Please provide your email address to receive an email when new articles are posted on . A 26-year-old woman with a past medical history significant for congenital heart disease, status-post multiple ...

Please provide your email address to receive an email when new articles are posted on . The patient is a 65-year-old white man with a past medical history significant for severe coronary artery ...

Pheochromocytoma is a catecholamine-producing tumor that originates from chromaffin cells of the adrenergic system, most commonly in the adrenal medulla. There are two main steps in the diagnosis of ...

A pheochromocytoma is an intra-adrenal paraganglioma; the current WHO nomenclature reserves the term 'pheochromocytoma' for paragangliomas of adrenal origin Measurements of plasma or urinary ...

Because of advances in medical imaging, incidental findings of adrenal tumors are increasingly common. These tumors are termed adrenal incidentalomas. In previous studies, adrenal incidentalomas have ...

June 23, 2004 (Philadelphia) — Positron emission tomography (PET) is more sensitive in detecting and localizing pheochromocytomas than conventional imaging, according to research presented here at the ...

Pheochromocytoma is a rare tumor of the adrenal medulla that secretes substances called catecholamines. The adrenal glands are a pair of small glands sitting on the top of the kidneys. An adrenal ...

Background A 55-year-old male with poorly controlled hypertension and a history of coronary artery disease presented with a large adrenal mass. The patient also reported a long-standing history of ...

Pheochromocytoma, a rare condition caused by a tumor in the adrenal medulla affecting the chromaffin cells, results in an excess production of catecholamines (epinephrine and norepinephrine) and ...

Headaches, palpitations, and diaphoresis are the classic triad of pheochromocytoma, but not all patients with pheochromocytoma are symptomatic. Pheochromocytoma crisis can occur spontaneously or be ...