首页> 外文期刊>Pediatric neurosurgery >Spinal seeding of a pilocytic astrocytoma in an adult, initially diagnosed 18 years previously.
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Spinal seeding of a pilocytic astrocytoma in an adult, initially diagnosed 18 years previously.

机译:成人成年的脊髓细胞星形细胞瘤的脊髓接种,最初在18年前被诊断出。

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摘要

Pilocytic astrocytoma (PA) is a slow-growing, well-circumscribed grade I glioma generally considered benign, with a low recurrence rate and an excellent prognosis following complete surgical resection. PA is the most common central nervous system glioma in the pediatric population and is rare in adults. We report a 26-year-old male with an intradural extramedullary PA at the thoracolumbar junction following subtotal cerebellar PA resection 18 years previously. Fifteen months after spinal PA resection, the patient is doing well, has regained the ability to stand independently, and has no evidence of any new or enlarging lesions. To our knowledge, this is the longest time reported from initial tumor resection of leptomeningeal dissemination to the distal spinal cord. PA patients with subtotal resection may benefit from continued follow-up for up to 20 years after the initial diagnosis and resection.
机译:上皮型星形细胞瘤(PA)是一种生长缓慢,界限分明的I级神经胶质瘤,通常被认为是良性的,复发率低,完全手术切除后预后良好。 PA是儿童人群中最常见的中枢神经系统神经胶质瘤,在成年人中很少见。我们报告了一位26岁男性,在18年前小脑PA切除后,在胸腰椎交界处有硬膜内髓外髓质PA。脊髓PA切除术后15个月,患者情况良好,恢复了独立站立的能力,并且没有任何新的或扩大的病变的证据。据我们所知,这是从最初的肿瘤切除术到脑脊髓扩散到远端脊髓以来最长的时间。初次诊断和切除后长达20年的持续随访可能会使次全切除的PA患者受益。

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