Kadiyala Vivek, Lee Linda S
Vivek Kadiyala, Linda S Lee, Division of Gastroenterology, Hepatology and Endoscopy, Brigham and Women's Hospital, Boston, MA 02115, United States.
World J Gastrointest Endosc. 2015 Mar 16;7(3):213-23. doi: 10.4253/wjge.v7.i3.213.
Rapid advances in radiologic technology and increased cross-sectional imaging have led to a sharp rise in incidental discoveries of pancreatic cystic lesions. These cystic lesions include non-neoplastic cysts with no risk of malignancy, neoplastic non-mucinous serous cystadenomas with little or no risk of malignancy, as well as neoplastic mucinous cysts and solid pseudopapillary neoplasms both with varying risk of malignancy. Accurate diagnosis is imperative as management is guided by symptoms and risk of malignancy. Endoscopic ultrasound (EUS) allows high resolution evaluation of cyst morphology and precise guidance for fine needle aspiration (FNA) of cyst fluid for cytological, chemical and molecular analysis. Initially, clinical evaluation and radiologic imaging, preferably with magnetic resonance imaging of the pancreas and magnetic resonance cholangiopancreatography, are performed. In asymptomatic patients where diagnosis is unclear and malignant risk is indeterminate, EUS-FNA should be used to confirm the presence or absence of high-risk features, differentiate mucinous from non-mucinous lesions, and diagnose malignancy. After analyzing the cyst fluid for viscosity, cyst fluid carcinoembryonic antigen, amylase, and cyst wall cytology should be obtained. DNA analysis may add useful information in diagnosing mucinous cysts when the previous studies are indeterminate. New molecular biomarkers are being investigated to improve diagnostic capabilities and management decisions in these challenging cystic lesions. Current guidelines recommend surgical pancreatic resection as the standard of care for symptomatic cysts and those with high-risk features associated with malignancy. EUS-guided cyst ablation is a promising minimally invasive, relatively low-risk alternative to both surgery and surveillance.
放射技术的飞速发展和横断面成像的增加,导致胰腺囊性病变的偶然发现急剧上升。这些囊性病变包括无恶性风险的非肿瘤性囊肿、恶性风险很小或无恶性风险的肿瘤性非黏液性浆液性囊腺瘤,以及恶性风险各异的肿瘤性黏液性囊肿和实性假乳头状肿瘤。由于治疗方案由症状和恶性风险决定,因此准确诊断至关重要。内镜超声(EUS)能够对囊肿形态进行高分辨率评估,并为囊肿液细针穿刺抽吸(FNA)提供精确引导,以便进行细胞学、化学和分子分析。首先,应进行临床评估和放射影像学检查,最好是胰腺磁共振成像和磁共振胰胆管造影。对于诊断不明确且恶性风险不确定的无症状患者,应使用EUS-FNA来确认高危特征的有无,区分黏液性和非黏液性病变,并诊断恶性肿瘤。在分析囊肿液的黏稠度后,应获取囊肿液癌胚抗原、淀粉酶和囊肿壁细胞学检查结果。当先前的研究结果不确定时,DNA分析可能会为诊断黏液性囊肿提供有用信息。目前正在研究新的分子生物标志物,以提高对这些具有挑战性的囊性病变的诊断能力和治疗决策水平。当前指南推荐手术切除胰腺作为有症状囊肿以及那些具有与恶性肿瘤相关的高危特征的囊肿的标准治疗方法。EUS引导下的囊肿消融是一种有前景的微创、相对低风险的替代手术和监测的方法。