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Transient biventricular apical ballooning: a unique presentation of the "broken heart"
Gregg Novak1, Kimberly Kross, Kristy Follmer
1General Internal Medicine, Geisinger Medical Center, Danville, Pennsylvania 17822-2160, USA.
Insights
Takotsubo cardiomyopathy typically involves left ventricular apical ballooning. This case highlights right ventricular dysfunction, challenging current understandings of the syndrome's pathophysiology.
Area of Science:
- Cardiology
- Pathophysiology
- Medical Science
Background:
- Takotsubo cardiomyopathy is characterized by transient left ventricular (LV) apical ballooning and normal epicardial coronary arteries.
- The syndrome is frequently triggered by emotional or physiological stress, with its exact pathogenesis remaining unclear.
- Existing hypotheses center on elevated catecholamines interacting with coronary artery endothelium, microcirculation, or LV geometry.
Observation:
- This report details a case of Takotsubo cardiomyopathy with concurrent right ventricular (RV) involvement.
- RV dysfunction is not a commonly reported feature in typical presentations of this condition.
- The presence of RV dysfunction was noted in the described patient.
Findings:
- The observed RV dysfunction in Takotsubo cardiomyopathy may influence immediate patient management strategies.
- This finding suggests a need to reconsider the universal applicability of proposed pathophysiologic mechanisms.
- The study indicates that current models may not fully encompass all presentations of the syndrome.
Implications:
- Further research is needed to elucidate the role of RV involvement in Takotsubo cardiomyopathy.
- Understanding RV dysfunction could lead to improved diagnostic and therapeutic approaches.
- This case broadens the perspective on the potential spectrum of Takotsubo cardiomyopathy and its underlying mechanisms.
Abstract:
Transient left ventricular (LV) apical ballooning and normal epicardial coronary arteries are the hallmarks of Takotsubo cardiomyopathy. The syndrome is often triggered by emotional or physiologic stress, and its pathogenesis is poorly understood. Current proposals focus on elevated cathecolamines in association with abnormal coronary artery endothelium, coronary microcirculation or LV geometry. Right ventricular (RV) involvement, as described in our patient, is not reported as a typical feature. Presence of RV dysfunction may affect the initial management of these patients and raises questions regarding the universal applicability of the currently proposed pathophysiologic mechanisms of this syndrome.
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