Kim Haeryoung, Jang Kee-Taek
Department of Pathology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
Department of Pathology and Translational Genomics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
J Pathol Transl Med. 2020 Sep;54(5):367-377. doi: 10.4132/jptm.2020.07.21. Epub 2020 Aug 31.
Pathologic interpretation of endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) cytology/biopsy specimens is one of the most challenging tasks in cytology and surgical pathology practice, as the procedure often yields minimal amounts of diagnostic material and contains contaminants, such as blood cells and normal intestinal mucosa. EUS-FNA cytology/biopsy will nevertheless become a more popular procedure for evaluation of various pancreatic lesions because they are difficult to approach with conventional endoscopic procedures. Pathologists should understand the structural differences and limitations of EUS-FNA that make pathologic diagnosis difficult. Ancillary tests are available for differential diagnosis of EUS-FNA for various pancreatic lesions. Immunostains are the most commonly used ancillary tests, and pathologists should able to choose the necessary panel for differential diagnosis. Pathologists should review clinical history and radiologic and/or EUS findings before selecting an immunostain panel and making a pathologic diagnosis. In addition, one's threshold of malignancy should be adjusted according to the appropriate clinical setting to avoid under-evaluation of pathologic diagnoses. Clinico-pathologic correlation is essential in pathologic evaluation of EUS-FNA for pancreatic lesions. Pathologists can reduce errors by correlating clinical and radiologic findings when evaluating EUS-FNA. Some molecular tests can be applied in differential diagnosis of pancreatic neoplastic and cystic lesions. Molecular data should be used as supportive evidence of a specific disease entity, rather than direct evidence, and should be correlated with clinico-pathologic findings to avoid errors in pathologic diagnosis.
内镜超声引导下细针穿刺抽吸术(EUS-FNA)细胞学/活检标本的病理诊断是细胞学和外科病理学实践中最具挑战性的任务之一,因为该操作通常只能获取少量的诊断材料,且含有血细胞和正常肠黏膜等污染物。然而,由于传统内镜检查难以对各种胰腺病变进行评估,EUS-FNA细胞学/活检将成为一种更常用的评估方法。病理学家应了解EUS-FNA的结构差异和局限性,这些因素使得病理诊断变得困难。辅助检查可用于各种胰腺病变的EUS-FNA鉴别诊断。免疫组化是最常用的辅助检查,病理学家应能够选择必要的免疫组化组合进行鉴别诊断。在选择免疫组化组合并做出病理诊断之前,病理学家应回顾临床病史以及放射学和/或EUS检查结果。此外,应根据适当的临床情况调整恶性肿瘤的诊断阈值,以避免对病理诊断评估不足。临床病理相关性在胰腺病变EUS-FNA的病理评估中至关重要。在评估EUS-FNA时,病理学家通过将临床和放射学检查结果相互关联,可以减少错误。一些分子检测可用于胰腺肿瘤性和囊性病变的鉴别诊断。分子数据应作为特定疾病实体的支持证据,而非直接证据,并且应与临床病理结果相关联,以避免病理诊断错误。