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pulmonary /pul·mo·nary/ (pool´mo-nar″e)
1. pertaining to the lungs. 2. pertaining to the pulmonary artery.
Pulmonary Relating to the opening leading from the right large chamber of the heart into the lung artery. Mentioned in: Altitude Sickness, Anthrax, Chest X Ray, Emphysema, Hantavirus Infections, Lung Transplantation, Pulmonary Edema, Pulmonary Hypertension, Pulmonary Valve Insufficiency, Pulmonary Valve Stenosis, Smoke Inhalation
pulmonary [poo͡l′məner′ē] Etymology: L, pulmo, lungs pertaining to the lungs or the respiratory system. Also pulmonic. pulmonary [pul´mo-ner″e] 2. pertaining to the pulmonary artery. pulmonary acid aspiration syndrome a disorder produced as a complication of inhalation of gastric contents; it may progress to a syndrome resembling acute respiratory distress syndrome. pulmonary alveolar proteinosis a disease of unknown etiology marked by chronic filling of the alveoli with a proteinaceous, lipid-rich, granular material consisting of surfactant and the debris of necrotic cells. Some patients have a history of exposure to irritating dusts or fumes. The condition is treated by whole lung lavage with balanced salt solution; most patients need repeated lavage. pulmonary artery the large artery originating from the superior surface of the right ventricle of the heart and carrying deoxygenated blood to the lungs for oxygenation; it starts as the pulmonary trunk, which divides between the fifth and sixth thoracic vertebrae to form the right pulmonary artery that enters the right lung and the left pulmonary artery that enters the left lung. See Appendix 3-1. pulmonary circulation the circulation of blood to and from the lungs. Unoxygenated blood from the right ventricle flows through the right and left pulmonary arteries to the right and left lungs. After entering the lungs, the branches subdivide, finally emerging as capillaries which surround the alveoli and release the carbon dioxide in exchange for a fresh supply of oxygen. The capillaries unite gradually and assume the characteristics of veins. These veins join to form the pulmonary veins, which return the oxygenated blood to the left atrium. See also circulatory system. pulmonary function tests tests used to evaluate lung mechanics, gas exchange, pulmonary blood flow, and blood gases and pH. They are used to evaluate patients in the diagnosis of pulmonary disease, assessment of disease development, or evaluation of the risk of pulmonary complications from surgery. Lung Volumes and Capacities. The total lung capacity (TLC) is divided into four volumes. The tidal volume (VT) is the volume inhaled or exhaled in normal quiet breathing. The inspiratory reserve volume (IRV) is the maximum volume that can be inhaled following a normal quiet inhalation. The expiratory reserve volume (ERV) is the maximum volume that can be exhaled following a normal quiet exhalation. The residual volume (RV) is the volume remaining in the lungs following a maximal exhalation. The vital capacity (VC) is the maximum volume that can be exhaled following a maximal inhalation; VC = IRV + VT + ERV. The inspiratory capacity (IC) is the maximum volume that can be inhaled following a normal quiet exhalation; IC = IRV + VT. The functional residual capacity (FRC) is the volume remaining in the lungs following a normal quiet exhalation; FRC = ERV + RV. The vital capacity and its components are measured using a spirometer, which measures the volumes of air inhaled and exhaled. The functional residual capacity is usually measured by the helium dilution method using a closed spirometry system. A known amount of helium is introduced into the system at the end of a normal quiet exhalation. When the helium equilibrates throughout the volume of the system, which is equal to the FRC plus the volume of the spirometer and tubing, the FRC is determined from the helium concentration. This test may underestimate the FRC of patients with emphysema. The FRC can be determined quickly and more accurately by body plethysmography. The residual volume and total lung capacity are determined from the functional reserve capacity. Forced Vital Capacity (FVC). In the forced vital capacity maneuver, the patient exhales as forcefully and rapidly as possible, beginning at maximal exhalation. Several parameters are determined from the spirogram. The forced vital capacity is the total volume of air exhaled during the maneuver; it is normally equal to the vital capacity. The forced expiratory volume (FEV) is the volume expired during a specified time period from the beginning of the test. The times used are 0.5, 1, 2, and 3 seconds; corresponding parameters are FEV0.5, FEV1.0, FEV2.0, and FEV3.0. The maximal expiratory flow is the slope of the line connecting the points where 200 ml and 1200 ml have been exhaled; it is also called FEF200–1200 (forced expiratory flow). The maximal midexpiratory flow is the slope of the line connecting the points where 25 per cent and 75 per cent of the forced vital capacity have been exhaled; it is also called FEF25–75%. Maximal Voluntary Ventilation (MVV). This is the maximal volume of air that can be breathed by the patient, expressed in liters per minute; it was formerly called maximal breathing capacity. The patient breathes as rapidly and deeply as possible for 12 to 15 seconds and the volume exhaled is determined by spirometry. Predicted Values. Because the results of pulmonary function tests vary with size and age, the normal values are calculated using prediction equations or nomograms, which give the normal value for a specific age, height, and sex. The prediction equations are derived using linear regression on the data from a population of normal subjects. The observed values are usually reported as a percentage of the predicted value. Interpretation. These tests provide evidence of impairment of ventilatory function; they do not point to specific disease processes. Abnormal test results may show either an obstructive or a restrictive pattern; sometimes both are present. The Obstructive Pattern. This pattern occurs when there is airway obstruction from any cause, as in asthma, bronchitis, emphysema, or advanced bronchiectasis; these conditions are grouped together in the nonspecific term chronic obstructive pulmonary disease. In this pattern, the residual volume is increased and the PV/TLC ratio is markedly increased. Owing to increased airway resistance, the flow rates are decreased. The FEV/FVC ratios, maximal midexpiratory flow, and maximal expiratory flow are all decreased; FEV1.0/FVC is less than 75 per cent. The Restrictive Pattern. This pattern occurs when there is a loss of lung tissue or when lung expansion is limited as a result of decreased compliance of the lung or thorax or of muscular weakness. This pattern occurs in conditions such as pectus excavatum, myasthenia gravis, diffuse idiopathic interstitial fibrosis, and space-occupying lesions (tumors, effusions). The vital capacity and forced vital capacity are less than 80 per cent of the predicted value, but the FEV/FVC ratios are normal. The total lung capacity is decreased and the RV/TLC ratio is normal. pulmonary vein any of the four large veins (two right and two left branches) that carry oxygenated blood from the lungs to the left atrium of the heart. See anatomic Table of Veins in the Appendices.
pulmonary pertaining to the lungs, or to the pulmonary artery. See also lung. pulmonary abscess causes a syndrome of chronic toxemia, cough, loss of body weight. Careful auscultation may elicit squeaky rales around the lesions. See also caudal vena caval thrombosis, aspiration pneumonia. pulmonary acinus basic structural unit of the lung parenchyma; the gas exchange unit, supplied by a single terminal bronchiole and includes branches of the terminal bronchiole, alveolar ducts, alveolar sacs, alveoli and associated blood vessels. A pulmonary lobule consists of many acini. pulmonary agenesis incompatible with life; found only in fetal or neonatal necropsy specimens. pulmonary alveolar microlithiasis see microlithiasis alveolaris pulmonum. pulmonary alveolar parenchyma include epithelial cells (pneumonocytes or pneumocytes), alveolar capillary endothelial cells, and interstitial cells (fibroblasts) and alveolar macrophages. pulmonary alveolar proteinosis a disease of unknown etiology marked by chronic filling of the alveoli with a proteinaceous, lipid-rich, granular material consisting of surfactant and the debris of necrotic cells. pulmonary arteriopathy see aelurostrongylus. pulmonary artery wedge pressure see wedge pressure. pulmonary atelectasis see atelectasis. pulmonary bed the network of capillaries in lung tissue. pulmonary calcinosis see microlithiasis alveolaris pulmonum. pulmonary calculus see bronchial calculus. pulmonary carcinomatosis see ovine pulmonary adenomatosis (below). pulmonary circulation the circulation of blood to and from the lungs. Deoxygenated blood from the right ventricle flows through the right and left pulmonary arteries to the right and left lung. After entering the lungs, the branches subdivide, finally emerging as capillaries which surround the alveoli and release the carbon dioxide in exchange for oxygen. The capillaries unite gradually and assume the characteristics of veins. These veins join to form the pulmonary veins, which return the oxygenated blood to the left atrium. See also circulatory system. pulmonary compliance a measure of the ability of the lung to distend in response to pressure without disruption. Expressed as the unit volume of change in the lung per unit of pressure. Compliance or distensibility of the lung is increased in conditions such as emphysema in which the lung distends more readily, and is decreased in fibrotic conditions in which the lung distends with difficulty. See also compliance. pulmonary congestion caused by engorgement of the pulmonary vascular bed and it may precede pulmonary edema when the intravascular fluid escapes into the parenchyma and the alveoli. There is a loss of air space and the development of respiratory embarrassment. pulmonary cysts may be congenital or acquired, caused by trauma, parasites (Paragonimus spp.), or associated with bronchiectasis. Rarely, metastatic tumors cavitate forming cysts. pulmonary defense mechanisms include aerodynamic filtration in nasal cavities, sneezing, local nasal antibody, laryngeal and cough reflexes, mucociliary transport mechanisms, alveolar macrophages, systemic and local antibody systems. pulmonary edema an effusion of serous fluid into the pulmonary interstitial tissues and alveoli. Preceded by pulmonary congestion (see above). If the extravascular exudation is sufficiently severe a critical level of hypoxia may be reached. The breathing will then be labored, the normal breath sounds on auscultation may be absent, and a frothy nasal discharge, often blood-tinged, may appear. At this stage the animal's life is about to terminate. pulmonary embolus obstruction of the pulmonary artery or one of its branches by an embolus. The embolus usually is a blood clot swept into circulation from a large peripheral vein. Signs vary greatly, depending on the extent to which the lung is involved. Simple, uncomplicated embolism produces such cardiopulmonary signs as dyspnea, tachypnea, persistent cough, pleuritic pain and hemoptysis. On rare occasions the cardiopulmonary signs may be acute, occurring suddenly and quickly producing cyanosis and shock. A septic embolus can lead to local pulmonary abscess or an extension to pneumonia as in caudal vena caval syndrome. See also caudal vena caval thrombosis, pulmonary abscess (above). pulmonary eosinophilic granulomatosis a lesion common in heartworm disease; eosinophiles and neutrophils surround trapped microfilariae causing nodules as large as 3 inches diameter. May be preceded by lesions of allergic pneumonitis. exercise-induced pulmonary hemorrhage traces of blood can be found in about 60% of horses after racing. Less than 1% of these bleed from the nostrils. See also epistaxis. pulmonary function tests tests used to evaluate lung mechanics, gas exchange, pulmonary blood flow and blood acid-base balance. Pulmonary function testing is used to detect emphysema and chronic obstructive bronchitis at an early stage. pulmonary hemorrhage as distinct from hemothorax, is recognized because of a syndrome of dyspnea, increased lung density radiographically, and hemorrhagic anemia. If a large vessel ruptures into an abscess cavity there is usually a massive hemoptysis and instant death. Frothy blood-stained nasal discharge is an indication of pulmonary edema rather than of pulmonary hemorrhage. See also exercise-induced pulmonary hemorrhage (above). pulmonary horse sickness the predominantly pulmonary form of african horse sickness. pulmonary hypertrophic osteoarthropathy see hypertrophic osteopathy. pulmonary hypoplasia a congenital defect resulting in decreased lung development. pulmonary infarction see pulmonary infarction, pulmonary embolus (above). pulmonary infiltration with eosinophilia (PIE) see pie syndrome. pulmonary malformation includes accessory lungs, pulmonary hypoplasia, pulmonary agenesis, congenital pulmonary cysts, endodermal heteroplasia, respiratory distress syndrome, neonatal maladjustment syndrome, immotile cilia syndrome. pulmonary mycoses includes aspergillosis, mortierellosis, blastomycosis, cryptococcosis, coccidioidomycosis. pulmonary neoplasm many types are recorded in all species but the prevalence is very low in food animals. A common site for metastases in companion animals. Characterized clinically by decreased exercise tolerance, progressive dyspnea, chronic cough and emaciation. Most diagnoses result from radiographic examination of the thorax for secondary growths. neurogenic pulmonary edema results from head trauma, central nervous system lesions and toxins, which may cause increased pulmonary blood pressure and alteration to sympathetic innervation leading to fluid leakage from vessels. overriding pulmonary artery ovine pulmonary adenomatosis a very chronic progressive pneumonia of sheep and goats caused by a retrovirus. Dyspnea, emaciation and a profuse nasal discharge are the cardinal signs, but coughing is not evident. The disease is always fatal. It is of great importance if it occurs in flocks that are housed for long periods. Characteristically the extensive lung involvement includes large areas of neoplastic tissue. Called also jaagsiekte, pulmonary carcinomatosis. pulmonary patterns re-expansion pulmonary edema edema, emphysematous bullae and serosanguinous fluid in the airways with generalized pulmonary capillary endothelial damage; associated with chronic pulmonary collapse and removal of pleural effusions or pneumothorax with rapid re-expansion. pulmonary rupture traumatic, especially when there is rib fracture, or spontaneous due to coughing and a weak parenchyma. The most common cause of pneumothorax. pulmonary thromboembolic disease thromboembolism causing blockage of large sections of the pulmonary vascular bed will result in at least temporary severe dyspnea. It may also lead to right heart congestive failure, i.e. cor pulmonale. pulmonary thrombosis see thromboembolism. pulmonary valve the pocket-like structure that guards the orifice between the right ventricle and the pulmonary artery. pulmonary valve stenosis causes right ventricular hypertrophy and a poststenotic dilatation of the pulmonary artery. There is a systolic murmur and thrill on the left side of the chest. A common congenital defect in dogs. pulmonary vein the large vein (right and left branches) that carries oxygenated blood from the lungs to the left atrium of the heart. pulmonary wedge pressure see wedge pressure. Patient discussion about pulmonary. Q. My grandfather died of lung cancer because of smoking. what is the probability of me getting a cancerous tumor? What procedure is done to see if a tumor is malignant? Is a simple MRI enough to make that conclusion? A. Sad.. my brother in law died from smoking, few years ago. Regardless of family history, smoking is not exactly helthy and does contribute to lung cancer. Even though the role of heredity in lung cancer is not as well-known, having a family history of lung cancer does increase our risk to some degree. Hereditary lung cancer is higher in women, nonsmokers and those with early onset lung cancer (lung cancer that occurs before the age of 60). Overall, it has been estimated that 1.7% of lung cancers up to the age of 68 are hereditary. Q. Does the risk for lung cancer remain the same after I stop smoking? I'm 55 years old woman and have been smoking since age 20 one pack a day. Fortunately, after numerous failures I succeeded to stop smoking 5 years ago. I'm happy and feel much better now, but I'm still worried about the possibility of lung cancer- I know that smoking cause lung cancer, but after I've stopped smoking, am I still at risk to have cancer? A. The answer is a little complicated: as former smoker, the risk for lung cancer does decrease with time. However, it may never return to the risk of someone similiar to you who never smoke to develop lung cancer. Q. Is it possible to have lung cancer without smoking? My 89 years-old grandfather was told by his doctor that he has lung cancer, after he had cough for almost two months. I thought that lung cancer happens because people smoke, but my grandfather never smoked or drank alcohol and is still in a very good shape (for his age, of course) – is it possible the doctor was wrong and he doesn’t have lung cancer? A. There are other things that increase the risk of lung cancer-. He may not be a smoker himself, but maybe he was living with a smoker, maybe he worked in an asbestos building, or exposed to substances that cause lung cancer. Read more or ask a question about pulmonaryWant to thank TFD for its existence? 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