Pathology Flashcards
(88 cards)
emryonic defect which results in tetralogy of fallot
anterosuperior displacement of the infundibular septum
exposure to what can cause ebstein anomaly
lithium exposure in utero
risk factors of persistent pulmonary hypertension in the newborn
aspiration of meconium-stained amniotic fluid
neonatal pnuemonia
neonate with diabetic mother may be at risk of what cardiac complications
transportation of great arteries
truncus arteriosus
tricuspid atresia
VSD
cardiac defect associated with williams syndromec
supravalvular aortic stenosis
cardiac defect associated with 22q11 deletion syndrome
truncus arteriosus, tetralogy of fallot
cardiac defects associated with downs syndrome
AVSD (endocardial cushion defect), ASD, VSD
cardiac defects associated with congenital rubella
PDA, pulmonary artery stenosis, septal defects
string of beads appearance of renal artery
fibromuscular displasia
most common cause of secondary HTN in females
2 main types of arteiolosclerosis
thickening of arteries and artioles
1. hyaline - vessel wall thickening due to leakage of protein into subendothelial due to diabetes and hypertension
- hyperplastic - ‘onion skinning’ in severe hypertension with proliferation of smooth muscle cells
stanford vs DeBakey classification of aortic dissection
stanford (2 syllables = 2 types)
type 1 - ascending +/- arch/descending
type 2 - descending only
DeBakey (3 syllables = 3 types)
type 1 - ascening + descening
type 2 - ascending only
type 3 - descending only
at what point does the asending become the descending aorta
becomes the descending aorta just below the left subclavian artery
subclavian steal syndrome pathophysiology
occlusion of the subclavian artery proximal to the vertebral artery = hypoperfusion distal to stenosis
causes reversed blood flow in the vertebral artery = reduced cerebral perfusion on exertion of affected arm
subclavian steal syndrome features
BP difference in L vs R arm
arm ischaemia, pain, paraesthesia
vertebrobasillar insufficiency = dizziness, vertigo
risk factors for coronary artery vasospams
tobacco (number 1 risk)
cocaine
amphetamines
alcohol
triptans
treatment for coronary artery vasospams
CCB
nitrates
smoking cessation
MI complication;
- acute mitral valve regurgitation –> cardiogenic shock, severe pulmonary oedema
papillary muscle rupture
MI complication;
- cardiac tamponade, sudden death
ventricular free wall rupture
pathophysiology of dresslers syndrome
autoimmune pericarditis which develops 2 weeks after MI
cardiac antigens released after injury -> deposition of immune complexes in pericardium -> inflammation
MI complication;
- chest pain, murmur, HF, embolus
pseudoaneurysm
what is more likely to rupture and why - ventricular pseudoaneurysm or true ventricular aneurysm
pseudoaneurysm as its not contained within endocardium or myocardium
most common gene in familial dilated cardiomyopathy
TTP gene encoding the sarcometric protein titin
type of hypertrophy found in dilated cardiomyopathy
eccentric hypertrophy (sarcomeres added in series)
mutations in genes encoding what are responsible for familial hypertrophic cardiomyopathy
mutations in genes encoding sarcometric proteins such as myosin binding protein C and beta-myosin heavy chain