Division of Hematology, Oncology and Bone Marrow Transplantation, British Columbia Children's Hospital, Vancouver, British Columbia, Canada.
Brain Pathol. 2012 Sep;22(5):625-35. doi: 10.1111/j.1750-3639.2011.00561.x. Epub 2012 Feb 13.
As "atypical teratoid rhabdoid tumors" (ATRTs) may mimic "small round blue cell tumors" (SRBCT), we reexamined our ATRT experience focusing upon INI-1 immunohistochemistry (IHC). All high-grade pediatric brain tumors occurring from 1986-2006 at our institution underwent INI-1 IHC. Clinicopathologic data from each INI-1 immunonegative case were reviewed. Additional genetic, epigenetic and IHC analyses (including interrogation of INI-1 and CLDN6) were performed on a subset of the INI-1 immunonegative cases. Twelve INI-1 IHC negative tumors were identified retrospectively, of which only two previously carried the diagnosis of ATRT. Overall, the clinicopathologic and genetic data supported the assertion that all 12 cases represented ATRT. Unexpectedly, three long-term survivors (4.2, 7.0 and 8.5 years) were identified. As hypothesized, "teratoid" and "rhabdoid" histologic features were relatively infrequent despite gross total resections in some cases. Methylation specific polymer chain reaction (PCR) (MSP) revealed a uniform methylation pattern across all cases and gene promoters tested (ie, MGMT, HIC1, MLH3 and RASSF1); notably, all cases demonstrated unmethylated MGMT promoters. Our data demonstate that a primitive non-rhabdoid histophenotype is common among ATRTs and highlights the diagnostic importance of INI-1 IHC. Epigenetically, the MGMT promoter is usually unmethylated in ATRT, suggesting that potential temozolomide-based chemotherapy may be of limited efficacy.
由于“非典型畸胎样/横纹肌样肿瘤”(ATRT)可能类似于“小圆细胞蓝色肿瘤”(SRBCT),我们重新检查了我们的 ATRT 经验,重点关注 INI-1 免疫组化(IHC)。本机构自 1986 年至 2006 年发生的所有高级别儿科脑肿瘤均进行了 INI-1 IHC。对每个 INI-1 免疫阴性病例的临床病理数据进行了回顾。对 INI-1 免疫阴性病例的一部分进行了额外的遗传、表观遗传和 IHC 分析(包括 INI-1 和 CLDN6 的检测)。回顾性鉴定出 12 例 INI-1 IHC 阴性肿瘤,其中仅 2 例之前被诊断为 ATRT。总的来说,临床病理和遗传数据支持所有 12 例均为 ATRT 的说法。出人意料的是,发现了 3 例长期存活者(4.2、7.0 和 8.5 年)。正如假设的那样,尽管一些病例进行了大体全切除,但“畸胎样”和“横纹肌样”组织学特征仍然相对少见。甲基化特异性聚合酶链反应(PCR)(MSP)显示所有病例和测试的基因启动子均具有均匀的甲基化模式(即,MGMT、HIC1、MLH3 和 RASSF1);值得注意的是,所有病例均显示未甲基化的 MGMT 启动子。我们的数据表明,ATRTS 中常见原始非横纹肌样表型,并强调了 INI-1 IHC 的诊断重要性。从表观遗传学上讲,MGMT 启动子在 ATRT 中通常未甲基化,这表明潜在的替莫唑胺为基础的化疗可能疗效有限。