Microscopic Findings of Myocardial Infarction
Myocardial infarction is characterized pathologically by coagulation necrosis and/or contraction band necrosis, with the presence of polymorphonuclear leukocytes defining acute MI histologically. 1
Temporal Evolution of Microscopic Changes
The microscopic appearance of MI evolves in a predictable sequence that depends critically on the time elapsed since ischemic injury:
Hyperacute Phase (<6 hours)
- Minimal or no polymorphonuclear leukocytes are present if death occurs within 6 hours of onset, making early histologic diagnosis challenging 1
- Waviness of myocardial fibers may be the only detectable microscopic finding in very early sudden death cases 1
- Cell death is not immediate after ischemia onset—it takes as little as 20 minutes to develop in some models, but standard microscopic examination cannot identify necrosis until approximately 6 hours have elapsed 2
Acute Phase (6 hours to 7 days)
- The defining histologic feature is the presence of polymorphonuclear leukocytes (neutrophils) infiltrating the necrotic myocardium 1, 3
- Cell death manifests as coagulation necrosis and/or contraction band necrosis, evolving primarily through oncosis and to a lesser degree through apoptosis 2, 1
- Complete necrosis of all at-risk myocardial cells requires at least 2-4 hours or longer, depending on collateral circulation, intermittent versus persistent occlusion, and individual oxygen demand 2, 1
Healing Phase (7 to 28 days)
- Mononuclear cells (macrophages and lymphocytes) and fibroblasts replace polymorphonuclear leukocytes as the dominant cellular infiltrate 1, 3
- The absence of polymorphonuclear leukocytes with presence of mononuclear cells is the key distinguishing feature of healing infarction 1
Healed Phase (≥29 days)
- Scar tissue without cellular infiltration characterizes the healed infarction 1, 3
- The entire process from acute injury to complete healing typically requires at least 5-6 weeks 2, 1
Special Microscopic Patterns
Reperfusion-Modified Infarction
- Reperfusion significantly alters the microscopic appearance, producing myocytes with prominent contraction bands and large quantities of extravasated erythrocytes 1
- This pattern differs markedly from non-reperfused infarction and must be recognized to avoid misinterpretation 1
Critical Diagnostic Pitfalls
Clinicopathologic Timing Discordance
- The clinical and electrocardiographic timing may not correspond exactly with pathological timing 1, 3
- ECG may show evolving ST-T changes and biomarkers may remain elevated when the infarction is pathologically already in the healing phase 1, 3
- This discordance occurs because biomarkers reflect ongoing myocyte death and membrane disruption, while histology reflects the tissue's inflammatory and reparative response 2