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66 Cards in this Set

  • Front
  • Back
the localized abnormal dilation of a vessel is known as what?
an aneurysm
what is the difference between a true and false aneurysm?
i. True aneurysm has complete arterial wall

ii. False aneurysm has a missing part of vessel wall
what are the 2 most common causes of an aneurysm
atherosclerosis, cystic medial degeneration are the most common
Where is the most common place for an aneurysm to occur?
Most common site for atherosclerotic plaques (and thus aneurysms) are abdominal aorta between renal arteries and iliac bifurcation or in common iliac
what population is most likely to have an aneurysm in the abdominal aorta?
i. Mostly in men older than 50

ii. Increased risk of rupture with increase in bulge over 5cm

iii. Operative risk increases with rupture
What stage of syphilis do Syphilitic aneurysms occur? Where in the body do they occur?
tertiary stage of syphilis

Usually involves only ascending and arch of aorta
what population are you likely to see aortic dissection?
i. Over 90% seen in hypertensive men 40-60
what problem is associated with Marfan's syndrome?
f. Aortic dissection
Pathology of vessel is elastic tissue fragmentation and disruption, focal separation of elastic and fibromuscular tissue; this describes?
Aortic Dissection
there are 2 types of aortic dissection...what are they, where do they occur, and which is more dangerous
Type A: proximal, more common and more dangerous, involves ascending aorta

Type B: distal to the subclavian
excruciating pain in anterior chest radiating to the back and down is the clinical presentation of what?
Aortic Dissection
what is the most common of the vasculitides?
Giant Cell Arteritis
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?
Giant Cell Arteritis

Treat with STEROIDS
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?
Takayasua Arteritis

Steroids
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
describe Microscopic polyangiitis
like PAN but involves smaller vessels, can involve the lungs
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
Kawasaki disease

**remember, with the fever, it must last at LEAST 5 DAYS in order to make the diagnosis***
What is the triad seen in Wegener granulomatosis
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
seen in heavy smokers before age 35; nodular phlebitis develops into Raynauds, cause in unknown, cause 4+ pain and gangrene of extremities
f. Thromboangiitis obliterans (buerger disease
unknown etiology but is an exaggeration of normal central and local vasomotor responses; found in young, healthy women
g. Raynauds disease
what is the commonest cause of superior vena cava syndrome?
most common is bronchogenic CA

or mediastinal lymphoma
what causes superior vena caval syndromes?
secondary to neoplasms that compress or invade the SVC, most common is bronchogenic CA or mediastinal lymphoma
patient presents with cyanosis and marked dilation of the veins of the head, neck and arms....what do they have?
SVC syndrome
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
IVC syndrome
what is the commonest cause of inferior vena cava syndrome?
secondary to neoplasm such as hepatocellular CA and renal cell CA
What are the 3 types of cardiomyopathy? which is most common?
Dilated--most common

hypertrophic

restrictive
what is characterized by gradual four chamber hypertrophy?
dilated cardiomyopathy
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
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)
hypertrophic cardiomyopathy
Clinically presents in young adults with dyspnea, angina, syncope, CHF, can see sudden death in young atheletes
hypertrophic cardiomyopathy (HCM)
what are the gross changes seen in HCM?
disproportionate thickening of septum vs. left ventricular free wall
the myocardium is infiltrated with a material that results in impaired ventricular filling and decreased cardiac output ...this describes
restrictive cardiomyopathy
what are the 2 most common causes of restrictive cardiomyopathy?
amyloidosis- stains orange/red/pink but seen blue/green in polarized light

hemochromatosis stains blue
what would be seen with endomyocardial fibrosis that occurs in children and young adults in Africa?
Eosinophilia
most common cause of myocarditis?
Coxsackievirus B (type 3/4)

[remember that adenovirus is second, and that these are enteroviruses]
myocardial inflammation, broad clinical spectrum from asymptomatic to abrupt onset of arrhythmia, CHF, or sudden death; most recover quickly without sequelae
myocarditis
what can occur after a group A infection?

what type of hemolysis does this step clear?
Rheumatic fever

beta
in addition to having a history of a strep infection, what else is necessary to diagnose rheumatic fever?
2 major jones criteria

OR

1 major and 2 minor
what is the most common symptom/jones criteria seen with RF? 2nd?
1: Poly arthritis

2. Carditis
what can recurrent attacks of rheumatic fever lead to?
congestive heart failure
what are the 5 acute types of pericarditis?
SPF Hates Cancer-

Serous, Purulent, Fibrinous, Hemorrhagic, Caseous
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
what type of pericarditis is associated with....

MI and produces friction rub; usually resolves without sequelae
b. Acute fibrinous and serofibrinous pericarditis
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
what type of pericarditis is associated with....

most often follows cardiac surgery or associated with TB or malignancy
d. Acute hemorrhagic pericarditis
what type of pericarditis is associated with....

secondary to TB and usually direct extension from lymph nodes
e. Acute caseous pericarditis
what type of pericarditis is most common?
b. Acute fibrinous and serofibrinous pericarditis
what are the 3 most common causative organisms for acute purulent pericarditis?
GRAM POSITIVE STAPH, STREP AND PNEUMOCOCCI
what is chronic pericarditis usually secondary to?
TB or purulent pericarditis
what is usually the cause of chronic pericarditis?
TB
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
what are the 4 types of hemangioma?
Capillary

Juvenile capillary

Cavernous

Pyogenic granuloma
ulcerated polypoid variant of capillary hemangioma secondary to trauma; PREGNANCY TUMOR, will regress after delivery
iv. Pyogenic granuloma
1-2cm, in addition to skin and mucous membranes, these lesions are common in the liver, CNS and other viscear;
Cavernous hemangioma


von hippel-Lindau disease is cavernous lesions of the cerebellum, brainstem or eyes
strawberry present at birth, grow rapidly for a few months, regress by age 7
juvenile capillary hemangioma
1-2mm lesion seen primarily in skin or mucous membrane and visecera
capillary hemangioma
benign, extremely painful tumor arising from smooth muscle cells, seen often in distal phalanges or beneath the nail bed
Glomus Tumor
birth mark, port wine stain of face and neck, grows with child, but most regress with age
Nevus flammus
facial port wine stain with associated mental retardation
sturge weber syndrome
minute focal subcutaneous arterioles arranged in radial fashion with central core; most often associated with hyperestrogenic states (pregnancy and cirrhosis)
ii. Spider telangiectasis
occurs in head, neck, axillary tissue, looks like hemangioma but NO blood cells
e. Simple lymphangioma
occur in the neck of axilla in children as large as 15cm, difficult to resect; looks like cavernous hemangioma, but no blood cells
Cystic hygroma
what is the most common adult heart tumor? where does it occur
Myxomas

fossa ovale in atria
what is the most common childhood heart tumor?
rhabdomyomas
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.
Hamartoma
a mass of histologically normal tissue in an abnormal location
Choristomas