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

Pheochromocytomas are rare neuroendocrine tumors that produce and store
catecholamines. Without adequate preparation, the release of excessive amounts of …

Objective: The aim was to formulate clinical practice guidelines for pheochromocytoma and
paraganglioma (PPGL). Participants: The Task Force included a chair selected by the …

Pheochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumors that
arise from chromaffin cells of the adrenal medulla and the sympathetic/parasympathetic …

An adrenal incidentaloma is an adrenal mass found in an imaging study performed for other
reasons unrelated to adrenal disease and often accompanied by obesity, diabetes, or …

Background Laparoscopic adrenalectomy (LA) has replaced open adrenalectomy as the
standard operation for non-malignant adrenal tumours. Retroperitoneoscopic …

BACKGROUND: This study evaluates the perioperative outcomes of robotic-assisted
adrenalectomy (RA) compared with lateral transperitoneal laparoscopic adrenalectomy (LA) …

Pheochromocytomas and sympathetic paraganglioma (PPGL) are rare chromaffin cell
tumors originating in the adrenal medulla and sympathetic paraganglia, respectively, which …

The terms paraganglioma (PGL) and pheochromocytoma (Pheo) were first mentioned in
1908 and 1912 respectively when pathologists Henri Alezais, Felix Peyron, and Ludwig Pick …

Hypothesis Pheochromocytoma can be safely treated laparoscopically;“subclinical”
pheochromocytoma is increasingly common. Design Retrospective review. Setting …