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87 Cards in this Set
- Front
- Back
where is the ligament of treitz
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between the 4th segment of the duodenum and the jejunum
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what is the nml small bowel diameter
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2.5 cm
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nml wall thickness of small bowel
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</ = 3mm
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ct appearance of crohn's dz in small bowel
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inflammation of bowel wall, mucosa, and mesentary (in skip lesion pattern)
TI often involved bowel wall enhances with contrast fistulas mesenteric abscess |
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ct findings of complete small bowel obstruction
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bowel diameter >2.5 cm
collapsed bowel distal to obx (= transition zone) |
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ct findings of small bowel ileus
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diffusely dilated bowel loops, no transition zone b/c everything is dilated
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what is the most common cause of sbo
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adhesions (but not commonly seen on ct)
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risk factors for intussusception
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seen with lymphoma, lipoma, carcinoma, mets
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describe appearance of intussusception on ct
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there is a bowel loop inside the lumen of another bowel loop, creating a target appearance, there is cecal mesentary (fat density) surrounding intussuseptum
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in sbo, what finding indicates that bowel wall is still viable
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contrast enhancement of bowel wall
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what is a closed sbo
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obstruction on 2 separate ends of bowel wall
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what causes closed sbo
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usually from adhesions or hernia
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on plain film, how to distinguish btwn ileus vs obstruction
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if you get an upright film, with an ileus, there will be equal air-fluid lvls at dependent portions of bowel loop
in obstruction, these levels are unequal (picture a manometer) |
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how big does appendix have to be for appendicitis to be considered
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>6mm
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describe the anatomy of the paracolic gutters
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the ascending and descending colon are retroperitoneal. the peritoneum sweeps anteriorly over these portions and extend laterally, forming the paracolic gutter
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t or f:
most diverticuli are along mesenteric surface |
true
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general findings of colitis
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thickening of bowel wall, if total wall width >3mm when distended
mural thickening with homogeneous enhancement or halo appearance |
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ct findings of ulcerative colitis
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wall thickening (7-8 mm) with lumen narrowing +/- inflammatory pseudopolyps
no skip lesions, starts in rectum, which is narrowed OUTER WALL IS SMOOTH! |
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ct findings of general crohn's dz
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TI and prox colon most often involved
bowel wall thickened (10-20mm) irregular outer wall |
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difference in ct findings btwn acute active crohn's and chronic dz
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target/halo sign seen in acute dz
chronic dz = fibrosis and fat prolif |
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ct findings of c diff
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pancoliits or segmental irregular wall thickening </= 30mm
wall has accordian like appearance |
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what is typhlitis
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neutropenic colitis
potentially fatal infx of cecum and ascending colon |
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toxic megacolon
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dilation of colon to 5cm, with thinning of colon wall
--> pneumatosis, perforation |
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`what are the 4 major causes of pneumatosis intestinalis
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bowel necrosis
mucosal disruption (from PUD, endoscopy, tubes, trauma, IBD) increased mucosal permeability from immunosup pulmonary causes (copd, cf, asthma, intubation) |
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cystic pneumatosis
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well-defined blebs or grapelike clusters with nml tissue surrounding
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what is a volvulus
what do you see on ct |
sigmoid colon twists on mesocolon, see "whirl sign"
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true or false:
centrolobular bronchioles are not visible in healthy pts |
true
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can you see the central artery within each lobule
where do these arteries extend to |
yes
they do not make it to the pleura unless there is atelectasis |
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causes of thickened intralobular septa
describe thickening for each cause |
lymphangitic spread of CA (smooth or nodular)
interstitial pulmonary edema (smooth) alveolar proteinosis (smooth thickening with ground glass opacity) sarcoidosis (nodular if granulomata are present, irregular in fibrotic or end stage) |
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findings of pulmonary fibrosis
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intralobular interstitial thickening (early, see fine reticular pattern)
honeycombing traction bronchiectasis visualization of intralobular bronchioles |
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describe honeycombing
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fibrosis with lung destruction and disorganization of lung architecture
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describe traction bronchiectasis
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dilated bronchi in region of fibrosis
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causes of fibrosis
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idiopathic (#1)
collagen vascular dz drug related asbestosis end stage hypersensitivity pneumoniti s end stage sarcoid |
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describe the pattern of distribution for multiple pulmonary nodules
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perilymphatic
random centrilobular |
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describe perilymphatic distribution of pulmonary nodule s
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nodules near pleural surfaces
large pulmonary vessels and bronchi interlobular septa centrilobular regions |
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describe pattern of random distribution of pulmonary nodules
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involve pleural surfaces
have diffuse, uniform distribution, but are randomly distrubuted throughout the lung structure |
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describe centrilobular distribution of pulmonary nodules
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spares pleural surfaces
nodules surrounding vessels no nodules will touch the pleural surface |
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which type of nodular pattern will also have tree in bud
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centrilobular
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etiology of tree in bud appearance
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mycoplasm infx
cf bronchiectasis |
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what can cause centrilobular nodular pattern
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small airway dz
endobronchial spread of bronchoalveolar CA BOOP TB |
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describe pathophys behind tree in bud
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mucous, pus in dilated centrilobular bronchioles
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what things can cause random nodular distribution
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miliary tb
hematogenous mets |
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what does a consolidation look like on ct
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obscured pulmonary vessls
air bronchograms +/- centrilobular nodules |
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ddx of consolidation
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depends on duration of sx
if acute: PNA, ARDS, edema, hemorrhage if chronic: BOOP, bronchoalveolar CA, chronic eosinophilic PNA |
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what is the difference btwn consolidation and ground glass opacity
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with ground glass opacity, you can still see the BV
lungs just look hazy |
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ddx for ground glass opacity
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depends on duration of sx
if acute: PCP/viral PNA edema hemorrhage acute hypersensitivity pneumonitis if chronic: BOOP bronchoalveolar CA lipoid PNA Pulmonary alveolar proteinosis |
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in a pt with acute sx, what does ground glass opacity indicate
and in chronic dz |
active dz
usually means active dz, but sometimes ground glass opacity can develop 2/2 fibrosis |
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appearance of mets that have lymphangitic spread
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interlobular septal thickening
peribronchial cuffing thickened fissures thin, patchy unilateral distribution |
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appearance of mets that have hematogenous spread
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randomly distributed small nodules
pleural and fissure thickening large nodules bilateral distribution |
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ct findings of idiopathic pulmonary fibrosis
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intralobular thickening
honeycombing traction bronchiectasis subpleural, postero/inferior lung involvement +/- ground glass opacity |
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NSIP
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non-specific interstitial PNA
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ct findings of NSIP
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ground glass opacitiyes in posterior lung region
spares immediate subpleural lung reticular formation traction bronchiectasis |
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ct findings of active sarcoid
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perilympatic nodules (1-10mm) +/- calcs
pathcy distribution, asymmetric upper lobe preodominance |
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ct findings of chronic sarcoid
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irregular septal thickenin g
architectural distortion ectatic bronchi |
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ct findings of silocosis and coal workers pneumoconiosis
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perilymphatic nodule s
symmetric distribution posterior lung fields superior lobes mases of nodules or fibrosis in upper lobes LAD |
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complication of pulmonary alveolar proteinosis
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nocardia or mycobacterial superinfx
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describe pathophys of pulmonary alveolar proteinosis
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filling of alveolar spaces with lipid rich, proteinaceous material, usually idiopathic, but can be 2/2 silica, malignancy or chemo
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ct findings of pulmonary alveolar proteinosis
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pathcy or geographic ground glass opacity
smooth interlobular septal thickening in regions of ground glass opacity (= crazy paving) |
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ct findings of hypersensitivity pneumonitis
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patchy or geographic ground glass opaity
poorly defied centrilobular nodules of ground glass opacitiy mosaic perfuson from bronchiolar abn air trapping |
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complications of pulmonary alveolar proteinosis
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suprainfection with nocardia or mycobacteria
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etiologies of boop
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idiopathic
2/2 toxins drug rxn autoimmune |
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clinical course of boop
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progressive sob
fever |
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ct findings of boop
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patchy nodular consolication/ground glass opacity
peripheral or peribronchial distribution |
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ct findings of histiocytosis
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centriolobular nodules early in course
cystic lesions late in course sparing of costophrenic angle upper lobe predominance |
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who gets lympahgiomyomatosis
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women of child bearing age who have had spont ptx, sob, cylous pleural effusion
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ct findings in lymphagiomyomatosis
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thin walled rounded cysts with intervening nml lung
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variant of lymphangiomyomatosis
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women with tuberous sclerosis get the same thing
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features of high risk pulm nodules
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irregular, spiculated edge
lobulated contour air bronchograms cavitation with cavitary wall (>15 m) diameter >2 cm |
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presentation of bronchoalveolar carcinoma
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can present as ground glass opacities or halo sign
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appearance of hamartoma
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smooth, rounded
contain either all fat, fat + calcs, or all calcs |
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where is rounded atelectasis usually found
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posterior paravertebral regions
can be bilateral seen mostly with pleural effusions or asbestosis |
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describe the comet tail sign
what is it associated with |
bending and bowing of adjacent bronchi and arteries towards the edge of atelectasis
will see air-bronchograms, displacement of fissures seen in rounded atelectasis |
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4 key criteria that must be present to dx rounded atelectasis
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ipsilateral pleural thickening/effusion
contact btwn lung lesion and abnormal pleural surface comet tail volume loss in lobe with opacity if these 4 things not present, do bx |
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describe appearance of halo sign
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soft tissue attenuation nodule surrounded by less dense rim or halo of ground glass opacity
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when is halo sign seen
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aspergillosis
tb legionella nocardia cmv bronchoalveolar ca lymphoma m kaposi infarction wegener's |
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describe air crescent sign
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mass within a cavity
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when is air crescent sign seen
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mycetoma
invasive aspergillosis clot/neoplasm within cavity echinococcal cyst |
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nml length of adrenal glands
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4-5 cm long
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nml thickness of adrenal glands
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<10 mm
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what is in a myelolipoma
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macroctic extracellular fat with interspersed bone marrow elements
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how to dx a myelolipoma
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should have same HU as fat
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differences btwn an adrenal true cyst and pseudocyst
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true cyst:
lined wiht endothelium/epithelium density same as fat pseudocyst : mass with visible wall higher density than simple fluid |
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how does adrenocorical ca present most often
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as cushing's dz
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ct findings of adrenocortical ca
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large (>5 cm)
central necrosis and irreg calcs possible post-contrast shows nodular areas of enancement, central hypoperfusion, delayed washout |
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complication of adrenocortical ca
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thrombus in renal vein or ivc --> pe
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differential for adrenal calcifications
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(the adrenals are like a HAAT on the kidney)
histoplasmosis/hemorrhage addison's/adenoma tb |
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clinical presentation of conn's syndrome
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primary hyperaldo
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