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成年晚期表现为岩骨脑膜瘤的硬脑膜后颅窝髓母细胞瘤

Dural-Based Posterior Fossa Medulloblastoma Mimicking a Petrous Meningioma in Late Adulthood.

作者信息

Griepp Daniel W, Miller Aaron, Klein Jonathan, Chaudhri Ali A, Moawad Stephanie, Rehmani Razia, Rahme Ralph

机构信息

Division of Neurosurgery, SBH Health System, Bronx, NY.

Department of Radiation Oncology, Albert Einstein College of Medicine and Montefiore Medical Center, Bronx, NY.

出版信息

Ochsner J. 2022 Summer;22(2):176-181. doi: 10.31486/toj.21.0064.

Abstract

Medulloblastoma of the posterior fossa is commonly encountered in pediatric populations but rarely reported in adults. Adult cases of medulloblastoma typically occur in younger patients, tend to arise intra-axially within the cerebellar hemisphere, and usually exhibit classic histopathologic features. A 54-year-old male presented with headaches, dizziness, gait instability, and frequent falls that had worsened during the prior 3 months. Imaging and histopathologic analysis revealed extra-axial, dural-based posterior fossa medulloblastoma with desmoplastic/nodular histopathology, mimicking a petrous meningioma. The mass occupied the left cerebellopontine angle. The patient underwent microsurgical gross total resection of the tumor followed by proton beam radiation therapy and was disease-free at 1-year follow-up. Few dural-based posterior fossa medulloblastomas resembling petrous meningiomas have been reported, and to our knowledge, this is the first description of a case to be treated successfully with proton beam therapy in an older adult. Although rare, medulloblastoma can occur extra-axially in the cerebellopontine angle of older adults, potentially mimicking a petrous meningioma. This rare possibility should always be kept in mind, especially if expectant, nonsurgical management is being considered. To optimize outcome, posterior fossa medulloblastoma should be treated with aggressive microsurgical resection followed by radiation therapy. When available, proton beam therapy should be considered.

摘要

后颅窝髓母细胞瘤常见于儿童群体,但在成人中鲜有报道。成人髓母细胞瘤病例通常发生于较年轻患者,倾向于起源于小脑半球轴内,且通常表现出典型的组织病理学特征。一名54岁男性出现头痛、头晕、步态不稳及频繁跌倒症状,在过去3个月中病情加重。影像学和组织病理学分析显示为轴外、硬膜起源的后颅窝髓母细胞瘤,具有促纤维增生/结节性组织病理学特征,酷似岩骨脑膜瘤。肿块占据左侧小脑脑桥角。患者接受了肿瘤显微手术全切,随后进行质子束放射治疗,1年随访时无疾病复发。鲜有类似岩骨脑膜瘤的硬膜起源后颅窝髓母细胞瘤的报道,据我们所知,这是首例在老年成人中成功接受质子束治疗的病例描述。尽管罕见,但髓母细胞瘤可发生于老年成人的小脑脑桥角轴外,可能酷似岩骨脑膜瘤。应始终牢记这种罕见可能性,尤其是在考虑进行观察性非手术治疗时。为优化治疗效果,后颅窝髓母细胞瘤应采用积极的显微手术切除,随后进行放射治疗。如有条件,应考虑质子束治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b8/9196958/8884aa59ea91/toj-21-0064-figure1.jpg

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