Evidence map›Paper›PMID 39244658›Full record

ArticleThe American journal of case reports2024

Complex Presentation of Pheochromocytoma: Hypertensive Encephalopathy and Takotsubo-Like Cardiomyopathy in a Young Female.

Nidhi Garg, Lekhya Raavi, Surabhi Maheshwari, Nafiye Busra Celik, Ashu Rastogi, Pankaj Garg

Abstract readCase Reports
In one paragraph

Article in The American journal of case reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Nidhi GargDivision of Endocrinology, University of Florida Health, Jacksonville, FL, USA.
Lekhya RaaviDivision of Critical Care Medicine, Mayo Clinic, Jacksonville, FL, USA.
Surabhi MaheshwariDivision of Internal Medicine, GMERS Medical College, Sola, Gujarat, India.ORCID 0009-0003-6798-7313
Nafiye Busra CelikDivision of Cardiothoracic Surgery, Mayo Clinic, Jacksonville, FL, USA.
Ashu RastogiDivision of Internal Medicine, PGIMER, Chandigarh, India.ORCID 0000-0002-9375-3102
Pankaj GargDivision of Cardiothoracic Surgery, Mayo Clinic, Jacksonville, FL, USA.ORCID 0000-0003-1569-6322

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Adrenal Gland NeoplasmsHypertensive EncephalopathyPheochromocytomaTakotsubo CardiomyopathyAdultFemaleHumans

Identifiers

PMID39244658
PMCPMC11393609

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