Primary Intraosseous Meningioma of the Sphenoid-Temporal Bone with Single-Stage, 3D-Planned Cranioplasty: Case Report.

IF 0.7 Q4 CLINICAL NEUROLOGY
Journal of Neurological Surgery Reports Pub Date : 2026-03-27 eCollection Date: 2026-01-01 DOI:10.1055/a-2813-1643
Arthur F de Mattos, Mariana S Shima, Lucas P Chaves, João V M Doro, Paulo Mácio Porto de Melo
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Abstract

Background: Primary intraosseous meningiomas (PIM) are rare extradural tumors, representing less than 2% of all meningiomas. They are often slow-growing and may present with nonspecific radiological features, complicating diagnosis.

Case report: We report the case of a 48-year-old female with progressive left frontotemporal bulging over 12 months, without neurological deficits. Imaging revealed an osteoblastic lesion in the left sphenoid and temporal bones, causing mild compression of adjacent structures. The patient underwent craniectomy with complete tumor resection and immediate cranioplasty using a preplanned customized prosthesis. Histopathology and immunohistochemistry confirmed a meningothelial meningioma, with tumor cells confined to intertrabecular bone spaces and free surgical margins, consistent with a primary intraosseous origin. Postoperative follow-up demonstrated excellent cosmetic results and no recurrence.

Conclusion: PIMs pose diagnostic and therapeutic challenges due to their rarity and nonspecific imaging features. Histopathology remains essential for definitive diagnosis. Preoperative 3D prototyping and customized prosthesis planning can optimize surgical reconstruction, reduce deformities, and improve cosmetic and functional outcomes. This case highlights the importance of integrating clinicoradiological evaluation, histopathology, and modern reconstructive techniques to achieve complete resection and minimize recurrence.

单期3d计划颅骨成形术治疗原发性蝶颞骨骨内脑膜瘤一例报告。
背景:原发性骨内脑膜瘤(PIM)是一种罕见的硬膜外肿瘤,占所有脑膜瘤的不到2%。它们通常生长缓慢,可能表现为非特异性放射学特征,使诊断复杂化。病例报告:我们报告一例48岁女性进行性左额颞膨出超过12个月,没有神经功能缺损。影像学显示左侧蝶骨和颞骨有成骨细胞病变,引起邻近结构轻度压迫。患者接受了颅骨切除术,完全切除肿瘤,并使用预先计划的定制假体立即进行颅骨成形术。组织病理学和免疫组织化学证实为脑膜上皮性脑膜瘤,肿瘤细胞局限于骨小梁间隙和游离手术缘,符合原发性骨内起源。术后随访显示良好的美容效果,无复发。结论:pim的罕见性和非特异性影像学特征给诊断和治疗带来了挑战。组织病理学仍然是明确诊断的必要条件。术前3D原型和定制假体规划可以优化手术重建,减少畸形,改善美容和功能结果。该病例强调了综合临床放射学评估、组织病理学和现代重建技术以实现完全切除和最小化复发的重要性。
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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