myocardial pathology 2 Flashcards

1
Q

mechanism of HF in dilated cardiomyopathy

A

impairment of contractility

systolic dysfunction

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2
Q

mechanism of HF in hypertrophic cardiomyopathy

A

impairment of compliance

diastolic dysfunction

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3
Q

mechanism of HF in restrictive cardiomyopathy

A

impairment of compliance

diastolic dysfunction

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4
Q

causes of dilated cardiomyopathy

A
  1. idiopathic
  2. alcohol
  3. peripartum
  4. genetic
  5. myocarditis
  6. anemia
  7. doxorubucin
  8. sarcoidosis
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5
Q

causes of hypertrophic cardiomyopathy

A
  1. genetic
  2. friedreich ataxia
  3. storage diseases
  4. infants of diabetic mothers
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6
Q

causes of restrictive cardiomyopathy

A
  1. idiopathic
  2. amyloidosis
  3. radiation induced fibrosis
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7
Q

indirect myodilated dysfunction: dilated cardiomyopathy

A
  1. ischemic heart disease
  2. valvular heart disease
  3. hypertensive heart disease
  4. congenital heart disease
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8
Q

indirect myodilated dysfunction: hypertrophic cardiomyopathy

A
  1. hypertensive heart disease

2. aortic stenosis

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9
Q

indirect myodilated dysfunction: restrcitive cardiomyopathy

A

pericardial constriction

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10
Q

dilated cardiomyopathy: mechanism

A

impaired contractility

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11
Q

dilated cardiomyopathy: microscopic changes

A

non specific

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12
Q

dilated cardiomyopathy: complication

A

mural thrombus formation

  1. systemic embolization
  2. arrhythmia
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13
Q

dilated cardiomyopathy: Hearts are

A

BIG and dilated (walls may be thick or thin)

30-40% of cases have associated genetic mutations, more yet to be discovered

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14
Q

hypertrophic cardiomyopathy is due to

A

100% due to genetic mutations

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15
Q

hypertrophic cardiomyopathy is

A
  1. thickened interventricular septum bulges into th eLV outflow tract during early systole
  2. outflow obstruction through aortic valve ejection murmur
  3. anterior leaflet of the mitral valve may also impinge on septal wall during systole
  4. cannot relax in diastole (impaired compliance)
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16
Q

hypertrophic cardiomyopathy complication:

A

sudden death (young athletes)

17
Q

hypertrophic cardiomyopathy pathologic changes:

A

hypertrophy and disarray of fibers

18
Q

restrictive cardiomyopathy

A
  1. cannot relax during diastole (impaired compliance)
  2. typically acquired (not really genetically linked)
  3. amyloid deposition and radiation-induced fibrosis are good examples
19
Q

dilated cardiomyopathy etiology

A

genetic, infection, alcoholic, peripartum

20
Q

restrictive cardiomyopathy etiology

A
  1. ayloidosis
  2. hemochromatosis
  3. scleroderma
  4. radiation therapy
21
Q

dilated cardiomyopathy pathophysiology

A

impaired systolic contriction

22
Q

hypertrophic cardiomyopathy pathophysiology

A
  1. impaired diastolic relaxation
  2. LV systolic function vigorious
  3. often with dynamic obstruction
23
Q

restrictive cardiomyopathy pathophysiology

A
  1. stiff LV with impaired diastolic relaxation

2. usually normal systolic function