Cleveland Clinic, Cleveland, OH, USA.
Int J Surg Pathol. 2021 Jun;29(4):443-446. doi: 10.1177/1066896920949675. Epub 2020 Aug 12.
Inflammatory pseudotumor-like follicular/fibroblastic dendritic cell sarcoma (IPT-like FFDCS) is a rare, indolent neoplasm that occurs in the spleen or liver and harbors Epstein-Barr virus (EBV) integrated into the host genome. The molecular genetic characteristics of IPT-like FFDCS have not been well studied and there are no established and actionable molecular features to guide treatment decisions or diagnosis beyond the recognition of viral genome integration. We subjected two cases of IPT-like FFDCS to a comprehensive next-generation sequencing analysis. Several variants of uncertain clinical significance were detected in both tumors. No variants of potential or strong clinical significance were detected within the targeted regions of the evaluated genes. Additionally, no fusion events were detected involving the genes in either tumor. The performed molecular analysis identified no genetic aberrations in IPT-like FFDCS and its genomic landscape remains, with the exception of a monoclonal EBV gene, largely undefined.
炎性假瘤样滤泡/纤维母细胞树突状细胞肉瘤(IPT 样 FFDCS)是一种罕见的、惰性的肿瘤,发生在脾脏或肝脏,携带整合到宿主基因组中的 Epstein-Barr 病毒(EBV)。IPT 样 FFDCS 的分子遗传学特征尚未得到很好的研究,除了识别病毒基因组整合之外,没有确定的、可操作的分子特征来指导治疗决策或诊断。我们对两例 IPT 样 FFDCS 进行了全面的下一代测序分析。在两个肿瘤中均检测到了几个具有不确定临床意义的变体。在评估基因的靶向区域内,没有检测到潜在或强烈临床意义的变体。此外,在这两个肿瘤中均未检测到涉及基因的融合事件。进行的分子分析未在 IPT 样 FFDCS 中发现遗传异常,其基因组图谱仍然存在,除了一个单克隆 EBV 基因外,基本尚未确定。