Cardio recal
| created: | 3 months ago by MirandaMarguerite | tags: | why use tags on flashcarddb? |
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Monckeberg |
calcification in the media of the aa, esp radial and ulnar. |
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Arteriolosclerosis |
Hyaline thickening of small aa in essential HTN. Hyperplastic "onion skinning" in malignant HTN |
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Atherosclerosis |
Fibrous plaques and atheromas form in intima of aa |
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corneal arcus |
ring of lipid in the cornea - nospecific can could demonstrate hyperlipidemia |
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atheroma |
plaque w/in a bd vessel wall (seen in atherosclerosis) |
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4 hrs post MI micro characteristics |
Coagulative necrosis: contraction bands |
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2-4 days post MI micro characteristics |
*risk for arrhythmia |
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5-10 days post MI micro characteristics |
*highest risk for free wall rupture |
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7 wks post MI micro characterisitics |
*risk ofr ventricular aneurysm |
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Cardiac troponin I time line (most sp protein marker for MI) |
rises after 4 hrs; peaks w/in 24 hrs; elevated fro a total of 7-10 days |
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Why aren't the following markers best for MI assessment: |
CK-MB: predominantly found in myocardium but also released from skeletal mm |
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At what time period post MI are these complications most likely: |
2-4 days post |
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Causes of pulsus paradoxus = Kussmaul's pulse = decreased amp of pulse during inspiration |
TAMPONADE |
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Signs of Bacterial endocarditis |
Fever |
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Causes of serous peicarditis |
SLE |
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Causes of fibrinous pericarditis |
Uremia |
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Causes of hemorrhagic pericarditis |
TB |
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Signs of the the hereditary hemorrhagic telangectasia (Osler-WEber-Tendu syn) |
frequent nosebleeds and skin discolorations |
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Wegener's pathophys triad: presenting signs |
*focal necrotizing vasculitis, necrotizing granulomas in teh lung and URT, necrotizing glomerulonephritis |
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Diagnostic findins in wegener's (3) |
c-ANCA |
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PAN notes |
*immune complex mediated fibrinoid necrosis of med aa |
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Takayasu's arteritis notes |
*granulomatous aorta and large aa w/ fibrosis and significant narrowing |
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Temporal arteritis / giant cell arteritis |
*granulomatous inflamm of med/large aa off the carotids, cranial aa, intimal fibrosis |
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Thromboangiitis obliterans aka Buerger's dx |
*no signs of inflamm or autoimmune attack (but usually HLA A9 or B5 +) |
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Hypercoaguable states |
*Inherited dx of coag: resistance of APC (factor V leidden); prothrombin gene mutation; AT III def; def of protein C or S |
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Kawasaki disease |
necrotizing vasculitis of sm/med vessels |
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Henoch-Schonlein purpura (most common form of childhood systemic vasculitis) triad: |
skin: (palpable purpura) *multiple lesions at same age* |
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Churg-Strauss syn |
Granulomatous vasculitis w/ eosinophila. Involves: lung, heart, skin, kidneys, nn |





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