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Chest Wall, Lung, Mediastinum, & Pleura
May 11, 2010
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Trachea
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Tracheal Injury Tracheal Stenosis Resection and primary anastomosis
Over-inflation of the cuff Ischemia, scarring, stricture Fistula development Incorrect placement of the tracheostomy through the first tracheal ring or the cricothyroid membrane Use of a large tracheostomy tube Stridor and dyspnea on exertion Resection and primary anastomosis
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TracheoInnominate Artery Fistula
Causes Too low placement of the tracheostomy (below the 4th ring) Hyperinflation of the tracheal cuff Typically occur 2 weeks after tracheostomy Signs Sentinel bleed Heavy bleed – blow up cuff Insert finger and press against manubrium Oral intubation and emergent resection of fistlua
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TracheoEsophageal Fistula
Causes ETT cuff compresses against NG tube Signs Gastric contents or tube feeds suctioned from airway Gastric distention from positive pressure ventilation Diagnosis Bronchoscopy or EGD Treatment Wean off vent Remove NG and place GT or JT Operative repair involves resection and primary repair of tracheal pathology, repair of esophagus, and interposition muscle flap
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Tracheal Neoplasms Rare SCC or adenoid cystic carcinoma
Cough, dyspnea, hemoptysis, stridor, or symptoms of invasion of contiguous structures 50% of patients have tracheal stenosis on Xray 50% have stage IV dz at time of diagnosis Overall 5-year survival is 40%, but falls to 15% for those with stage IV disease
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Surgical Approaches to the Thoracic Cavity
Posterior Thoracotomy – most common approach for pulmonary resections, esophageal procedures, posterior mediastinal access, and vertebral procedures Patient in lateral decubitus – risk of injury to brachial plexus or axillary vascular structure Anteriolateral Thoracotomy – trauma victims Median sternotomy – cardiac procedures VATS – improved pain and functional recovery Improved ability to tolerate chemotherapy Quicker return of respiratory function in elderly and COPD
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Post-operative Care Chest Tube Pain Control
Evacuation of air Evacuation of blood/pleural fluid Check the system regularly Pain Control Epidural at T6 with ropivicaine Hypotension and urinary retention Narcotics and Toradol Aggressive Pulmonary Toilet
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Post-operative Complications
Air leak Bronchopleural fistula Diagnose by bronchoscopy Continued chest tube mgmt Operative closure with intercostal muscle flap Bronchoscopic fibrin glue application (<4mm) Concomitant empyema may require open drainage Post-pneumonectomy pulmonary edema Decreased lympnatic drainage Mechanical ventilation & diuresis
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Lung Solitary Pulmonary Nodule
A single, well-circumscribed, spherical lesion ≤3 cm in diameter Completely surrounded by normal aerated lung parenchyma Detected incidentally on chest radiographs or CT scans DDx – malignancy, hamartoma (10%), granulomatous dz (70%) 20 to 40% likelihood of being malignant 50% or higher in smokers growth over time, density of the lesion on CT associated symptom age, sex, cigarette smoking history, occupational history, prevalence of endemic granulomatous disease
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Lung Cancer Leading cause of cancer-related death (30%)
Second most common diagnosed cancer Women – breast Men – prostate
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Lung Cancer Epidemiology
Leading risk factor – smoking (polycyclic aromatic hydrocarbons) Secondhand smoke also increases risk Environmental exposures - asbestos, arsenic, and chromium compounds COPD h/o tuberculosis
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Lung Cancer Non-small cell carcinoma vs neuroendocrine tumors
NSCLC - large cell carcinoma, squamous cell carcinoma, adenocarcinoma, and BAC Clinical behavior and treatment options are similar and thought of as a uniform group Neuroendocrine - typical carcinoid, atypical carcinoid, large cell neuroendocrine carcinoma, and small cell carcinoma
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Squamous Cell Carcinoma
30 to 40% of lung cancers Highly associated with cigarette smoking Primarily located centrally and arises in the major bronchi Typical symptoms are hemoptysis, bronchial obstruction with atelectasis, dyspnea, and pneumonia Peripherally based SCC will develop in a tuberculosis scar or in the wall of a bronchiectatic cavity Central necrosis is frequent and may lead to the radiographic findings of a cavity (air-fluid level) May become infected & form an abscess
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Adenocarcinoma Incidence has increased over the last several decades & now 25 to 40% of all lung cancers. Most frequent histologic type found in women Peripherally based tumor Frequently discovered incidentally on routine chest radiographs Symptoms of chest wall invasion or malignant pleural effusions Composed of glands with or without mucin production and destruction of contiguous lung architecture
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Bronchoalveolar Carcinoma
Unusual (5% of all lung cancers) subtype of adenocarcinoma Unique growth pattern Rather than invading and destroying contiguous lung parenchyma, tumor cells multiply and fill the alveolar spaces Because of their growth within alveoli, BAC tumor cells from one site can aerogenously seed other parts of the same lobe or lung, or the contralateral lung. Three radiographic presentations: a single nodule multiple nodules (in single or multiple lobes) diffuse form with an appearance mimicking that of a lobar pneumonia Air bronchograms can be seen
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Large Cell Carcinoma 10 to 20% of lung cancers and may be located centrally or peripherally Often admixed with other cell types such as squamous cells or adenocarcinoma May be confused with a large cell variant of neuroendocrine carcinoma, with immunohistochemical staining usually allowing diagnostic distinction between the two
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Neuroendocrine Carcinoma
Grade I NEC (classic or typical carcinoid) is a low-grade NEC primarily in the central airways primarily in younger patients. classically presents with hemoptysis, with or without airway obstruction and pneumonia Regional lymph node metastases are seen in 15% of patients but rarely spread systemically or cause death Grade II NEC (atypical carcinoid) tumors with a degree of aggressive clinical behavior linked to cigarette & peripherally located Much higher malignant potential. Lymph node metastases found in 30 to 50% of patients At the time of diagnosis, 25% have remote metastases Grade III NEC large cell–type tumors occur primarily in heavy smokers Grade III NEC small cell type [small cell lung carcinoma (SCLC)] is the most malignant NEC and accounts for 25% of all lung cancers Immunohistochemical stains distinguish from NSCLC Leading producer of paraneoplastic syndromes
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Paraneoplastic Syndromes
Table 19-5 Hypercalcemia (ectopic parathyroid hormone) Cushing's syndrome Syndrome of inappropriate secretion of antidiuretic hormone Carcinoid syndrome Gynecomastia Hypercalcitoninemia Elevated growth hormone level Elevated levels of prolactin, follicle-stimulating hormone, luteinizing hormone Hypoglycemia Hyperthyroidism Neuropathy
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Metastatic Symptoms Lung cancer metastases occur most commonly to the CNS, vertebral bodies, bone, liver, adrenal glands, lungs, skin, and soft tissue At diagnosis, 10% of patients have CNS metastases another 10 to 15% will go on to develop CNS metastases after diagnosis. Focal symptoms are most common and include headache, nausea and vomiting, seizures, hemiplegia, and speech difficulty Most common cause of spinal cord compression Invasion of an intervertebral foramen from a primary tumor contiguous with the spine Direct extension of a vertebral metastasis. Bony metastases, are identified in 25% - lytic and painful Liver & adrenal metastases are typically asymptomatic and discovered by routine CT scan Skin and soft tissue metastases occur in 8% of patients dying of lung cancer and generally present as painless subcutaneous or intramuscular masses
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Assessment of Primary Lung Cancer
History and directed questions regarding the presence or absence of pulmonary, nonpulmonary, thoracic, and paraneoplastic symptoms Imaging Nodes and invasion Tissue diagnosis Bronchoscopy or percutaneous biopsy Thoracoscopy or rarely thoracotomy
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Staging Mediastinal nodes Distant mets Stations 4 & 7
CT scan & perc biopsy PET Bronchoscopy Mediastinoscopy EUS w FNA Distant mets PET-CT
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Staging System
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Chest Wall Tumors
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Mediastinal Tumors Anterior (thymus) Thymoma – always resect
50% malignant 50% have symptoms 50% have myasthenia gravis Thyroid cancer and goiter T-cell lymphoma – treat with XRT and chemo Teratoma – resection and chemo Seminoma – resectiona and XRT Parathyroid adenoma
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Mediastinal Tumors Middle (heart, trachea, ascending aorta)
Bronchiogenic cyst – posterior to the carina - resect Pericardial cyst – at right costophrenic angle – resect Enteric cyst - resect Lymphoma Posterior (esophagus, descending aorta) Enteric cysts Neurogenic tumors – cause pain and neurologic deficit – resect – 10% have intraspinal involvement
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Pleural Disease Pleural effusion - any significant collection of fluid within the pleural space Transudative vs exudative Chylothorax – injury to thoracic duct
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Pleural Tumors Malignant mesothelioma Fibrous Tumors
50% associated with asbestos exposure Patients present with dyspnea and chest pain Treatment options include supportive care only, surgical resection, and multimodality approaches Fibrous Tumors Unrelated to asbestos exposure or malignant mesothelioma Single pedunculated mass arising from the visceral pleura Found incidnetally Benign or malignant Symptoms such as cough, chest pain, and dyspnea occur in 30 to 40% of patients Less common are fever, hypertrophic pulmonary osteoarthropathy, hemoptysis, and hypoglycemia Cured by complete surgical resection
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