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Basic level for allied health students. Prepared specifically for Physician assistant course.
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Pathology of Respiratory System Disorders MX1002-PAS-Wk7-RSThe only place wheresuccess comes beforework is in a dictionary…!Vidal Sassoon
MX1002-PAS-Wk7-RSPathophysiologyRespiratory SystemDr. Venkatesh M. Shashidhar.Associate Professor & Head of Pathology MX1002-PAS-Wk7-RSPathophysiologyRespiratory SystemDr. Venkatesh M. Shashidhar.Associate Professor & Head of Pathology
PAS-Respiratory PathophysiologyIntroduction to Resp. Sys:• 10,000L/day of air – filtered, moistened,warmed, O2/Co2. exchanged.!• Full capacity 6L. (500ml at rest)• Sinusitis, pharyngitis, laryngitis…* URI• Pneumonia: Inflammation of lung * LRI• Chronic: COPD, Fibrosis – Smoking.• Commonest internal Cancer.• Respiratory tract inflammations -commonest in medical practice.• Enormous morbidity & mortality.• Important medical learning. Doctors daily bread….! PAS-Respiratory PathophysiologyIntroduction to Resp. Sys:• 10,000L/day of air – filtered, moistened,warmed, O2/Co2. exchanged.!• Full capacity 6L. (500ml at rest)• Sinusitis, pharyngitis, laryngitis…* URI• Pneumonia: Inflammation of lung * LRI• Chronic: COPD, Fibrosis – Smoking.• Commonest internal Cancer.• Respiratory tract inflammations -commonest in medical practice.• Enormous morbidity & mortality.• Important medical learning. Doctors daily bread….!
PAS-Respiratory PathophysiologyRespiration – Respiratory system:5 PAS-Respiratory PathophysiologyRespiration – Respiratory system:5
PAS-Respiratory PathophysiologyRespiration – Respiratory system:6 PAS-Respiratory PathophysiologyRespiration – Respiratory system:6
PAS-Respiratory PathophysiologyAlveolar Gas Exchange:8Co2O2 PAS-Respiratory PathophysiologyAlveolar Gas Exchange:8Co2O2
PAS-Respiratory PathophysiologyLung Function testing:9Expiration0 ------- Volume ---------------6LInspiration PAS-Respiratory PathophysiologyLung Function testing:9Expiration0 ------- Volume ---------------6LInspiration
. PAS-Respiratory PathophysiologyLung Function Testing:• Total Lung Capacity (TLC) 6L male/4.7L fem.• Tidal Volume (TV) – 500 / 390ml• Forced Vital Capacity (FVC) 4.8L / 3.7L• Forced Expiratory Volume in 1 Sec - FEV1• FEV1/FVC (FEV1%) - 75–80% normal.1. In Obstructive diseases (COPD) FEV1 low& FVC high. So FEV1/FVC is low (<80%).2. In Restrictive diseases (fibrosis) the FEV1and FVC are both low proportionally and theFEV1/FVC value normal or high. Volume (%FYC)
. MX1002-PAS-Wk7-RSFirst step to make yourdreams come trueis to wake up!— Paul Valery
. PAS-Respiratory PathophysiologyPneumonia: Infection of lung (LRT)• Inflammation of alveoli• Etiology: pathogens vs defence.• Types: Bacterial, viral, fungal, other.• Clinical: Lobar / Broncho pneumonia.• Symptoms: Fever, cough, dyspnoea.• Complications: Spread septicemia,abscess, scarring.
. PAS-Respiratory PathophysiologyPneumonia Types:Etiologic Types:• Infective– Viral– Bacterial– Fungal– Tuberculosis• Non Infective– Toxins– chemical– AspirationMorphologic types:• Lobar• Broncho• InterstitialDuration:• Acute• ChronicClinical:• Primary / secondary.
. 1. Congestion 2.Red HepatisationNormal 4. Resolution 3. Grey HepatizationPathogenesis of Pneumonia
. PAS-Respiratory PathophysiologyLobar Pneumonia - Primaryin healthy people in community. Gram Positive Cocci, wholelobe unilateral. heals without scar. Rare complications.
. PAS-Respiratory PathophysiologyBronchopneumonia - Secondaryin Sick patients, Gram Negative bacilli, bilateral,basal. More complications, heals by scarring.
. PAS-Respiratory PathophysiologyBroncho-pneumonia – Lobar-pneumonia• Extremes of age.• Secondary, in sick.• Both genders.• Klebsiella, E.coli• Patchy, basal, bilateral.• Around Small Bronchi• Not limited by anatomicboundaries.• Usually bilateral.• Middle age – 20-50• Primary in a healthy adult.• males common.• 95% pneumococcus• Entire lobe consolidation• Diffuse• Limited by anatomicboundaries.• Usually unilateral
. PAS-Respiratory PathophysiologyTuberculosis:• Mycobacterium tuberculosis (typical)• Primary & Secondary,• Chronic, Hypersensitivity to bacteria,• Caseating Granuloma + Fibrosis.• debilitating, weight loss.• Upperlobe, cavity + fibrosing.• Systemic spread, miliary spread.• Tuberculin Test – hypersensitivity.
. MX1002-PAS-Wk7-RS“Whether you think that youcan or that you cant,you are right…!”– Henry Ford
. MX1002-PAS-Wk7-RSChronic Lung disorders:Obstructive & Restrictive
. PAS-Respiratory PathophysiologyRestrictive vs Obstructive• Interstitial fibrosis• Stiff hard lung• Increased tissue• Normal FEV1:FVC ratio• Normal PEFR.• Types:– Fibrosis,– Pneumoconiosis• Obstruction to air flow.• Soft lung• Loss of tissue.• Low FEV1:VC ratio• Low PEFR.• Types:–COPD–Asthma
. PAS-Respiratory PathophysiologyRestrictive - Obstructive
. PAS-Respiratory Pathophysiology• Irreversible, fibrotic pulmonarydisease due to the inhalationof large amounts of silica dustover time.• Road, civil & mining workers.• Toxic Inflam fibrosis.• dyspnea, fatigue, weight loss,fever, and pleuritic pain.• Multiple small, fibrotic Nodulesbilateral + emphysema.• Restrictive pattern of PFT.• TB association common.Silicosis: Restrictive COPDFine nodular shadows
. PAS-Respiratory Pathophysiology• Beaded protein coveredneedle like microscopic .Asbestos bodies• Within alveoli & sputum.• Dyspnoea, dry cough• Diffuse fibrosis: Honey comblung Pulmonary failure.• Mesothelioma – pleuralcancer.Asbestosis: Restrictive
. MX1002-PAS-Wk7-RSPathology ofChronic ObstructivePulmonary Diseases (COPD)Dr. Venkatesh M. ShashidharAssociate Professor of Pathology
. PAS-Respiratory PathophysiologyObstructive Airway Disease:• Localized: Foreign body, aspiration, tumor..• Diffuse – Distal airway diseases– Transient reversible spasm - Asthma– Chronic irreversible permanent – COPD.
. PAS-Respiratory PathophysiologyAsthma Clinical Pathology:Chronic hypersensitivity inflammatorydisease of bronchi excess mucousand spasmodic occlusion.Causes• Allergic: allergens, infection• non-allergic:neurogenic,psychogenicSigns and symptoms• dyspnea, wheezing, catching for air.• cough – viscous thick sputum• Tachycardia & chest pain
. BronchialInflammationTRIGGERSAllergens, Exercise,Cold Air, SO2 ParticulatesAirwayHyperresponsivenessGenetic*INDUCERSAllergens,Chemical sensitisers,Air pollutants, Virus infectionsAirflow Limitation
. PAS-Respiratory PathophysiologyChronic Obstr. Pulm Disease: COPD• Chronic, irreversible airway obstruction withdestruction of bronchi & alveoli.• Clinical: Chronic bronchitis, Emphysema orCOPD (combined).• Smoking / pollution – commonest cause• 15% smokers develop COPD.• Finally leads to lung failure or Cancer.
. PAS-Respiratory PathophysiologySmoking – Pathogenesis• Increase in– Alveolar marcrophages– CD8 Lymphocytes– Neutrophils– Proteases.• Tissue irritation / destruction• Airway damage- Bronchitis• Alveoli damage- Emphysema.Emphysema Bronchitis
. PAS-Respiratory PathophysiologySmoking effects: FEV 1 & Age
. PAS-Respiratory PathophysiologyPathogenesis – Smoke - Lung Dis.CancerInflam COPDIrritation Inflammation Mucous Infections destr. COPD Cancer
. PAS-Respiratory PathophysiologyCombined COPD (common)
. PAS-Respiratory PathophysiologyLung Normal & in Smokers:
. PAS-Respiratory PathophysiologySmokers lung – COPD Bronchitis
. PAS-Respiratory PathophysiologyEmphysema:Pink Puffer:• Lean/weight loss• Forward stooping• Barrel chest• Flat diaphragm• Hyperlucent Lung
. PAS-Respiratory PathophysiologyComplications of COPD:1. Cor Pulmonale – Heart failure.2. Acute Exacerbations.3. Recurrent pneumonia.4. End-stage lung disease.5. Polycythemia – hypoxia.6. Bronchiectasis.7. Lung Cancer.
. PAS-Respiratory PathophysiologyBronchiectasis:• Permanent dilatation ofbronchi with pus.• Cough, copious purulentsputum (pus).• Lower lobes common• Complications -Pneumonia, septicemia,meningitis.• Management – surgicalresection.
. MX1002-PAS-Wk7-RS“Get me well so I can get ontelevision and tell people tostop smoking…!”-- Nat King Cole
. “Troubles are often the tools by whichnature fashions us for better things”- Henry Ward Beecher
. Life’s battles don’t go always to the stronger orfaster man, sooner or later, The man who wins isthe man who thinks he can….!
. MX1002-PAS-Wk7-RSPathology ofLung tumors(Lung Cancer)Dr. Venkatesh M. ShashidharA/Prof. & Head of PathologySchool of Medicine45
. PAS-Respiratory PathophysiologyLung Cancer Intro:• Most common & fatal cancer (internalmalignancy)• Kills more people than colorectal,breast, and prostate cancers combined.• Significant increase in incidence..(developing countries*)• Now Increasing in females > breastcancer.• 90% of lung cancers are related tosmoking..! (passive smoking in 5%)• Mutagen sensitive genotype : P-450enzyme• Poor prognosis ~ 5% 5y survival *46
. PAS-Respiratory PathophysiologyLung Cancer Incidence:47
. PAS-Respiratory PathophysiologyLung Cancer & Smoking:• Proportional to duration, amount & quality of smoking &deep inhaling.• 90% are smokers and 10% are non smokers• 20 fold risk if >40cigarettes per day• >100 fold combined with Asbestos, coal, radon, etc.• Atypical cells in sputum in 96.7% of smokers - 0.9% in nonsmokers.• Smoke has several irritants & carcinogens.– Initiators – Benzo[o]pyrenes– Promoters – Phenol derivatives– Radioactive substances – Polonium, C14, K4048
. PAS-Respiratory PathophysiologyLung tumors Classification:• Benign tumours – rare (Adenoma, Hamartoma)• Malignant (common):– Bronchogenic Carcinoma: (95%)– Bronchial Carcinoid Tumor (5%)– Other Tumors (<1%)– Metastasis (common)• Tumors of Pleura– Mesothelioma – asbestosis *49
. PAS-Respiratory PathophysiologyTypes of Bronchogenic Ca.:• Bronchogenic Carcinoma (95%)– Small cell ca. SCC – 15-20% (oat cell carcinoma)– Non Small cell NSCC– 80%• Squamous cell carcinoma – 20-30%• Adeno carcinoma – 30-40%• Large cell anaplastic carcinoma• Clinical / prognostic classification:SCC - small cell CaEarly spreadSurgery not possible.Responds to chemo50Non-SCCLate spread – localizedStaging & SurgeryDoes not respond to chemo.