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Updated: Sep 2, 2025

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Published on: November 29, 2018
Isolated extreme right ventricular hypertrophy: A case report
Daiki Shako1, Tatsuya Kawasaki1, Michiyo Yamano1,2
1Department of Cardiology, Matsushita Memorial Hospital, Osaka, Japan.
This study presents a rare case of extreme right ventricular (RV) hypertrophic cardiomyopathy (HCM) in a 72-year-old man. The findings highlight the diverse presentations of HCM, including isolated RV involvement with significant wall thickening and calcification.
Area of Science:
- Cardiology
- Cardiovascular Imaging
- Genetics
Background:
- Hypertrophic cardiomyopathy (HCM) is typically characterized by left ventricular (LV) hypertrophy.
- Right ventricular (RV) involvement can occur but is usually less severe than LV hypertrophy.
Observation:
- A 72-year-old male presented with an abnormal electrocardiogram.
- Echocardiography revealed isolated hypertrophy of the RV apex.
- Multidetector computed tomography showed partial calcification within the RV hypertrophy, surrounded by hypoperfused myocardium.
Findings:
- Diagnosis of HCM was confirmed based on myocardial imaging characteristics, including systolic thickening.
- The patient exhibited an extreme RV hypertrophy with a maximum wall thickness of 40 mm.
- This case represents an isolated extreme RV HCM phenotype.
Implications:
- This case underscores the importance of recognizing diverse phenotypes in HCM.
- It highlights the possibility of isolated and extreme RV hypertrophy as a presentation of HCM.
- Awareness of such presentations is crucial for accurate diagnosis and management of hypertrophic cardiomyopathy.
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