Malignant Pleural Effusion Pneumothorax Malignant Mesothelioma and Other Primary Pleural Tumors
PLEURAL EFFUSION A pleural effusion is present when there is an excess quantity of fluid in the pleural space. Bilateral pleural effusions Heart failure or ascites. Occasionally, they are due to collagen vascular disease or metastatic tumor. Unilateral pleural effusions Tuberculosis, pneumonia, pulmonary infarction, metastatic tumor, primary pleural tumor, lymphoma, collagen vascular disease, chest trauma, ascites, and intra-abdominal inflammatory processes, such as subphrenic abscess or pancreatitis Etiology Pleural fluid accumulates when pleural fluid formation exceeds pleural fluid absorption. Normally, fluid enters the pleural space from the capillaries in the parietal pleura and is removed via the lymphatics situated in the parietal pleura. Fluid can also enter the pleural space from the interstitial spaces of the lung via the visceral pleura or from the peritoneal cavity via small holes in the diaphragm. The lymphatics have the capacity to absorb 20 times more fluid than is normally formed. Accordingly, a pleural effusion may develop when there is excess pleural fluid formation (from the interstitial spaces of the lung, the parietal pleura, or the peritoneal cavity) or when there is decreased fluid removal by the lymphatics.
Diagnostic Approach Transudative pleural effusion occurs when systemic factors that influence the formation and absorption of pleural fluid are altered. Causes left ventricular failure and cirrhosis. Exudative pleural effusion occurs when local factors that influence the formation and absorption of pleural fluid are altered. Causes bacterial pneumonia, malignancy, viral infection, and pulmonary embolism. If one or more of the exudative criteria are met and the patient is clinically thought to have a condition producing a transudative effusion, the difference between the protein levels in the serum and the pleural fluid should be measured. If this gradient is greater than 31 g/L (3.1 g/dL), the exudative categorization can be ignored because almost all such patients have a transudative pleural effusion. Diagnosis Thoracentesis and pleural biopsy may be necessary to establish the nature of a pleural effusion that has been recognized radiographically. CT and MRI are usually not useful in determining the exact cause of a pleural effusion. Differential Diagnosis
Fishmans Pulmonary Disease 4 th edition Harrison Internal Medicine 18 th edition MALIGNANT PLEURAL EFFUSION Malignancies Associated with Pleural Effusion Most common malignancy to invade the pleura and produce effusion is Carcinoma of the lung 2 nd cause is by Breast cancer Metastatic carcinoma of lymphoma (10%), Ovarian and gastric cancer (5%). Less common is primary tumor of the pleura, malignant mesothelioma. Clinical Presentation Pleural effusion (effusions is greater than 500 mL), cough and dyspnea on exertion (depends on size of effusion and patient underlying pulmonary function). Thoracentesis results in relief of dyspnea in most patients Chest pain may be present because of involvement of the parietal pleura, ribs, or chest wall Weight loss and appear chronically ill Cachexia and lymphadenopathy 25% patient with metastatic carcinoma is asymptomatic About 20 percent of patients with lymphoma have no respiratory symptoms when the malignant pleural effusion is diagnosed. Malignant mesothelioma usually related to asbestos exposure, patient with mesothelioma present with chest pain and shortness of breath. The chest radiograph reveals a pleural effusion, generalized pleural thickening, and a shrunken hemithorax (thoracostomy is needed for diagnosis) Chest Radiographic Pleural effusion ipsilateral to the primary lesion is the rule in carcinoma of the lung Interstitial infiltrates with effusions (lymphangitic carcinomatosis) and multiple nodules with effusions also suggest malignant disease. Mesothelioma may show a moderate to large pleural effusion (early) or a nodular, thickened pleura with extension to the apex of the hemithorax (late). Pleural fluid may be serous, serosanguinous, or grossly bloody an exudate with a protein concentration of about 4 g/dl. However, protein concentrations have been reported in the range of 1.5 to 8.0 g/dl. The number of nucleated cells in the pleura fluid is modest (1500 to 4000/l) and consists of lymphocytes macrophages, and mesothelial cells. In about one-half of malignant pleural effusions, lymphocytes predominate (5 to 70 percent of nucleated cells). Malignant cells in pleural fluid are rare in some patients Polymorphonuclear leukocytes usually represent less than 25 percent of the cell population pleural fluid pH is low (less than 7.30), ranging from 6.95 to 7.29 glucose concentration is also low (less than 60 mg/dL, or the ratio of pleural fluid to serum glucose is below 0.5, lactate concentration is high, the PcO2 is high, and the PO2 is low Diagnosis: Detecting exfoliated malignant cells in pleural fluid or in pleural tissue obtained by percutaneous pleural biopsy, thoracoscopy, or thoracotomy, or at autopsy immunohistochemistry in the diagnosis of malignant pleural effusions secondary to adenocarcinoma, mesothelioma, and lymphoma has been established. Flow cytometry, a technique used to quantitate nuclear DNA levels, is useful in the evaluation of lymphocytic pleural effusions in which lymphoma is a possible diagnosis Treatment *Radiation of the hemithorax is contraindicated in malignant pleural effusions from lung cancer, since the adverse effects from radiation pneumonitis outweigh possible benefits of therapy.
Prognosis The diagnosis of a malignant pleural effusion signals a poor prognosis. Patients with carcinoma of the lung, stomach, and ovary tend to have a survival time of only a few months from the time that the malignant effusion is diagnosed; patients with breast cancer may survive longer, several months to years, depending on the response to chemotherapy. pH and glucose concentrations in the malignant pleural effusion are low (below 7.30 and 60 mg/dl, respectively), the survival time is less (average 2 months) than in those with a normal pH and glucose (average 10 months).
NON MALIGNANT PLEURAL EFFUSION PLEURAL EFFUSION SECONDARY TO PULMONARY EMBOLIZATION Dyspnea is the most common symptom. The pleural fluid is almost always an exudate. The diagnosis is established by spiral CT scan or pulmonary arteriography. Treatment is the same as for any patient with pulmonary emboli. If the pleural effusion increases in size after anticoagulation, the patient probably has recurrent emboli or another complication such as a hemothorax or a pleural infection. TUBERCULOUS PLEURITIS Usually associated with primary TB and are thought to be due primarily to a hypersensitivity reaction to tuberculous protein in the pleural space. S&S: fever, weight loss, dyspnea, and/or pleuritic chest pain. The pleural fluid is an exudate with predominantly small lymphocytes. Diagnosis: high levels of TB markers in the pleural fluid (adenosine deaminase > 40 IU/L, interferon > 140 pg/mL, or positive polymerase chain reaction (PCR) for tuberculous DNA). Alternatively, by culture of the pleural fluid, needle biopsy of the pleura, or thoracoscopy. Treatment: identical with TB PARAPNEUMONIC EFFUSION Associated with bacterial pneumonia, lung abscess, or bronchiectasis and are probably the most common cause of exudative pleural effusion in the United States. Empyema refers to a grossly purulent effusion aerobic bacterial pneumonia acute febrile illness consisting of chest pain, sputum production, and leukocytosis. anaerobic infections a subacute illness with weight loss, a brisk leukocytosis, mild anemia, and a history of some factor that predisposes them to aspiration.
PLEURAL EFFUSION DUE TO HEART FAILURE The most common cause of pleural effusion is left ventricular failure. The effusion occurs because the increased amounts of fluid in the lung interstitial spaces exit in part across the visceral pleura. This overwhelms the capacity of the lymphatics in the parietal pleura to remove fluid Thoracentesis should be performed if the effusions are not bilateral and comparable in size, if the patient is febrile, or if the patient has pleuritic chest pain, Best treated with diuretics. If the effusion persists despite diuretic therapy, a diagnostic thoracentesis should be performed. A pleural fluid N-terminal probrain natriuretic peptide (NT-proBNP) >1500 pg/mL is virtually diagnostic of an effusion secondary to congestive heart failure. VIRAL PLEURAL EFFUSION Viral infections are probably responsible for a sizable percentage of undiagnosed exudative pleural effusions. In many series, no diagnosis is established for ~20% of exudative effusions, and these effusions resolve spontaneously with no long-term residua. Pleural fluid cell count usually reveals a predominance of mononuclear cells. AIDS Uncommon. The most common cause is Kaposis sarcoma, followed by parapneumonic effusion. Other common causes are TB, cryptococcosis, and primary effusion lymphoma. Pleural effusions are very uncommon with Pneumocystis carinii infection. CHYLOTHORAX A chylothorax occurs when the thoracic duct is disrupted and chyle accumulates in the pleural space. Cause : Trauma, tumors in the mediastinum. S&S : Dyspnea, and a large pleural effusion is present on the chest radiograph. Thoracentesis reveals milky fluid, and biochemical analysis reveals a triglyceride level that exceeds 1.2 mmol/L (110 mg/dL). Patients with chylothorax and no obvious trauma should have a lymphangiogram and a mediastinal CT scan to assess the mediastinum for lymph nodes. Treatment: Insertion of a chest tube plus the administration of octreotide. If fail, a pleuroperitoneal shunt should be placed unless the patient has chylous ascites. Should not undergo prolonged tube thoracostomy with chest tube drainage because this will lead to malnutrition and immunologic incompetence. HEMOTHORAX Diagnosis: If there is bloody pleural fluid, a hematocrit should be obtained on the pleural fluid. If the haematocrit is more than half of that in the peripheral blood, the patient is considered to have a hemothorax. Cause: of trauma; other causes include rupture of a blood vessel or tumor. Treatment: tube thoracostomy MISCELLANEOUS CAUSES OF PLEURAL EFFUSION