Purpose Diverse radionuclide imaging techniques are available for the diagnosis, staging,
and follow-up of phaeochromocytoma and paraganglioma (PPGL). Beyond their ability to …

Phaeochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumors with
clinical heterogeneity and a high association with hereditary disease, affecting …

Background Pheochromocytoma and paraganglioma (PPGL) are neuroendocrine tumors
with frequent mutations in genes linked to the tricarboxylic acid cycle. However, no …

Paragangliomas (PGL) of the adrenal (also known as pheochromocytomas) or extra-adrenal
neural crest-derived cells are highly heritable tumors, usually driven by single pathogenic …

Abstract Context Pheochromocytomas/paragangliomas (PPGLs) are neuroendocrine tumors
that can secrete norepinephrine (NE). Brown adipose tissue (BAT) activation is mediated …

Context The behavior of locally advanced pheochromocytoma (LAP) remains unknown.
Objective We characterized the population with LAP and recurrence-free survival (RFS) …

Abstract About 30%–40% of patients with pheochromocytoma (PCC) and paraganglioma
(PGL) have underlying germline mutations in certain susceptibility genes despite absent …

Increasingly common, neuroendocrine tumors (NETs) are regarded nowadays as
neoplasms potentially causing debilitating symptoms and life-threatening medical …

Simple Summary Pheochromocytomas and paragangliomas (PPGLs) are neuroendocrine
tumors arising from chromaffin cells of the adrenal medulla, or extra-adrenal paraganglia …

Apart from the oncometabolite succinate, little studies have appeared on extra-mitochondrial
pathways in Succinate Dehydrogenase (SDH) genetic deficiency. The role of NADH/NAD+ …