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Endocardial fibroelastosis with coronary artery thromboembolus and myocardial infarction

K L Lane1, A J Herzberg, K A Reimer

  • 1Department of Pathology, Duke University Medical Center, Durham, North Carolina.

Clinical Pediatrics
|October 1, 1991
PubMed

Insights

Endocardial fibroelastosis can lead to unusual thromboembolic complications, such as myocardial infarction in pediatric patients. This case highlights the importance of suspecting coronary artery thromboemboli in children with cardiomyopathy.

Area of Science:

  • Pediatric Cardiology
  • Cardiovascular Pathology

Background:

  • Congenital heart conditions in infants can present with severe symptoms like congestive heart failure and respiratory distress.
  • Early life febrile illness in the mother may be a risk factor for fetal cardiac anomalies.

Observation:

  • An 18-month-old male presented with symptoms suggestive of cardiomyopathy and myocarditis, initially responding to pharmacologic therapy.
  • The patient later experienced respiratory distress and cardiogenic shock, with electrocardiographic (ECG) evidence of myocardial infarction.

Findings:

  • Autopsy revealed endocardial fibroelastosis with left ventricular mural thrombi.
  • Thromboembolism to the left anterior descending coronary artery resulted in transmural myocardial infarction.

Implications:

  • Myocardial infarction is an uncommon but serious thromboembolic complication of endocardial fibroelastosis.
  • Pediatric patients with cardiomyopathy and suspected myocardial infarction require a high index of suspicion for coronary artery thromboemboli.

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