Goldin Robert David, Roa Juan Carlos
Department of Histopathology, Imperial College Faculty of Medicine at St Mary's, London, UK.
Histopathology. 2009 Aug;55(2):218-29. doi: 10.1111/j.1365-2559.2008.03192.x. Epub 2009 Mar 12.
Gallbladder cancer (GBC) shows a marked geographical variation in its incidence, with the highest figures being seen in India and Chile and relatively low levels in many Western countries. Risk factors for its development include the presence of gallstones, infection and the presence of an anomalous pancreatobiliary ductal junction. It can arise from either a pathway involving metaplasia or dysplasia or one in which there is a pre-existing adenoma. The former is the more common and, because it is often not associated with a macroscopically recognizable lesion, leads to the recommendation that all gallbladders need to be examined microscopically. Accurate staging of invasive cancers is essential to determine prognosis and treatment, and this requires extensive tumour sampling. A number of genetic alterations have been identified in the preinvasive and invasive stages of GBC and they support the morphological evidence of there being two pathways by which tumours develop. Some of these genetic changes are associated with particular risk factors. For example, cases with anomalous pancreatobiliary ductal junction show a higher frequency of K-ras mutations. Some changes are associated with differences in prognosis. For example, cancers without expression of p21 but with expression for p27 have a better prognosis, whereas those that express c-erb-B2 have a worse one. Work has also been done on identifying clinical, imaging and other factors that indicate that patients have a higher risk of having GBC. This is particularly important in high-incidence areas in which GBC is a significant public health problem.
胆囊癌(GBC)的发病率在地域上存在显著差异,印度和智利的发病率最高,而在许多西方国家相对较低。其发病的危险因素包括胆结石的存在、感染以及胰胆管异常汇合。它可以起源于化生或发育异常途径,也可以起源于先前存在腺瘤的途径。前者更为常见,并且由于它通常与肉眼可识别的病变无关,因此建议对所有胆囊进行显微镜检查。侵袭性癌症的准确分期对于确定预后和治疗至关重要,这需要广泛的肿瘤取样。在GBC的浸润前期和浸润期已经发现了一些基因改变,它们支持肿瘤发展存在两种途径的形态学证据。其中一些基因变化与特定的危险因素有关。例如,胰胆管异常汇合的病例K-ras突变频率较高。一些变化与预后差异有关。例如,不表达p21但表达p27的癌症预后较好,而表达c-erb-B2 的癌症预后较差。在识别表明患者患GBC风险较高的临床、影像学和其他因素方面也开展了相关工作。这在GBC是重大公共卫生问题的高发病率地区尤为重要。