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18F-FDG PET/CT Imaging of Primary Hepatic Neuroendocrine Tumor

机译:肝原发性神经内分泌肿瘤的18F-FDG PET / CT成像

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摘要

Primary hepatic neuroendocrine tumors (PHNETs) are extremely rare neoplasms. Herein, we report a case of a 70- year-old man with a hepatic mass. The non-contrast computed tomography (CT) image showed a low-density mass, and dynamic CT images indicated the enhancement of the mass in the arterial phase and early washout in the late phase. F-18 fluorodeoxyglucose (18F-FDG) positron emission tomography (PET) and fused PET/CT images showed increased uptake in the hepatic mass. Whole-body 18F-FDG PET images showed no abnormal activity except for the liver lesion. Presence of an extrahepatic tumor was also ruled out by performing upper gastrointestinal endoscopy, total colonoscopy, and chest and abdominal CT. A posterior segmentectomy was performed, and histologic examination confirmed a neuroendocrine tumor (grade 1). The patient was followed up for about 2 years after the resection, and no extrahepatic lesions were radiologically found. Therefore, the patient was diagnosed with PHNET. To the best of our knowledge, no previous case of PHNET have been detected by 18F-FDG PET imaging.
机译:原发性肝神经内分泌肿瘤(PHNETs)是极为罕见的肿瘤。在此,我们报告一例70岁的男子患有肝脏肿块。非对比计算机断层扫描(CT)图像显示低密度肿块,动态CT图像显示动脉期肿块增加,晚期则早期洗脱。 F-18氟脱氧葡萄糖( 18 F-FDG)正电子发射断层扫描(PET)和融合的PET / CT图像显示肝脏团块的摄取增加。全身 18 F-FDG PET图像除肝脏病变外均无异常活动。还可以通过进行上消化道内窥镜检查,全结肠镜检查以及胸部和腹部CT来排除肝外肿瘤的存在。进行了后段切除术,并且组织学检查证实为神经内分泌肿瘤(1级)。切除后对该患者进行了约2年的随访,未在放射学上发现肝外病变。因此,患者被诊断出患有PHNET。据我们所知, 18 F-FDG PET成像未发现任何PHNET病例。

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