Lévy Philippe, Rebours Vinciane
Department of Gastroenterology and Pancreatology, Pôle des Maladies de l'Appareil Digestif, DHU Unity, Hôpital Beaujon, Faculté Denis Diderot, AP-HP, Clichy, France.
Centre de référence des maladies rares du pancréas (PAncreatic RAre DISeases), Hôpital Beaujon, Clichy, France.
Visc Med. 2018 Jul;34(3):192-196. doi: 10.1159/000489242. Epub 2018 Jun 8.
A precise diagnosis of the nature of pancreatic cystic neoplasm (PCN) is crucial since it determines the patients in need of rapid surgical resection as well as those who can be followed up, and, accordingly, the frequency and modalities of surveillance. Endoscopic ultrasound (EUS) and especially fine needle aspiration (FNA) are invasive methods, with specific adverse events occurring in 2.7-5%. Thus, they should only be used as a third-line tool in the absence of characteristic radiographic features on computed tomography (CT) scan and magnetic resonance imaging (MRI). The most difficult aspects of differential diagnosis are: intraductal papillary mucinous neoplasm (IPMN) versus chronic pancreatitis; unifocal IPMN versus serous cystic neoplasm (SCN); macrocystic SCN versus mucinous cystic neoplasm (MCN); cystic neuroendocrine tumors versus MCN; solid serous cystadenoma versus neuroendocrine tumors versus small solid pseudopapillary tumors; pseudocyst versus MCN; low-grade, high-grade, or invasive IPMN. When classical radiological and EUS features are not conclusive, EUS-FNA may be helpful by analyzing cytological, chemical, and/or molecular data. The addition of EUS-FNA to CT scan and MRI increased the overall accuracy for diagnosing PCN by 36 and 54%, respectively. Analysis of molecular markers in pancreatic cyst fluid might increase the limited accuracy of EUS-FNA by using cytology and chemical and/or tumor marker analysis alone. Current evidence suggests that contrast-enhanced EUS (CH-EUS) is highly accurate for distinguishing non-neoplastic cysts from neoplastic cysts. CH-EUS might also be useful for distinguishing mural epithelial nodules from mucinous clots. Needle-based confocal laser endomicroscopy (nCLE) images a target tissue at a subcellular level of resolution, providing real-time in-vivo optical biopsy. nCLE is feasible during EUS-FNA and allows in-vivo diagnosis of PCN with high accuracy. In conclusion, EUS is a third-line tool in the diagnosis of PCN. Clinical context as well as careful evaluation of CT scan and magnetic resonance cholangiopancreatography images by specialized radiologists are crucial in the diagnosis process. Nowadays it is inconceivable to skip these steps.
准确诊断胰腺囊性肿瘤(PCN)的性质至关重要,因为这决定了哪些患者需要快速手术切除,哪些患者可以进行随访,进而决定了监测的频率和方式。内镜超声(EUS),尤其是细针穿刺抽吸(FNA)是侵入性方法,特定不良事件的发生率为2.7%-5%。因此,只有在计算机断层扫描(CT)和磁共振成像(MRI)上没有特征性影像学表现时,才应将它们用作三线工具。鉴别诊断最困难的方面包括:导管内乳头状黏液性肿瘤(IPMN)与慢性胰腺炎;单灶性IPMN与浆液性囊性肿瘤(SCN);大囊型SCN与黏液性囊性肿瘤(MCN);囊性神经内分泌肿瘤与MCN;实性浆液性囊腺瘤与神经内分泌肿瘤与小实性假乳头状肿瘤;假性囊肿与MCN;低级别、高级别或浸润性IPMN。当经典的放射学和EUS特征不明确时,EUS-FNA通过分析细胞学、化学和/或分子数据可能会有所帮助。在CT扫描和MRI中加入EUS-FNA分别将诊断PCN的总体准确率提高了36%和54%。单独使用细胞学、化学和/或肿瘤标志物分析时,胰腺囊液中分子标志物的分析可能会提高EUS-FNA有限的准确率。目前的证据表明,对比增强EUS(CH-EUS)在区分非肿瘤性囊肿和肿瘤性囊肿方面具有很高的准确性。CH-EUS也可能有助于区分壁上皮结节和黏液凝块。基于针的共聚焦激光内镜显微镜(nCLE)在亚细胞分辨率水平对目标组织进行成像,提供实时体内光学活检。nCLE在EUS-FNA期间是可行的,并且能够以高准确率对PCN进行体内诊断。总之,EUS是诊断PCN的三线工具。临床背景以及专业放射科医生对CT扫描和磁共振胰胆管造影图像的仔细评估在诊断过程中至关重要。如今跳过这些步骤是不可想象的。