原发性和转移性脑尤文氏肉瘤:罕见病例报告与文献综述。

Surgical neurology international Pub Date : 2024-10-11 eCollection Date: 2024-01-01 DOI:10.25259/SNI_316_2024
Mariem Mhiri, Amal Abbes, Rihab Ben Dhia, Narjes Gouta, Mahbouba Frih Ayed
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引用次数: 0

摘要

背景:尤文氏肉瘤(ES)是一种罕见的恶性肿瘤,主要影响年轻人,颅内定位尤其少见。颅内转移性 ES 并不常见,文献中仅报道了四例颅内转移性 ES;这给诊断和治疗带来了独特的挑战:我们介绍了一例独特的 ES 病例,以描述其临床、放射学和组织病理学特征。患者 33 岁,表现为颅内高压和步态障碍。神经系统检查发现了静态和动态小脑综合征。影像学检查和立体定向活检证实了原发性和转移性脑 ES 的诊断。治疗方案包括化疗和放疗:我们的病例强调了在鉴别诊断硬脑膜病变(表现为囊性成分和异质造影剂增强)时考虑 ES 的重要性,尤其是在年轻人中。早期识别和干预有望优化患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary and metastatic cerebral Ewing's sarcoma: A case report about a rare entity and literature review.

Background: Ewing's sarcoma (ES) is a rare malignant tumor primarily affecting young individuals, with cranial localization being particularly uncommon. While intracranial metastatic ES is infrequent, only four cases of intracranial metastatic ES are reported in the literature; it presents unique diagnostic and therapeutic challenges.

Case description: We present a distinctive case of ES to delineate its clinical, radiological, and histopathological characteristics. Our patient, a 33-year-old, manifested symptoms of intracranial hypertension and gait disturbance. Neurological examination revealed a static and kinetic cerebellar syndrome. Imaging studies and stereotactic biopsy confirmed the diagnosis of primary and metastatic cerebral ES. The treatment regimen encompassed chemotherapy and radiation therapy.

Conclusion: Our case underscores the importance of considering ES in the differential diagnosis of dural-based lesions exhibiting cystic components and heterogeneous contrast enhancement, particularly in young individuals. Early recognition and intervention hold promise for optimizing patient outcomes.

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