Related Experiment Video
Updated: Sep 27, 2025

Author Spotlight: Enhancing Coronary Artery Revascularization
Published on: September 15, 2023
Hypertrophic obstructive cardiomyopathy complicated with acute myocardial infarction and diffuse fibrosis: surgery or
Yunhong Wang1, Xuemei Zhao1, Mei Zhai1
1Heart Failure Center, State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, 167 North Lishi Road, Beijing, 100037, People's Republic of China.
Insights
Hypertrophic cardiomyopathy with myocardial infarction without coronary artery disease is rare. Septal reduction surgery may cautiously treat this condition, improving patient outcomes.
Area of Science:
- Cardiology
- Cardiovascular Imaging
- Interventional Cardiology
Background:
- Hypertrophic cardiomyopathy (HCM) with extreme hypertrophy, biventricular obstruction, and myocardial fibrosis is a rare phenotype.
- Myocardial infarction in the absence of obstructive coronary artery disease (MINOCA) complicates this presentation.
- Limited evidence and guidelines exist for managing this rare condition.
Observation:
- A 38-year-old male with a 2-year history of nonobstructive HCM presented with acute myocardial infarction.
- Coronary angiography revealed no obstructive lesions but showed slow flow in the left descending artery.
- Diagnostic workup confirmed anterior wall myocardial infarction, severe biventricular hypertrophy, and outflow tract obstruction.
Findings:
- Cardiac MRI confirmed a concentric HCM subtype with diffuse left ventricular late gadolinium enhancement.
- The patient underwent extended septal myectomy one month after diagnosis.
- The patient experienced a good recovery following the surgical intervention.
Implications:
- Acute myocardial infarction in hypertrophic obstructive cardiomyopathy warrants coronary angiography.
- Septal reduction surgery may be a viable, albeit cautious, treatment option for select HCM patients with MINOCA.
- This case highlights a potential therapeutic strategy for a rare and complex cardiovascular presentation.
Background:
Hypertrophic cardiomyopathy with extreme hypertrophy, biventricular obstruction and diffuse myocardial fibrosis complicated by myocardial infarction in the absence of obstructive coronary artery disease (MINOCA) is a rare phenotype. Evidence and guideline recommendations are still lacking for a treatment strategy.
Case Presentation:
Emergency coronary angiography was performed in a 38-year-old man with a 2-year history of nonobstructive hypertrophic cardiomyopathy (HCM) presenting with acute myocardial infarction. The coronary angiogram yielded no stenotic lesions but showed a diffusely dilated left descending artery with slow blood flow. All evidence from biomarker analysis, electrocardiography, echocardiography, and imaging supported the diagnosis of acute myocardial infarction in the left ventricular anterior wall. The echocardiogram demonstrated severe interventricular and apical hypertrophy, severe left ventricular outflow tract obstruction and mild right ventricular outflow tract obstruction. Cardiac magnetic resonance imaging showed a concentric morphological subtype of HCM with diffuse late gadolinium enhancement in the left ventricle. Extended septal myectomy was performed 1 month later, and the patient recovered well.
Conclusions:
Hypertrophic obstructive cardiomyopathy with acute myocardial infarction is an indication for coronary angiography. Septal reduction surgery could be performed cautiously in HCM patients with extreme hypertrophy, biventricular obstruction and diffuse myocardial fibrosis complicated by MINOCA to improve the patient's symptoms.
Related Concept Videos
Cardiomyopathy V: Interprofessional Care
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Cardiomyopathy II: Dilated Cardiomyopathy
Cardiomyopathy IV: Restrictive Cardiomyopathy
Myocarditis III: Medical Management
Cardiomyopathy VII: Pre and Post Operative Nursing Management

