Hypertension was not an independent risk factor for postoperative complications among patients undergoing surgery for pheochromocytoma.

Pheochromocytomas are slow-growing tumors in the adrenal gland. Learn how much they grow each year and how long they take double.

The panel of experts at the ISP felt strongly that localization of pheochromocytoma or paraganglioma should only be initiated if the clinical evidence for the presence of tumor is reasonably ...

A pheochromocytoma tumor ... went through with treatment for the tumor in October and suffered a setback post-surgery, but earlier today, she provided an uplifting update on her X account.

The patient underwent surgery, which confirmed a malignant neck paraganglioma with metastasis to a cervical lymph node. He had no family history of carotid body tumors or pheochromocytoma.

Measurement of both metanephrine and normetanephrine, therefore, had a sensitivity of 100% in identifying pheochromocytoma. Overall, 17 patients were assessed before and after surgery ...

A metaiodobenzylguanidine scan showed positive uptake within the mass, which supported a diagnosis of pheochromocytoma. The patient underwent a laparoscopic right suprarenal adrenalectomy after ...

At the Baylor College of Medicine Endocrine Surgery Clinics, Drs ... hyperparathyroidism, adrenal masses, pheochromocytoma, Cushing’s syndrome and Conn’s syndrome. A new procedure allows surgeons, ...

Treatment for pheochromocytoma involves blood pressure medications followed by surgery, usually laparoscopic (minimally invasive) removal of one or both adrenal glands. Cushing’s syndrome is a ...

Monitor HR during therapy. Bronchospastic disease. Pheochromocytoma. Surgery. Diabetes. May mask signs and increase risk for hypoglycemia. Hyperthyroidism. Avoid abrupt cessation. Hepatic impairment.