Myocardial Pathology Flashcards
most common primary cardiac neoplasms in (a) infants/children and (b) teens/adults
a) rhabdomyoma (benign)
b) cardiac myxoma (benign)
most common location and possible complications of cardiac myxoma
This is the most common primary cardiac tumor in adults. Arises most often in the Left atrium as a pedunculated or sessile myxoid lesion. Although benign, they can cause significant problems if fragments embolize or they cause a “ball valve” obstruction of the mitral valve with syncopal episodes and even sudden death. Resected when detected.
what types of organisms may infect the myocardium?
viruses (coxsackievirus, ECHO, influenza, HIV, cytomegalovirus), bacteria (chlamydiae, Rickettsiae, etc.), fungi (candida), parasites (protazoa and helminths)
Name at least one autoimmune disease that may affect the heart and identify the components of the heart that can be affected
Lupus, scleroderma, RA
Collagen vascular disease/connective tissue disease
1. Variable involvement of pericardium, myocardium, endocardium
2. Can have heart blood vessel-focused attack: vasculitis leading to small infarcts
medication associated with toxic cardiomyopathy and name at least one non-medication substance associated with toxic cardiomyopathy
Toxic medication: Adiamycin (chemo drug, cumulative dose-dependent toxicity)
Toxic non-medication: ethanol, cobalt from artificial joint prostheses
what is amyloidosis?
- proteins deposited as “beta-pleated sheets” around blood vessels and in the parenchyma of various organs
- organs involved (wax-like consistency) can be: heart, kidneys, nerves, liver, spleen
what is a neoplasm commonly associated with amyloidosis?
commonly associated with Plasma Cell Neoplasm/Dyscrasia (multiple myeloma)
dilated cardiomyopathy: macroscopic appearance, prob with contraction or relaxation and prevalence of genetic mutation
dilated chambers, impaired contractility, 30-40% have genetic mutations
hypertrophic cardiomyopathy: macroscopic appearance, prob with contraction or relaxation and prevalence of genetic mutation
thickened interventricular septum bulges into the LV outflow tract during early systole -> outflow obstruction through aortic valve – hypertrophy and disarray of fibers; cannot relax during diastole, 100% due to genetic mutations
restrictive cardiomyopathy: macroscopic appearance, prob with contraction or relaxation and prevalence of genetic mutation
fibrotic or infiltrative; cannot relax during diastole; acquired
causes of restrictive cardiomyopathy
Amyloidosis, hemochromatosis, scleroderma, radiation therapy