Jallo G I, Kothbauer K F, Silvera V M, Epstein F J
Division of Pediatric Neurosurgery, Institute for Neurology and Neurosurgery, Beth Israel Medical Center, New York, New York 10028, USA.
Neurosurgery. 2001 Jan;48(1):218-21; discussion 221-2. doi: 10.1097/00006123-200101000-00042.
Intraspinal clear cell meningioma is a rare morphological variant of meningioma. Only 13 case reports are found in the literature; therefore, no management strategy has been defined for this tumor type. This article describes two patients, reviews the literature, and proposes a treatment plan for clear cell meningioma.
Two female patients, 22 months and 8 years of age, respectively, presented with localized neck and leg pain that limited their ability to walk. Magnetic resonance imaging revealed intradural tumors, a cervical intramedullary neoplasm in the younger patient, and a cauda equina tumor in the older child.
Both patients underwent radical resection of their intradural tumor. Both tumors, however, recurred shortly (5 and 6 mo) after the initial operation. During the second operation, a radical removal was performed on each patient. Both patients received adjuvant radiotherapy. In addition, the younger patient developed posterior fossa metastasis 20 months after intraspinal surgery.
Intraspinal clear cell meningiomas are very uncommon tumors. The clinical course in our two patients supports the reported 40% recurrence rate within 15 months. These tumors also can disseminate within the central nervous system. We recommend serial imaging studies every 3 months. For recurrent tumors, we recommend localized radiation therapy after reoperation.
脊髓内透明细胞型脑膜瘤是一种罕见的脑膜瘤形态学变异类型。文献中仅发现13例病例报告;因此,尚未针对该肿瘤类型确定治疗策略。本文描述了两名患者,回顾了文献,并提出了透明细胞型脑膜瘤的治疗方案。
两名女性患者,年龄分别为22个月和8岁,均表现为局限性颈部和腿部疼痛,影响行走能力。磁共振成像显示硬膜内肿瘤,年幼患者为颈髓内肿瘤,年长儿童为马尾肿瘤。
两名患者均接受了硬膜内肿瘤的根治性切除术。然而,两个肿瘤在初次手术后不久(5个月和6个月)均复发。在第二次手术中,对每名患者进行了根治性切除。两名患者均接受了辅助放疗。此外,年幼患者在脊髓手术后20个月出现后颅窝转移。
脊髓内透明细胞型脑膜瘤是非常罕见的肿瘤。我们两名患者的临床病程支持文献报道的15个月内40%的复发率。这些肿瘤也可在中枢神经系统内播散。我们建议每3个月进行系列影像学检查。对于复发性肿瘤,我们建议再次手术后进行局部放射治疗。