Pheochromocytoma and Paraganglioma: Current Functional and Future Molecular Imaging

Paragangliomas are neural crest-derived tumors, arising either from chromaffin sympathetic tissue (in adrenal, abdominal, intra-pelvic or thoracic paraganglia) or from parasympathetic tissue (in head and neck paraganglia). They have a specific cellular metabolism, with the ability to synthesize, sto...

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Main Authors: Elise M Blanchet, Victoria eMartucci, Karel ePacak
Format: Article
Language:English
Published: Frontiers Media S.A. 2012-01-01
Series:Frontiers in Oncology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fonc.2011.00058/full
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author Elise M Blanchet
Victoria eMartucci
Karel ePacak
author_facet Elise M Blanchet
Victoria eMartucci
Karel ePacak
author_sort Elise M Blanchet
collection DOAJ
description Paragangliomas are neural crest-derived tumors, arising either from chromaffin sympathetic tissue (in adrenal, abdominal, intra-pelvic or thoracic paraganglia) or from parasympathetic tissue (in head and neck paraganglia). They have a specific cellular metabolism, with the ability to synthesize, store and secrete catecholamines (although most head and neck paragangliomas do not secrete any catecholamines). This disease is rare and also very heterogeneous, with various presentations (e.g., in regards to localization, multifocality, potential to metastasize, biochemical phenotype, and genetic background). With growing knowledge, notably about the pathophysiology and genetic background, guidelines are evolving rapidly. In this context, functional imaging is a challenge for the management of paragangliomas.Nuclear imaging has been used for exploring paragangliomas for the last three decades, with MIBG historically as the first-line exam. Tracers used in paragangliomas can be grouped in three different categories. Agents that specifically target catecholamine synthesis, storage, and secretion pathways include: 123 and 131I-metaiodobenzylguanidine (123/131I-MIBG), 18F-fluorodopamine (18F-FDA), and 18F-fluorodihydroxyphenylalanine (18F-FDOPA). Agents that bind somatostatin receptors include 111In-pentetreotide and 68Ga-labelled somatostatin analog peptides. The non-specific agent most commonly used in paragangliomas is 18F-fluorodeoxyglucose (18F-FDG). This review will first describe conventional scintigraphic exams that are used for imaging paragangliomas. In the second part we will emphasize the interest in new PET approaches (specific and non-specific), considering the growing knowledge about genetic background and pathophysiology, with the aim of understanding how tumors behave, and optimally adjusting imaging technique for each tumor type.
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spelling doaj.art-8f7ce339b7e74fc5be982a26cf3d232e2022-12-21T19:17:16ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2012-01-01110.3389/fonc.2011.0005816042Pheochromocytoma and Paraganglioma: Current Functional and Future Molecular ImagingElise M Blanchet0Victoria eMartucci1Karel ePacak2Centre Hospitalier d'AngersNational Institutes of HealthNational Institutes of HealthParagangliomas are neural crest-derived tumors, arising either from chromaffin sympathetic tissue (in adrenal, abdominal, intra-pelvic or thoracic paraganglia) or from parasympathetic tissue (in head and neck paraganglia). They have a specific cellular metabolism, with the ability to synthesize, store and secrete catecholamines (although most head and neck paragangliomas do not secrete any catecholamines). This disease is rare and also very heterogeneous, with various presentations (e.g., in regards to localization, multifocality, potential to metastasize, biochemical phenotype, and genetic background). With growing knowledge, notably about the pathophysiology and genetic background, guidelines are evolving rapidly. In this context, functional imaging is a challenge for the management of paragangliomas.Nuclear imaging has been used for exploring paragangliomas for the last three decades, with MIBG historically as the first-line exam. Tracers used in paragangliomas can be grouped in three different categories. Agents that specifically target catecholamine synthesis, storage, and secretion pathways include: 123 and 131I-metaiodobenzylguanidine (123/131I-MIBG), 18F-fluorodopamine (18F-FDA), and 18F-fluorodihydroxyphenylalanine (18F-FDOPA). Agents that bind somatostatin receptors include 111In-pentetreotide and 68Ga-labelled somatostatin analog peptides. The non-specific agent most commonly used in paragangliomas is 18F-fluorodeoxyglucose (18F-FDG). This review will first describe conventional scintigraphic exams that are used for imaging paragangliomas. In the second part we will emphasize the interest in new PET approaches (specific and non-specific), considering the growing knowledge about genetic background and pathophysiology, with the aim of understanding how tumors behave, and optimally adjusting imaging technique for each tumor type.http://journal.frontiersin.org/Journal/10.3389/fonc.2011.00058/fullRadionuclide Imagingpositron emission tomography18F-fluorodeoxyglucose18F-fluorodopamine18F-fluorodyhydroxyphenylalaninegenetic mutation
spellingShingle Elise M Blanchet
Victoria eMartucci
Karel ePacak
Pheochromocytoma and Paraganglioma: Current Functional and Future Molecular Imaging
Frontiers in Oncology
Radionuclide Imaging
positron emission tomography
18F-fluorodeoxyglucose
18F-fluorodopamine
18F-fluorodyhydroxyphenylalanine
genetic mutation
title Pheochromocytoma and Paraganglioma: Current Functional and Future Molecular Imaging
title_full Pheochromocytoma and Paraganglioma: Current Functional and Future Molecular Imaging
title_fullStr Pheochromocytoma and Paraganglioma: Current Functional and Future Molecular Imaging
title_full_unstemmed Pheochromocytoma and Paraganglioma: Current Functional and Future Molecular Imaging
title_short Pheochromocytoma and Paraganglioma: Current Functional and Future Molecular Imaging
title_sort pheochromocytoma and paraganglioma current functional and future molecular imaging
topic Radionuclide Imaging
positron emission tomography
18F-fluorodeoxyglucose
18F-fluorodopamine
18F-fluorodyhydroxyphenylalanine
genetic mutation
url http://journal.frontiersin.org/Journal/10.3389/fonc.2011.00058/full
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AT victoriaemartucci pheochromocytomaandparagangliomacurrentfunctionalandfuturemolecularimaging
AT karelepacak pheochromocytomaandparagangliomacurrentfunctionalandfuturemolecularimaging