A molecular biology–based taxonomy has been proposed for pheochromocytoma and
paraganglioma (PPGL). Data from the Cancer Genome Atlas revealed clinically relevant …

Pheochromocytoma and paraganglioma (PPGL) are rare neuroendocrine tumors,
characterized by excessive release of catecholamines (CAs), and manifested as the classic …

By definition, an adrenal incidentaloma is an asymptomatic adrenal mass detected on
imaging not performed for suspected adrenal disease. In most cases, adrenal …

This first part of a two-part review of pheochromocytoma and paragangliomas (PPGLs)
addresses clinical presentation, diagnosis, management, treatment, and outcomes. In this …

The discovery of an adrenal mass in the course of abdominal imaging performed for other
reasons,“adrenal incidentaloma,” is a common clinical problem that poses a challenging …

Context: The per-operative hemodynamic behavior of normotensive incidentally discovered
pheochromocytomas is poorly documented. Objective: To compare the per-operative …

Objective Pheochromocytoma (PHEO) may occur in 0.1–5.7% of patients presenting with a
neurofibromatosis type 1 (NF1). Current recommendations are to explore only symptomatic …

Resection of phaeochromocytoma and paraganglioma (PPGL) is traditionally preceded by
alpha‐blockade to prevent complications of haemodynamic instability intraoperatively. While …

Introduction: An adrenal incidentaloma (AI) is an adrenal neoplasm incidentally discovered
during an imaging unrelated to suspected adrenal disease. The aim of the present review is …

Phaeochromocytoma and extra adrenal paraganglioma are rare neuroendocrine tumours
and have the potential to secrete adrenaline, noradrenaline and dopamine causing a myriad …