脊髓非典型嗜酸性粒细胞星形细胞瘤--采用埃尔斯伯格和啤酒技术分两期切除。病例报告和文献综述。

IF 1 4区 医学 Q4 CLINICAL NEUROLOGY British Journal of Neurosurgery Pub Date : 2024-06-05 DOI:10.1080/02688697.2024.2357349
Sebastian Victor Trifoi, Shubhabrata Biswas, Rafal Szylak, Nicholas Carleton-Bland
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引用次数: 0

摘要

在儿童群体中,嗜酸性星形细胞瘤通常表现为世卫组织 1 级颅内肿块,预后良好。在较少见的情况下,脊髓中也会发现这种肿瘤。颅内嗜酸性粒细胞星形细胞瘤的无弹性变异型也有罕见病例。我们报告了一例罕见的具有无弹性特征的颈脊髓髓细胞星形细胞瘤成人患者。患者有6个月的颈部疼痛和右手麻痹病史,对类固醇治疗有部分反应。颈椎核磁共振成像显示颈脊髓明显扩张,水肿向头顶延伸至延髓,向尾部延伸至中胸脊髓。钆 T1 加权后图像显示,髓内强化主要集中在 C3 椎体水平。弥散张量成像断层扫描显示,肿瘤的中心位置使脊髓扩张,并使脊髓束向四周移位。手术切除按照埃尔斯伯格和比尔技术分两期进行,有助于安全边缘肿瘤剥离。组织学切片显示,该肿瘤为神经胶质细胞系肿瘤,ATRX 核表达保留,GFAP 阳性,Ki-67 估计为 10%,甲基化类别与无弹性嗜碱性星形细胞瘤相符。随后,患者接受了辅助放疗和化疗(10 个周期的替莫唑胺和 6 个周期的氯硝柳胺)。患者在首次手术后18个月出现症状进展,34个月出现放射学进展,总生存期为40个月。我们查阅了相关文献,发现只有四例病例具有类似的组织学特征。
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Spinal cord anaplastic Pilocytic Astrocytoma - two stage resection with elsberg and beer technique. Case report and literature review.

Pilocytic Astrocytomas are generally presenting as WHO grade 1 intracranial masses in the paediatric population with a favourable prognostic. In less common instances they can be found in the spinal cord. There have been rare cases of Anaplastic variants of the Cranial Pilocytic Astrocytomas. We report a rare instance of an adult patient with pilocytic astrocytoma of the cervical cord with anaplastic features. Our patient presented with 6 months history of neck pain and right-hand paraesthesia which partially responded to steroid treatment. MRI of the cervical spine demonstrated marked expansion of the cervical cord with oedema extending cranially to the medulla and caudally to the mid-thoracic cord. Post-gadolinium T1-weighted images showed intense intramedullary enhancement mainly centred at the level of the C3 vertebra. Diffusion Tensor Imaging Tractography showed the central location of the tumour expanding the cord and displacing the tracts circumferentially. Surgical resection was performed in two stages according to the Elsberg and Beer technique that assisted with safe margin tumour debulking. The histological sections revealed a glial lineage tumour with retained ATRX nuclear expression, positive for GFAP, Ki-67 estimated to 10% and a methylation class corresponding to an Anaplastic Pilocytic Astrocytoma. Subsequently, our patient underwent adjuvant radiotherapy and chemotherapy (10 cycles of Temozolamide and 6 cycles of CCNU). Symptomatic progression developed at 18 months from the initial surgery, radiological progression at 34 months and the overall survival was 40 months. We reviewed the literature and found only four other cases with similar histology.

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来源期刊
British Journal of Neurosurgery
British Journal of Neurosurgery 医学-临床神经学
CiteScore
2.30
自引率
9.10%
发文量
139
审稿时长
3-8 weeks
期刊介绍: The British Journal of Neurosurgery is a leading international forum for debate in the field of neurosurgery, publishing original peer-reviewed articles of the highest quality, along with comment and correspondence on all topics of current interest to neurosurgeons worldwide. Coverage includes all aspects of case assessment and surgical practice, as well as wide-ranging research, with an emphasis on clinical rather than experimental material. Special emphasis is placed on postgraduate education with review articles on basic neurosciences and on the theory behind advances in techniques, investigation and clinical management. All papers are submitted to rigorous and independent peer-review, ensuring the journal’s wide citation and its appearance in the major abstracting and indexing services.
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