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在具有新型NF1-SCIMP融合的恶性外周神经鞘瘤中,USP6荧光原位杂交出现异常的绿色-橙色分裂信号:一个潜在的诊断陷阱。

Unusual split green-orange signals in USP6 fluorescence in situ hybridization in a malignant peripheral nerve sheath tumor with a novel NF1-SCIMP fusion: a potential diagnostic pitfall.

作者信息

Qiu Yan, Jing Wenyi, Zhou Ying, Chen Huijiao, Chen Min, Zhang Hongying

机构信息

Department of Pathology, West China Hospital, Sichuan University, Guoxuexiang 37, Chengdu, 610041, Sichuan, China.

Department of Pathology, Neijiang Hospital of Traditional Chinese Medicine, Neijiang, China.

出版信息

Virchows Arch. 2022 Jun;480(6):1255-1260. doi: 10.1007/s00428-021-03179-2. Epub 2021 Aug 19.

Abstract

Deletion of the neurofibromatosis 1 (NF1) gene is common, but NF1 rearrangement or fusion has rarely been reported in peripheral nerve sheath tumors. Here, we present a case of malignant peripheral nerve sheath tumor (MPNST) in a 36-year-old Chinese female. Histologically, the lesion was composed of spindle cells with moderate atypia, immature bone, and atypical cartilage elements. Fluorescence in situ hybridization (FISH) for USP6 revealed green-orange split signals, strongly suggesting the presence of USP6 rearrangement. Subsequent next-generation sequencing-based technology analyses revealed t(17,17) (p13.2, q11.2) intrachromosomal translocation resulting in a novel NF1-SCIMP fusion gene along with NF1 deletion. However, USP6 fusion was not identified. To the best of our knowledge, this is the first case with a confirmed NF1 gene fusion partner in a peripheral nerve sheath tumor. Notably, rearrangement of the SCIMP may cause a pitfall in the interpretation of USP6 FISH results.

摘要

神经纤维瘤病1型(NF1)基因缺失很常见,但外周神经鞘瘤中NF1重排或融合鲜有报道。在此,我们报告1例36岁中国女性的恶性外周神经鞘瘤(MPNST)。组织学上,病变由中度异型的梭形细胞、未成熟骨和非典型软骨成分组成。针对USP6的荧光原位杂交(FISH)显示绿色-橙色分裂信号,强烈提示存在USP6重排。随后基于新一代测序的技术分析显示17号染色体内部t(17,17)(p13.2,q11.2)易位,导致一个新的NF1-SCIMP融合基因以及NF1缺失。然而,未发现USP6融合。据我们所知,这是外周神经鞘瘤中首例证实有NF1基因融合伴侣的病例。值得注意的是,SCIMP重排可能会在USP6 FISH结果的解读中造成陷阱。

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