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Updated: Jul 7, 2026
06:08
A Novel Method: Super-selective Adrenal Venous Sampling
Published on: September 15, 2017
[Hypertension and hyperhidrosis. Pheochromocytoma].
J Mettler1, E Battegay, T Egelhof
1Medizinische Poliklinik/Hypertoniesprechstunde, Universitätsspital Basel. julian.mettler@unibas.ch
Praxis
|February 29, 2008
Summary
Refractory hypertension in a 39-year-old woman was diagnosed as pheochromocytoma. Surgical removal of the tumor successfully treated the condition.
Area of Science:
- Endocrinology
- Nephrology
- Oncology
Background:
- Refractory hypertension poses a significant clinical challenge, often necessitating investigation into secondary causes.
- Pheochromocytoma, a rare neuroendocrine tumor, is a critical, treatable cause of secondary hypertension.
Observation:
- A 39-year-old woman presented with severe, difficult-to-control hypertension.
- Clinical history suggested potential underlying endocrine abnormalities, specifically pheochromocytoma.
Findings:
- Diagnostic workup confirmed pheochromocytoma through elevated plasma metanephrine levels.
- Computer tomography imaging localized the adrenal tumor.
Implications:
- Early diagnosis and surgical intervention are crucial for managing pheochromocytoma-induced hypertension.
- This case highlights the importance of considering rare endocrine causes in refractory hypertension cases.
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