Holocord pilocytic astrocytoma in a young woman with intracranial extension: case report and review of the MRI characteristics.

IF 0.7 Q4 CLINICAL NEUROLOGY Spinal Cord Series and Cases Pub Date : 2024-06-22 DOI:10.1038/s41394-024-00656-z
Sima Kiani Salmi, Amirreza Dehghanian, Ali Taherifard, Alireza Dehghan
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Abstract

Introduction: Pilocytic astrocytoma is a low-grade glioma more frequently seen in patients <20. It is pretty uncommon in the spinal cord. Rarely, astrocytoma may involve the most or total length of the spinal cord; in that case, they are called "holo-cord astrocytoma." In this case report, we are reporting the third holo-cord pilocytic astrocytoma in an adult patient and the first with an extension to the Magendie foramen.

Case presentation: We presented a 24-year-old woman with complaints of progressively worsening neck and back pain since one year ago. The patient's MRI showed a very large intradural and intramedullary cystic lesion with a solid component within the spinal cord extending from the medulla to the conus medullaris. Partial resection of the solid part of the cervical portion of the tumor was performed. Histopathological evaluation of the resected tumor segments was compatible with grade I pilocytic astrocytoma. After one year of follow-up, neck and back pain has reduced, and neurological functions have improved.

Conclusion: Spinal cord pilocytic astrocytoma may present as a holo-cord tumor and can rarely extend to the intracranial fossa. Although this tumor does not arise from the central canal, in this case, it was extended through the Magendie foramen. Symptoms could be subtle despite extensive cord involvement. On MRI, this tumor presents as an intramedullary holo-cord cystic lesion intermixed with a solid component with a variable enhancement of the solid component.

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一名年轻女性罹患伴颅内扩展的 Holocord 型朝粒细胞星形细胞瘤:病例报告和磁共振成像特征回顾。
导言:嗜酸性星形细胞瘤是一种低级别胶质瘤,多见于病例中的患者:我们接诊了一名 24 岁的女性患者,她主诉自一年前以来颈部和背部疼痛逐渐加重。患者的磁共振成像显示,脊髓内有一个非常大的硬膜内和髓内囊性病变,其中有一个实性部分从髓质延伸至髓圆。医生对肿瘤颈椎部分的实性部分进行了部分切除。对切除的肿瘤部分进行的组织病理学评估显示,该肿瘤属于I级柔毛细胞性星形细胞瘤。经过一年的随访,颈背部疼痛减轻,神经功能也有所改善:结论:脊髓柔毛细胞性星形细胞瘤可能表现为全脊髓肿瘤,很少会扩展到颅内窝。虽然这种肿瘤并非来自中央管,但在本病例中,它通过马氏孔扩展。尽管广泛累及脊髓,但症状可能并不明显。在核磁共振成像中,这种肿瘤表现为髓内全脊髓囊性病变与实性成分混杂,实性成分呈不同程度的强化。
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来源期刊
Spinal Cord Series and Cases
Spinal Cord Series and Cases Medicine-Neurology (clinical)
CiteScore
2.20
自引率
8.30%
发文量
92
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