孤立的神经结节病与脑膜瘤病合并多发性颅神经病变的处理:一种罕见的临床情况。

Surgical neurology international Pub Date : 2025-08-15 eCollection Date: 2025-01-01 DOI:10.25259/SNI_579_2025
Ashish Mishra, Ved Prakash Maurya, Nandita Chaudhary, Arun Kumar Srivastava
{"title":"孤立的神经结节病与脑膜瘤病合并多发性颅神经病变的处理:一种罕见的临床情况。","authors":"Ashish Mishra, Ved Prakash Maurya, Nandita Chaudhary, Arun Kumar Srivastava","doi":"10.25259/SNI_579_2025","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Sarcoidosis is an immune-mediated disorder characterized by granulomatous inflammation of the affected organ. Isolated neurosarcoidosis presents as aseptic granulomatous meningitis or focal mass lesions due to granulomas. This case is notable for its radiological resemblance to meningiomatosis, which has a substantial disease burden.</p><p><strong>Case description: </strong>A 47-year-old man presented with symptoms of vertigo and right-sided hearing impairment for the past year. After 6 months, he experienced progressive visual impairment in the right eye and a headache associated with dural stretching on the right side. Neurological evaluation revealed significant visual impairment in the right eye, limited to finger counting at 1 m. The right-sided primary optic atrophy was due to mass effect from the sarcoid granuloma on the optic nerve. Pure-tone audiometry indicated mild sensorineural hearing loss on the right side. Radiological investigations showed multiple intracranial lesions, with the largest lesion located at the right anterior clinoid, exhibiting pial breach, and perilesional edema. The institutional tumor board diagnosed cerebral meningiomatosis. Due to rapidly progressive visual deterioration caused by the right clinoidal lesion, a right pterional craniotomy with gross total excision of the lesion was performed. The histopathology evaluation report revealed neurosarcoidosis. The patient was started on glucocorticoids and immunosuppressant medication by clinical immunology. Follow-up magnetic resonance imaging of the brain after 1 year showed stable disease without any recurrence.</p><p><strong>Conclusion: </strong>Surgical removal of lesions causing mass effect should be regarded as the primary therapy. Insufficient response to medical treatment may result in permanent deficits. When dealing with multiple intracranial lesions, the aim should be to achieve optimal results through surgical intervention.</p>","PeriodicalId":94217,"journal":{"name":"Surgical neurology international","volume":"16 ","pages":"345"},"PeriodicalIF":0.0000,"publicationDate":"2025-08-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12482805/pdf/","citationCount":"0","resultStr":"{\"title\":\"Management of isolated neurosarcoidosis mimicking cerebral meningiomatosis with multiple cranial neuropathies: An uncommon clinical scenario.\",\"authors\":\"Ashish Mishra, Ved Prakash Maurya, Nandita Chaudhary, Arun Kumar Srivastava\",\"doi\":\"10.25259/SNI_579_2025\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Sarcoidosis is an immune-mediated disorder characterized by granulomatous inflammation of the affected organ. Isolated neurosarcoidosis presents as aseptic granulomatous meningitis or focal mass lesions due to granulomas. This case is notable for its radiological resemblance to meningiomatosis, which has a substantial disease burden.</p><p><strong>Case description: </strong>A 47-year-old man presented with symptoms of vertigo and right-sided hearing impairment for the past year. After 6 months, he experienced progressive visual impairment in the right eye and a headache associated with dural stretching on the right side. Neurological evaluation revealed significant visual impairment in the right eye, limited to finger counting at 1 m. The right-sided primary optic atrophy was due to mass effect from the sarcoid granuloma on the optic nerve. Pure-tone audiometry indicated mild sensorineural hearing loss on the right side. Radiological investigations showed multiple intracranial lesions, with the largest lesion located at the right anterior clinoid, exhibiting pial breach, and perilesional edema. The institutional tumor board diagnosed cerebral meningiomatosis. Due to rapidly progressive visual deterioration caused by the right clinoidal lesion, a right pterional craniotomy with gross total excision of the lesion was performed. The histopathology evaluation report revealed neurosarcoidosis. The patient was started on glucocorticoids and immunosuppressant medication by clinical immunology. Follow-up magnetic resonance imaging of the brain after 1 year showed stable disease without any recurrence.</p><p><strong>Conclusion: </strong>Surgical removal of lesions causing mass effect should be regarded as the primary therapy. Insufficient response to medical treatment may result in permanent deficits. When dealing with multiple intracranial lesions, the aim should be to achieve optimal results through surgical intervention.</p>\",\"PeriodicalId\":94217,\"journal\":{\"name\":\"Surgical neurology international\",\"volume\":\"16 \",\"pages\":\"345\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-08-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12482805/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Surgical neurology international\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.25259/SNI_579_2025\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Surgical neurology international","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.25259/SNI_579_2025","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

背景:结节病是一种免疫介导的疾病,以受累器官的肉芽肿性炎症为特征。孤立性神经结节病表现为无菌性肉芽肿性脑膜炎或肉芽肿引起的局灶性肿块病变。该病例的放射学特征与具有重大疾病负担的脑膜瘤病相似。病例描述:47岁男性,过去一年出现眩晕和右侧听力障碍的症状。6个月后,患者出现右眼进行性视力损害,并出现与右侧硬脑膜拉伸相关的头痛。神经学评估显示右眼视力明显受损,仅限于手指计数1米。右侧原发性视神经萎缩是由于视神经肉芽肿的肿块效应。纯音测听显示右侧轻度感音神经性听力损失。影像学检查显示颅内多发病变,最大的病变位于右侧前斜突,表现为脑膜破裂,病灶周围水肿。机构肿瘤委员会诊断为脑膜瘤病。由于右斜向病变引起的视力迅速恶化,我们进行了右翼点开颅术,并全部切除病变。组织病理学检查报告显示为神经结节病。临床免疫学给予糖皮质激素和免疫抑制药物治疗。随访1年后脑磁共振成像显示病情稳定,无复发。结论:应以手术切除引起肿块效应的病灶为主要治疗方法。对医疗反应不足可能导致永久性缺陷。在处理颅内多发病变时,应以手术干预达到最佳效果为目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Management of isolated neurosarcoidosis mimicking cerebral meningiomatosis with multiple cranial neuropathies: An uncommon clinical scenario.

Background: Sarcoidosis is an immune-mediated disorder characterized by granulomatous inflammation of the affected organ. Isolated neurosarcoidosis presents as aseptic granulomatous meningitis or focal mass lesions due to granulomas. This case is notable for its radiological resemblance to meningiomatosis, which has a substantial disease burden.

Case description: A 47-year-old man presented with symptoms of vertigo and right-sided hearing impairment for the past year. After 6 months, he experienced progressive visual impairment in the right eye and a headache associated with dural stretching on the right side. Neurological evaluation revealed significant visual impairment in the right eye, limited to finger counting at 1 m. The right-sided primary optic atrophy was due to mass effect from the sarcoid granuloma on the optic nerve. Pure-tone audiometry indicated mild sensorineural hearing loss on the right side. Radiological investigations showed multiple intracranial lesions, with the largest lesion located at the right anterior clinoid, exhibiting pial breach, and perilesional edema. The institutional tumor board diagnosed cerebral meningiomatosis. Due to rapidly progressive visual deterioration caused by the right clinoidal lesion, a right pterional craniotomy with gross total excision of the lesion was performed. The histopathology evaluation report revealed neurosarcoidosis. The patient was started on glucocorticoids and immunosuppressant medication by clinical immunology. Follow-up magnetic resonance imaging of the brain after 1 year showed stable disease without any recurrence.

Conclusion: Surgical removal of lesions causing mass effect should be regarded as the primary therapy. Insufficient response to medical treatment may result in permanent deficits. When dealing with multiple intracranial lesions, the aim should be to achieve optimal results through surgical intervention.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信