Saito Yoshito, Ishida Masanori, Sukeda Aoi, Mukai Shuntaro, Wakabayashi Yukari, Arizono Elly, Utsumi Yoshitaka, Nagakawa Yuichi, Itoi Takao, Nagao Toshitaka, Saito Kazuhiro
Radiology, Tokyo Medical University Hospital, Tokyo, JPN.
Pathology, Tokyo Medical University Hospital, Tokyo, JPN.
Cureus. 2024 Nov 26;16(11):e74486. doi: 10.7759/cureus.74486. eCollection 2024 Nov.
Neuroendocrine tumors (NETs) of the biliary tract are extremely rare due to a paucity of Kulchitsky cells. While their preoperative diagnosis remains challenging due to the lack of specific diagnostic markers and imaging findings, there have been no detailed reports describing the diagnostic utility of various imaging modalities for bile duct NETs at the junction of the cystic and common hepatic ducts. We report a case of a woman in her 40s who presented with jaundice and elevated hepatobiliary enzymes. Imaging studies identified a 17 mm × 15 mm × 13 mm nodule at the junction of the cystic and common hepatic ducts. Contrast-enhanced computed tomography (CT) demonstrated a well-enhanced nodule from the early phase, while magnetic resonance imaging showed slightly high intensity on T2-weighted images and strong diffusion restriction. Fluorine-18-fluorodeoxyglucose (18F-FDG) positron emission tomography/CT revealed mild 18F-FDG uptake with a maximum standardized uptake value of 3.5. Endoscopic retrograde cholangiopancreatography (ERCP) suggested extramural compression by a submucosal tumor, and endoscopic ultrasonography (EUS) and intraductal ultrasound (IDUS) revealed a well-circumscribed, homogeneous, hypoechoic submucosal nodule. This comprehensive multimodal approach allowed for the inclusion of NET in the preoperative differential diagnosis. The patient underwent cholecystectomy and extrahepatic bile duct resection, and histopathological examination confirmed a World Health Organization grade 1 NET at the junction of the cystic and common hepatic ducts. The patient remains recurrence-free after two years of follow-up. This is the first detailed report demonstrating the potential utility of a multimodal approach, including ERCP, EUS, and IDUS, in the preoperative diagnosis of biliary tract NET at this specific anatomical location, particularly in identifying the characteristic features of a submucosal tumor.
由于库氏细胞数量稀少,胆道神经内分泌肿瘤(NETs)极为罕见。尽管由于缺乏特异性诊断标志物和影像学表现,其术前诊断仍具有挑战性,但尚无详细报告描述各种影像学检查方法对胆囊管与肝总管交界处胆管NETs的诊断效用。我们报告一例40多岁女性患者,表现为黄疸和肝胆酶升高。影像学检查在胆囊管与肝总管交界处发现一个17 mm×15 mm×13 mm的结节。对比增强计算机断层扫描(CT)显示该结节在早期强化良好,而磁共振成像在T2加权图像上显示为略高信号强度且有强烈的扩散受限。氟-18-氟脱氧葡萄糖(18F-FDG)正电子发射断层扫描/CT显示18F-FDG摄取轻度增高,最大标准化摄取值为3.5。内镜逆行胰胆管造影(ERCP)提示为黏膜下肿瘤引起的壁外压迫,内镜超声检查(EUS)和导管内超声检查(IDUS)显示为边界清晰、均匀、低回声的黏膜下结节。这种综合多模态方法有助于在术前鉴别诊断中考虑NETs。患者接受了胆囊切除术和肝外胆管切除术,组织病理学检查证实胆囊管与肝总管交界处为世界卫生组织1级NETs。患者随访两年无复发。这是第一份详细报告,展示了包括ERCP、EUS和IDUS在内的多模态方法在该特定解剖部位胆道NETs术前诊断中的潜在效用,特别是在识别黏膜下肿瘤的特征方面。