胰腺神经内分泌肿瘤伴导管内生长和静脉浸润的影像学特征:1例报告并文献复习。

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Journal of the Korean Society of Radiology Pub Date : 2025-05-01 Epub Date: 2025-02-25 DOI:10.3348/jksr.2024.0064
Yoon Kyung Jung, Hyun Jeong Park, Hye Won Hwang, Eun Sun Lee, Rae Rim Ryu
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引用次数: 0

摘要

胰腺神经内分泌肿瘤(PanNETs)是一种罕见的胰腺肿瘤。导管内生长的PanNETs被认为是极其罕见的,据报道,NETs的导管累及与侵略性临床行为相关。一位67岁男性因胰脏肿瘤转介至本院作进一步评估。超声、增强CT、MRI和超声内镜(EUS)等多种影像学检查均显示患者头部和身体有一个明确的胰腺肿块,主要位于主胰管内,并延伸至门静脉主干。eus引导下活检的组织学诊断显示3级高分化NET。病人被安排进行手术;然而,在18f -氟脱氧葡萄糖PET/CT上发现了多个额外的骨转移灶。虽然导管内生长和门静脉侵犯在PanNETs中并不常见,但在这种情况下,积极的检查和治疗是必不可少的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Imaging Features in Pancreatic Neuroendocrine Tumor with Intraductal Growth and Venous Invasion: A Case Report and Literature Review.

Pancreatic neuroendocrine tumors (PanNETs) are a rare type of pancreatic neoplasm. PanNETs with intraductal growth are considered extremely rare, and ductal involvement in NETs has been reported to correlate with aggressive clinical behavior. A 67-year-old male was referred to our hospital for further evaluation of a pancreatic tumor. Various imaging modalities, including ultrasonography, contrast-enhanced CT, MRI, and endoscopic ultrasonography (EUS), demonstrated a well-defined pancreatic mass in the head and body, primarily located within the main pancreatic duct with extension to the main portal vein. Histological diagnosis from an EUS-guided biopsy revealed a grade 3 well-differentiated NET. The patient was scheduled for surgery; however, multiple additional bone metastases were identified on 18F-fluorodeoxyglucose PET/CT. Although the presence of intraductal growth and portal vein invasion is uncommon in PanNETs, aggressive workup and treatment are essential in such cases.

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