Abstract
Patient presenting following the incidental detection of a 9 mm nodule at the pancreatic tail. 68Ga-DOTA-NOC PET/CT documented a focal area of uptake (red arrow) in the nodule confirming its neuroendocrine nature
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68Ga-DOTA-peptide PET/CT imaging is accurate for the characterisation of even very small well differentiated neuroendocrine lesions.
FormalPara Teaching PointPET/CT provides accurate staging (T,N,M) of well differentiated NEN.
FormalPara Teaching PointNeuroendocrine differentiation in other solid tumours may occur. 68Ga-DOTA-NOC PET/CT may provide data on SSTR expression.
FormalPara Teaching Point68Ga-DOTA-NOC is accurate to study patients with paraganglioma, providing data on somatostatin receptor expression and on disease localization in the whole body.
FormalPara Teaching Point68Ga-DOTA-NOC PET/CT is accurate for the detection of relapse.
FormalPara Teaching PointNEN patients may relapse a long time after primary surgery. 68Ga-DOTA-NOC PET/CT can identify relapse undetected by CT.
FormalPara Teaching Point68Ga-DOTA-peptide PET/CT delayed imaging may be useful for better localisation of equivocal imaging findings at standard acquisition time.
FormalPara Teaching PointDiffuse non-pathologic 68Ga-DOTA-peptides uptake at the pancreatic head may be encountered and may be transient in the same patient.
FormalPara Teaching PointAlthough the head of the pancreas can present a faint diffuse non-pathologic uptake, in the presence of a nodule with increased uptake of the 68Ga-DOTA-peptide, the presence of disease should be suspected.
FormalPara Teaching Point68Ga-DOTA-peptides imaging can be useful to detect the unknown primary tumour site in patients with documented neuroendocrine secondary lesions.
FormalPara Teaching CaseIn patients with NEN presenting lesions without significant somatostatin receptor expression, 18F-FDG PET/CT should be considered as additional examination.
FormalPara Teaching CaseIn patients with NEN secondary lesions and unknown primary, 18F-FDG PET/CT may provide valuable information on primary site in cases with undifferentiated tumours.
FormalPara Teaching PointAlthough generally well differentiated, undifferentiated NET may be encountered, are clinically more aggressive and generally show preferential 18F-FDG uptake.
FormalPara Teaching PointA cold central lesion area may be encountered in both 68Ga-DOTA-NOC and 18F-FDG PET/CT images, especially in large lesions representing necrosis (in case of concordant findings). It must also be mentioned that in some cases a lesion with a peripheral rim and a cold core at 68Ga-DOTA-NOC PET/CT may present with 18F-FDG uptake only in the 68Ga-DOTA-peptide-negative area; in this case disease differentiation should be suspected.
FormalPara Teaching PointAlthough most NEN are well differentiated, aggressive forms showing FDG avidity are encountered. High-grade tumours show preferential FDG uptake.
FormalPara Teaching Point68Ga-DOTA-peptides uptake correlates with SSTR expression and is useful to select candidate patients for PRRT. 68Ga-DOTA-peptides PET/CT is also useful to guide further treatment planning after PRRT.
FormalPara Teaching PointAlthough ideally a metabolic tracer should be employed to assess disease after therapy, correlating with SSTR expression, 68Ga-DOTA-peptides may be useful to guide further treatment planning.
FormalPara Teaching Point18F-DOPA is accurate for the detection of pheochromocytoma lesions (on the contrary 68Ga-DOTA-peptides have shown suboptimal sensitivity due to the generally low/variable expression of somatostatin receptors)
FormalPara Teaching PointAlthough pheochromocytoma may be well differentiated, aggressive undifferentiated forms can be encountered and show a preferential 18F-FDG uptake.
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© 2016 Springer International Publishing Switzerland
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Ambrosini, V., Fanti, S. (2016). Neuroendocrine Tumours Pictorial Atlas. In: Ambrosini, V., Fanti, S. (eds) PET/CT in Neuroendocrine Tumors. Clinicians’ Guides to Radionuclide Hybrid Imaging(). Springer, Cham. https://doi.org/10.1007/978-3-319-29203-8_8
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DOI: https://doi.org/10.1007/978-3-319-29203-8_8
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