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Imp Points:- Most common cardiomyopathy (90%)
- AD(35%)
- Inherited cytoskeletal mutations
- Men 20-60 (young)
- Most common cause of transplant
Risk Factors/Causes:
- Often Unknown
- Alcohol cardiomyopathy, thiamine defficiency (Beriberi heart), or prior myocarditis (late stage myocarditis?)
- Peripartum cardiomyopathy (late 3rd trimester or post partum) – 50% of these pts recover
- Mutations - Dystrophin gene (occurs with Duchenne’s MD), Ox phos mito genes
- Drug toxicity (adriamycin)
- Hemochromatosis
Clincal/Pathological Features:
- 4 chamber dilation with R and L sided SYSTOLIC heart failure Viruses have been identified in these hearts
- Normal wall thickness
- Enlarged flabby heart which is dilated and hypertrophied, stretched myocytes with enlarged nuclei
- Lack of contraction → formation of mural thrombi
- Myocyte hypertrophy, interstitial fibrosis, wavy fiber changes, mono infiltrate
- ↓ EF → CHF
Inflammatory infiltrate not common
Category:
Pathology Notes
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