While somatostatin receptors (sst), through somatostatin-radiolabeled analogs, are used, mainly in second line, in the diagnosis and treatment of pheochromocytomas (PCC) and paragangliomas (PGL), the clinical significance of dopamine receptor subtype 2 (D 2 ) in PCC/PGL is unknown. Indeed, radiolabeled dopamine (DA) analogs such as fluorine 18 ( 18 F)-DA, used for positron emission tomography in PCC localization, are mainly correlated to the presence of noradrenaline transporter (NAT) and vesicular monoamine transporters (VMAT) but not to D 2 . The aim of this study was to quantitate D 2 and sst expression in 52 PCC/PGL and to compare it with that of 35 gastroenteropancreatic neuroendocrine tumors (GEP-NETs). Quantitative RT-PCR of sst 1-3 and sst 5 , D 2 , NAT, VMAT1/2 was performed in all tumors, while immunohistochemistry analysis of sst 2 and D 2 was performed in seven tumors. D 2 mRNA was expressed in all PCC/PGL. Mean expression was significantly higher in PCC/PGL than in GEP-NETs (4.8 vs 0.5 copy/copy b-glucuronidase (Gus)). sst 2 and sst 1 were expressed in most PCC/PGL, with sst 2 -dominant expression (mean mRNA: 1.6 vs 0.4 copy/copy b-Gus). sst 2 expression level was similar to that of GEP-NETs, whereas sst 5 expression level was significantly lower (0.12 vs 0.78 copy/copy b-Gus). Our study evidenced strong D 2 mRNA expression in PCC and for the first time in PGL. PCC/PGL express sst 2 mRNA at levels similar to those of GEP-NETs. New drugs can target ssts and D 2 more efficiently than current somatostatin analogs. Moreover, transporters like NAT and VMAT1/2, could be co-targeted with sst, as a basis of new radionuclide compounds in the imaging and treatment of these tumors.