Multicentric primary ectopic meningiomas involving lung and cranial bone barrier: A rare case report.

IF 1.4 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Medicine Pub Date : 2025-01-31 DOI:10.1097/MD.0000000000041294
Huiyang Zhang, Xiang Li, Yan Jiang
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Abstract

Rationale: Primary ectopic meningiomas (PEMs) are extremely rare, with limited literature available on the subject. Understanding their clinical and radiological characteristics is crucial for accurate diagnosis and treatment.

Patient concerns: This study presents a case of a multicentric PEM involving the lungs and cranial bone barrier, aiming to provide new insights into its clinical and diagnostic features.

Diagnoses: A 46-year-old woman with no prior history of intracranial meningiomas or other tumors was found to have multiple lobulated nodules in the lungs during a routine physical examination. Computed tomography scans revealed well-defined lesions with mild to moderate heterogeneous enhancement. Magnetic resonance imaging showed a lesion at the cranial bone barrier, which presented as a high-signal area on T2-weighted FLAIR images and mild to moderate enhancement on T1-weighted images. The magnetic resonance spectroscopy displayed a broad Lip peak but lacked N-acetylaspartate or creatine peaks. Histopathological and immunohistochemical analyses confirmed the diagnosis of multicentric PEMs.

Interventions: We performed surgical resection of the lesion on the cranial bone plate and conducted follow-up examinations for the multiple lesions in the lungs.

Outcomes: This case highlights the diagnostic challenges of multicentric PEMs involving the lungs and cranial bone barrier. Due to their extremely low incidence and nonspecific clinical manifestations, a comprehensive evaluation combining radiological, pathological, and immunophenotypic data is essential for accurate diagnosis.

Lessons: This case underscores the importance of a thorough, multidisciplinary approach to diagnosis and treatment and provides valuable insights for managing similar rare cases.

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累及肺及颅骨屏障的多中心原发性异位脑膜瘤1例。
理由:原发性异位脑膜瘤(PEMs)极为罕见,文献资料有限。了解其临床和放射学特征对准确诊断和治疗至关重要。患者关注:本研究报告一例涉及肺和颅骨屏障的多中心PEM,旨在为其临床和诊断特征提供新的见解。诊断:46岁女性,无颅内脑膜瘤或其他肿瘤病史,在常规体检中发现肺部多发分叶结节。计算机断层扫描显示病灶明确,轻度至中度不均匀强化。磁共振成像显示颅骨屏障病变,在t2加权FLAIR像上表现为高信号区,在t1加权像上表现为轻度至中度强化。磁共振波谱显示较宽的Lip峰,但缺乏n -乙酰天冬氨酸和肌酸峰。组织病理学和免疫组织化学分析证实了多中心PEMs的诊断。干预措施:手术切除颅骨板病变,随访肺部多发病变。结果:本病例强调了涉及肺和颅骨屏障的多中心PEMs的诊断挑战。由于其发病率极低且临床表现非特异性,因此结合放射学、病理学和免疫表型资料进行综合评估对于准确诊断至关重要。经验教训:本病例强调了全面、多学科的诊断和治疗方法的重要性,并为管理类似罕见病例提供了宝贵的见解。
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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来源期刊
Medicine
Medicine 医学-医学:内科
CiteScore
2.80
自引率
0.00%
发文量
4342
审稿时长
>12 weeks
期刊介绍: Medicine is now a fully open access journal, providing authors with a distinctive new service offering continuous publication of original research across a broad spectrum of medical scientific disciplines and sub-specialties. As an open access title, Medicine will continue to provide authors with an established, trusted platform for the publication of their work. To ensure the ongoing quality of Medicine’s content, the peer-review process will only accept content that is scientifically, technically and ethically sound, and in compliance with standard reporting guidelines.
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