Bancu Andrei, Hanks Matthew, Ackroyd Lauren, Venkatachalapathy Suresh, Lobo Dileep N, Zaitoun Abed M
Department of Cellular Pathology, Nottingham University Hospitals NHS Trust, Queen's Medical Centre, Nottingham, UK.
Division of Translational Medical Sciences, School of Medicine, Nottingham Digestive Diseases Centre, University of Nottingham, Queen's Medical Centre, Nottingham, UK.
J Cytol. 2025 Jul-Sep;42(3):151-162. doi: 10.4103/joc.joc_6_25. Epub 2025 Aug 29.
Cytological appearances may be insufficient to establish the diagnosis of pancreatic cystic lesions, especially for premalignant neoplasms. This study aimed to evaluate three commonly used cytological grading systems [C1-C5, Papanicolaou (Pap), and World Health Organization (WHO) classification systems] in assessing pancreatic cystic lesions.
A total of 210 pancreatic cytology specimens were classified based on the aforementioned grading systems, 127 of which had supporting histology reported across 6 years, at a single-tertiary referral center.
We excluded 26 cases because of inadequate cytology. The most common cystic lesions were intraductal papillary mucinous neoplasms (IPMNs, = 71) and pseudocysts ( = 55). Among IPMN, 27 were moderate/high-grade, and 44 were low-grade. There were 12 mucinous cystic neoplasms, 75 benign cysts (pseudocysts, serous cystadenomas, lymphoepithelial cysts, and others), and 15 malignant cases, with 11 cysts being of uncertain etiology. There were 21 high-risk and potentially malignant (WHO grade V) cases in comparison with 42 cases using the C grading (C4 and C5). However, according to Pap grading, 87 had varying risks of malignancy (Category IVB). According to the WHO classification, 63 cases were classified as low-risk pancreaticobiliary neoplasms (WHO grade IV). The remaining cases 85 were benign to very low-risk malignant potential and, therefore, were less likely to be considered for surgical intervention. Diagnostic concordance was higher between cytology and core biopsies in low-grade IPMN.
The WHO system provides better risk stratification for neoplasms, optimizing surgical management. However, the C1-C5 system does not recognize cystic lesions with malignant potential.
细胞学表现可能不足以确诊胰腺囊性病变,尤其是对于癌前肿瘤。本研究旨在评估三种常用的细胞学分级系统[C1 - C5、巴氏(Pap)和世界卫生组织(WHO)分类系统]在评估胰腺囊性病变中的应用。
在一个单一的三级转诊中心,共210份胰腺细胞学标本根据上述分级系统进行分类,其中127份在6年期间有配套的组织学报告。
因细胞学检查不充分,我们排除了26例。最常见的囊性病变是导管内乳头状黏液性肿瘤(IPMNs,n = 71)和假性囊肿(n = 55)。在IPMN中,27例为中/高级别,44例为低级别。有12例黏液性囊性肿瘤、75例良性囊肿(假性囊肿、浆液性囊腺瘤、淋巴上皮囊肿等)和15例恶性病例,11例囊肿病因不明。与C分级(C4和C5)的42例相比,有21例高危和潜在恶性(WHO V级)病例。然而,根据巴氏分级,87例有不同程度的恶性风险(IVB类)。根据WHO分类,63例被归类为低风险胰腺胆管肿瘤(WHO IV级)。其余85例病例为良性至极低风险恶性潜能,因此不太可能考虑手术干预。低级别IPMN的细胞学检查与核心活检之间的诊断一致性更高。
WHO系统为肿瘤提供了更好的风险分层,优化了手术管理。然而,C1 - C5系统未识别出具有恶性潜能的囊性病变。