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66 Cards in this Set
- Front
- Back
the localized abnormal dilation of a vessel is known as what?
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an aneurysm
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what is the difference between a true and false aneurysm?
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i. True aneurysm has complete arterial wall
ii. False aneurysm has a missing part of vessel wall |
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what are the 2 most common causes of an aneurysm
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atherosclerosis, cystic medial degeneration are the most common
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Where is the most common place for an aneurysm to occur?
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Most common site for atherosclerotic plaques (and thus aneurysms) are abdominal aorta between renal arteries and iliac bifurcation or in common iliac
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what population is most likely to have an aneurysm in the abdominal aorta?
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i. Mostly in men older than 50
ii. Increased risk of rupture with increase in bulge over 5cm iii. Operative risk increases with rupture |
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What stage of syphilis do Syphilitic aneurysms occur? Where in the body do they occur?
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tertiary stage of syphilis
Usually involves only ascending and arch of aorta |
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what population are you likely to see aortic dissection?
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i. Over 90% seen in hypertensive men 40-60
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what problem is associated with Marfan's syndrome?
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f. Aortic dissection
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Pathology of vessel is elastic tissue fragmentation and disruption, focal separation of elastic and fibromuscular tissue; this describes?
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Aortic Dissection
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there are 2 types of aortic dissection...what are they, where do they occur, and which is more dangerous
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Type A: proximal, more common and more dangerous, involves ascending aorta
Type B: distal to the subclavian |
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excruciating pain in anterior chest radiating to the back and down is the clinical presentation of what?
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Aortic Dissection
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what is the most common of the vasculitides?
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Giant Cell Arteritis
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patient presents with a headache, and facial pain....later he complains of visual problems. What does this patient have? What do you treat them with?
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Giant Cell Arteritis
Treat with STEROIDS |
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this vascular problem is most common in Asian women, unknown cause; involves medium to large arteries including aortic arch and major branches...what is it? Treatment?
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Takayasua Arteritis
Steroids |
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affects young adults, may be associated with Hep B antigen, affects any organ but LUNG..what is this?
treatment? |
b. Polyarteritis nodosa (PAN)
immunosuppresive therapy provides 90% cure rate |
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describe Microscopic polyangiitis
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like PAN but involves smaller vessels, can involve the lungs
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illness of infants and children, 20% have coronary arteritis; etiology unknown but patients have immunoregulatory problems --> t cell activation, auto antibodies to endothelial cells, circulating immune complexes; will see fever
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Kawasaki disease
**remember, with the fever, it must last at LEAST 5 DAYS in order to make the diagnosis*** |
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What is the triad seen in Wegener granulomatosis
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triad of focal necrotizing vasculitis of lung, necrotizing granulomas of upper respiratory tract, necrotizing glomerulitis;
lesions like PAN but with granulomas, greatest occurrence in 40s, 90% have C-ANCA antibodies, w/o treatment 80% die in a year |
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seen in heavy smokers before age 35; nodular phlebitis develops into Raynauds, cause in unknown, cause 4+ pain and gangrene of extremities
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f. Thromboangiitis obliterans (buerger disease
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unknown etiology but is an exaggeration of normal central and local vasomotor responses; found in young, healthy women
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g. Raynauds disease
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what is the commonest cause of superior vena cava syndrome?
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most common is bronchogenic CA
or mediastinal lymphoma |
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what causes superior vena caval syndromes?
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secondary to neoplasms that compress or invade the SVC, most common is bronchogenic CA or mediastinal lymphoma
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patient presents with cyanosis and marked dilation of the veins of the head, neck and arms....what do they have?
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SVC syndrome
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i. Clinically presents with marked edema of legs, distention of superficial collateral veins of lower abdomen; when renal veins involved, massive protein urea...what do they have
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IVC syndrome
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what is the commonest cause of inferior vena cava syndrome?
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secondary to neoplasm such as hepatocellular CA and renal cell CA
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What are the 3 types of cardiomyopathy? which is most common?
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Dilated--most common
hypertrophic restrictive |
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what is characterized by gradual four chamber hypertrophy?
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dilated cardiomyopathy
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May occur at any age as slow progressive CHF;
Unknown etiology, but genetic defects, etOH, viral myocarditis may contribute Gross changes include cardiomegaly, thrombi, endocardial thickening |
dilated cardiomyopathy
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this is characterized by a heavy, muscular, hypercontractile heart with poor diastolic relaxation resulting from asymmetric interventricular septal hypertrophy (on the left side, resulting in left ventricular outflow obstruction)
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hypertrophic cardiomyopathy
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Clinically presents in young adults with dyspnea, angina, syncope, CHF, can see sudden death in young atheletes
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hypertrophic cardiomyopathy (HCM)
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what are the gross changes seen in HCM?
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disproportionate thickening of septum vs. left ventricular free wall
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the myocardium is infiltrated with a material that results in impaired ventricular filling and decreased cardiac output ...this describes
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restrictive cardiomyopathy
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what are the 2 most common causes of restrictive cardiomyopathy?
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amyloidosis- stains orange/red/pink but seen blue/green in polarized light
hemochromatosis stains blue |
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what would be seen with endomyocardial fibrosis that occurs in children and young adults in Africa?
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Eosinophilia
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most common cause of myocarditis?
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Coxsackievirus B (type 3/4)
[remember that adenovirus is second, and that these are enteroviruses] |
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myocardial inflammation, broad clinical spectrum from asymptomatic to abrupt onset of arrhythmia, CHF, or sudden death; most recover quickly without sequelae
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myocarditis
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what can occur after a group A infection?
what type of hemolysis does this step clear? |
Rheumatic fever
beta |
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in addition to having a history of a strep infection, what else is necessary to diagnose rheumatic fever?
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2 major jones criteria
OR 1 major and 2 minor |
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what is the most common symptom/jones criteria seen with RF? 2nd?
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1: Poly arthritis
2. Carditis |
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what can recurrent attacks of rheumatic fever lead to?
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congestive heart failure
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what are the 5 acute types of pericarditis?
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SPF Hates Cancer-
Serous, Purulent, Fibrinous, Hemorrhagic, Caseous |
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what type of pericarditis is associated with....
slowly accumulating fluid typically secondary to nonbacterial involvement; unknown etiology; only about 200cc of fluid |
a. Acute serous pericarditis
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what type of pericarditis is associated with....
MI and produces friction rub; usually resolves without sequelae |
b. Acute fibrinous and serofibrinous pericarditis
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what type of pericarditis is associated with....
usually secondary to bacterial, fungal or parasitic infection which has reached the pericardium by direct extension...produces 500cc of fluid that can cause constrictive pericarditis |
c. Acute purulent pericarditis
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what type of pericarditis is associated with....
most often follows cardiac surgery or associated with TB or malignancy |
d. Acute hemorrhagic pericarditis
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what type of pericarditis is associated with....
secondary to TB and usually direct extension from lymph nodes |
e. Acute caseous pericarditis
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what type of pericarditis is most common?
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b. Acute fibrinous and serofibrinous pericarditis
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what are the 3 most common causative organisms for acute purulent pericarditis?
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GRAM POSITIVE STAPH, STREP AND PNEUMOCOCCI
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what is chronic pericarditis usually secondary to?
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TB or purulent pericarditis
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what is usually the cause of chronic pericarditis?
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TB
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i. Healing of acute lesions could form a thick nonadherent epicardial plaque in this problem...
what is a name for this plaque? |
Chronic pericarditis
Soldier's plaque |
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what are the 4 types of hemangioma?
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Capillary
Juvenile capillary Cavernous Pyogenic granuloma |
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ulcerated polypoid variant of capillary hemangioma secondary to trauma; PREGNANCY TUMOR, will regress after delivery
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iv. Pyogenic granuloma
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1-2cm, in addition to skin and mucous membranes, these lesions are common in the liver, CNS and other viscear;
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Cavernous hemangioma
von hippel-Lindau disease is cavernous lesions of the cerebellum, brainstem or eyes |
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strawberry present at birth, grow rapidly for a few months, regress by age 7
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juvenile capillary hemangioma
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1-2mm lesion seen primarily in skin or mucous membrane and visecera
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capillary hemangioma
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benign, extremely painful tumor arising from smooth muscle cells, seen often in distal phalanges or beneath the nail bed
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Glomus Tumor
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birth mark, port wine stain of face and neck, grows with child, but most regress with age
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Nevus flammus
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facial port wine stain with associated mental retardation
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sturge weber syndrome
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minute focal subcutaneous arterioles arranged in radial fashion with central core; most often associated with hyperestrogenic states (pregnancy and cirrhosis)
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ii. Spider telangiectasis
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occurs in head, neck, axillary tissue, looks like hemangioma but NO blood cells
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e. Simple lymphangioma
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occur in the neck of axilla in children as large as 15cm, difficult to resect; looks like cavernous hemangioma, but no blood cells
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Cystic hygroma
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what is the most common adult heart tumor? where does it occur
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Myxomas
fossa ovale in atria |
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what is the most common childhood heart tumor?
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rhabdomyomas
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what is A benign (noncancerous) tumor-like growth consisting of a disorganized mixture of cells and tissues normally found in the area of the body where the growth occurs.
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Hamartoma
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a mass of histologically normal tissue in an abnormal location
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Choristomas
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