了解伸长细胞室管膜瘤:一种罕见的室管膜瘤亚型

IF 0.5 Q4 CLINICAL NEUROLOGY
Mitrajit Sharma, Aanchal Datta, Chhitij Srivastava
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引用次数: 0

摘要

摘要脊髓髓内伸长细胞型室管膜瘤(TE)是一种罕见的室管膜瘤,至今仅报告约60例。放射学诊断是繁琐的,其独特的组织病理学鉴定是明确诊断所必需的。仅凭放射学和术中发现常被误诊。由于其发病率极低(占所有脊髓肿瘤的1%),迄今为止仅记录了少量髓内TE病例。我们报告一位成年女性,她表现为背侧髓内TE,并在术中神经监测下接受了全切除术。此外,我们还回顾了已经发表的关于该实体的文献。细微的放射鉴别可能有助于考虑TE作为鉴别诊断。这些病例的长期存活是非常有利的。我们的病例描述了文献中已知的少数脊髓髓内TE病例之一,也是南亚地区极少数病例之一。我们强调在放射学和术中对这种实体进行准确诊断所涉及的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Understanding tanycytic ependymoma: A rare subtype of ependymoma
Spinal intramedullary tanycytic ependymoma (TE) is a rare variant of ependymoma with only about 60 cases reported till date. Radiological diagnosis is tedious and identification of its unique histopathology is required for definitive diagnosis. It is often misdiagnosed solely on radiology as well as intra-operative findings. Because of its exceedingly low incidence (1% of all spinal cord neoplasms), only a small number of cases of intramedullary TE have been recorded so far. We report an adult female who presented with dorsal intramedullary TE and underwent gross total resection under intraoperative nerve monitoring. Additionally, we have also reviewed the literature already published on this entity. Subtle radiological differentiations may assist in considering TE as a differential diagnosis. Long term survival in these cases is extremely favorable. Our case depicts one of the few cases of spinal intramedullary TE known in literature and one of the very few in Southern Asian region. We highlight the challenges involved in making an accurate diagnosis of this entity radiologically and intra-operatively.
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来源期刊
CiteScore
1.00
自引率
0.00%
发文量
236
审稿时长
15 weeks
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