Pulmonary Diseases. We Move A Lot of Air. Basic Categories. Alveolar Level. Developmental

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Transcription:

Pulmonary Diseases We Move A Lot of Air Alveolar Level Functions Oxygenation CO 2 & ph Basic defenses Nose hairs Cilia Mucus Cough reflex Immune system Basic Categories Congenital Infectious Neoplastic Nutritional Trauma Immunologic Vascular Developmental Diaphragmatic defect Intestines in chest No room for lung to develop The newborn needs two. Depending on the degree of lung hypoplasia, may not be compatible with life. Today can surgical fix inutero.

Gene Defect Related Cystic fibrosis Bronchial infections Pancreatic destruction Thick mucus Alpha-1 1 antitrypsin deficiency Emphysema Cirrhosis Can t neutralized activated proteases Immune system failure Atelectasis (Collapse) Obstructive vs. Restrictive Obstructive Air passage patency Increased resistance Acute asthma Chronic Chronic bronchitis Emphysema Restrictive Ability of lung to expand Decreased total lung capacity Chronic Obstructive Pulmonary Disease COPD Lasting longer than 3 months Chronic cough with mucus production Restriction to air movement Two basic forms Emphysema Chronic bronchitis Actually most patients have a mix Emphysema Loss of pulmonary elastic tissue. Inflammatory Smoking Can t keep small airways open. Reduced surface area Reduced air volume exchange COPD

Emphysema Emphysema Emphysema Large airspaces Trapped in air the dilated alveoli causes compression of smaller airways Hyperinflation Changes are irreversible Emphysema Pink puffer Barrel chest Hyperinflation Trapped air Thin Lots of calories just to breath Rapid respirations Pursed lips COPD Chromic Bronchitis Also a chronic obstructive disease Chronic cough with mucus production for 3 months. May lead to emphysema (especially in smokers). COPD Larger airway narrowing Increased secretions Goblet cell hyperplasia Blue bloater Cyanotic Asthma Bronchoconstriction Episodic Reversible Various stimuli Extrinsic Asthma Type I hypersensitivity IgE Atopic most frequent Other manifestations Intrinsic Triggers are nonimmune Aspirin Viral infections Cold Stress

Asthma, Sensitization Sensitization of CD4 cells The T H 2 class T H 2 cells release cytokines IL-4, IL-5 5 & IL-13 Cause production IgE Growth of mast cells Histamine producers Activation of eosinophils Typically see 2 phases to an attack Early, 30-60 minutes Late, 4-84 8 hours Asthma, Reaction Asthma, Long-term Bronchiectasis Dilated and inflamed bronchi Repeat infections Lots of mucus Foul smelling breath Unbelievable, productive morning cough Restrictive Lung Disease Reduced compliance Acute, surfactant problem Chronic, fibrosis

Acute Respiratory Distress Endothelial injury Loss of fluid and proteins Injury to Type II epi Lack of surfactant Accumulation of protein in the form of hyaline membranes within alveoli. Hyaline Membrane Formation Initiation of inflammatory response Neutrophils play significant role Oxidant injury Leakage of proteins Formation of hyaline membrane Reduces O 2 diffusion Reduced surfactant Alveolar wall becomes rigid. Hyaline Membranes Chronic Restrictive Lung Disease Occupational Asbestos Silicosis Coal miner s lung Chemotherapy Busulfan Immunological Rheumatoid arthritis Sarcoid Scleroderma and other collagen vascular diseases Idiopathic Pulmonary Fibrosis Silicosis

Sarcoidosis Sarcoidosis Hypersensitivity Pneumonitis Idiopathic Pulmonary Fibrosis Vascular Related Pulmonary Disease Acute alterations in blood flow. Congestion and edema PE Chronic congestion Eisenminger reaction Primary Pulmonary hypertension Inflammatory Autoimmune vasculitis

Pulmonary Edema Pulmonary Embolus Pulmonary Infarct Ventricular Septal Defect Left to right shunt Depending on size will lead to Eisenminger reaction. Later becomes right to left shunt. Possible infections. Pulmonary Hypertension

Pulmonary Infections Bacterial Pneumonia Pneumonia Infection in the alveolar spaces Bacteria TB Interstitial tissue Virus Mycoplasma Abscess Bronchitis Bronchiolitis Pleuritis Streptococcal pneumoniae Acute Bacterial Pneumonia Gram Negative Bugs Typically from body flora Opportunistic infections Compromised host Alcoholic Aspiration Chemotherapy Tracheostomy Broad spectrum antibiotics that change host flora

Klebsiella Pneumonia Gram negative rod Very mucoid capsule Aspiration Head down in the gutter Rusty sputum High fever Pulmonary Abscess Staphylococcus Aspiration of gastric material Hole with Air-fluid level Fungal Pneumonias Typically means something wrong with immune system Histoplasmosis is very common Ohio River valley Virtually all of us beat the bug HIV has changed things a lot Histoplasmosis Dimorphic yeast Fungal growth phase Oral or pulmonary infection Granulomas Most people lock it down. Forms of the disease Pulmonary Systemic Pneumocystis carinii Immune failure Organism is very common Immunosuppression Starvation HIV Chemotherapy Can t culture Bronchial wash Stain for the bug Tuberculosis Mycobacterium tuberculosis (most cases) Type IV hypersensitivity Granuloma Primary infection Pulmonary Perhaps goes lymphatics Hopefully it stops here. Secondary TB Internal reactivation Perhaps years later Not all patients

Granuloma Formation Primary TB Secondary or Reactivation TB Tuberculosis TB Chest X-RayX TB Chest X-RayX

Caseous granulomas Giant cells Inert bug Granulomas of TB Disseminated TB Skin Test PPD Injected intradermally Read in 2 days Measure swelling Not redness Positivity maybe life long CMV Pneumonia Common virus Infant and neonate Immune suppressed HIV Chemotherapy Characteristic inclusion Lung Tumors Mass on X-RayX Space occupying lesion Granuloma Neoplasm Benign Malignant Primary vs. Metastatic

Benign Rare Hamartoma A rest of tissue from development Cartilage most times Malignant Primary, so called bronchiogenic. Squamous cell Small cell Adenocarcinoma Metastatic, just about any source Kidney Breast Colon Reproductive Even the other lung Bronchiogenic Carcinoma Squamous in most cases Chronic irritant leads to squamous metaplasia. Continued exposure leads to dysplasia and eventually cancer. Very aggressive. Surgery is about it. Poor response to chemotherapy ands radiation Exfoliative cytology Cough it up Wash it out Bronchoscopic biopsy Pulmonary Cytology Metaplasia, Dysplasia, Cancer Basic Patterns of Bronchiogenic Carcinoma

What Lung Cancer Can Do Obstruct bronchus causing pneumonia Spread widely Odd hormonal activity Small cell makes ADH and ACTH Squamous cell makes PTH Multiple sclerosis like symptoms Even without brain mets Pancoast s tumor -> Horner s syndrome Metastatic Cancer to Lung Can come from anywhere Microscopic looks like tumor of origin Spreads by blood Isolated masses -> Spreads by lymphatics Diffuse involvement Pleura Membranes surrounding lung and Lining chest cavity Inflammation, Pleuritis Sterile Renal failure Infectious Bacteria, Lyme, Virus, TB Either may lead to scarring and trapping of lung Hemothorax Pneumothroax -> Pleural Tumors Metastatic About anywhere Primary, mesothelioma Mesothelial cells Asbestos workers Slow growing Traps & invades lung Upper Airway Allergic disease Sinusitis Larynx Infections Polyps Squamous cancer