Clinical Laboratory Services, University Hospitals Birmingham NHS Foundation Trust, Queen Elizabeth Hospital Birmingham, Birmingham, UK.
Ann Clin Biochem. 2014 Mar;51(Pt 2):151-66. doi: 10.1177/0004563213503819. Epub 2013 Oct 4.
Diagnosis and management of pancreatic cyst lesions is challenging as there is currently no investigation that offers both high diagnostic sensitivity and high specificity for the identification of potentially malignant lesions. Accurate classification of these lesions is vital in order to avoid unnecessary treatment of benign lesions and missed opportunities for early treatment of lesions that are malignant/pre-malignant. Pancreatic cyst fluid analysis has an important role in diagnosis, although all currently available investigations based on fluid analysis have significant limitations. Cytological analysis can reveal features that are specific for a certain class of cyst, but offers limited sensitivity in detecting malignant/pre-malignant cysts. Measurement of tumour markers, particularly carcinoembryonic antigen can also be informative. Concentrations of cyst fluid carcinoembryonic antigen tend to be higher in malignant/pre-malignant cysts, although there is a wide overlap between the various classes of cyst. A number of studies have suggested that diagnostic carcinoembryonic antigen cut-offs can be chosen that provide a high degree of specificity but limited sensitivity. Studies of the analytical validity of tumour marker assays in pancreatic cyst fluid analysis have highlighted discrepancies in some fluid specimens, which require further investigation. DNA analysis also has a role. In particular, K-Ras-2 mutational analysis appears to provide high specificity for detection of malignant/pre-malignant lesions. A number of diagnostic algorithms have been published, integrating use of available investigations in order to achieve the optimum discrimination of benign and potentially malignant cysts. Research into new biochemical markers and optimal use of available pancreatic cyst fluid analyses is ongoing.
胰腺囊性病损的诊断和处理极具挑战性,因为目前尚无一种检查手段能同时具备高诊断灵敏度和高特异性,以识别出可能恶性的病损。准确分类这些病损至关重要,可避免对良性病损进行不必要的治疗,以及错失对恶性/癌前性病损进行早期治疗的机会。胰腺囊液分析在诊断中具有重要作用,尽管目前所有基于囊液分析的检查都存在明显的局限性。细胞学分析可以揭示出某些特定类型囊液的特征,但在检测恶性/癌前性囊液方面灵敏度有限。肿瘤标志物的测量,特别是癌胚抗原,也具有一定的提示作用。癌胚抗原在恶性/癌前性囊液中的浓度往往较高,但各种类型的囊液之间存在广泛的重叠。多项研究表明,选择诊断用癌胚抗原截断值可以提供高度的特异性,但灵敏度有限。对胰腺囊液分析中肿瘤标志物检测的分析性能的研究突出了一些液体标本之间存在的差异,需要进一步研究。DNA 分析也具有一定作用。特别是 K-Ras-2 突变分析似乎对检测恶性/癌前性病变具有高度特异性。已发表了一些诊断算法,整合了各种现有检查手段,以最佳地区分良性和可能恶性的囊液。目前正在对新的生化标志物和最佳利用现有的胰腺囊液分析进行研究。