Department of Diabetes, Endocrinology and Nutrition, Kyoto University Graduate School of Medicine, Kyoto 606-8507, Japan.
Department of Metabolism and Endocrinology, Kishiwada City Hospital, Kishiwada 596-8501, Japan.
Endocr J. 2024 Sep 2;71(9):925-933. doi: 10.1507/endocrj.EJ24-0187. Epub 2024 Jun 5.
Insulinomas are the most common functional pancreatic neuroendocrine neoplasm; when treatment is delayed, they induce hyperinsulinemic hypoglycemia, which is life-threatening. As surgical resection is the only curative treatment for insulinoma, preoperative localization is crucial; however, localization based on conventional imaging modalities such as computed tomography (CT) and magnetic resonance imaging is often inconclusive. Somatostatin receptor-targeted imaging is another option for detecting pancreatic neuroendocrine neoplasms but has low sensitivity and is not specific for insulinoma. The clinical application of other localizing approaches such as selective arterial calcium stimulation and endoscopic ultrasonography-guided fine needle aspiration (EUS-FNA) is limited by their being invasive and/or technically complex. Moreover, an EUS-FNA specimen of an insulinoma may be negative on insulin immunostaining. Thus, a noninvasive and clinically practical insulinoma-specific diagnostic tool to discriminate insulinomas with high accuracy is anticipated. Glucagon-like peptide-1 receptor (GLP-1R)-targeted imaging has emerged in the effort to fulfill this need. We recently developed the novel fluorine-18-labeled exendin-4-based probe conjugated with polyethylene glycol, [F]FB(ePEG12)12-exendin-4 (F-exendin-4) for positron emission tomography (PET) imaging and reported its clinical benefit in a case of insulinoma in the pancreatic tail. We report here a case of insulinoma in the pancreatic head in which an EUS-FNA specimen was negative on insulin immunostaining while precise preoperative localization and conclusive evidence for curative enucleation was provided by F-exendin-4 PET/CT (Japan Registry of Clinical Trials; jRCTs051200156).
胰岛素瘤是最常见的功能性胰腺神经内分泌肿瘤;若治疗延误,可导致危及生命的胰岛素诱导低血糖症。由于手术切除是胰岛素瘤的唯一治愈性治疗方法,因此术前定位至关重要;然而,基于计算机断层扫描(CT)和磁共振成像等常规成像方式的定位往往不明确。生长抑素受体靶向成像也是检测胰腺神经内分泌肿瘤的另一种选择,但敏感性低,且对胰岛素瘤特异性不强。其他定位方法,如选择性动脉钙刺激和内镜超声引导下细针抽吸(EUS-FNA)的临床应用受到其侵袭性和/或技术复杂性的限制。此外,胰岛素瘤的 EUS-FNA 标本在胰岛素免疫染色上可能呈阴性。因此,人们期望有一种非侵入性的、临床上实用的、具有高度准确性的胰岛素瘤特异性诊断工具来进行区分。为满足这一需求,胰高血糖素样肽-1 受体(GLP-1R)靶向成像应运而生。我们最近开发了一种新型氟-18 标记的外啡肽-4 基探针,与聚乙二醇偶联,[F]FB(ePEG12)12-外啡肽-4(F-外啡肽-4),用于正电子发射断层扫描(PET)成像,并在胰尾胰岛素瘤的病例中报告了其临床获益。我们在此报告了一个胰头胰岛素瘤的病例,该病例的 EUS-FNA 标本在胰岛素免疫染色上呈阴性,而 F-外啡肽-4 PET/CT 则提供了精确的术前定位和明确的治愈性切除证据(日本临床试验注册;jRCTs051200156)。