Dietary Recommendations for Pheochromocytoma Patients: Foods …
网页2024年2月10日 · Instead of processed and fast foods, pheochromocytoma patients should focus on consuming a well-balanced diet consisting of fresh fruits, vegetables, whole grains, lean proteins, and healthy fats. These nutrient-dense foods provide essential vitamins, minerals, and antioxidants that support overall health and help manage the symptoms of ...
Pheochromocytoma - Diagnosis and treatment - Mayo Clinic
网页2024年3月1日 · You also may be told to eat a high-sodium diet. Medicines such as alpha blockers, beta blockers and calcium channel blockers keep smaller veins and arteries open and relaxed. This improves blood flow and lowers blood pressure.
Pheochromocytoma - Symptoms and causes - Mayo Clinic
网页2024年3月1日 · With a pheochromocytoma, the tumor releases hormones that can cause various symptoms. They include high blood pressure, headache, sweating and symptoms of a panic attack. If a pheochromocytoma isn't treated, serious or life-threatening damage to other body systems can happen.
Pheochromocytoma > Fact Sheets > Yale Medicine
网页Surgical removal of the tumor is the main treatment for pheochromocytoma. Usually, several weeks before the surgery, patients begin taking medications to lower and stabilize their blood pressure and heart rate. They may also need to follow a high-sodium diet and drink plenty of fluids to increase blood volume in the weeks leading up to the surgery.
Pheochromocytoma: An Adrenal Gland Tumor - Johns Hopkins …
网页A pheochromocytoma is a rare type of tumor in the middle of the adrenal gland. The adrenal glands make different hormones. These hormones help keep your heart rate and blood pressure normal. A pheochromocytoma causes the adrenal glands to make too much of these hormones.
网页Preparation should include a high-sodium diet and fluid intake to prevent postoperative hypotension. We recommend minimally invasive adrenalectomy for most pheochro-mocytomas with open resection for most paragangliomas.
Treatment of pheochromocytoma in adults - UpToDate
网页2024年4月22日 · INTRODUCTION. Pheochromocytoma is a rare neuroendocrine tumor, occurring in less than 0.2 percent of patients with hypertension [1,2]. In approximately 60 percent of patients, the tumor is discovered incidentally during computed tomography (CT) or magnetic resonance imaging (MRI) of the abdomen for unrelated symptoms [3].
Update on Modern Management of Pheochromocytoma and …
网页2017年6月23日 · To prevent this postsurgical hypotension, it is mandatory to prescribe a high-sodium diet and high fluid intake during the preparation period although this advice is not evidence-based . The first 24 hours after tumor removal the patient should be strictly monitored to detect and treat hypertension, hypotension, or hypoglycemia [ 58 ].
Management of Pheochromocytoma - Endocrine Society
网页2021年9月13日 · Abstract. Pheochromocytomas/paragangliomas are characterized by a unique molecular landscape that allows their assignment to clusters based on underlying genetic alterations.
Multidisciplinary practice guidelines for the diagnosis, genetic ...
网页2021年5月6日 · Pheochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumors that arise from chromaffin cells of the adrenal medulla and the sympathetic/parasympathetic neural ganglia, respectively. The heterogeneity in its etiology makes PPGL diagnosis and treatment very complex.