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脊索样胶质瘤:一种第三脑室的新型肿瘤。

Chordoid glioma: a novel tumor of the third ventricle.

作者信息

Castellano-Sanchez A A, Recine M A, Restrepo R, Howard L H, Robinson M J

机构信息

Arkadi M. Rywlin, MD Department of Pathology and Laboratory Medicine, Mount Sinai Medical Center of Greater Miami, FL 33140, USA.

出版信息

Ann Diagn Pathol. 2000 Dec;4(6):373-8. doi: 10.1053/adpa.2000.19369.

DOI:10.1053/adpa.2000.19369
PMID:11149969
Abstract

Chordoid glioma of the third ventricle is a recently characterized primary neoplasm of the central nervous system. We present a case and discuss the pathologic and radiologic features. We are aware of only 16 other cases documented in the world literature. This radiologic-pathologic correlation alerts pathologists and radiologists to recognize chordoid glioma as a distinct clinicopathologic entity restricted to the third ventricular area of adult patients.

摘要

第三脑室脊索样胶质瘤是一种最近才被明确特征的中枢神经系统原发性肿瘤。我们报告一例并讨论其病理和放射学特征。据我们所知,世界文献中仅记载了另外16例。这种放射学与病理学的相关性提醒病理学家和放射学家,要将脊索样胶质瘤识别为一种仅限于成年患者第三脑室区域的独特临床病理实体。

相似文献

1
Chordoid glioma: a novel tumor of the third ventricle.脊索样胶质瘤:一种第三脑室的新型肿瘤。
Ann Diagn Pathol. 2000 Dec;4(6):373-8. doi: 10.1053/adpa.2000.19369.
2
Test and teach. A recurrent third ventricular brain tumour. Diagnosis: Chordoid glioma of the third ventricle.检测与诊断。复发性第三脑室脑肿瘤。诊断:第三脑室脊索样胶质瘤。
Pathology. 2006 Jun;38(3):254-7. doi: 10.1080/00313020600699151.
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Origin of chordoid glioma of the third ventricle.第三脑室脊索样胶质瘤的起源。
Arch Pathol Lab Med. 2006 Apr;130(4):460-4. doi: 10.5858/2006-130-460-OOCGOT.
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Chordoid glioma: report of two rare examples with unusual features.脊索样胶质瘤:两例具有不寻常特征的罕见病例报告。
Acta Neurochir (Wien). 2008 Mar;150(3):295-300; discussion 300. doi: 10.1007/s00701-008-1420-x. Epub 2008 Feb 4.
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Chordoid glioma of the third ventricle: immunohistochemical and molecular genetic characterization of a novel tumor entity.第三脑室脊索样胶质瘤:一种新型肿瘤实体的免疫组织化学和分子遗传学特征
Brain Pathol. 1999 Oct;9(4):617-26. doi: 10.1111/j.1750-3639.1999.tb00543.x.
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Chordoid glioma of the third ventricle: a report of two new cases, with further evidence supporting an ependymal differentiation, and review of the literature.第三脑室脊索样胶质瘤:两例新病例报告,有进一步证据支持室管膜分化,并文献复习
Am J Surg Pathol. 2002 Oct;26(10):1330-42. doi: 10.1097/00000478-200210000-00010.
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Intracranial chordoid glioma: A clinical, radiological and pathological study of 14 cases.颅内脊索样胶质瘤:14 例临床、放射学和病理学研究。
J Clin Neurosci. 2020 Oct;80:267-273. doi: 10.1016/j.jocn.2020.09.019. Epub 2020 Sep 18.
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Chordoid glioma: a rare radiologically, histologically, and clinically mystifying lesion.脊索样胶质瘤:一种在放射学、组织学和临床上均罕见且令人困惑的病变。
World J Surg Oncol. 2015 May 28;13:188. doi: 10.1186/s12957-015-0603-9.
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Third ventricular chordoid glioma: clinicopathological study of two cases with evidence for a poor clinical outcome despite low grade histological features.第三脑室脊索样胶质瘤:两例临床病理研究,尽管组织学特征为低级别,但仍有临床预后不良的证据
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Immunohistochemical and ultrastructural study of chordoid glioma of the third ventricle: its tanycytic differentiation.第三脑室脊索样胶质瘤的免疫组织化学和超微结构研究:其室管膜细胞分化
Acta Neuropathol. 2003 Aug;106(2):176-80. doi: 10.1007/s00401-003-0713-2. Epub 2003 May 14.

引用本文的文献

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Concurrence of chordoid gliomas with Rosai-Dorfman component: report of two rare cases.脉络丛样胶质瘤合并Rosai-Dorfman成分:两例罕见病例报告。
Int J Clin Exp Pathol. 2017 Nov 1;10(11):11260-11266. eCollection 2017.
2
Prognostic factors for recurrence and complications in the surgical management of primary chordoid gliomas: A systematic review of literature.原发性脉络丛胶质瘤手术治疗中复发和并发症的预后因素:文献系统评价
Clin Neurol Neurosurg. 2015 Nov;138:129-36. doi: 10.1016/j.clineuro.2015.08.011. Epub 2015 Aug 19.
3
Chordoid glioma: ten years of a low-grade tumor with high morbidity.
脊索样胶质瘤:一种具有高致残率的低级别肿瘤的十年研究
Skull Base. 2010 Mar;20(2):125-38. doi: 10.1055/s-0029-1246223.
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Chordoid glioma : a case report of unusual location and neuroradiological characteristics.脊索样胶质瘤:一例位置特殊及具有神经放射学特征的病例报告
J Korean Neurosurg Soc. 2010 Jul;48(1):62-5. doi: 10.3340/jkns.2010.48.1.62. Epub 2010 Jul 31.
5
Chordoid glioma: report of a case with unusual histologic features, ultrastructural study and review of the literature.
J Neurooncol. 2003 May;63(1):39-47. doi: 10.1023/a:1023752717042.