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106 Cards in this Set
- Front
- Back
What are the five causes of Right to left shunting in the heart?
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1. Tetralogy of Fallot 2. Transposition of great vessels. 3. Truncus arteriosus 4. Tricuspid atresia 5. Total anomalous pulmonary venous return (TAPVR)
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What is Truncus arteriosus?
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Single artery from RV and LV give rise to aorta and pulmonary artery resulting in intermixing blood. Right to left shunt
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What is Total anomalous pulmonary venous return (TAPVR)?
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Rare defect where all 4 pulmonary veins are malpositioned and make anomalous connections with systemic venous connections (right atrium alsi) right to left shunt.
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What are the three types of left to right shunts?
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1. VSD 2. ASD 3. PDA
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What is the most common congenital cardiac anomaly?
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VSD
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What is heard on ascultation with ASD?
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loud S1; wide, fixed split S2
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What is the Tetralogy of Fallot?
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1. Pulmonary stenosis (most important for prognosis) 2. RVH 3. Overlying aorta (overrides the VSD) 4. VSD
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What embryologic defect causes Tetralogy of Fallot?
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Anterosuperior displacement of the infundibular septum
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How do patients compensate for Tetralogy of Fallot and what effect does it have?
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Squat: compression of femoral arteries: Compression increases resistance increasing pressure decreasing the right to left shunt and directing more blood from RV to the lungs.
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What is the lutembacher syndrome?
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Atrial septic defect with mitral stenosis
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Aorta leaves RV and pulmonary trunk leaves LV (what condition?)
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Transposition of great vessels
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Why does transposition of great vessels occur?
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Failure of aorticopulmonary septum to spiral (neural crest)
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What congential heart condition is incompatible with life unless a shunt is present?
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Transposition of great vessels
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What is the difference between infantile type and adult type coarctations of the aorta?
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Infantile: aortic stenosis proximal to insertion of ductus arteriosus. Adult type: distal to ductus arteriosus.
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Check femoral pulses for what cardiac disease?
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Coarctation of the aorta
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What 2 things is coarctation of the aorta associated with?
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1. Turner's syndrome (45, XO) 2. Bicuspid aortic valve
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What valvular problem can coarctation of the aorta lead to?
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Aortic regurgitation
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What is used to end the patency of a ductus arteriosus?'
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Indomethacin
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How is patency of ductus arteriosus maintained?
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PGE synthesis and low O2 tension
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22q11 syndromes
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Truncus arteriosus, tetralogy of Fallot
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Down syndrome is associated with what congenital cardiac defects
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ASD, VSD, AV septal defect (endocardial cushion defect)
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Congenital rubella is associated with what congenital cardiac defects
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Septal defects, PDA, pulmonary artery stenosis
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Marfan's syndrome is associated with what cardiac defect
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Aortic insufficiency (late complication)
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Offspring of diabetic mothers have what congenital cardiac defect association
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Transposition of great vessels
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What is an atheroma?
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Plaque in blood vessel walls
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Xanthelasma is
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Plaque/nodule composed of lipid-laden histiocytes on eyelid (sign of hyperlipidemia)
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Lipid desposit in cornea
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Corneal arcus (arcus senilis)
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Monckeberg arteriosclerosis: what is it, and where does it usually occur, PE finding
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Calcification in the media of the arteries, especially radial or ulnar. Usually benign; "pipestem" arteries. Intima not involved.
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What are the two types of arteriolosclerosis?
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1. Hyaline thickening of small arteries in essential HTN. 2. Hyperplastic "onion skinning" in malignant HTN.
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In hyalin arteriosclerosis: what is pathogenesis and what are common causes?
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Increased protein deposited in vessel wall and occludes lumen. Common causes: diabetes and HTN
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In hyperplastic arteriolosclerosis, what is pathogenesis and what are common causes?
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Pathogenesis: Smooth muscle hyperplasia and basement membrane duplication. Causes: Malignant HTN, bad pulmonary HTN, scleroderma, HUS
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What does a CXR show in aortic dissection?
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Mediastinal widening
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What is the order of prevelance of atherosclerosis by location?
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Abdominal aorta > coronary artery > popliteal artery > carotid artery
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Basic pathogenesis of atherosclerosis
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Endothelial cell injury --> Macrophages and platelets adhere to damaged endothelium --> Medial SM hyperplasia, SM cells migrate to intima, Cholesterol enters SM and macrophages --> Fatty streaks --> Fibrous cap
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What is seen with stable angina on ECG? With Prinzmetal's angina?
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ST depression for stable angina. ST elevation for Prinzmetal's
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Red infarcts vs. pale infarcts: what'st he difference
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Red (hemorrhagic) infacts: loose tissues with collaterals (liver, lungs, intestines) or following reperfusion. Pale infarcts: solid tissues with single blood supply (heart, kidney, and spleen)
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Reperfusion injury is due to
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Free radical damage
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What is the order of coronary artery occlusion in most likely to least likely
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LAD > RCA > circumflex
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What is there risk for 2-4 days after MI?
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Arrhythmia
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What is there risk for 5-10 days after MI?
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Free wall rupture, tampoade, papillary muscle rupture, ventricular septal rupture
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What color is the area of infarct by 10 days?
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Hyperemic border; central yellow-brown softening - maximally yellow and soft by 10 days
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ST elevation on ECG is indicative of what type of infarct?
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Transmural infarct
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Subendocardial infarcts occur because of what and display what on eCG?
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Fewer collaterals, higher pressure; ST depression on ECG
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MI complication involving pericardium
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Fibrinous pericarditis causing friction rub (3-5 days post MI); Dressler's syndrome - autoimmune phenomenon resulting in fibrinous pericarditis (several weeks post MI)
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What is the most common cardiomyopathy?
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Dilated cardiomyopathy (90%)
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Etiologies of dialted cardiomyopathies
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chronic Alcohol abuse, wet Beriberi, Coxsackie B virus mycoarditis, chronic Cocain use, Chagas' disease, Doxorubicin toxicity, and peripartum cardiomyopathy
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What are common findings of dilated cardiomyopathy on exam? CXR? US?
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S3, dilated heart on US, ballooon appearance on cxr
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Dilated cardiomyopathy: systolic or diastolic dysfx
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Systolic dysux (Dec contractility with decreased EF)
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What are the exam findings for hypertrophic cardiomyopathy?
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Normal sized heart, S4, apical impulses, systolic murmur
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Pathophys of hypertrophic cardiomyopathy - what causes sudden death in young athletes?
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Disoriented, tangled, hypertrophied myocardial fibers - leading to sudden death in athletes due to conduction disturbances. Hypertrophied IV septum "too close" to anterior mitral valve leaflet, leading to outflow tract obstruction
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Tx for hypertrophic cardiomyopathy
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B-blocker or heart specific calcium channel blocker
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Hypertrophic cardiomyopathy: systolic or diastolic dysfunction
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Diastolic
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Thick fibroelastic tissue in endocardium of young children
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Endocardial fibroelastosis
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Some major causes of restrictive cardiomyopathy
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Sarcoidosis, amyloidosis, postradiation fibrosis, and hemochromatosis
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In pulmonary edema due to LV failure, what characteristic cells are present in the lungs?
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Hemosiderin laden macrophages
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Fat emboli are associated with
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Long bone fractures and liposuction
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Virchow's triad
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Stasis, hypercoagulability, endothelial damage
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Round white spots on retina surrounded by hemorrhage seen in bacterial endocarditis
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Roth spots
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Tender raised lesions on finger or toe pads in bacterial endocarditis
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Osler's nodes
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Small erythematous lesions on palm or sole in bacterial endocarditis
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Janeway lesions
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What type of endocarditis is associated with IV drug abuse?
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Tricuspid valve endocarditis
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What is Libman-Sacks endocarditis?
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Verrucous (wartlike), sterile vegetations occur on both sides of the valve - seen in SLE
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What is Marantic endocarditis?
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Paraneoplastic syndrome. Sterile fibrin deposits randomly arranged along line of closure of valve leaflets
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Verrucous (wartlike), sterile vegetations occur on both sides of cardiac valves - seen in SLE
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Libman-Sacks endocarditis
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What is the histological features of Rheumatic heart disease?
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Aschoff bodies (granuloma with giant cells) surrounded by Anitschkow's cells (activated histiocytes)
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Signs of rheumatic fever
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Fever, Erythema marginatum, Valvular damage (vegetation and fibrosis), ESR Inc, Migratory polyarthritis (Red-hot joints), Subcutaneous nodules, St. Vitus dance (chorea) FEVERSS
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What 4 other things can pulsus paradoxus signify besides severe cardiac tamponade?
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Asthma, obstructive sleep apnea, pericarditis, and croup
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Equilibrium of diastolic pressures in all 4 chambers
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Cardiac tamponade
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What are the causes of serous pericarditis?
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SLE, RA, viral infection, uremia
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What are causes of hemorrhagic pericarditis?
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TB, malignancy
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ECG changes with pericarditis
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ST segment elevation
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Findings with pericarditis
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Pericardial pain, friction rub, pulsus paradoxus, distant heart sounds
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Most common location of cardiac myxomas
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left atrium
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Most common cardiac tumors in adult; children
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Adult myxoma. Children: rhabdomyomas (tuberous sclerosis)
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What is the most common heart tumor?
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Metastases
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What sign is seen with cardiac tumors?
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Kussmaul's sign: increase in JVP on inspiration
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Vascular, red peduncled mass that ulcerates and bleeds easily like rotten cherry. Post traumatic or associated with pregnancy
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Pyogenic granuloma
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Bengn tumor derved from arteriovenous shunts in glomus bodies. Painful red subungual (under fingernail) nodule in a digit.
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Glomus tumor
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Osler Weber Rendu syndrome
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Hereditary hemorrhagic telangiectasias. Autosomal dominant inheritance. Nosebleeds and skin discolorations
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Pathophys of Raynaud's disease
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Decreased blood flow to skin due to arteriolar vasospasm in response to cold temperature or emotional stress.
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Triad seen in Wegener's granulomatosis
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Focal necrotizing vasculitis, necrotizing granulomas in the lung and upper airway, necrotizing glomerulonephritis
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Cavernous hemangiomas in cerebellum and retina. Increased incidence of pheochromocytoma and bilateral renal cell carcinomas
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von Hippel-Lindau syndrome
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Angiomyolipomas are located where and composed of what. associated with?
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Kidney hamartoma composed of blood vessels, muscle, and mature adipose tissue. Assoc with tuberous sclerosis
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Perforation of nasal septum, chronic sinusitis, otitis media, mastoiditis, cough, dyspnea, hemoptysis, hematuria - sx of which vasculitis
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Wegener's granulomatosis
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Marker of Wegener's
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c-ANCA
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Tx for Wegener's
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Cyclophosphamide and corticosteroids
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What type of glomerular nephritis is wegener's and microscopic polangiitis associated with?
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Rapidly progressing crescentic glomerulonephritis
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Granulomatous vasculitis with eosinophilia. p-ANCA.
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Churg-Strauss syndrome
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What is the Churg-strauss syndrome
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Granulomatous vasculitis with eosinophilia. p-ANCA.
3 stages: 1) allergic rhinitis, sinusitis. 2) acute asthma 3) various organ systems |
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Congenital vascular disorder that affects capillary sized blood vessels with port wine stian (nervus flammeus) and leptomeningeal angiomatosis (intracerebral AVM)
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Sturge-Weber disease
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Sturge-Weber disease
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Congenital vascular disorder that affects capillary sized blood vessels with port wine stian (nervus flammeus) and leptomeningeal angiomatosis (intracerebral AVM)
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Most common form of childhood systemic vasculitis
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Henoch-Schonlein purpura
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Skin rashon buttocks and legs with palpable purpura, arthralgia, intestinal hemorrhage, abdominal pain, and melana
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Henoch-Schonlein purpura
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What type of immune complexes are seen in Henoch-Schonlein
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IgA immune complexes - Ssociation with IgA nephropathy
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Buerger's disease: another name, pathophys, and type of vessels seen in
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Thromboangiitis obliterans: idiopathic, segmental, thrombosing vasculitis of small and medium peripheral arteries and veins. Seen in heavy smokers.
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Another name for thromboangiitis obliterans: idiopathic, segmental, thrombosing vasculitis of small and medium peripheral arteries and veins. Seen in heavy smokers.
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Buerger's disease
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Kawasaki's disease: pathophys, who it's found in, common complication, and clinical pres
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Necrotizing vasculitis of small/medium-sized vessels; Asian infants/kids; May develop coronary aneurysms. Fever, congested conjunctiva, changes in lips/oral mucosa "strawberry tongue", lymphadenitis
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Necrotizing immune complex inflammation of medium sized muscular arteries typically invovling renal, heart, bowel vessels. Hepatitis B seropositivity in 30% of pts. Multiple aneurysms and constrictions on angiogram
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Polyarteritis nodosa
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Polyarteritis nodosa: pathophys, what organs, seropositivity of what pathogen, angiogram finding
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Focal vasculitis; Necrotizing immune complex inflammation of medium sized muscular arteries typically invovling renal, heart, bowel vessels. Hepatitis B seropositivity in 30% of pts. Multiple aneurysms and constrictions on angiogram
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Tx for polyarteritis nodosa
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Corticosteroids, cyclophosphamide
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"Pulseless disease"
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Takayasu's arteritis
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Pathophys behind Takayasu's arteritis
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Granulomatous thickening of aortic arch and/or prox great vessels. Affects medium and large vessels.
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Vasculitis associated with an increased ESR, primarily affects Asian females < 40 yrs old
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Takayasu's arteritis
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Most common vasculitis that affects medium and large arteries, usually branches of carotid artery
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Temporal arteritis (giant cell arteritis)\
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Symptoms of temporal arteritis
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Unilateral headache, jaw claudication, impaired vision (occlusio of ophthalmic artery that may lead to irreversible blindness)
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Temporal arteritis is associated with
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Increased ESR. Half of pts have systemic involvement and polymyalgia rheumatica
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