{"title":"Cauda equina myxopapillary ependymoma in von Hippel-Lindau disease: A case report","authors":"Lucas Ribeiro, Valérie Rigau, Luc Bauchet","doi":"10.25259/sni_104_2024","DOIUrl":null,"url":null,"abstract":"\n\nPatients affected by Von Hippel-Lindau (VHL) are prone to develop central nervous system neoplasms such as hemangioblastomas (HBs). Myxopapillary ependymoma (MPE) is not commonly associated with VHL disease.\n\n\n\nWe present the first case of a VHL patient affected by simultaneous silent cauda equina MPE and a symptomatic conus medullaris HB. The patient was first operated for systemic tumors and followed for asymptomatic HBs. Simple surveillance was maintained until neurological symptoms appeared. Regular follow-up demonstrated objective growth of the cystic conus medullaris tumor while the cauda equina lesion remained stable. Surgery was performed to avoid further neurological worsening. Histopathological examination showed conus medullaris HB and a nearby cauda equina MPE.\n\n\n\nSimultaneous spinal HBs and isolated MPE may exceptionally occur in VHL patients.\n","PeriodicalId":38981,"journal":{"name":"Surgical Neurology International","volume":" 9","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-06-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Surgical Neurology International","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.25259/sni_104_2024","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
Patients affected by Von Hippel-Lindau (VHL) are prone to develop central nervous system neoplasms such as hemangioblastomas (HBs). Myxopapillary ependymoma (MPE) is not commonly associated with VHL disease.
We present the first case of a VHL patient affected by simultaneous silent cauda equina MPE and a symptomatic conus medullaris HB. The patient was first operated for systemic tumors and followed for asymptomatic HBs. Simple surveillance was maintained until neurological symptoms appeared. Regular follow-up demonstrated objective growth of the cystic conus medullaris tumor while the cauda equina lesion remained stable. Surgery was performed to avoid further neurological worsening. Histopathological examination showed conus medullaris HB and a nearby cauda equina MPE.
Simultaneous spinal HBs and isolated MPE may exceptionally occur in VHL patients.
Von Hippel-Lindau(VHL)患者易患血管母细胞瘤(HBs)等中枢神经系统肿瘤。我们报告了第一例同时患有无症状马尾MPE和无症状圆锥髓质HB的VHL患者。患者首先接受了系统性肿瘤手术,并对无症状的 HB 进行了随访。在出现神经系统症状之前,患者一直接受简单的监测。定期随访显示,囊性延髓肿瘤有客观生长,而马尾病变保持稳定。为避免神经功能进一步恶化,患者接受了手术治疗。组织病理学检查显示,锥髓HB和附近的马尾MPE同时存在。