Polydorides Alexandros D, Mukherjee Bhramar, Gruber Stephen B, McKenna Barbara J, Appelman Henry D, Greenson Joel K
Department of Pathology, University of Michigan Health System, Ann Arbor, MI 48109-0054, USA.
Am J Surg Pathol. 2008 Nov;32(11):1661-6. doi: 10.1097/PAS.0b013e31816ffa80.
Patients with hereditary nonpolyposis colorectal cancer syndrome (HNPCC) develop microsatellite-unstable colorectal cancers that tend to be more proximally located and are histologically more likely to show high numbers of tumor-infiltrating lymphocytes, a lack of dirty necrosis, mucinous or poor differentiation, and a Crohn-like host immune response, when compared with microsatellite-stable cancers. However, histologic features that are characteristic of and can perhaps distinguish colorectal adenomas in HNPCC patients from those occurring in the general population have not been previously reported. We compared 16 adenomas endoscopically removed from patients with genetically proven HNPCC to 32 control adenomas, group-matched for patient age and sex, along with endoscopic size, shape, anatomic location, and presence of high-grade dysplasia. Adenomas from HNPCC patients were more likely to contain high numbers of adenoma-infiltrating lymphocytes (AILs) with 12 of 16 (75%) adenomas having >or=5 AILs per high-power field (HPF) as opposed to 4 of 32 (12%) adenomas in the control group (P=0.00003). HNPCC adenomas were also less likely to contain increased numbers of apoptotic bodies: 7 of 16 (44%) contained >or=5 apoptoses per HPF, compared with 27 of 36 (84%) control adenomas (P=0.006). The presence of necrosis or serrated architecture, percent villous component, and numbers of mitotic figures per HPF did not differ significantly between the 2 groups. Therefore, increased numbers of AILs and decreased numbers of apoptoses in colorectal adenomas are simple and inexpensive markers that raise the possibility of HNPCC.
遗传性非息肉病性结直肠癌综合征(HNPCC)患者会发生微卫星不稳定的结直肠癌,与微卫星稳定的癌症相比,这些癌症往往更靠近近端,并且在组织学上更有可能表现出大量肿瘤浸润淋巴细胞、无脏坏死、黏液性或低分化以及克罗恩样宿主免疫反应。然而,此前尚未报道过HNPCC患者结直肠腺瘤所特有的、或许能将其与普通人群中发生的腺瘤区分开来的组织学特征。我们将16例经基因检测证实为HNPCC患者内镜切除的腺瘤与32例对照腺瘤进行了比较,对照腺瘤在患者年龄、性别、内镜下大小、形状、解剖位置以及高级别异型增生的存在情况方面进行了组间匹配。HNPCC患者的腺瘤更有可能含有大量腺瘤浸润淋巴细胞(AILs),16例腺瘤中有12例(75%)每高倍视野(HPF)有≥5个AILs,而对照组32例腺瘤中只有4例(12%)如此(P=0.00003)。HNPCC腺瘤也不太可能含有增多的凋亡小体:16例中有7例(44%)每HPF有≥5个凋亡,而对照腺瘤36例中有27例(84%)如此(P=0.006)。两组之间坏死或锯齿状结构的存在、绒毛成分百分比以及每HPF有丝分裂象数量没有显著差异。因此,结直肠腺瘤中AILs数量增多和凋亡小体数量减少是简单且廉价的标志物,提示可能存在HNPCC。