椎管内ASPSCR1: TFE3重排肿瘤伴神经分化。

IF 2.7 3区 医学 Q2 CLINICAL NEUROLOGY
Yue-E Wang, Wei Wang, An-Li Zhang, Yuan Li, Sibai Sun, Wenchao Zhou, Haibo Wu
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引用次数: 0

摘要

ASPSCR1::TFE3重排已在肺泡软组织肉瘤、MiT家族易位性肾细胞癌以及血管周围上皮样细胞瘤(PEComas)中被描述。然而,这种重排尚未在初级椎管中报道。在此,我们报告一例18岁男性左下肢疼痛2个月的病例。神经影像学显示从胸椎12号到腰椎1号椎管有病变。组织病理学检查显示,肿瘤呈巢状结构,伴有大量沙质钙化。肿瘤细胞TFE3和SOX10呈强烈弥漫性阳性,HMB-45和S100呈斑片状阳性,其他免疫标志物呈阴性染色。RNA测序证实ASPSCR1::TFE3基因重排。Heidelberg DNA甲基化分类器将该病例归类为“颅和棘旁神经肿瘤”。该病例可能代表了一种新的椎管内肿瘤实体,通过独特的组织病理学特征和潜在的神经分化,扩大了ASPSCR1:: tfe3重排肿瘤的范围。我们将该病例命名为脊柱内ASPSCR1::TFE3重排肿瘤,并表达SOX10。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intraspinal ASPSCR1::TFE3 rearranged tumor with nerve differentiation.

The ASPSCR1::TFE3 rearrangement has been described in alveolar soft part sarcoma, MiT family translocation renal cell carcinomas as well as perivascular epithelioid cell tumors (PEComas). However, this rearrangement has not been reported in the primary spinal canal. Here, we report a case of an 18-year-old male who had pain in his left lower limb for 2 months. Neuroimaging revealed a lesion in the spinal canal from thoracic 12 to lumbar 1. Histopathological examination showed the tumor consisting of nested architectural pattern with abundant psammomatous calcification. Tumor cells exhibited strong and diffuse positivity for TFE3 and SOX10, patchy positivity for HMB-45 and S100, while other immunomarkers were negatively stained. RNA sequencing confirmed the ASPSCR1::TFE3 gene rearrangement. The Heidelberg DNA methylation classifier classified this case as "Cranial and Paraspinal Nerve Tumor". This case may represent a novel intraspinal neoplasm entity that expands the spectrum of ASPSCR1::TFE3-rearranged neoplasms by unique histopathological features and potential neural differentiation. We named this case as intraspinal ASPSCR1::TFE3 rearranged tumor with SOX10 expression.

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来源期刊
Brain Tumor Pathology
Brain Tumor Pathology 医学-病理学
CiteScore
5.40
自引率
9.10%
发文量
30
审稿时长
>12 weeks
期刊介绍: Brain Tumor Pathology is the official journal of the Japan Society of Brain Tumor Pathology. This international journal documents the latest research and topical debate in all clinical and experimental fields relating to brain tumors, especially brain tumor pathology. The journal has been published since 1983 and has been recognized worldwide as a unique journal of high quality. The journal welcomes the submission of manuscripts from any country. Membership in the society is not a prerequisite for submission. The journal publishes original articles, case reports, rapid short communications, instructional lectures, review articles, letters to the editor, and topics.Review articles and Topics may be recommended at the annual meeting of the Japan Society of Brain Tumor Pathology. All contributions should be aimed at promoting international scientific collaboration.
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