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起源于锁骨下臂丛神经内正中神经的原发性无BAP1非典型脑膜瘤:病例说明

Primary BAP1-absent atypical meningioma arising from median nerve within infraclavicular brachial plexus: illustrative case.

作者信息

Wu Adela, Ring Adam C, Ziskin Jennifer, Nguyen Tina, Pezeshkian Patrick

机构信息

Department of Neurosurgery, Stanford University Medical Center, Stanford, California.

Departments of Neurosurgery, Kaiser Permanente Redwood City Medical Center, Redwood City, California.

出版信息

J Neurosurg Case Lessons. 2024 Jul 29;8(5). doi: 10.3171/CASE24226.

Abstract

BACKGROUND

The authors present the only known case of a World Health Organization grade II ectopic meningioma occurring in the infraclavicular brachial plexus, causing pain within the axilla not associated with a primary malignant meningioma of the central nervous system. Peripheral nerve sheath tumors are rare entities, the majority of which are schwannomas or neurofibromas. Ectopic meningiomas only represent 1%-2% of all meningiomas. To date, there is one other published case specifically of a primary ectopic meningioma located in the brachial plexus.

OBSERVATIONS

Following the dissection of the left axilla, a dominant rubbery tumor involving the median nerve was encountered. The tumor capsule contained areas of hemorrhage and a soft core with nerve fascicles coursing through, which were not compromised during internal tumor debulking. The tumor lacked a clear pseudocapsule that is characteristically seen in schwannomas. Histopathological studies confirmed an atypical epithelioid neoplasm with elevated numbers of mitotic figures and BAP1 gene deletion.

LESSONS

Primary meningiomas arising outside the central nervous system are exceedingly rare. For this unusual higher-grade primary ectopic meningioma located in the distal brachial plexus, surgery with the goal of gross-total resection, adjuvant radiation, additional imaging, and genetics screening were recommended. Close follow-up is warranted. https://thejns.org/doi/10.3171/CASE24226.

摘要

背景

作者报告了世界卫生组织二级异位脑膜瘤发生于锁骨下臂丛神经的唯一已知病例,该病例导致腋窝疼痛,且与中枢神经系统原发性恶性脑膜瘤无关。周围神经鞘瘤是罕见的实体瘤,其中大多数是神经鞘瘤或神经纤维瘤。异位脑膜瘤仅占所有脑膜瘤的1%-2%。迄今为止,另有一例已发表的病例专门报道了位于臂丛神经的原发性异位脑膜瘤。

观察结果

在解剖左腋窝后,发现一个主要的橡皮样肿瘤累及正中神经。肿瘤包膜内有出血区域和一个软芯,有神经束穿过,在肿瘤内部减瘤过程中神经束未受损害。该肿瘤缺乏神经鞘瘤典型的清晰假包膜。组织病理学研究证实为非典型上皮样肿瘤,有丝分裂象数量增加且存在BAP1基因缺失。

经验教训

中枢神经系统外发生的原发性脑膜瘤极为罕见。对于位于臂丛神经远端的这种不寻常的高级别原发性异位脑膜瘤,建议进行以大体全切为目标的手术、辅助放疗、进一步的影像学检查和基因筛查。需要密切随访。https://thejns.org/doi/10.3171/CASE24226

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a7e/11301597/1470cbbbc10f/CASE24226_figure_1.jpg

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