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98 Cards in this Set
- Front
- Back
Seemingly normal CXR:
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tracheomegaly, dilated esophagus, PTX, lobar collapse
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Interstitial (general/perihilar) on CXR:
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interstitial pulmonary edema, lymphangitic spread of CA (colon, lung, breast, gastric), infectious (viral/Mycoplasma, miliary TB, fungal, PCP)…
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Apical Cap
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(if smooth, think extrapleural): subpleural fat extending from mediastinal lipomatosis (smooth), lymphoma/infection extending from the neck or mediastinum (smooth), extrapleural hematoma (smooth), nonspecific apical/subpleural scarring (not smooth), superior sulcus tumor, radiation fibrosis
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Bronchiectasis (irreversible dilitation of the bronchi - may be cylindrical, varicoid, or cystic ):
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postinfectious (most common), congenital (CF, Kartageners, William Campbell, Mounier-Kuhn); ABPA (usually central and varicoid bronchiectasis – not seen until finger and glove clear; classic additional findings are mucoid impaction, patchy migratory atelectasis and consolidation)
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Crazy Paving (smoothly thickened septal lines superimposed on ground glass opacities):
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PAP, edema, infection…esp viral or PCP (look for cysts)
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Collapse of entire lung:
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mucous plug, aspirated FB, malpositioned ETT, obstructing neoplasm (bronchogenic CA, carcinoid, mets)
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Mosaic pattern
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Air trapping 2o small airways disease (get expiration view): BO, URI with bronchiolitis, asthma
Decreased perfusion 2o small vessels disease: vasculitis, microemboli Imflammatory: infection, hypersensitivity pneumonitis |
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Miliary nodules (look for superior medistinal mass – thyroid):
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(3-5mm) Infection (TB, fungi – disseminated histo or blasto [may or may not be immunocompromised], varicella) , mets (melanoma, RCC, chorioCA, thyroid), silicosis, healed varicella, Langerhans cell histiocytosis
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Multiple cavitary lesions:
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Septic emboli (Staph secondary to IVDA or indwelling line, Apergillus/Mucor in immunocompromised), mets (usually SCC), Wegener’s (appears angiocentric!)
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Solitary Cavity:
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TB, fungal (cocci…which is usually thin grapeskin walled, histo, blasto) pyogenic abscess (Staph, Klebsiella, E coli, Pseudomonas, anaerobes), bronchogenic CA (usu sq cell), Nocardia, secondary Aspergillus infection of cavity, septic emboli (Staph aureus), mets (usu sq cell), lymphoma (Hodgkin’s), rheumatoid nodule, Wegener’s, large hiatal hernia, silicosis, lymphomatoid granulomatosis, Echinococcus (also thin wall)
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Smooth or nodular centrilobular and interlobular septal thickening on HRCT (with preservation of architecture):
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Lymphangitic spread of CA (colon, lung, breast, gastric), lymphoma, sarcoidosis, and Kaposi’s
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Solitary pulmonary nodule:
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granuloma (TB, fungus ESPECIALLY HISTO…fungal nodules account for 30% solitary pulmonary nodules per Galvin), hamartoma, lung CA, carcinoid, met, lymphoma, abscess, bronchogenic cyst, AVM, and if immunocompromised: Nocordia, Aspergillus, and PTLD…
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Large thoracic mass:
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tumor (bronchogenic CA, lymphoma), mets, infection (abscess, round PNA), rounded atelectasis, sequestration, hematoma; extrapulmonary – fibrous tumor of pleura, loculated effusion , chest wall mass, mediastinal mass, AAA
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Tubular opacity on CXR or CT:
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Mucoid impaction (ABPA, CF, obstructed bronchus distal to mass, congenital bronchial atresia) versus vascular malformation
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HIV with lung nodule:
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: fungal, mycobacterial (TB), septic infarct, Kaposi’s, lymphoma
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Post-transplant lung nodule(s):
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infection – Aspergillus, Nocardia, CMV (usually no LAD with infections) versus PTLD (4-6 mos post transplant with assd LAD)
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Post-lung transplant complications:
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reperfusion edema (fist 1-5 days), acute rejection (1st 3 mos), infection (1st month = bacterial, after 1st month – CMV)
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Endobronchial spread of infection (tree-and-bud):
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Bacterial: TB, MAC, Staph, H. flu; Fungal: Apergillus; Viral: CMV, RSV
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Unilateral absence of perfusion on Tc99-MAA scan:
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hilar/mediastinal mass, ascending aortic aneurysm, hypoplastic pulmonary artery, s/p pneumonectomy, large PE
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Interstitial upper zone:
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CASSETP – CF (not an interstitial disease), AS, sarcoid, silicosis, EG, TB, PCP, chronic hypersensitivity pneumonitis, radiation fibrosis, chronic fungal infection
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Interstitial lower zone:
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BADARDS – bronchiectasis (not an interstitial disease), asbestosis, drugs (amiodarone, bleomycin, MTX), aspiration (chronic), RA, DIP/UIP, SLE/scleroderma, neurofibromatosis
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Peripheral consolidation:
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BOOP/COP (cryptogenic organizing pneumonia – peripheral AND peribronchovascular consolidation), eosinophilic PNA (often biapical/biaxillary distribution), pulmonary infarcts, vasculitis
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Cardiophrenic angle mass:
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prominent pericardial fat pad (most common), pericardial cyst, Morgagni hernia, epicardial lymph nodes (common site of recurrence for Hodgkins), thymic mass
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Mediastinal widening (look at trachea):
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tortuous brachiocephalic vessels or aorta, fatty deposition (mediastinal lipomatosis), mediastinal hemorrhage, malignant adenopathy, lymphoma, enlarged thyroid, mediastinitis, lung CA, thymic lesion, teratoma
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Mediastinal Adenopathy:
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General – metastatic LAD, lymphoma, TB, fungal infection (especially Histo which classically mimicks sarcoidosis), sarcoidosis
Low attenuation – TB or fungal infection esp in AIDS, necrotic mets, lymphoma, seminoma; Enhancing/Vascular – Castleman’s, vascular mets (RCC, thyroid, melanoma, carcinoid, small cell, KS, chorioCA); Calcified – TB, fungal, sarcoid, silicosis, lymphoma post radiation, disseminated PCP (immunocompromised) Intrathoracic nodal mets – GU (renal, testicular), head and neck (skin, larynx, thyroid), breast, melanoma, KS |
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Peribronchovascular/axial nodules:
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sarcoid, lymphangitic carcinomatosis, KS, lymphoma, bronchiolitis obliterans.
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Reterosternal nodular opacity on lateral CXR:
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metastatic LN’s (breast CA or lymphoma), enlarged internal mammary vessels secondary to aortic coarctation (associated with rib notching) or SVC syndrome (associated with right suprahilar mass)
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Tracheobronchomalacia
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(excessive airway collapsibility – must be diagnosed by comparing inspiration and expiration films – >50% narrowing is abnl): prolonged ETT, COPD, congenital cartilaginous deficiency, relapsing polychondritis, Wegener’s, amyloidosis, sarcoidosis, TB, tracheopathia osteochondroplastica (submucosal cartilaginous and osseous nodules of various sizes that cause a narrowing of the upper respiratory tract)
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Tracheal lumen:
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Increased (>2.5 cm AP at 2 cm above arch) – congenital tracheobronchomegaly (mounier Kuhn), pulmonary fibrosis, tracheomalacia;
Decreased – saber-sheath (COPD), tracheomalacia, relapsing polychondritis, sarcoid, amyloid, Wegener’s, TB and fungal stenosis, tracheopathia osteochondroplastica |
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Tracheal masses (intraluminal):
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#1 papilloma, #2 amyloidosis (low T1 and T2), TB, SSC, adenoid cystic CA, mets (any vascular met)
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Lobar Pneumonia
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(initial site of inflammation is alveolus, secondary pulmonary lobule completely opacified; spread occurs at intra-alveolar level hence may not conform to segmental anatomy): Strep pneumonia (#1), Klebsiella (#2 – lobar expansion aka Friedlanders pneumonia), Haemophilus
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Lobar pneumonia with necrosis/cavitation:
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Strep pneumonia (#1), Klebsiella (#2)
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“atypical pneumonia”
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= bronchiolitis ± bronchopneumonia; causes include Mycoplasma pneumonia (#1), viral infection (influenza, adenovirus), Legionella (#2)
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Bronchopneumonia
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(initial site of inflammation is bronchiole, secondary pulmonary lobule incompletely opacified): Staph, gram negatives, anaerobes, mycoplasma, legionella
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Nodular or masslike infectious consolidation:
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round pneumonia (Strep pneumonia), TB, fungus (blasto likes to do this), actinomycosis (likes to cross pleura into ribs and chest wall), nocardia (will also cross pleura into chest wall!)
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Complications of pneumonia
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necrosis secondary to vascular thrombosis, bronchopleural fistula, lung abscess, pneumatocele (ball valve effect, assocated with Staph in pediatric patients), bronchiectasis
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PAH
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systolic >30mmHg, primary (young female), secondary (chronic lung dz, chronic PE, L to R shunts, mitral stenosis, LV failure, vasculitis, drugs)
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PA stenosis
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congenital pulmonary valve stenosis (enlarged main and left PA with sparing of right PA), “TOF with absent pulmonary valves” (implies a hypoplastic pulmonic annulus and is associatd with TOF), Takayasu, rubella, Williams syndrome;
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PA dilatation
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poststenotic jet, Osler-Weber-Rendu;
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PA Aneurysm
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Takayasu, Behcets, vasculitis, trauma, infection
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Aortic aneurysm types:
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In a true aortic aneurysm, all layers of the aortic wall are intact (usually secondary to atherosclerosis but also seen with Marfans, Ehlers Danlos, syphilis, aortc valve disease). In a false aneurysm there is focal disruption of one or more layers.
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Partial absence of the pericardium
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can look just like left atrial appendage enlargement (as seen with rheumatic heart disease). Slight leftward shift of the entire cardiac silhouette (but not trachea) and lung/air extending into AP window favor former dx.
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Pneumopericardium:
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barotraumas in childrem, s/p pericardiocentesis or cardiac surgery in adults, penetrating trauma, esophageal fistula (look for fluid level) usually secondary to ulcerating mass
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Pericardial nodularity + effusion:
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metastatic disease usually from breast, lung, melanoma, or lymphoma and may be via hematogenous OR lymphatic spread. Effusion may be hemmorhagic.
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Right Hilar Convex mass on frontal CXR:
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include Sinus of Valsalva aneurysm with diff dx (as they most frequently arise from the right or the noncoronary sinus)!!! LAD, bronchogenic cyst, PA aneurysm, maybe ascending aortic aneurysm
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Sinus of Valsalva aneurysm:
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most frequently arise from the right or the noncoronary sinus; associated with aortic regurg and supracristal VSD.
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2 types of aortic coarcatation:
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Congenital = focal and juxtaductal
Acquired = segmental usually from Takayasus or (rarely) giant cell arteritis |
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Types of VSD:
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Membranous
Muscular AVSD Supracristal – between the aortic root and RV outflow tract; associated with aortic insufficiency, sinus of valsalva aneurysm, and left to right shunt |
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Cardiac viability by MRI:
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ascertained by delayed post-gad images (7-10 minutes), which demonstrate hyperenhancement in scarred (non-viable) myocardium. Normal myocardium enhances early and washes out. MRI is better than PET in that it allows better spatial resolution so that subendocardial infarct/scar can be distinguished from transmural infarct/scar. Revascularization may be of benefit if the nonviable region is <50% myocardial thickness.
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Aortic stenosis:
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Enlargement of the ascending aorta ONLY (jet phenomena), with NORMAL aortic knob and descending aorta. (With aortic regurgitation, see enlargement of all 3). 3 main causes are (1) Congenital aortic stenosis, (2) Degeneration of a bicuspid or tricuspid AV, and (3) Rheumatic heart disease
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Mitral annulus Ca+:
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Circular, C or J shaped, atherosclerotic and age-related, assoc with mitral regurgitation
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Left atrial wall calcifications:
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Due to chronic outflow obstruction (MV stenosis) and can result in Afib
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Alveolar OPACITY:
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pneumonia, aspiration, pulmonary edema, pulmonary hemorrhage; less common – bronchogenic TB, fungus, sarcoid, bronchioloalveolar CA, lymphoma, alveolar proteinosis, aspiration of blood or lipid, leukemia, BOOP, eosinophilic PNA; (blood, pus, water, cells, protein); chronic ASD – bronchioloalveolar CA, lymphoma, alveolar proteinosis, lipoid PNA, alveolar sarcoid, BOOP, eosinophilic PNA
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Pulmonary hemorrhage:
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anticoagulation, hemophilia, contusion, PE, vasculitis (Goodpasture’s, Wegener’s), CVD, infectious (TB, GNB, Aspergillus, Mucor), drugs, bronchiectasis, tumor
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HRCT: ground glass opacity
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hypersensitivity pneumonitis, all acute interstitial disease (IPF, viral), PCP, BOOP, eosinophilic PNA, pulmonary edema, alveolar proteinosis
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centrilobular nodules
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endobronchial spread of infection or tumor (TB, MAI, bronchoPNA), airways diseases (CF, bronchiectasis, TB, MAI), hypersensitivity pneumonitis, silicosis, histiocytosis, BOOP, pulmonary edema, talc
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tree-in-bud
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endobronchial spread of infection, airways diseases
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perilymphatic nodules
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sarcoid, silicosis, lymphangitic spread
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diffuse random nodules
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miliary TB, fungus, mets
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Kerley B lines:
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CHF, lymphangitic spread of CA; less common – viral, asbestosis, sarcoid, lymphoma
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Pulmonary fibrosis:
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IPF, sarcoid, pneumoconiosis, histiocytosis, CVD, talc, radiation, drugs, chronic hypersensitivity pneumonitis, NF
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Lymphangitic carcinomatosis:
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lung, breast, stomach, pancreas, prostate, thyroid
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Hematogenous pulmonary mets:
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lung, breast, kidney, thyroid, colon, uterus, head&neck, testes, melanoma, lymphoma, osteosarcoma
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Calcified nodules:
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thyroid mets, mucinous mets, osteogenic mets, varicella, TB, histo, cocci, silicosis, alveolar microlithiasis
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Eggshell calcifications in hilar nodes:
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silicosis, CWP, treated lymphoma, granulomatous dz, sarcoid (rare)
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Conglomerate masses:
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silicosis, CA, TB, fungus, sarcoid, berylliosis
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Hilar mass:
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bilateral + symmetric (TB, fungal, sarcoid, mets, lymphoma, silicosis, PA enlargement), bilateral + asymmetric (TB, fungal, sarcoid, mets, lymphoma, silicosis, PA enlargement), unilateral (TB, fungal, sarcoid, mets, lymphoma, lung CA, carcinoid Castleman’s, PA enlargement, bronchogenic cyst); (per UCSD -5 infections) – TB, Histo, Anthrax, Brucellosis, Plague
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Superior mediastinal mass:
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thyroid, adenopathy, cystic hygroma, lymphoma, mets, vascular, parathyroid
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Anterior mediastinal mass:
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thymic lesion (thymoma), lymphoma (Hodgkin’s), germ cell tumor (teratoma), thyroid (intrathoracic goiter), vascular (aneurysm), bronchogenic cyst, pericardial cyst, lymphangioma, hemangioma, lipoma, TB, fungus, sarcoid, mets
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Middle mediastinal mass:
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thyroid (intrathoracic goiter), esophageal lesion (leiomyoma, duplication cyst), bronchogenic cyst, pericardial cyst, vascular lesion (aneurysm, aberrant vessel), mets (head and neck, GU, breast, melanoma), lung CA (small cell), lymphoma, leukemia, KS, TB, fungus, sarcoid, hiatal hernia, Castleman’s disease
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Posterior mediastinal mass:
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neurogenic tumor (neurofibroma, schwannoma, ganglioneuroma, neuroblastoma, pheochromocytoma, paraganglioma), anterior or lateral thoracic meningocele, bronchogenic cyst, gastroenteric cyst, neuroenteric cyst, TB spine, paraspinal lymphoma, vascular, hematoma, extramedullary hematopoeisis, Bochdalak hernia, sequestration, mets, sarcoid
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Fatty mediastinal mass:
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mediastinal lipomatosis, hernia, lipoma, liposarcoma, thymolipoma, teratoma
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Densely enhancing mediastinal mass:
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vascular, hypervascular tumors, goiters, Castleman’s
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Cyst:
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traumatic cyst, hematoma cyst, bronchogenic cyst, hydatid cyst, emphysematous bullae, bronchiectasis, end-stage interstitial disease, sequestration, CAM, pneumatocele; small cystic dz – EG, LAM, cystic PCP, honeycombing, emphysema
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Air crescent sign in cavity:
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Aspergillus, Mucor, Actinomycosis, septic emboli, Klebsiella, TB, tumors (KS)
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Endobronchial:
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tumor (usu sq cell > small cell, carcinoid), mets, TB, hamartoma, papilloma, hemangioma, foreign body, mucus plug, trauma, broncholith
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Scarring:
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prior TB, prior pneumonia, prior PE, prior trauma, prior surgery, radiation, fibrosis
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Calcification:
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granuloma (TB, fungus), hamartoma, lung CA, vascular, pleural (asbestos exposure, prior pyothorax or hemothorax), sarcoid, silicosis, varicella, mitral stenosis, mets (bone tumor, mucinous tumors, post-chemotherapy), alveolar microlithiasis, parasites
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Air fluid level:
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lung (abscess, tumor, cyst), mediastinum (esophageal lesion, bronchogenic cyst), pleural (hydroPTX, hemoPTX, pyoPTX, bronchopleural fistula), hiatal hernia, achalasia,
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Atelectasis:
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poor diaphragmatic excursion, hypoventilation, PE; central obstruction – endobronchial mass (bronchogenic CA, mucus plug, foreign body), extrinsic mass (large lymph nodes, large heart, aneurysm, mediastinal mass); peripheral obstruction – pneumonia, post-surgery (LLL after cardiac surgery); compression – pleural effusion, PTX; contraction – scarring from chronic TB or any pulmonary fibrosis
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Complete opacification of one hemithorax:
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complete atelectasis (bronchogenic CA, mucus plug, ETT too low), large effusion (mets, lymphoma), prior pneumonectomy, malignant mesothelioma, unilateral pneumonia or pulmonary edema
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PTX:
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emphysema (ruptured bulla), trauma (rib puncture, ruptured bronchus), iatrogenic (line placement, thoracentesis), any chronic interstitial lung disease or pneumoconiosis, pulmonary fibrosis, spontaneous, ventilator, bronchopleural fistula, infection (Staph), neoplasm (metastatic osteosarcoma), LAM, EG, asthma, PCP, catamenial
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Pneumomediastinum:
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asthma, trauma, alveolar rupture, ruptured bronchus or esophagus, post endoscopy, Boerhaave syndrome, positive pressure ventilation, chest tube placement, ruptured abdominal viscus, post surgical, pneumo(retro)peritoneum
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Pleural effusion:
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infectious, tumor (lung CA, mets, lymphoma), CHF (R>L), nephrotic syndrome, renal failure, liver failure, post-surgery (L post-cardiac surgery), post-trauma, mesothelioma, asbestosis, ovarian CA (Meig’s syndrome), pancreatitis, Dressler syndrome, CVD, sarcoid, drugs, ascites, PE, leukemia
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Chylothorax:
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tumor (esp lymphoma), trauma, iatrogenic, idiopathic, LAM, filariasis
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Pleural mass:
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mesothelioma, benign fibrous tumor, malignant thymoma/lymphoma, mets (esp lung CA), lipoma, rib tumors (children – EG, ABC, Ewing’s, neuroblastoma; adults – mets>myeloma>Paget’s, fibrous dysplasia), neurofibromas, infection (TB, fungus, Actinomycosis), asbestos-related, trauma, surgery
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Calcified pleural plaques:
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TB, asbestos exposure, fluid (empyema, hematoma), talc
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Pleural thickening + calcification:
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old infection, old trauma, asbestos exposure, loculated effusion, empyema, pleural mets, mesothelioma, talc
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Extrapleural lesions:
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CA (mets, myeloma, esp rib mets), infection (TB, fungus, Actinomycosis), trauma (hematoma), diaphragmatic rupture or paralysis, pectus excavatum, kyphoscoliosis, cervical ribs, congenital fusion of ribs
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Elevated diaphragm:
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localized eventration, atelectasis, subpulmonic effusion, diaphragmatic paralysis, hernia (hiatal, Morgagni, Bochdalak), ascites, subphrenic mass, pleural mass
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Oligemia and/or overinflation:
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infection (TB, Staph pneumatocele, viral, parasite), pulmonary HTN, asthma, emphysema, bullae, lobar atelectasis with compensatory hyperinflation, Swyer-James-Macleod syndrome = bronchiolitis obliterans (unilateral hyperlucent lung), PE (Westermark’s sign), foreign body or mucus plug (air trapping), lung hypoplasia, scimitar syndrome, mastectomy, congenital bronchial atresia, congenital lobar emphysema, Poland’s syndrome (congenital absence of pectoralis muscle), PA stenosis/hypoplasia
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Bronchiolitis obliterans:
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postinfectious, CVD (esp RA), toxic fumes, post transplant (BMT), lymphoma, lung CA, idiopathic
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Mosaic attenuation (air trapping):
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BO, sarcoid, hypersensitivity pneumonitis, chronic PE, asthma, emphysema
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Small lung:
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hypogenetic lung syndrome, PA agenesis, chronic atelectasis, BO
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Small hilum:
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PA compression/invasion/hypoplasia, lobar atelectasis/resection, emphysema
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Enlarged cardiac silhouette:
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cardiomegaly, pericardial effusion
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Blunted CPA
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pleural effusion, pleural thickening
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SVC syndrome:
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bronchogenic CA (#1), lymphoma, mets, long term IV devices, fibrosing mediastinitis
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