Montravers Françoise, Arnoux Jean-Baptiste, Ribeiro Maria-Joao, Kerrou Khaldoun, Nataf Valérie, Galmiche Louise, Aigrain Yves, Bellanné-Chantelot Christine, Saint-Martin Cécile, Ohnona Jessica, Balogova Sona, Huchet Virginie, Michaud Laure, Talbot Jean-Noël, de Lonlay Pascale
a Service de médecine nucléaire, Hôpital Tenon, AP-HP and Université Pierre et Marie Curie-Paris 6, Paris, France.
b Centre de référence des maladies héréditaires du métabolisme de l'enfant, et l'adulte, AP-HP Hôpital Necker-Enfants Malades, Université Paris Descartes, Paris, France.
Expert Rev Endocrinol Metab. 2014 Sep;9(5):477-485. doi: 10.1586/17446651.2014.949240. Epub 2014 Aug 13.
fluorine-fluorodihydroxyphenylalanine (FDOPA) PET/CT is currently the first-line imaging technique to distinguish between focal and diffuse forms of congenital hyperinsulinism (CHI) and to accurately localize focal forms. However, this technique has a number of limitations, mainly the very small size of focal forms or inversely a very large focal form mimicking a diffuse form, and misinterpretation of physiologic uptake masking hot spots or inversely mimicking focal forms. The other limitation is the limited availability of the radiopharmaceutical. FDOPA PET/CT has no recognized competitor to date among the available morphologic and functional imaging techniques. Other potential approaches using specific tracers for positron emission tomography (PET) are discussed, using radiopharmaceuticals specific for β cell mass or targeting somatostatin receptors. These radiopharmaceuticals can be labeled with gallium-68, a PET emitter readily available in PET centers equipped with 68Ge/68Ga generators.
氟代二羟基苯丙氨酸(FDOPA)正电子发射断层扫描/计算机断层扫描(PET/CT)目前是区分先天性高胰岛素血症(CHI)局灶性和弥漫性形式并准确定位局灶性形式的一线成像技术。然而,该技术存在一些局限性,主要是局灶性形式非常小,或者相反,非常大的局灶性形式类似于弥漫性形式,以及对生理性摄取的错误解读掩盖了热点或相反地模拟了局灶性形式。另一个局限性是放射性药物的供应有限。迄今为止,在现有的形态学和功能成像技术中,FDOPA PET/CT没有公认的竞争对手。还讨论了使用针对正电子发射断层扫描(PET)的特定示踪剂的其他潜在方法,这些示踪剂是针对β细胞量的放射性药物或靶向生长抑素受体的药物。这些放射性药物可以用镓-68标记,镓-68是一种正电子发射体,在配备68Ge/68Ga发生器的PET中心很容易获得。