Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
39 Cards in this Set
- Front
- Back
Which organs/body parts are affected by ischemia from atherosclerosis
|
Heart (ischemic HD/MI), brain (stroke), bowel (ischemic bowel dz), limbs (peripheral vascular occlusive disease => claudication), kidney (renal arterial ischemia, 2° htn)
|
|
risk factors for atherosclerosis
|
age, gender (men, post menopausal women), hypercholesterolemia (w/ high LDL/HDL ratio > 4:1), htxn, DM, cigarettes. Also: obseisty, physical inactivity, stress, hyperuricemia, hyperhomocysteinemia, chlamydia pneumoniae, OC w/ smoking
|
|
Pathogensis of atherosclerotic plaques (vaguely)
|
vascular injury => moncyte accumulation with cholesterol deposits = foam cells => fibrous cap rupture => thrombus/emolism
|
|
Where do atherosclerotic aneurysms most frequently occur?
|
abdominal aorta (also found in iliac arters, arch, thoracic aorta)
|
|
Berry aneurysms: where? Relation to atherosclerosis? Consequence?
|
Circle of willis. No relation to atherosclerosis; they occur at points congenital weakness. Subarachnoid hemorrhage.
|
|
Syphilitic aneurysm. What stage of syphilis? What part of the aorta? Complication?
|
Tertiary syphilis. Ascending aorta. Aortic value insufficiecny
|
|
Aortic dissction. What is it? A/w? Radiographic finding? Complication?
|
Longitudinal intraluminal tear. Hypertension, marfan syndrome. Widening of the mediastinum. Aortic rupture (e.g. into pericardial sac => cardiac tamponade)
|
|
Predisposing factors for venous thrombosis
|
(Virchow's triad) pregnancy, cardiac failure, physical inactivity, varicose veins
|
|
Describe pulmonary infarct from pulmonary embolism
|
Hemorrhagic, subpleural, wedge-shaped
|
|
Predisposing factors for varicose veins
|
Increased venous pressure from pregnancy, obesity, thrombophlebitis, prolonged standing
|
|
Spider telangiectasia. What is it? When does it happen?
|
Small dilated vessel with radiating channels. Hyperestrinism (e.g. chronic liver dz or pregnancy)
|
|
Osler-Weber-Rendu syndrome. Other name? Complications?
|
Hereditary Hemorrhagic Telangiectasia. Epistaxis and GI bleed.
|
|
Capillary hemangioma. What is it
|
proliferation of tangled capillaries in skin or organs. Benign vascular neoplasm
|
|
Cavernous hamangioma. What is it? A/w with what dz (other findings of the dz)
|
Carvernous vascular space in skin or organs. Benign vascular neoplasm. A/w von Hippel Lindau disease (CNS hemangioblastomas, cysts and adenomas in multiple organs, RCC)
|
|
Glomangioma (glomus tumor). What is it
|
painful subungal benign vascular tumor
|
|
Cystic hygroma. What is it? Where does it occur
|
cavernous lympangioma in neck or axilla
|
|
kaposi sarcoma, what is it? who gets it?
|
malignant vascular tumor. Old european men, young african men, immunocompromisd (AIDS, transplant pt). HHV8
|
|
Name 9 vasculidities.
|
Polyarteritis nodosa, Churg-Strauss syndrome, Henoch-Schonlein purprua (hypersensitivity vasculidities), Wegeners granulomatosis, Giant cell (temporal arteritis), Takayasu arteritis, Kawasaki disease (mucocutaenous lymph node syndrome), Buerger dz (thromboangiitis obliterans), Lymphomatoid granulomatosis
|
|
Which vasculidities affect kids?
|
Henoch-Schnolein purpura and Kawasaki dz
|
|
In which vasculidities are giant cells in the lesions?
|
Churg-strauss syndrome, Wegeners granulomatosis, Giant cell (temporal) arteritis, Temporal arteritis, Lymphomatoid granulomatosis
|
|
Which vasculidities are caused by IC deposition?
|
Polyarteritis nodosa, Henoch-Schonlein purpura (other hypersensitivity vasculidities too)
|
|
Which vasculidities cause visual disturbances?
|
temporal (giant cell) arteritis, takayasu arteritis
|
|
Polyarteritis nodosa. Pathophys? What size arteries? A/w? Manifestations/organs? What organ does it not affect?
|
IC deposition in small/medium arteries => necrosis, thrombosis. A/w ab vs. HBV. Ischemia/infarction: coronary arteries => IHD, msk => pain, GI => n/v/pain, melena. Does not affect lungs.
|
|
Churg-Strauss syndrome. What is it/what organ does it affect? Blood cell finding? A/w?
|
"allergic granulomatous angiitis". vasculitis of pulmonary vasculature. Eosinophilia. Asthma.
|
|
Henoch-Schonlein purpura. What is it? Who gets it? Cause of exacerbation?
|
Hypersensitivity vasculitis leading to hemorrhagic purpura in kids. Precipitated by exogenous antigens: drugs, food, upper repsiratory tract infection (e.g. strep).
|
|
Wegeners granulomatosis. What is it? What organs are affected? Autoabs?
|
Granulomatous vasculitis of small/med vessels in repsiratory tract and kidneys. A/w c-ANCA
|
|
Temporal (giant cell) arteritis. Which arteries? Manifesations? Physical finding? A/w
|
Granulomatous vasculitis of branches of caroid artery. Temporal => h/a, jaw claudication, ophthalmic artery => visual disturbances. Palpable nodules along temporal artery. A/w polymyalgia rheumatica (proximal musc pain/stiffness but not weakness… weakness is polymyositis or dermatomyositis)
|
|
Takayasu arteritis. Nickname? Which arteries, manifestations? Who gets this?
|
"Pulseless dz". Vasculitis of aortic arch and branches => stenosis => Absent pulse in carotid/ulnar/radial, visual disturbances. Young azn F
|
|
Kawasaki disease. Other name? Manifestations? Who gets it?
|
Mucocutaneous lymph node syndrome. 1) Hemorrhagic edema of conjunctivae, lips/oral mucosa. 2) Coronary artery vasculitis w/ aneurysm formation. Kids.
|
|
Breuger disease. Other name? What is it, manifestations? Who?
|
Thromboangiitis obliterans. Vasculitis of extermities => hand/foot pain. Especially tibial and radial artery. Smokers, jewish peope.
|
|
Lymphomatoid granulomatosis. What is it?
|
Granulomatous vasculitis with lymphocyte-like cell infiltrate. May progress to T-cell non-Hodgkin lymphoma
|
|
Which is the most common vasculitis
|
Temporal arteritis (giant cell)
|
|
Distinguish between Raynaud dz and Raynaud phenomenon
|
Raynaud dz is recurrent vasospasm of arteries in fingers toes => cyanosis, usu precip by cold. Phenonemon is 2° to underlying disorder (clasically, SLE or scleroderma [progressive systemic sclerosis])
|
|
Kidney changes in essential hypertension?
|
benign nephrosclerosis (hardening/thickening of renal vasculature)
|
|
Kidney changes in malignant hypertension?
|
malignant nephrosclerosis: necrosis => capillary rupture ("flea-bitten" kidney)
|
|
Causes of 2° hypertension of renal origin (2). Mechanism
|
any dz of renal parenchyma, unilateral renal artery stenosis. Macula densa's juxtaglomerular cells sense less flow => renin => angiotensin I converted to angiotensin II (vasconstriction + aldo secretion) => aldo promotes Na/water reabs.
|
|
Name 6 endocrine disorders that cause 2° hypertension
|
Conn syndrome (1° aldosteronism from adrenocortical adenoma or bilateral adrenal hyperplasia; also see in Na dec K), acromegaly, cushing syndrome (pituitary or adrenocortical origin, or CVS), pheochromocytoma, hyperthyroidism, DMII (diabetic glomeruloscerlosis)
|
|
where is the hypertension in coarctation of the aorta
|
upper limbs only
|
|
Malignant hypertension. What is it, manifestations, who gets it. Death by?
|
Complication of 1° or 2° htn => inc diastolic bp, papilledema (edema of optic disc, focal retinal hemorrhages, LVH, malignant nephrosclerosis. Young black males. Death: CHF, cerebrovascular accident, renal failure.
|