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首页> 外文期刊>Journal of clinical neuroscience: official journal of the Neurosurgical Society of Australasia >Primary epidural hemangiopericytoma of the thoracic spine: Case report and literature review
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Primary epidural hemangiopericytoma of the thoracic spine: Case report and literature review

机译:胸脊柱的原发性硬膜外血管瘤:案例报告和文献综述

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Hemangiopericytoma (HPC) is a rare tumor originating from pericapillary cells. Rarely found in the central nervous system, it is extremely rare in the spinal canal. Because of the low incidence of this tumor, its radiographic features and clinical manifestations have not been extensively studied and reported, therefore, it is often misdiagnosed as a schwannoma or spinal meningioma. We describe an unexpected HPC in a 35-year-old woman who was admitted to the Peking Union Medical College Hospital with a severe backache, sensory abnormalities, and muscle weakness. Magnetic resonance imaging showed an enhancing lesion at T6-7 with severe compression of the spinal cord. Gross total resection was achieved, and subsequently, a marked neurologic improvement was observed. The diagnosis of primary extradural HPC in our patient was confirmed based on postoperative histopathology and immunohistochemistry. Neither recurrence nor metastasis of the tumor was found during the 14-month follow-up, which did not include radiotherapy. To describe the demography, radiologic features, treatment, and prognosis of spinal HPC, a comprehensive literature review was performed and 105 cases of primary spinal HPC from 1958 to 2017 were collected from 39 articles. Although rare, HPC should be considered in the differential diagnosis of intraspinal lesions. Immunohistologic examination is of decisive importance in making the diagnosis. Adequate surgical resection, when feasible, is the first choice of treatment for all cases of HPC; however, the outcomes of radiotherapy and chemotherapy have yet to be determined. Individualized treatment combined with long-term follow-up for each patient is recommended. (C) 2018 Elsevier Ltd. All rights reserved.
机译:血醋酸血育瘤(HPC)是源自植物细胞的罕见肿瘤。很少在中枢神经系统中发现,它在脊柱管中非常罕见。由于这种肿瘤的发生率低,其放射线照相特征和临床表现尚未被广泛研究和报道,因此,它通常被误诊为施瓦南瘤或脊髓脑膜瘤。我们在一名35岁的女性中描述了一个意外的HPC,他们被占据了北京联盟医学院医院,严重的腰痛,感官异常和肌肉无力。磁共振成像显示T6-7的增强病变,具有严重压缩脊髓。实现总分解,随后,观察到显着的神经系统改善。基于术后组织病理学和免疫组织化学证实了我们患者初级外抗HPC的诊断。在14个月的随访期间没有发现肿瘤的复发性和转移,其不包括放射疗法。为了描述脊髓HPC的人口统计学,放射学特征,治疗和预后,综合文献综述,从39篇文章中收集了1958年至2017年的105例原发性脊髓HPC。虽然罕见,但应考虑HPC在静脉内部病变的鉴别诊断中。免疫组织学检查对诊断具有决定性的重要性。适当的手术切除,可行,是所有HPC治疗的首选。然而,尚未确定放疗和化疗的结果。建议使用个性化治疗每位患者的长期随访。 (c)2018年elestvier有限公司保留所有权利。

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