Ahmed Habib, Hansen Deng, N. F. Hameed, Scott Kulich, Pascal Zinn
{"title":"巨型颈胸椎上皮瘤显微手术切除术:二维手术视频","authors":"Ahmed Habib, Hansen Deng, N. F. Hameed, Scott Kulich, Pascal Zinn","doi":"10.25259/sni_317_2024","DOIUrl":null,"url":null,"abstract":"\n\nEpendymomas, rare glial brain tumors, account for <5% of all brain tumors. Interestingly, over 60% of ependymomas occur in the spinal cord of adults, including those originating from the filum terminale, while the rest are found within the brain. The World Health Organization (WHO) categorizes ependymomas into three grades: subependymomas and myxopapillary ependymomas ([MEPNs]; WHO grade I), classic ependymomas (WHO grade II), and anaplastic ependymomas (WHO grade III). Spinal ependymomas generally exhibit a more favorable prognosis compared to their intracranial counterparts and are primarily treated through gross total resection, which is considered the most effective surgical approach. As such, they are recognized as a distinct clinical entity that demands tailored management strategies. MEPNs, which constitute 13% of ependymomas, typically occur in the cauda equina and sometimes extend into the conus medullaris. Most other spinal ependymomas are of the classic type and predominantly arise in the cervical and thoracic regions of the spine. The mean age at diagnosis is 45 years of age. While prognosis varies based on molecular subtypes, complete resection is associated with improved survival.\n\n\n\nHere, we demonstrate the technical nuances to safely achieve gross total resection of a giant spinal ependymoma in a 29-year-old female with a medical history notable for sept-optic dysplasia, and panhypopituitarism. The patient presented with progressive neck pain, upper and lower extremity weakness, and numbness for 1 year. On physical examination, she demonstrated mild weakness in her left arm. The preoperative magnetic resonance imaging revealed a cervicothoracic intramedullary mass extending from C4 to T2 with an associated syrinx at C4. Under intraoperative neural monitoring (somatosensory evoked potentials, motor-evoked potentials, and epidural direct wave recordings), the patient underwent a C4 – T2 laminectomy. In addition, spinal ultrasonography helped differentiate solid tumor mass from syrinx formation, thus guiding the focus and extent of the decompression .\n\n\n\nGross total resection was achieved; at 18 postoperative months, the patient had mild residual motor deficit. The pathological evaluation revealed a WHO grade II ependymoma. Subsequent sequential enhanced MR studies at 3, 6, and 12 months confirmed no tumor recurrence.\n","PeriodicalId":38981,"journal":{"name":"Surgical Neurology International","volume":"31 12","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Microsurgery resection of giant cervicothoracic spinal ependymoma: Two-dimensional operative video\",\"authors\":\"Ahmed Habib, Hansen Deng, N. F. Hameed, Scott Kulich, Pascal Zinn\",\"doi\":\"10.25259/sni_317_2024\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n\\nEpendymomas, rare glial brain tumors, account for <5% of all brain tumors. Interestingly, over 60% of ependymomas occur in the spinal cord of adults, including those originating from the filum terminale, while the rest are found within the brain. The World Health Organization (WHO) categorizes ependymomas into three grades: subependymomas and myxopapillary ependymomas ([MEPNs]; WHO grade I), classic ependymomas (WHO grade II), and anaplastic ependymomas (WHO grade III). Spinal ependymomas generally exhibit a more favorable prognosis compared to their intracranial counterparts and are primarily treated through gross total resection, which is considered the most effective surgical approach. As such, they are recognized as a distinct clinical entity that demands tailored management strategies. MEPNs, which constitute 13% of ependymomas, typically occur in the cauda equina and sometimes extend into the conus medullaris. Most other spinal ependymomas are of the classic type and predominantly arise in the cervical and thoracic regions of the spine. The mean age at diagnosis is 45 years of age. While prognosis varies based on molecular subtypes, complete resection is associated with improved survival.\\n\\n\\n\\nHere, we demonstrate the technical nuances to safely achieve gross total resection of a giant spinal ependymoma in a 29-year-old female with a medical history notable for sept-optic dysplasia, and panhypopituitarism. The patient presented with progressive neck pain, upper and lower extremity weakness, and numbness for 1 year. On physical examination, she demonstrated mild weakness in her left arm. The preoperative magnetic resonance imaging revealed a cervicothoracic intramedullary mass extending from C4 to T2 with an associated syrinx at C4. Under intraoperative neural monitoring (somatosensory evoked potentials, motor-evoked potentials, and epidural direct wave recordings), the patient underwent a C4 – T2 laminectomy. 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引用次数: 0
摘要
附肢瘤是一种罕见的胶质脑肿瘤,占所有脑肿瘤的5%以下。有趣的是,超过 60% 的附肢瘤发生在成人的脊髓中,包括那些起源于终丝的肿瘤,而其余的则发生在大脑中。世界卫生组织(WHO)将附殖瘤分为三个等级:亚独立瘤和肌乳头状附肢瘤([MEPNs];WHO I 级)、典型附肢瘤(WHO II 级)以及无弹性附肢瘤(WHO III 级)。脊柱上皮瘤的预后一般比颅内上皮瘤好,主要通过全切除术治疗,这被认为是最有效的手术方法。因此,它们被认为是一种独特的临床实体,需要量身定制的治疗策略。脊髓内皮瘤占脊髓外皮瘤的 13%,通常发生在马尾,有时会扩展到延髓。其他大多数脊柱外皮瘤属于典型类型,主要发生在颈椎和胸椎部位。确诊时的平均年龄为 45 岁。虽然预后因分子亚型而异,但完全切除与生存率的提高有关。在此,我们展示了在一名29岁女性患者身上安全实现巨大脊柱外胚瘤大体全切除的细微技术差别,该患者的病史有明显的视神经隔发育不良和泛垂体功能障碍。患者出现进行性颈部疼痛、上下肢无力和麻木已有一年。体格检查显示,她的左臂轻度无力。术前磁共振成像显示,颈胸椎髓内肿块从C4延伸至T2,C4处伴有鞘膜积液。在术中神经监测(体感诱发电位、运动诱发电位和硬膜外直接波记录)下,患者接受了 C4 - T2 椎板切除术。此外,脊柱超声波检查有助于区分实性肿瘤肿块和鞘膜积液,从而指导减压的重点和范围。 术后 18 个月,患者出现轻度残余运动障碍。病理评估显示为 WHO II 级上皮瘤。随后在 3 个月、6 个月和 12 个月进行的连续增强磁共振检查证实肿瘤没有复发。
Microsurgery resection of giant cervicothoracic spinal ependymoma: Two-dimensional operative video
Ependymomas, rare glial brain tumors, account for <5% of all brain tumors. Interestingly, over 60% of ependymomas occur in the spinal cord of adults, including those originating from the filum terminale, while the rest are found within the brain. The World Health Organization (WHO) categorizes ependymomas into three grades: subependymomas and myxopapillary ependymomas ([MEPNs]; WHO grade I), classic ependymomas (WHO grade II), and anaplastic ependymomas (WHO grade III). Spinal ependymomas generally exhibit a more favorable prognosis compared to their intracranial counterparts and are primarily treated through gross total resection, which is considered the most effective surgical approach. As such, they are recognized as a distinct clinical entity that demands tailored management strategies. MEPNs, which constitute 13% of ependymomas, typically occur in the cauda equina and sometimes extend into the conus medullaris. Most other spinal ependymomas are of the classic type and predominantly arise in the cervical and thoracic regions of the spine. The mean age at diagnosis is 45 years of age. While prognosis varies based on molecular subtypes, complete resection is associated with improved survival.
Here, we demonstrate the technical nuances to safely achieve gross total resection of a giant spinal ependymoma in a 29-year-old female with a medical history notable for sept-optic dysplasia, and panhypopituitarism. The patient presented with progressive neck pain, upper and lower extremity weakness, and numbness for 1 year. On physical examination, she demonstrated mild weakness in her left arm. The preoperative magnetic resonance imaging revealed a cervicothoracic intramedullary mass extending from C4 to T2 with an associated syrinx at C4. Under intraoperative neural monitoring (somatosensory evoked potentials, motor-evoked potentials, and epidural direct wave recordings), the patient underwent a C4 – T2 laminectomy. In addition, spinal ultrasonography helped differentiate solid tumor mass from syrinx formation, thus guiding the focus and extent of the decompression .
Gross total resection was achieved; at 18 postoperative months, the patient had mild residual motor deficit. The pathological evaluation revealed a WHO grade II ependymoma. Subsequent sequential enhanced MR studies at 3, 6, and 12 months confirmed no tumor recurrence.