Atypical Congenital Meduloblastoma: Case Report

Sabina Oblitas López, Edgar Pinto Garcia, Mauro Toledo Aguirre
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Abstract

Medulloblastomas are WHO grade 4 embryonal neuroepithelial tumors that typically occur in the posterior fossa in the pediatric population. They represent 68% of embryonal tumors. The study of congenital cases is scarce due to the rarity of reported patients. There is also no specific bibliography, however histologically and molecularly they can be classified. On the other hand, due to the young age of these patients, they are difficult to manage and have a higher risk of complications in the treatment. In addition to this, patients are born with alterations in the development of the central nervous system due to chronic intracranial hypertension caused by said tumor and have little functional development. The objective of this study is to teach us to recognize the diagnosis early, the evolution of the disease to lead to better treatment for these patients in the future.
非典型先天性髓母细胞瘤:病例报告
髓母细胞瘤是世卫组织 4 级胚胎性神经上皮肿瘤,通常发生在儿童后窝。它们占胚胎性肿瘤的 68%。由于报告的患者很少,对先天性病例的研究也很少。也没有专门的参考书目,但可以从组织学和分子学上对其进行分类。另一方面,由于这些患者年龄较小,因此难以管理,治疗过程中出现并发症的风险也较高。此外,由于上述肿瘤导致的慢性颅内高压,患者出生时中枢神经系统的发育就已发生改变,功能发育不完善。这项研究的目的是让我们学会早期识别诊断,了解疾病的演变过程,以便将来更好地治疗这些患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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