First Department of Internal Medicine, Gifu University Hospital, 1-1 Yanagido, Gifu, 502-0061, Japan.
J Med Ultrason (2001). 2024 Apr;51(2):219-226. doi: 10.1007/s10396-023-01389-6. Epub 2023 Dec 5.
Advancements in diagnostic radiology have amplified the incorporation of these techniques into routine clinical practice. Concurrently, the frequency of incidentally identifying pancreatic cystic lesions (PCLs) has surged. PCLs encompass diverse categories contingent upon their origin. Among them, branch duct-intraductal papillary mucinous neoplasms (BD-IPMN) and mucinous cystic neoplasms (MCN) are categorized as mucinous cystic lesions that have malignant potential. Even solid neoplasms occasionally show cystic degeneration. Therefore, precise differential PCL diagnosis is crucial to optimize clinical management strategies and detect malignant transformations. Endoscopic ultrasound (EUS) affords comprehensive visualization of the pancreas with high-resolution ultrasound, complemented by fine-needle aspiration (FNA) under real-time EUS guidance, which is a minimally invasive procedure for obtaining pathological samples. This synergy has established EUS and EUS-FNA as vital procedures in the management of PCLs, enabling differentiation of PCLs. Cyst fluid analysis has played a pivotal role in deciding the optimal management strategy. The efficacy of cytological analysis is limited by scant cytologic material. The "string sign" test evaluates fluid viscosity, and its simplicity warrants initial consideration. Amylase and tumor markers, such as CEA, have been studied, but they yield varied sensitivity and specificity. Glucose and genetic mutations (KRAS, GNAS) exhibit promise, while comprehensive genomic profiling underscores genetic insights. Through-the-needle biopsy and needle-based confocal laser endomicroscopy also show high diagnostic yield. EUS-FNA, however, entails risks like infection and needle tract seeding, emphasizing the need for proper utilization. Pancreatic cyst fluid analysis augments diagnostic accuracy and informs clinical decisions, making it a valuable adjunct to imaging.
诊断放射学的进步推动了这些技术在常规临床实践中的应用。与此同时,偶然发现胰腺囊性病变(PCL)的频率也急剧上升。PCL 依据其起源可分为不同类别。其中,分支胰管内乳头状黏液性肿瘤(BD-IPMN)和黏液性囊腺瘤(MCN)被归类为具有恶性潜能的黏液性囊性病变。即使是实性肿瘤偶尔也会出现囊性变性。因此,准确鉴别 PCL 对于优化临床管理策略和检测恶性转化至关重要。
内镜超声(EUS)通过实时 EUS 引导下的细针抽吸(FNA)提供胰腺的高分辨率超声综合可视化,这是一种微创获取病理样本的方法。这种协同作用使 EUS 和 EUS-FNA 成为 PCL 管理的重要程序,能够区分 PCL。囊液分析在决定最佳管理策略方面发挥了关键作用。细胞学分析的效果受到细胞数量稀少的限制。“字符串征”试验评估液体粘度,其简单性值得初步考虑。淀粉酶和肿瘤标志物,如 CEA,已被研究,但它们的敏感性和特异性差异较大。葡萄糖和基因突变(KRAS、GNAS)显示出前景,而全面的基因组分析突显了遗传见解。经皮穿刺活检和基于针的共聚焦激光内窥镜检查也具有较高的诊断率。然而,EUS-FNA 存在感染和针道种植的风险,强调了正确使用的必要性。
胰腺囊性液分析提高了诊断准确性并为临床决策提供信息,是影像学的有力辅助手段。
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