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

Phaeochromocytomas are rare neuroendocrine tumours with a highly variable clinical
presentation but most commonly presenting with episodes of headaches, sweating …

Neuroendocrine tumors (NETs) constitute a heterogeneous group of neoplasms that
originate from endocrine glands such as the pituitary, the parathyroids, and the …

Pheochromocytomas are rare neuroendocrine tumors with a highly variable clinical
presentation, but they most commonly present as spells of headaches, sweating …

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

Abstract The First International Symposium on Pheochromocytoma, held in October 2005,
included discussions about developments concerning these rare catecholamine-producing …

Purpose To assess the yield and the clinical value of systematic screening of susceptibility
genes for patients with pheochromocytoma (pheo) or functional paraganglioma (pgl) …

Pheochromocytoma or secreting paraganglioma may recur after initial surgery. Diagnostic
methods have improved in recent decades. We determined whether features at presentation …

Pheochromocytomas and paragangliomas are tumors derived from chromaffin cells in the
adrenal medulla or extra-adrenal paraganglia. 1 Pheochromocytomas and sympathetic …

Pheochromocytomas (PHEO)(1–3) are catecholamineproducing tumors that arise from
chromaffin cells. PHEO are mostly situated within the adrenal medulla, although in about 9 …