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

IF 1.3 Q2 MEDICINE, GENERAL & INTERNAL
Daniel W Griepp, Aaron Miller, Jonathan Klein, Ali A Chaudhri, Stephanie Moawad, Razia Rehmani, Ralph Rahme
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引用次数: 0

Abstract

Background: 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. Case Report: 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. Conclusion: 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.

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成年晚期以硬脑膜为基础的后窝髓母细胞瘤与岩状脑膜瘤相似。
背景:后窝髓母细胞瘤常见于儿科人群,但在成人中很少报道。成神经管细胞瘤的成人病例通常发生在年轻患者中,倾向于出现在小脑半球的轴内,通常表现出典型的组织病理学特征。病例报告:一名54岁男性,表现为头痛、头晕、步态不稳和频繁跌倒,在过去3个月内病情加重。影像学和组织病理学分析显示轴外,硬脑膜为基础的后窝髓母细胞瘤,伴有韧带增生/结节状组织病理学,类似于岩状脑膜瘤。肿块占据左桥小脑角。患者接受显微外科手术切除肿瘤后再进行质子束放射治疗,随访1年无肿瘤复发。结论:很少有类似岩状脑膜瘤的硬脑膜后窝髓母细胞瘤的报道,据我们所知,这是第一例用质子束治疗老年人成功的病例。虽然罕见,但髓母细胞瘤可发生在老年人的桥小脑角轴外,可能类似于岩状脑膜瘤。这种罕见的可能性应始终牢记,特别是如果期待,非手术治疗正在考虑。后窝髓母细胞瘤应采用积极的显微手术切除配合放射治疗。如果可行,应考虑质子束治疗。
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来源期刊
Ochsner Journal
Ochsner Journal MEDICINE, GENERAL & INTERNAL-
CiteScore
2.10
自引率
0.00%
发文量
71
审稿时长
24 weeks
期刊介绍: The Ochsner Journal is a quarterly publication designed to support Ochsner"s mission to improve the health of our community through a commitment to innovation in healthcare, medical research, and education. The Ochsner Journal provides an active dialogue on practice standards in today"s changing healthcare environment. Emphasis will be given to topics of great societal and medical significance.
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