Paragangliomas are rare neuroendocrine tumors that may arise anywhere along the
paraganglial system, with a high frequency of hereditary forms or multifocal disease. Most …

Aim and methods Paragangliomas (PGL) are neural crest-derived tumours that are found
along the autonomic neural network throughout the body and can be multiple and/or …

Phaeochromocytomas and paragangliomas (PPGLs) are rare tumours that arise from the
adrenal medulla or extra‐adrenal sympathetic or parasympathetic paraganglia. Recent …

Paragangliomas are neural crest-derived tumors, arising either from chromaffin sympathetic
tissue (in adrenal, abdominal, intra-pelvic, or thoracic paraganglia) or from parasympathetic …

Although anatomic imaging to assess the precise localization of pheochromocytomas/
paragangliomas (PHEOs/PGLs) is unavoidable before any surgical intervention on these …

With improvements in genetics and oncology, and increased cross-sectional imaging, there
is rapid expansion in the existing knowledge regarding diagnosis and management of …

Purpose Paragangliomas (PGLs) are tumors that can metastasize and recur; therefore,
lifelong imaging follow-up is required. Hybrid PET/CT is an essential tool to image PGLs …

After establishing a biochemical diagnosis, pheochromocytomas and extra-adrenal
paragangliomas (PPGLs) can be localized using different anatomical and functional imaging …

Abstract Pheochromocytomas (PCCs) and paragangliomas (PGLs) are rare, heterogeneous
neuroendocrine neoplasms of the autonomous nervous system of chromaffin cell origin that …

Aims and methods The aim of this prospective study was to compare the diagnostic value of
[18F] FDOPA‐PET and [111In] pentetreotide‐SPECT somatostatin receptor scintigraphy …