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Updated: Aug 13, 2026

Morphological and Functional Assessment of the Right Ventricle Using 3D Echocardiography
Published on: October 28, 2020
Left ventricular involvement in right ventricular dysplasia/cardiomyopathy
F V Lobo1, M D Silver, J Butany
1Hamilton General Hospital, Hamilton, Canada. lobof@hamcivhos.on.ca
Insights
Left ventricular (LV) involvement is common in arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C), often affecting the LV free wall and septum. Pathologists must carefully examine hearts for these subtle LV changes.
Area of Science:
- Cardiovascular Pathology
- Cardiac Morphology
- Histopathology
Background:
- Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is a primary myocardial disease.
- Left ventricular (LV) involvement is increasingly recognized but less understood than right ventricular pathology.
Purpose of the Study:
- To define the pathological characteristics of LV involvement in ARVD/C.
- To assess the prevalence and patterns of LV myocardial changes in a cohort of ARVD/C patients.
Main Methods:
- Retrospective morphological analysis of 17 hearts from individuals with ARVD/C.
- Inclusion of cases with sudden cardiac death and explanted hearts due to arrhythmias or heart failure.
- Detailed gross and microscopic examination of both right and left ventricles.
Main Results:
- All 17 hearts exhibited typical right ventricular features of ARVD/C and evidence of LV wall involvement.
- LV free wall was affected in all cases, and the ventricular septum (VS) in 15.
- Histological findings included myocyte atrophy and inflammation, with more severe LV changes in older patients.
Conclusions:
- LV free wall and frequent VS involvement are likely in ARVD/C patients with longer survival.
- LV involvement may be missed on gross examination and requires diligent histological assessment.
- Examination of appropriate histological sections from both LV free wall and septum is crucial for accurate diagnosis.
Objective:
To characterize pathological features of left ventricular (LV) involvement in right ventricular dysplasia/cardiomyopathy (RVD/C).
Design:
Retrospective morphological case study.
Setting:
Two referral-based university medical centres.
Materials:
Seventeen hearts were studied: 15 from sudden cardiac deaths outside hospital and two explanted hearts, one removed for intractable arrhythmias and the other for right-sided heart failure. The subjects (three female) were aged 16 to 60 years.
Main Results:
All had typical right ventricular features of RVD/C and morphological evidence of LV wall involvement, seven with microscopic changes only. Of 10 hearts with gross and microscopic lesions, nine had large or laminar segments involved. The LV free wall was affected in all cases and the ventricular septum (VS) in 15. Sixteen hearts were hypertrophied. In involved areas, the LV or VS walls were of 'normal' thickness or slightly thinned. Five histological patterns of involvement were recognized, of which four were found in the LV. More severe LV involvement was seen in the hearts of older patients. Complete transmural fatty replacement of the myocardium was not observed, nor were the LVs aneurysmal. Minimal or mild focal aggregates of inflammatory cells were seen in nine hearts and moderate inflammatory changes in two. Inflammation was usually associated with myocyte atrophy and only rarely with myonecrosis.
Conclusions:
This study suggests that patients with RVD/C who live long enough will likely have LV free wall involvement with frequent VS involvement. Pathologists may miss LV involvement on gross examination. It should be sought diligently in patients dying of the condition or receiving transplants for heart failure. Appropriate histological sections from both free wall and septum must be examined.
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