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Multiple Schwannomas of the Spine: Review of the Schwannomatosis or Congenital Neurilemmomatosis: A Case Report

机译:多发性脊柱神经鞘瘤:神经鞘瘤病或先天性神经膜瘤病的回顾:一例报告

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Schwannomas are the most common benign nerve sheath tumors originating in Schwann cells. With special conditions like neurofibromatosis type 2 or entity called schwannomatosis, patients develop multiple schwannomas. But in clinical setting, distinguishing schwannomatosis from neurofibromatosis type 2 is challengeable. We describe 58-year-old male who presented with severe neuropathic pain, from schwannomatosis featuring multiple schwannomas of spine and trunk, and underwent surgical treatment. We demonstrate his radiologic and clinical findings, and discuss about important clinical features of this condition. To confirm schwannomatosis, we performed brain magnetic resonance imaging, and took his familial history. Staged surgery was done for pathological confirmation and relief of the pain. Schwannomatosis and neurofibromatosis type 2 are similar but different disease. There are diagnostic hallmarks of these conditions, including familial history, pathology, and brain imaging. Because of different prognosis, the two diseases must be distinguished, so diagnostic tests that are mentioned above should be performed in caution.
机译:雪旺氏瘤是起源于雪旺氏细胞的最常见的良性神经鞘瘤。患有2型神经纤维瘤病或称为神经鞘瘤病的特殊疾病,患者会发展为多发神经鞘瘤。但是在临床环境中,将神经鞘瘤病与2型神经纤维瘤病区分开来是有挑战性的。我们描述了58岁的男性,患有严重的神经性疼痛,来自以多发性脊柱和躯干神经鞘瘤为特征的神经鞘瘤病,并接受了手术治疗。我们证明他的放射学和临床发现,并讨论这种疾病的重要临床特征。为了证实神经鞘瘤病,我们进行了脑磁共振成像,并记录了他的家族史。进行了分期手术以病理确认和减轻疼痛。 Schwannomatosis和2型神经纤维瘤病相似但不同。这些疾病有诊断标志,包括家族史,病理学和脑成像。由于预后不同,必须区分这两种疾病,因此应谨慎进行上述诊断测试。

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