Chordoid meningioma: a retrospective study of 17 cases at a single institution

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摘要Chordoid meningioma (CM),characterized by its resemblance to chordoma,was first described by Kepes et al1 in 1988,and classified histologically as a WHO grade Ⅱ neoplasm in the 2000 revision of the WHO grading system,featured by its aggressive clinical course,great risk of recurrence,and infrequent association with hematological conditions.2 This article describes the clinical course,radiological characteristics,postoperative treatment,and prognosis of 17 patients with CM who underwent surgical treatment at our hospital.

作者单位 Department of Neurosurgery,Huashan Hospital, Fudan University,Shanghai 200040, China ^[1] Department of Neuropathology,Huashan Hospital, Fudan University,Shanghai 200040, China ^[2]

关键词 chordoid meningioma outcomes postoperative treatment

栏目名称 SHORT COMMUNICATION

DOI 10.3760/cma.j.issn.0366-6999.20122880

发布时间 2013-04-19

基金项目

This study was supported by grants from the National Natural Science Foundation of China Science and Technology Commission of Shanghai Municipality

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