Lung cancer and mesothelioma: Pathology review

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Lung cancer and mesothelioma: Pathology review

Cardiothoracic Disease

Cardiothoracic Disease

Respiratory system anatomy and physiology
Lung volumes and capacities
Anatomic and physiologic dead space
Ventilation
Alveolar gas equation
Compliance of lungs and chest wall
Combined pressure-volume curves for the lung and chest wall
Alveolar surface tension and surfactant
Airflow, pressure, and resistance
Breathing cycle
Breathing control
Pulmonary chemoreceptors and mechanoreceptors
Ideal (general) gas law
Boyle's law
Dalton's law
Henry's law
Fick's laws of diffusion
Graham's law
Diffusion-limited and perfusion-limited gas exchange
Hypoxia
Oxygen binding capacity and oxygen content
Oxygen-hemoglobin dissociation curve
Erythropoietin
Carbon dioxide transport in blood
Regulation of pulmonary blood flow
Zones of pulmonary blood flow
Pulmonary shunts
Ventilation-perfusion ratios and V/Q mismatch
Pulmonary changes during exercise
Pulmonary changes at high altitude and altitude sickness
Diffuse parenchymal lung disease: Clinical
Restrictive lung diseases: Pathology review
Restrictive lung diseases
Idiopathic pulmonary fibrosis
Sarcoidosis
Lung cancer: Clinical
Lung cancer and mesothelioma: Pathology review
Mesothelioma
Cardiovascular system anatomy and physiology
Lymphatic system anatomy and physiology
Cardiac cycle
Normal heart sounds
Abnormal heart sounds
Blood pressure, blood flow, and resistance
Resistance to blood flow
Laminar flow and Reynolds number
Compliance of blood vessels
Pressures in the cardiovascular system
Physiological changes during exercise
Cardiovascular changes during hemorrhage
Cardiovascular changes during postural change
Measuring cardiac output (Fick principle)
Cardiac and vascular function curves
Altering cardiac and vascular function curves
Stroke volume, ejection fraction, and cardiac output
Frank-Starling relationship
Pressure-volume loops
Changes in pressure-volume loops
Cardiac work
Cardiac preload
Cardiac afterload
Law of Laplace
Baroreceptors
Renin-angiotensin-aldosterone system
Chemoreceptors
Cardiac conduction system
Action potentials in pacemaker cells
Action potentials in myocytes
Cardiac conduction velocity
Excitability and refractory periods
Cardiac excitation-contraction coupling
Cardiac contractility
Cerebral circulation
Coronary circulation
Control of blood flow circulation
Microcirculation and Starling forces
Cardiomyopathies: Clinical
Cardiomyopathies: Pathology review
Hypertrophic cardiomyopathy
Dilated cardiomyopathy
Restrictive cardiomyopathy
Sleep apnea
Apnea of prematurity
Aortic aneurysms and dissections: Clinical
Aortic dissections and aneurysms: Pathology review
Aortic dissection
Aneurysms
Marfan syndrome
Peripheral vascular disease: Clinical
Peripheral artery disease: Pathology review
Peripheral artery disease
Arterial disease
Deep vein thrombosis
Leg ulcers: Clinical
Chronic venous insufficiency
Thrombophlebitis
Vasculitis: Pathology review
Vasculitis
Kawasaki disease
Behcet's disease
Nutcracker syndrome
Superior mesenteric artery syndrome
Subclavian steal syndrome
Coronary steal syndrome
Lymphedema
ECG basics
ECG normal sinus rhythm
ECG rate and rhythm
ECG intervals
ECG axis
ECG QRS transition
ECG cardiac hypertrophy and enlargement
ECG cardiac infarction and ischemia
Heart blocks: Pathology review
Premature ventricular contraction
Premature atrial contraction
Atrial fibrillation
Atrial flutter
Atrioventricular nodal reentrant tachycardia (AVNRT)
Wolff-Parkinson-White syndrome
Atrioventricular block
Bundle branch block
Long QT syndrome and Torsade de pointes
Ventricular tachycardia
Brugada syndrome
Ventricular fibrillation
Pulseless electrical activity
Class I antiarrhythmics: Sodium channel blockers
Class II antiarrhythmics: Beta blockers
Class III antiarrhythmics: Potassium channel blockers
Class IV antiarrhythmics: Calcium channel blockers and others
Positive inotropic medications
Sympatholytics: Alpha-2 agonists
Adrenergic antagonists: Alpha blockers
Adrenergic antagonists: Beta blockers
Adrenergic antagonists: Presynaptic
cGMP mediated smooth muscle vasodilators
Calcium channel blockers
Heart failure: Clinical
Heart failure: Pathology review
Heart failure
Cor pulmonale
Pulmonary hypertension
Pulmonary edema
Anatomy of the coronary circulation
Asthma: Clinical
Obstructive lung diseases: Pathology review
Asthma
Chronic obstructive pulmonary disease (COPD): Clinical
Chronic bronchitis
Emphysema
Alpha 1-antitrypsin deficiency
Bronchodilators: Beta 2-agonists and muscarinic antagonists
Bronchodilators: Leukotriene antagonists and methylxanthines
Pulmonary corticosteroids and mast cell inhibitors
Non-corticosteroid immunosuppressants and immunotherapies
Cystic fibrosis: Pathology review
Cystic fibrosis
Bronchiectasis
Anatomy of the heart
Anatomy clinical correlates: Heart
Cardiac muscle histology
Marfan syndrome
Ehlers-Danlos syndrome
Arteriole, venule and capillary histology
Cardiac muscle histology
Artery and vein histology
Trachea and bronchi histology
Bronchioles and alveoli histology
Nasal cavity and larynx histology
Coarctation of the aorta
Mitral valve disease
Pulmonary valve disease
Tricuspid valve disease
Aortic valve disease
Ventricular arrhythmias: Pathology review
Supraventricular arrhythmias: Pathology review
Coronary artery disease: Clinical
Atherosclerosis and arteriosclerosis: Pathology review
Coronary artery disease: Pathology review
Arterial disease
Angina pectoris
Unstable angina
Myocardial infarction
Prinzmetal angina
Coronary steal syndrome

Transcript

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Two people came to the clinic one day. First is a 65-year-old named Alex, who presents with a two-month history of dry, persistent cough and weight loss of around 7 pounds without dieting. He also says he coughs up blood sometimes but denies fever, dyspnea, sore throat, rhinorrhea or any chest pain. Alex has a history of asthma and hypertension, and smoked 1 pack of cigarettes daily for 45 years. On examination, his breath sounds are diminished at the right lung base.

The other individual is Clara, who’s an 80-year-old retiree. Before her retirement, Clara was a construction site supervisor. She complains of increasing shortness of breath, which started ten months ago, and new onset of myalgia located on the right side of her chest. Physical examination reveals decreased breath sounds in the right lung base along with dullness to percussion. Chest X-rays were ordered for both people. In Alex’s case, it showed a single, coin-like lesion on the right lung base. Clara’s scan showed pleural effusion, irregular pleural thickening, and two ivory white, calcified pleural plaques at the base of her right lung.

Both people have cancer involving the lung. But first, a bit of physiology. Lining the airways are several types of epithelial cells that serve multiple functions. These include ciliated cells that have hair-like project called cilia that work to sweep foreign particles and pathogens back to the throat to be swallowed. Another type, called goblet cells secrete mucin to moisten the airways and trap foreign pathogens. There are also basal cells that are thought to be able to differentiate into other cells in the epithelium, club cells that act to protect the bronchiolar epithelium, and neuroendocrine cells that secrete hormones into the blood. On the outside, the lungs are covered by the mesothelium which consists of the parietal pleura and the visceral pleura. Between them, there’s the pleural space, where the fluid produced by the epithelial cells is released, which acts as a lubricant to allow the layers to slide effortlessly against each other during respiratory movements.

Now, let’s begin with lung cancer. The two most common types are small cell lung cancer and non-small cell cancer, both sharing common pathophysiology. Cells of the lungs can undergo mutations that cause them to divide uncontrollably and replace the normal healthy lung tissue. Eventually these cells will form a tumor. To supply it, new blood vessels also develop and this is called angiogenesis. Sometimes the tumor can metastasize and spread via blood vessels or lymphatics and establish secondary sites throughout the body. Particularly at risk for lung cancer metastasis are the mediastinum and hilar lymph nodes because of their proximity to the lungs, so remember this as it’s very high yield! Other common sites include the liver, adrenal glands, bones, and brain.

There are many risk factors for lung cancer. Tobacco smoking is the most important one, which accounts for more than 90% of cases of lung cancer. This usually comes in the form of cigarettes, but also includes cigars, pipes, and hookah. There is a dose-dependent linear relationship between lung cancer risk and pack-years, which is the number of cigarette packs per day times the number of years of smoking. Second-hand smoke also increases the risk of lung cancer. The second leading risk factor for lung cancer is exposure to radon, a colorless, odorless gas which is a natural breakdown product of uranium found in the soil, so it sometimes accumulate in basements. Other environmental factors include asbestos, a mineral made of long, fibrous crystals that was commonly used for construction until the 1980s in the US. The most common type of cancer caused by asbestos is adenocarcinoma. Next there’s air pollution and ionizing radiation from medical imaging with chest X rays and CT scans, or during radiation therapy.

The symptoms of lung cancer vary based on the size and location of the tumor, whether or not it has spread to other organs, and whether or not it secretes hormones. Initially, individuals may be completely asymptomatic. Over time, in response to the cancer, the body mounts an immune response to fight it off. This results in the release of inflammatory chemokines like TNF-alpha, IL1-beta, and IL-6. The chemokines cause unintentional weight loss, fever, malaise, and night sweat. If the primary tumor physically obstructs the airway and presses on surrounding tissue, it can cause coughing, shortness of breath, wheezing. Since the obstruction can decrease the clearance of mucus, it also increase the risk of developing pneumonia. Sometimes, the tumor obstructs the bronchus and prevents the ventilation for a lobe, or even an entire lung! This will cause obstruction atelectasis where the lung could collapse. Compression of nearby nerves can cause pain, and compression of specific nerves like the recurrent laryngeal nerve and phrenic nerves can cause hoarseness or difficulty breathing, respectively. Another high yield fact is that compression of nearby vessels, like the superior vena cava, can prevent blood from draining from the head, leading to facial swelling or puffiness. If the swelling occurs in the epiglottis, it could cause difficulty breathing and if there’s swelling in the brain, it could cause headaches and altered mental status; both of which can be medical emergencies! Finally, if tumor necrosis occurs or if cancer cells invade a blood vessel, individuals can experience hemoptysis. A high yield fact is that sometimes a tumor can arise in the superior sulcus, which is the space formed by the subclavian vessels, and these are called Pancoast tumors. These are most often non-small cell carcinomas and can compress the blood vessels and nerves located in the region. Some important symptoms to remember include arm muscle weakness and paresthesia due to compression of the brachial plexus, and pain that irradiates to the scapula and arm on the affected side. Since Pancoast tumors near the thoracic inlet can compress cervical sympathetic ganglia, it can lead to Horner syndrome which causes constricted pupil, drooping upper eyelid, which is called ptosis, and anhidrosis, or the inability to sweat.

Ok, now let’s discuss small cell carcinomas, which account for a small percentage of lung cancer. They are associated with amplification of the Myc oncogene and originate from small, ovoidal, neuroendocrine cells. These tumors usually develop centrally in the lung, near a main bronchus. They also grow the fastest and tend to rapidly metastasize to other organs when compared to non-small cell lung cancers. Small cell carcinomas can sometimes secrete hormones and that can lead to what is called a paraneoplastic syndrome. One example is they can releases adrenocorticotropic hormone or ACTH. This leads to bilateral adrenal enlargement and an increase in cortisol production. The result is Cushing’s syndrome and some symptoms include elevated blood glucose, high blood pressure, skin hyperpigmentation, easy bruising, osteoporosis, frequent infections from a weakened immune system, and weight gain. Next, these tumors can also release antidiuretic hormone. This is called syndrome of inappropriate antidiuretic hormone or SIADH, which increases water reabsorption in the renal collecting ducts, leading to high blood pressure, hyponatremia, edema, and concentrated urine. Finally, small cell carcinoma can trigger the production of autoantibodies against neurons. If cerebellar neurons are affected, it leads to symptoms like ataxia and nystagmus. If neurons in the cerebrum are affected, then it can lead to symptoms like dementia and seizures. There’s also Lambert-Eaton syndrome where the autoantibodies target voltage gated calcium channels on the presynaptic membrane at the neuromuscular junction. This condition results in muscle weakness, especially the proximal muscles in the legs, but it also causes double vision, drooping of the eyelids, and difficulty swallowing.

Sources

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