Abstract 4364678: A Rare Case of Self-Resolving Pheochromocytoma-Induced Reverse Takotsubo Cardiomyopathy Due to Tumor Hemorrhagic Conversion

Case: A 38-year-old woman with a history of migraine headaches, a stable intracranial aneurysm, no recent stressors and a prior normal echocardiogram and ECG presented with 2 years of episodic headaches, palpitations, chest pain and worsening dyspnea. She was found to be hypertensive and electrocardiogram showed inferolateral ST segment depressions, QT interval prolongation, and elevated troponins concerning for myocardial infarction. She underwent cardiac catheterization which revealed normal coronary arteries and left ventricular basal hypokinesis with apical hyperkinesis, suggestive of reverse Takotsubo cardiomyopathy (rTTC). This left ventriculogram was confirmed with an echocardiogram and cardiac MRI. In addition, computed tomography revealed a 3 cm adrenal nodule and 24-hour urine metanephrine levels were greater than eight times the upper limit of normal, concerning for pheochromocytoma (PCC). Follow-up abdominal MRI a few days later showed the nodule had shrunk to 2.3 cm, with hemorrhagic contents. 2 weeks later, catecholamines normalized. Adrenalectomy was deferred. Repeat echocardiogram 6 months later showed normalized LV wall motion. Repeat abdominal CT showed marked adrenal mass reduction with findings consistent with nodule hemorrhage. She remains asymptomatic with normal catecholamines. Discussion: rTTC is characterized by transient basal LV hypokinesis with apical hyperkinesis and no coronary obstruction. It is attributed to catecholamine surges causing myocardial stunning. PCCs, though rare, have been documented as reversible triggers of rTTC. In this case, elevated metanephrines and an adrenal mass suggested PCC-induced rTTC that resolved after tumor hemorrhage. Early recognition and treatment of PCC is vital. Rarely, PCCs may auto-infarct or hemorrhage, becoming nonfunctional—a scenario that can shift management strategy and avoid unnecessary surgery. While rTTC is often reversible, its 10% recurrence rate underscores the importance of addressing underlying causes and ensuring appropriate follow-up.

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Publication Details

Journal
Circulation
Published
2025-11-03
DOI
https://doi.org/10.1161/circ.152.suppl_3.4364678
Primary Topic
Adrenal and Paraganglionic Tumors
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article
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Abstract 4364678: A Rare Case of Self-Resolving Pheochromocytoma-Induced Reverse Takotsubo Cardiomyopathy Due to Tumor Hemorrhagic Conversion

Felipe Contreras Yametti, Daniel Sims, Daniel Lorenzatti, Christy Joseph et al.
Circulation
Adrenal and Paraganglionic Tumors
article

Abstract 4364678: A Rare Case of Self-Resolving Pheochromocytoma-Induced Reverse Takotsubo Cardiomyopathy Due to Tumor Hemorrhagic Conversion

Felipe Contreras Yametti, Daniel Sims, Daniel Lorenzatti, Christy Joseph, Shaunak Mangeshkar, David Carruthers, N. Morales, Juan Cedeno Serna, Girish Jayant
article en

Abstract

Case: A 38-year-old woman with a history of migraine headaches, a stable intracranial aneurysm, no recent stressors and a prior normal echocardiogram and ECG presented with 2 years of episodic headaches, palpitations, chest pain and worsening dyspnea. She was found to be hypertensive and electrocardiogram showed inferolateral ST segment depressions, QT interval prolongation, and elevated troponins concerning for myocardial infarction. She underwent cardiac catheterization which revealed normal coronary arteries and left ventricular basal hypokinesis with apical hyperkinesis, suggestive of reverse Takotsubo cardiomyopathy (rTTC). This left ventriculogram was confirmed with an echocardiogram and cardiac MRI. In addition, computed tomography revealed a 3 cm adrenal nodule and 24-hour urine metanephrine levels were greater than eight times the upper limit of normal, concerning for pheochromocytoma (PCC). Follow-up abdominal MRI a few days later showed the nodule had shrunk to 2.3 cm, with hemorrhagic contents. 2 weeks later, catecholamines normalized. Adrenalectomy was deferred. Repeat echocardiogram 6 months later showed normalized LV wall motion. Repeat abdominal CT showed marked adrenal mass reduction with findings consistent with nodule hemorrhage. She remains asymptomatic with normal catecholamines. Discussion: rTTC is characterized by transient basal LV hypokinesis with apical hyperkinesis and no coronary obstruction. It is attributed to catecholamine surges causing myocardial stunning. PCCs, though rare, have been documented as reversible triggers of rTTC. In this case, elevated metanephrines and an adrenal mass suggested PCC-induced rTTC that resolved after tumor hemorrhage. Early recognition and treatment of PCC is vital. Rarely, PCCs may auto-infarct or hemorrhage, becoming nonfunctional—a scenario that can shift management strategy and avoid unnecessary surgery. While rTTC is often reversible, its 10% recurrence rate underscores the importance of addressing underlying causes and ensuring appropriate follow-up.

CirculationVol. 152(Suppl_3)
Montefiore Medical Center (US), Jacobi Medical Center (US)
Openalex Percentile: Top 50%
Adrenal and Paraganglionic Tumors
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