Pheochromocytoma and Paraganglioma Pheochromocytoma and paraganglioma are
related tumors that differ mainly in location; pheochromocytomas are adrenal, and …

Phaeochromocytoma and paraganglioma (PPGL) are chromaffin cell tumours that require
timely diagnosis because of their potentially serious cardiovascular and sometimes life …

Adrenal incidentalomas are adrenal masses detected on imaging performed for reasons
other than suspected adrenal disease. In most cases, adrenal incidentalomas are …

Adrenal tumors are commonly discovered incidentally on cross-sectional abdominal
imaging performed for reasons other than adrenal mass. Incidence of adrenal tumors …

Pheochromocytoma and paraganglioma (PPGL) require prompt consideration and efficient
diagnosis and treatment to minimize associated morbidity and mortality. Once considered …

Abstract Context Pheochromocytomas and paragangliomas (PPGLs) are believed to harbor
malignant potential; about 10% to 15% of pheochromocytomas and up to 50% of abdominal …

Pheochromocytomas and paragangliomas (PPGLs) are rare neuro-endocrine tumors. The
catecholamine surge causes paroxysmal or chronic secondary hypertension. PPGLs may …

Context Pheochromocytoma and sympathetic paraganglioma (PPGL) are rare
catecholamine-secreting tumors but recent studies suggest increasing incidence …

Objective Hypertension and symptoms of catecholamine excess are features of
pheochromocytomas and paragangliomas (PPGLs). This prospective observational cohort …

Simple Summary Pheochromocytomas and abdominal paragangliomas (PPGLs) are rare.
They can be discovered incidentally by imaging with computed tomography or magnetic …