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首页> 外文期刊>Journal of clinical neuroscience: official journal of the Neurosurgical Society of Australasia >Clinical features and surgical outcomes of spinal clear cell meningioma: An institutional experience
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Clinical features and surgical outcomes of spinal clear cell meningioma: An institutional experience

机译:脊柱透明细胞脑膜瘤的临床特征和外科结果:一种制度经验

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摘要

Clear cell meningiomas are uncommon tumors in the spinal canal. The clinical and radiological features, clinicopathological characteristics, treatment results, and long-term outcomes of this rare entity are still uncertain. The authors review their experience in a surgical series of 10 patients with histologically proven spinal clear cell meningioma treated at a single institution and discuss clinical features, radiological findings, and surgical outcomes. There were 3 male and 7 female patients with a mean age of 25.5 +/- 17.7 years. The mean follow-up period was 68.4 +/- 32.7 months. One tumor was in the cervical spine, 2 were in the thoracic spine, 2 were in the thoracolumbar spine, and 5 were in the lumbar or lumbosacral spine. Gross total resection of the tumor with a well-demarcated dissection plane was achieved in 9 patients, while subtotal resection was achieved in 1 patient, and no patients underwent postoperative radiotherapy. Symptoms present before surgery had improved in 9 patients at the last follow-up. Postoperative follow-up magnetic resonance imaging showed no recurrence/regrowth in the 9 patients with total removal and 1 patient with subtotal removal during the mean follow-up periods of 68.4 months and 56.0 months, respectively. Clear cell meningiomas should be considered in the differential diagnosis of young female patients with spinal tumors involving the lower thoracic, lumbar or sacral region. Although the nature of this disease is aggressive, spinal clear cell meningiomas are amenable to surgery. The risk of long-term lesion recurrence is low if complete removal can be achieved, and followup imaging is still needed. (C) 2019 Elsevier Ltd. All rights reserved.
机译:透明细胞脑膜瘤是脊柱管中罕见的肿瘤。这种罕见实体的临床和放射性特征,临床病理特征,治疗结果和长期结果仍然不确定。作者审查了在一个机构治疗的组织验证脊柱透明细胞脑膜瘤的10名患有10名患者的手术系列中的经验,并讨论临床特征,放射性调查结果和手术结果。有3名男性和7名女性患者平均年龄为25.5 +/- 17.7岁。平均随访时间为68.4 +/- 32.7个月。一个肿瘤在颈椎中,2位于胸椎,2位胸椎脊柱,5位腰椎或腰骶脊柱。在9名患者中达到了患有良好划分的解剖平面的肿瘤总切除术,而1例患者患者映射,并且没有术后放射治疗的患者。在最后一次随访的9名患者中,手术前的症状存在于9例。术后随访磁共振成像显示出9例患者没有复发/再生,分别在68.4个月和56.0个月的平均随访期内出现过量去除1例患者。应在涉及​​下胸部,腰椎或骶骨区的脊柱肿瘤的年轻女性患者的鉴别诊断中考虑透明细胞脑膜瘤。虽然这种疾病的性质是侵略性的,但脊柱透明细胞脑膜瘤均可用于手术。如果可以实现完全拆卸,长期病变复发的风险很低,并且仍需要跟踪成像。 (c)2019年elestvier有限公司保留所有权利。

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