Pathological Anatomy and Cytopathology · MU Plovdiv

7. Myocardial infarction. Risk factors. Species. Evolution and complications.

Inside: 3 sections · 2 labelled pictures · 13 flashcards · 3 min

Topic 70 of 163 in the MU Plovdiv syllabus for Pathological Anatomy and Cytopathology (Medicine, Years 3 and 4). The free AceMed note covers it in 3 sections, about 582 words (3 min of reading), with 13 flashcards.

In this note

  1. Ischemic heart disease: myocardial infarction. Microscopic & gross pathomorphology. Stages, complications, outcomes
  2. Stages
  3. Complications/Outcomes

Ischemic heart disease: myocardial infarction. Microscopic & gross pathomorphology. Stages, complications, outcomes

Cardiomyocytes generate energy via oxidative phosphorylation, so oxygen is a must. IHD is a term that encompasses all conditions where there is an imbalance between cardiac perfusion and myocardial oxygen required. 90% of IHD cases are reduced coronary blood flow due to obstructive atherosclerosis, and this is what the term generally means. Manifestations of IHD are:

  • Angina pectoris (stable, unstable, Prinzmetal)
  • Acute MI
  • Chronic IHD with CHF (see below)
  • Sudden cardiac death (can occur due to MI but commonly due to lethal arrhythmia)

Here we will focus on Myocardial Infarction

  • The vast majority of MIs are caused by acute coronary artery thrombosis, generally where there is disruption of a pre existing atherosclerotic plaque that provides thrombus generation, vascular occlusion and transmural infarction of downstream myocardium
  • 10% of MIs are due to coronary artery vasospasm or embolism from other thrombi.
  • In typical MI the following events occur
  • Atheromatous plaque is disrupted exposing endothelium collagen and necrotic plaque
  • Platelets adhere, aggregate and are activated
  • Activation causes coagulation and the thrombus is generated
  • Myocardial response to MI
  • Loss of ATP production has rapid functional effect with ultrastructural changes (including myofibrillar relaxation and mitochondrial swelling). These early stages are reversible
  • Ischemia after 20-40 minutes is irreversible and leads to coagulative necrosis
  • MIs also commonly trigger arrhythmias (e.g. ventricular fibrillation)
  • We can describe infarcts as transmural or non-transmural. Transmural means that the necrosis spreads through the whole thickness of the myocardium, non-transmural does not.

Remember: which artery, which wall:

  • Left anterior descending (40–50% of MIs): anterior wall of the left ventricle, apex, anterior two-thirds of the septum
  • Right coronary (30–40%): inferior/posterior wall, posterior third of the septum, right ventricle
  • Left circumflex (15–20%): lateral wall of the left ventricle

Myocardial infarcts less than 12 hours old are not grossly apparent, however, those more than 2-3 hours old can be visualised by staining. 12-24 hours after the event, a red-blue discolouration should be visible caused by stagnated blood, over the following weeks, a fibrous scar will evolve.

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