Complex Presentation of Pheochromocytoma: Hypertensive Encephalopathy and Takotsubo-Like Cardiomyopathy in a Young Female.
Nidhi GargLekhya RaaviSurabhi MaheshwariNafiye Busra CelikPankaj MalhotraPankaj GargPublished in: The American journal of case reports (2024)
BACKGROUND Pheochromocytoma, a rare catecholamine-secreting tumor, often presents with paroxysmal or sustained hypertension, tachycardia, headache, and diaphoresis. Timely diagnosis is essential to prevent adverse complications. Less common presentations include pheochromocytoma crisis, with severe neurological and cardiac complications. CASE REPORT We report a unique case of a 25-year-old woman who initially presented with pheochromocytoma-induced hypertensive encephalopathy and acute coronary syndrome. Echocardiography revealed takotsubo-like cardiomyopathy, and magnetic resonance imaging of the brain revealed posterior reversible encephalopathy syndrome. Initial treatment focused on controlling her blood pressure and supporting cardiac function. Due to her recovering from immediate crisis and absence of further symptoms, the patient refused further follow-up. However, she eventually experienced another episode of hypertensive crisis 2 years later. Subsequent investigations with 24-h urine tests revealed elevated vanillylmandelic acid levels (7.93 mg/24 h), normetanephrine (2638.72 µg/24 h), and nor-metanephrine to creatinine ratio (3546.67) and normal urine metanephrine levels (195.92 µg/24 h) and metanephrine to creatinine ratio (263.33). Contrast-enhanced computed tomography of the abdomen revealed a 4.3×3.1×4-cm mass in the right adrenal gland. A DOTATATE positron emission tomography scan revealed a 3.9×4.3×2.7-cm localized right adrenal pheochromocytoma. Biochemical testing and adrenal imaging revealed a previously undiagnosed pheochromocytoma. Following targeted medical therapy and right adrenalectomy, the patient achieved complete resolution of her hypertension and associated symptoms. CONCLUSIONS Our case is a unique simultaneous presentation of posterior reversible encephalopathy syndrome and takotsubo-like cardiomyopathy, highlighting the importance to consider pheochromocytoma in acute neurological and cardiac presentations, even in the absence of typical symptoms.
Keyphrases
- computed tomography
- blood pressure
- case report
- positron emission tomography
- magnetic resonance imaging
- contrast enhanced
- single cell
- early onset
- acute coronary syndrome
- public health
- hypertensive patients
- heart rate
- heart failure
- dual energy
- left ventricular
- drug induced
- pet ct
- high resolution
- percutaneous coronary intervention
- magnetic resonance
- hepatitis b virus
- stem cells
- healthcare
- type diabetes
- sleep quality
- liver failure
- mesenchymal stem cells
- brain injury
- adipose tissue
- oxidative stress
- emergency department
- combination therapy
- uric acid
- bone marrow
- insulin resistance
- aortic dissection
- antiplatelet therapy
- extracorporeal membrane oxygenation