| Literature DB >> 30042056 |
A S Kroiss1, C Uprimny2, R Pichler3, R W Gasser4, I J Virgolini2.
Abstract
Pheochromocytoma (PHEO) is rare and belongs to the group of neuroendocrine tumours (NETs). These tumours can be found anywhere from the neck to the pelvis associated with sympathetic ganglia. Morphological imaging, for example CT, provides excellent anatomical detail and high sensitivity but lacks specificity as difficulties may occur when distinguishing between tumours derived from the sympathetic nervous system and other tumour entities. In contrast to anatomical imaging, functional imaging (123I-MIBG, 68Ga-DOTA-TOC PET) provides high sensitivity and specificity in detecting NETs. Early detection of PHEO is crucial and has a major effect on treatment and prognosis. This case report describes the important role of anatomical and functional imaging in a patient with a neuroendocrine tumour of unusual origin.Entities:
Keywords: (123)I-MIBG SPECT/CT; (123)I-MIBG SPECT/TC; (68)Ga-DOTA-TOC PET/CT; (68)Ga-DOTA-TOC PET/TC; Feocromocitoma; Pheochromocytoma
Mesh:
Substances:
Year: 2018 PMID: 30042056 DOI: 10.1016/j.remn.2018.02.001
Source DB: PubMed Journal: Rev Esp Med Nucl Imagen Mol (Engl Ed) ISSN: 2253-8089