A Rare Presentation of Adult Primary Leptomeningeal Medulloblastoma: Case Report.

IF 0.5 Q4 PATHOLOGY
Case Reports in Pathology Pub Date : 2025-09-08 eCollection Date: 2025-01-01 DOI:10.1155/crip/8937543
Grace E Hey, Megan E H Still, Rachel S F Moor, Amanda Stanton, Duane A Mitchell, Brent A Orr, Jesse L Kresak, Anthony A Yachnis, Tara Massini, Ashley P Ghiaseddin
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Abstract

Medulloblastomas are tumors of the posterior fossa that have a propensity to develop leptomeningeal metastases along the spinal cord, commonly known as "drop metastases." Medulloblastoma accounts for approximately 1%-2% of all adult brain tumors, and reports of primary leptomeningeal medulloblastoma are extremely limited. Herein, we present a rare case of a 34-year-old woman diagnosed with multifocal primary spinal leptomeningeal medulloblastoma without cranial involvement.

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罕见的成人原发性轻脑膜髓母细胞瘤1例。
髓母细胞瘤是后颅窝的肿瘤,有沿脊髓发展为轻脑膜转移的倾向,通常称为“滴状转移”。髓母细胞瘤约占所有成人脑肿瘤的1%-2%,原发性脑脊膜髓母细胞瘤的报道非常有限。在此,我们提出一个罕见的病例,34岁的女性诊断为多灶性原发性脊髓轻脑膜髓母细胞瘤,没有颅脑受累。
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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