about enlarged lymph nodes or
metastases suitable for biopsy
3. MRI Used to answer specific questions relating to tumour invasion/ borders.
4. Bone scan Indicated if any suggestion of metastatic disease such as bony pain,
pathological fracture, hypercalcaemia, raised ALP,highly suggestive of bony
metastases if multiple areas of increased uptake.
5. CT head Indicated if any neurological evidence of metastatic
6. Positron Emission Tomography (PET) scanning Imaging technique
INVESTIGATIONS
• Radiology (CXR)
INVESTIGATIONS
• Radiology (CXR)
INVESTIGATIONS
• Radiology (CXR)
INVESTIGATIONS
• Radiology (CXR)
INVESTIGATIONS
• Radiology (CXR)
INVESTIGATIONS
• Radiology (CXR)
INVESTIGATIONS
• Radiology (CXR)
INVESTIGATIONS
• Bronchoscopy
INVESTIGATIONS
• Bronchoscopy
INVESTIGATIONS
• Bronchoscopy
INVESTIGATIONS
• Bone Scan
INVESTIGATIONS
• Positron Emission
Tomography (PET)
INVESTIGATIONS
• Positron Emission
Tomography (PET)
MANAGEMENT
1. Surgical resection in patients with ipsilateral
peribronchial or hilar node involvement
2. Radiotherapy
3. Chemotherapy
4. Laser therapy
5. General managment
MANAGEMENT
• Radiotherapy
SVCO
Recurrent hemoptysis
Pain caused by chest wall invasion or skeletal
metastasis
To relieve obstruction of trachea & main bronchi
With chemotherapy,it can prevent brain
metastasis in small cell carcinoma
MANAGEMENT
• Chemotherapy
Small cell carcinoma – Combined treatment with
cytotoxic drugs & radiotherapy
IV Cyclophosphamide
Doxorubicin
Vincristine
Etoposide
IV Cisplatin
MANAGEMENT
•Laser Therapy
Via fiber optic bronchoscopy
Palliative treatment
To destroy tumour tissue occluding major
airways & to allow re aeration of collapsed
lung
MANAGEMENT
•General Management
Pain relief
Good diet
Specific therapy to treat anxiety & depression
Treat Hypercalcemia
Manage malignant pleural effusions.
Bronchogenic Carcinoma by Dr. Sookun Rajeev Kumar

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Bronchogenic Carcinoma by Dr. Sookun Rajeev Kumar

  • 1. BRONCHOGENIC CARCINOMA DR. SOOKUN RAJEEV. K (MD) DEPT OF GENERAL MEDICINE ANNA MEDICAL COLLEGE
  • 2. INTRODUCTION • Malignant proliferation of cells arising from the bronchial epithelium or mucous glands. • Although largely preventable, carcinoma of the lung kills about 8.8 million people each year globally. • It is the most common cause of cancer death in men and the second most common cause in women, after breast cancer.
  • 3. ETIOLOGY 1. Cigarette smoking – both active and passive smoking • White area shows lung cancer. • Blackish area shows discolouration due to tobacco smoke
  • 4. ETIOLOGY 2. Radon gas – Colourless and odourless gas generated by breakdown of radium which is a radioactive substance. 3. Asbestos – Has a synergistic effect with cigarette smoking in causing lung cancer. Also causes mesothelioma(different from lung cancer) 4. Air pollution – Fine particulates and sulphate aerosols. 5. Genetics - ~ 8%. Polymorphism on chromosomes 5, 6 and 15 6. Others – Ionisation radiation, arsenic and inorganic arsenic compounds, hemalite, vincristine-prednisone-nitrogen mustard-procarbazine mixture
  • 5. CLASSIFICATION 1. Squamous (35%) 2. Adenosquamous (30%) 3. Small Cell (20%) 4. Large Cell (15%)
  • 7. SPREAD 1. Direct Invades pleura Invades Chest wall Invades Intercostal nerves Invades Brachial plexus
  • 8. SPREAD 2. Lymphatics Mediastinal lymph nodes Compressing: •Pericardium •Esophagus •Superior vena cava •Trachea •Phrenic/ left recurrent laryngeal nerve
  • 11. TNM CLASSIFICATION • Tumour (T) T1: <3 cm and not involving main bronchus or pleura T2: >3 cm, or involving main bronchus and visceral pleura T3: any size, invading chest wall, or within 2 cm of carina T4: invading mediastinum, great vessels, trachea • Node (N) N0: no regional node metastases N1: ipsilateral hilar node metastases N2: ipsilateral mediastinal or subcarinal node metastases N3: contralateral mediastinal or hilar nodes • Metastases (M) M0: no distant metastasis M1: distant metastasis
  • 12. CLINICAL FEATURES • These may be due to: 1. Local tumour effects 2. Metastatic tumour effects 3. Paraneoplastic manifestations. • Many patients have no specific signs. • In some, the lung cancer may be an incidental finding on CXR or CT performed for another reason.
  • 13. CLINICAL FEATURES • Local Tumour effects Persistent cough or change in usual cough Haemoptysis Chest pain (suggests chest wall or pleural involvement) Unresolving pneumonia or lobar collapse Unexplained dyspnoea (due to bronchial narrowing or obstruction) Wheeze or stridor Shoulder pain (due to diaphragm involvement) Pleural effusion (due to direct tumour extension or pleural metastases)
  • 14. CLINICAL FEATURES • Local Tumour effects Hoarse voice (tumour invasion of the left recurrent laryngeal nerve) Dysphagia Raised hemidiaphragm (phrenic nerve paralysis) SVCO Horner’s syndrome (miosis, ptosis, enophthalmos, anhydrosis) due to apical or pancoast’s tumour damaging sympathetic chain Pancoast’s tumours can also directly invade the rib and brachial plexus, causing C8–T1 dermatome numbness, shoulder pain, and weakness of small muscles of the hand.
  • 15. CLINICAL FEATURES • Metastatic Tumour effects Cervical/supraclavicular lymphadenopathy (common, present in 30%, and may be an easy site for diagnostic biopsy) Palpable liver edge Bone pain/pathological fracture due to bone metastases Neurological sequelae 2° to cerebral metastases Hypercalcaemic effects (due to bony metastases or direct tumour production of parathyroid hormone (PTH)-related peptide or PTH) Dysphagia (compression from large mediastinal nodes).
  • 16. CLINICAL FEATURES •Paraneoplastic syndromes • Endocrine syndromes are due to the ectopic production of hormones or hormonally active peptides. • Neurological syndromes are due to antibody-mediated CNS damage. Cachexia and wasting Clubbing (up to 29% of patients; any cell type, more common in squamous and adenocarcinoma) Hypertrophic pulmonary osteoarthropathy
  • 17. CLINICAL FEATURES Gynaecomastia Ectopic ACTH (Cushing’s syndrome) Cerebellar syndrome (usually SCLC) Limbic encephalitis (SCLC, also breast, testicular, other cancers). Dermatomyositis/polymyositis Glomerulonephritis.
  • 19. INVESTIGATIONS • In outpatients 1. History and examination, including smoking and occupational histories 2. Spirometry pre-biopsy or surgery 3. CXR (PA and possibly lateral)—location of lesion, pleural involvement, pleural effusion, rib destruction, intrathoracic metastases, mediastinal lymphadenopathy. CXR can be normal 4. Blood tests, including sodium, calcium, and LFTs. Check clotting if biopsy planned 5. Sputum cytology only indicated in patients who are unfit for bronchoscopy or biopsy 6. Diagnostic pleural tap, if effusion present 7. FNA of enlarged supraclavicular or cervical lymph nodes.
  • 20. INVESTIGATIONS • Radiology 1. CT neck, chest, liver, adrenals (contrast-enhanced) to assess tumour site and size 2. USG of neck or liver may provide information about enlarged lymph nodes or metastases suitable for biopsy 3. MRI Used to answer specific questions relating to tumour invasion/ borders. 4. Bone scan Indicated if any suggestion of metastatic disease such as bony pain, pathological fracture, hypercalcaemia, raised ALP,highly suggestive of bony metastases if multiple areas of increased uptake. 5. CT head Indicated if any neurological evidence of metastatic 6. Positron Emission Tomography (PET) scanning Imaging technique
  • 34. MANAGEMENT 1. Surgical resection in patients with ipsilateral peribronchial or hilar node involvement 2. Radiotherapy 3. Chemotherapy 4. Laser therapy 5. General managment
  • 35. MANAGEMENT • Radiotherapy SVCO Recurrent hemoptysis Pain caused by chest wall invasion or skeletal metastasis To relieve obstruction of trachea & main bronchi With chemotherapy,it can prevent brain metastasis in small cell carcinoma
  • 36. MANAGEMENT • Chemotherapy Small cell carcinoma – Combined treatment with cytotoxic drugs & radiotherapy IV Cyclophosphamide Doxorubicin Vincristine Etoposide IV Cisplatin
  • 37. MANAGEMENT •Laser Therapy Via fiber optic bronchoscopy Palliative treatment To destroy tumour tissue occluding major airways & to allow re aeration of collapsed lung
  • 38. MANAGEMENT •General Management Pain relief Good diet Specific therapy to treat anxiety & depression Treat Hypercalcemia Manage malignant pleural effusions.

Notas del editor

  1. Anophthalmos – Posterior dislocation of the eye Anhydrosis – inability to perspire Pancoast tumor- tumot in the superior sulcus of the lung