颅内多发性骨髓瘤伪装成硬膜下血肿:说明性病例。

Stephanie A Ihezie, Vishva Natarajan, George Zanazzi, Swaroopa PonnamReddy, Fredrick Lansigan, Linton T Evans, Jennifer Hong
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引用次数: 0

摘要

背景:多发性骨髓瘤(MM)累及颅内是一种罕见的临床表现,通常与其他疾病如硬膜下血肿(SDH)相似,导致预后不良。观察:本病例系列突出了2例老年女性患者,其中1例先前诊断为MM,发展为类似SDH的硬膜下肿块。两例患者均伴有明显的脑水肿和肿块效应。活检证实为浆细胞肿瘤,两名患者均接受了量身定制的治疗,包括皮质类固醇、放射治疗和全身化疗。治疗后患者的临床和影像学表现均有改善。结论:这些病例强调了在硬膜下积液患者中保持广泛鉴别的重要性,特别是如果伴有明显的血管源性水肿或有MM病史的患者。尽管有肿块效应,非手术治疗是有效的。https://thejns.org/doi/10.3171/CASE25347。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intracranial multiple myeloma masquerading as subdural hematoma: illustrative cases.

Background: Intracranial involvement in multiple myeloma (MM) is a rare clinical presentation, often mimicking other conditions such as subdural hematoma (SDH) and resulting in poor prognosis.

Observations: This case series highlights 2 older female patients, one with a prior diagnosis of MM, who developed subdural masses resembling SDH. Both cases were associated with significant cerebral edema and mass effect. Biopsies confirmed plasma cell neoplasms, and both patients underwent tailored treatment, including corticosteroids, radiation therapy, and systemic chemotherapy. The patients showed clinical and radiographic improvement posttreatment.

Lessons: These cases underscore the importance of maintaining a broad differential in patients with subdural collections, particularly if associated with significant vasogenic edema or in those with a history of MM. Nonoperative management is effective, despite mass effect. https://thejns.org/doi/10.3171/CASE25347.

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