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成人期髓母细胞瘤在未治疗的脊柱裂背景下出现:病例说明

Adult-onset medulloblastoma presenting in the setting of untreated spina bifida: illustrative case.

作者信息

Patel Devan, Riea Sanjida, Lim Jaims, Khan Hamid S, Gugino Lauren, Carver Chloe, Snyder Kenneth V, Algattas Hanna N

机构信息

Department of Neurosurgery, University at Buffalo Jacobs School of Medicine and Biomedical Sciences, Buffalo, New York.

出版信息

J Neurosurg Case Lessons. 2025 Mar 31;9(13). doi: 10.3171/CASE24897.

Abstract

BACKGROUND

Adult-onset medulloblastoma in the setting of untreated spina bifida and Chiari type II malformation is exceptionally rare and has not been previously reported. The relationship between medulloblastoma and spina bifida remains poorly understood.

OBSERVATIONS

An adult male with untreated spina bifida presented to the emergency department with headaches and was found to have a left cerebellar medulloblastoma and obstructive hydrocephalus. He underwent preoperative catheter-based angiography, which revealed inferior displacement of the venous sinuses. A suboccipital craniotomy for resection was performed, followed by radiation therapy and chemotherapy. Follow-up imaging at 3 months postoperatively demonstrated no evidence of residual tumor.

LESSONS

Given the abnormal posterior fossa development in patients with spina bifida and Chiari type II malformation, posterior fossa surgery requires a thorough understanding of the patient's venous sinus anatomy to achieve a maximal safe resection and prevent venous sinus injury or thrombosis. While the role of CSF diversion in adults with untreated spina bifida is unknown, the authors opted to proceed with postresection ventriculoperitoneal shunt placement given the persistent mass effect on the fourth ventricle from peritumoral swelling. Additional studies are needed to establish a molecular and/or genetic relationship between medulloblastoma and spinal dysraphism. https://thejns.org/doi/10.3171/CASE24897.

摘要

背景

在未经治疗的脊柱裂和Chiari II型畸形背景下发生的成人髓母细胞瘤极为罕见,此前未见报道。髓母细胞瘤与脊柱裂之间的关系仍知之甚少。

观察结果

一名患有未经治疗的脊柱裂的成年男性因头痛就诊于急诊科,被发现患有左侧小脑髓母细胞瘤和梗阻性脑积水。他接受了术前导管血管造影,显示静脉窦下移。进行了枕下开颅切除术,随后进行放射治疗和化疗。术后3个月的随访影像学检查未发现残留肿瘤的迹象。

经验教训

鉴于脊柱裂和Chiari II型畸形患者后颅窝发育异常,后颅窝手术需要全面了解患者的静脉窦解剖结构,以实现最大程度的安全切除并防止静脉窦损伤或血栓形成。虽然脑脊液分流在未经治疗的脊柱裂成人中的作用尚不清楚,但鉴于肿瘤周围肿胀对第四脑室持续产生占位效应,作者选择在切除术后进行脑室腹腔分流术。需要进一步研究以确定髓母细胞瘤与脊柱发育异常之间的分子和/或遗传关系。https://thejns.org/doi/10.3171/CASE24897

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0a2/11959635/f1ff3225c0cb/CASE24897_figure_1.jpg

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