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Massive intratumoral hemorrhage following ventriculoperitoneal shunting procedure in an 8-year-old boy: A case report. 脑室-腹膜分流术后肿瘤内大量出血一例8岁男童。
Pub Date : 2024-11-29 eCollection Date: 2024-01-01 DOI: 10.25259/SNI_690_2024
Riky Novriansyah Wibowo, Wihasto Suryaningtyas, Muhammad Arifin Parenrengi

Background: Pineal region tumors comprise 0.4% of all central nervous system tumors in adults and 2.8% in children aged up to 19 years. Pineal gland tumors exhibit histological variability and necessitate a multidisciplinary approach. The first step in managing hydrocephalus is to treat it with either endoscopic third ventriculostomy (ETV) or a shunt surgery.

Case description: We present a case of a child with a massive intratumoral hemorrhage located in the pineal region. An 8-year-old boy with a suspected germinoma in the pineal area accompanying noncommunicating hydrocephalus underwent a right ventriculoperitoneal shunt procedure. He experienced a sudden decline of consciousness following the procedure. The subsequent imaging showed an extensive hyperdense lesion within the brain ventricles, indicating intratumoral hemorrhage. Given that intratumoral hemorrhage in pineocytoma following the placement of ventriculoperitoneal shunt surgery is uncommon, it is a significant factor contributing to morbidity and mortality. It should be considered when cerebrospinal fluid (CSF) diversion is performed before a craniotomy.

Conclusion: A hypothesis suggests that changes in CSF flow after diverting CSF can be the main trigger for intratumoral hemorrhage although uncommon. In this study, we present our experience with our patients and provide a comprehensive evaluation of the existing literature.

背景:松果体区肿瘤占成人中枢神经系统肿瘤的0.4%,在19岁以下儿童中占2.8%。松果体肿瘤表现出组织学变异性,需要多学科联合治疗。治疗脑积水的第一步是内窥镜第三脑室造口术(ETV)或分流手术。病例描述:我们报告一例儿童在松果体区有大量瘤内出血。一个8岁的男孩,怀疑松果体区有生殖细胞瘤并伴有非交通性脑积水,接受了右心室-腹膜分流术。手术后他突然意识下降。随后的影像学显示脑室内有广泛的高密度病变,表明肿瘤内出血。鉴于脑室-腹膜分流术后松果体细胞瘤内出血并不常见,这是导致发病率和死亡率的一个重要因素。在开颅手术前进行脑脊液(CSF)分流时应考虑到这一点。结论:一种假说提示脑脊液分流后脑脊液流量的变化可能是肿瘤内出血的主要触发因素,尽管这种情况并不常见。在这项研究中,我们介绍了我们与患者的经验,并对现有文献进行了全面的评估。
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引用次数: 0
Impacts of type 1 Chiari malformation on elderly. 1型Chiari畸形对老年人的影响。
Pub Date : 2024-11-29 eCollection Date: 2024-01-01 DOI: 10.25259/SNI_832_2024
Amr Badary, Oday Atallah

Background: This study aims to evaluate the surgical outcomes of elderly patients with Chiari malformation (CM) who underwent suboccipital craniectomy (SC) with duraplasty (DP) or dural splitting (DS). The focus is on symptom relief, changes in syrinx size, hospital admission duration, and postoperative complications.

Methods: A retrospective study was performed to evaluate the outcomes of elderly CM patients who underwent SC with DP or dural splitting (DS). Patients older than 60 years who underwent posterior fossa decompression (PFD) together with DP or DS who underwent surgery from 1989 to 2022 were included in the study. Patients were divided into two categories based on their surgical approach - SC with DP and SC with dural splitting (DS) surgery. Demographic details, co-morbidities, clinical features, management details, Chicago Chiari Outcome Scale (CCOS), complications, and follow-up details were obtained.

Results: Of the seven patients, five were females, and two were males. The mean age at the time of the operation is 65.14 years. Among the seven patients, six had syrinx, with a mean diameter of 6.17 mm; one patient had hydrocephalus, and one had scoliosis. All the patients underwent PFD; six patients also underwent DP, and one patient underwent DS. The median CCOS at the time of discharge is 13.

Conclusion: In elderly CM patients, surgery improved symptoms for most but led to reoperations in two cases. Despite a slight increase in syrinx diameter and a drop in the CCOS score, better outcomes were associated with smaller syrinxes. Further research is needed to optimize treatment strategies for this population.

背景:本研究旨在评价老年Chiari畸形(CM)患者行枕下颅骨切除术(SC)联合硬脑膜成形术(DP)或硬脑膜劈裂(DS)的手术效果。重点是症状缓解,鼻腔大小的变化,住院时间和术后并发症。方法:回顾性研究老年CM患者行SC合并DP或硬脊膜裂(DS)的预后。年龄大于60岁、1989年至2022年间接受后颅窝减压(PFD)合并DP或DS手术的患者被纳入研究。根据手术入路将患者分为两类- SC合并DP和SC合并硬脊膜劈裂(DS)手术。统计资料、合并症、临床特征、管理细节、芝加哥Chiari结果量表(CCOS)、并发症和随访细节。结果:7例患者中,女性5例,男性2例。手术时平均年龄65.14岁。7例患者中有6例有鸣管,平均直径为6.17 mm;1例患有脑积水,1例患有脊柱侧凸。所有患者均行PFD;6例患者还接受了DP, 1例患者接受了DS。出院时的中位CCOS为13。结论:在老年CM患者中,手术改善了大多数患者的症状,但导致2例再次手术。尽管导管直径略有增加,CCOS评分下降,但导管越小,预后越好。需要进一步的研究来优化针对这一人群的治疗策略。
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引用次数: 0
Surgical treatment of tuberculum sellae meningioma: A retrospective review of single institutional experience. 鞍结节脑膜瘤的外科治疗:单一机构经验的回顾性回顾。
Pub Date : 2024-11-29 eCollection Date: 2024-01-01 DOI: 10.25259/SNI_685_2024
Roland Sidabutar, Yulius Hermanto, Agung Budi Sutiono, Guata Naibaho, Ahmad Faried

Background: Tuberculum sellae meningiomas (TSMs) represent a distinct entity among intracranial meningiomas. Both transcranial approaches (TCAs) and endoscopic endonasal approaches (EEAs) have provided neurosurgeons with options for managing these difficult tumors. Still, controversies persist regarding the selection criteria for the most optimal approach.

Methods: The authors retrospectively reviewed 45 patients treated surgically for TSM between 2018 and 2023. The clinical reports of all subjects were assessed pre-and post-operatively, encompassing demographic information, clinical symptoms, imaging results, ophthalmological evaluations, operative details, and any complications.

Results: A total of 45 patients were included in this study, with 21 patients undergoing EEAs and 24 TCAs. TSMs treated with EEA are smaller than TCA (P = 0.0014), less prevalent in optic canal invasion (P = 0.0291) and in arterial encasement (P = 0.0050), and have no lateral extension (P < 0.0001). The majority of patients (36/45) had visual improvement or stabilization following the surgery, with the rate of achieving gross total resection (GTR) was higher in the EEA group (17/21) than in the TCA group (9/24) (P = 0.0032). The mortality tends to be higher in the TCA group and is related to arterial encasement, although statistically insignificant.

Conclusion: Both traditional TCAs and EEAs offer options for the surgical management of TSM, each with its advantages and limitations. Based on our experiences, several factors (lateral extension and arterial encasement) may guide the suitable approach, and multidisciplinary considerations, with the overarching goals of achieving maximal tumor resection and minimizing postoperative complications.

背景:鞍结节脑膜瘤(TSMs)是颅内脑膜瘤中一个独特的实体。经颅入路(TCAs)和内窥镜鼻内入路(EEAs)为神经外科医生提供了治疗这些困难肿瘤的选择。然而,关于最优方法的选择标准的争议仍然存在。方法:作者回顾性分析了2018年至2023年接受TSM手术治疗的45例患者。评估所有受试者术前和术后的临床报告,包括人口统计信息、临床症状、影像学结果、眼科评估、手术细节和任何并发症。结果:本研究共纳入45例患者,其中21例接受EEAs, 24例接受TCAs。经EEA治疗的tsm小于TCA (P = 0.0014),在视管侵犯(P = 0.0291)和动脉包膜(P = 0.0050)中较少出现,且无外侧延伸(P < 0.0001)。大多数患者(36/45)术后视力改善或稳定,其中EEA组(17/21)的总全切除率(GTR)高于TCA组(9/24)(P = 0.0032)。TCA组死亡率较高,与动脉闭塞有关,但无统计学意义。结论:传统的tca和EEAs均为TSM的手术治疗提供了选择,各有其优势和局限性。根据我们的经验,几个因素(外侧延伸和动脉包裹)可以指导合适的入路,并考虑多学科因素,以实现最大限度的肿瘤切除和减少术后并发症为首要目标。
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引用次数: 0
Neurosurgical treatment of cerebellar infarct: Open craniectomy versus endoscopic surgery. 小脑梗死的神经外科治疗:开颅手术与内窥镜手术。
Pub Date : 2024-11-29 eCollection Date: 2024-01-01 DOI: 10.25259/SNI_740_2024
Keyvan Mostofi, Kamran Shirbache, Ali Shirbacheh, Morad Peyravi

Background: Cerebellar infarction can lead to severe morbidity and mortality. Current surgical options include decompressive craniectomy (DC) and endoscopic minimally invasive evacuation of necrotic tissue (MEN), but no randomized studies compare their outcomes.This study compares outcomes between DC and MEN in patients with cerebellar infarct using the Glasgow Coma Scale (GCS) and Scale for the Assessment and Rating of Ataxia (SARA) scores.

Methods: Retrospective review of 37 patients treated for cerebellar infarct between 2010 and 2020. Patients were divided into DC and MEN groups, with outcome measures assessed postoperatively.

Results: Both techniques produced similar improvements in GCS and SARA scores, though MEN showed faster healing time and shorter surgery duration.

Conclusion: MEN may offer advantages over traditional surgery in terms of healing and shorter operative time, warranting further investigation.

背景:小脑梗死可导致严重的发病率和死亡率。目前的手术选择包括减压颅骨切除术(DC)和内窥镜微创坏死组织清除术(MEN),但没有随机研究比较它们的结果。本研究使用格拉斯哥昏迷量表(GCS)和共济失调评定量表(SARA)评分比较DC和MEN在小脑梗死患者中的结果。方法:回顾性分析2010 ~ 2020年收治的37例小脑梗死患者。将患者分为DC组和MEN组,并对术后结果进行评估。结果:两种技术对GCS和SARA评分的改善相似,但MEN的愈合时间更快,手术时间更短。结论:MEN在愈合和缩短手术时间方面可能比传统手术有优势,值得进一步研究。
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引用次数: 0
Management of complex vertebral artery anatomy in craniocervical surgery: A case report. 颅颈外科复杂椎动脉解剖的处理:1例报告。
Pub Date : 2024-11-22 eCollection Date: 2024-01-01 DOI: 10.25259/SNI_781_2024
Yasir Hassan Elhassan, Asheesh Tandon, Yasser Seddeg Abdulghani

Background: The surgery on the craniocervical junction is associated with complex techniques that endanger the vertebral artery (VA), especially if there are some anatomical variations present, thereby increasing the risk of vascular injury, particularly during cervical decompression or instrumentation.

Case description: A case of a 60-year-old female with progressive myelopathy and craniocervical junction malformation is presented. Key preoperative imaging findings included basilar invagination, C1 assimilation, and os odontoideum, along with VA anomalies such as a tortuous, hypoplastic left VA arising anomalously from the aortic arch and a right VA with a V2 segment forming a high-riding medial loop into the C2 vertebral body. The surgical procedure was performed through a posterior approach using C-arm fluoroscopy, Doppler ultrasound, and intraoperative neurophysiologic monitoring, which achieved adequate deformity fixation and anterior decompression.

Conclusion: Computed tomography angiography is the gold standard for assessing the preoperative VA anatomy at the craniocervical junction. Intraoperative Doppler ultrasound is invaluable because it minimizes the risk of sudden accidental injury to VAs in cases with abnormal anatomies.

背景:颅颈交界的手术涉及复杂的技术,危及椎动脉(VA),特别是当存在一些解剖变异时,从而增加血管损伤的风险,特别是在颈椎减压或内固定时。病例描述:一个病例60岁的女性进行性脊髓病和颅颈交界处畸形提出。术前主要影像学表现包括颅底内陷、C1同化和齿状突,以及室间隔异常,如主动脉弓异常出现的扭曲、发育不全的左室间隔,以及右室间隔与V2节段形成高位内侧环进入C2椎体。手术通过后路c臂透视、多普勒超声和术中神经生理监测进行,获得了足够的畸形固定和前路减压。结论:ct血管造影是评估颅颈交界区VA术前解剖的金标准。术中多普勒超声是非常宝贵的,因为它最大限度地减少意外伤害的风险突发性输精管解剖异常的情况下。
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引用次数: 0
Tubercular arachnoiditis: A rare culprit of paraparesis in a young adult - A case report and review of literature. 结核性蛛网膜炎:一个罕见的罪魁祸首,在一个年轻人的截瘫-一个病例报告和文献复习。
Pub Date : 2024-11-22 eCollection Date: 2024-01-01 DOI: 10.25259/SNI_598_2024
Jiwesh Kumar, Kaushik Roy, Abhirup Chakraborty, Ritankar Patra

Background: The prevalence of central nervous system tuberculosis (TB) is about 1-2% of all TB cases. Atypical cases like the present case, being interpreted as leptomeningeal metastasis in magnetic resonance imaging (MRI), can pose a dilemma, delaying or even leading to mistreatment.

Case description: A 19-year-old male presented with acute onset paraparesis and bowel bladder involvement presented with an MRI lumbar spine suggesting leptomeningeal metastasis from D11-L5 levels who underwent decompression biopsy which on histopathological examination revealed to be tubercular granulomatous infection. Anti-tubercular drug (ATD) started, and significant improvement was seen in the lower limb power and tone. The outcome of treatment has been unpredictable. Previous case studies having neurological deficits due to severe compression, including ours, show good recovery after surgical decompression and ATD regime.

Conclusion: Such cases should be managed with high suspicion as they can be easily misdiagnosed to be tumors, leading to mistreatment or delayed treatment.

背景:中枢神经系统结核(TB)的患病率约占所有结核病例的1-2%。像本病例这样的非典型病例,在磁共振成像(MRI)中被解释为脑轻脑膜转移,可能会造成困境,延迟甚至导致不当治疗。病例描述:一名19岁男性患者表现为急性麻痹和膀胱受累,腰椎MRI提示从D11-L5水平的轻脑膜转移,经减压活检,组织病理学检查显示为结核性肉芽肿感染。开始使用抗结核药物(ATD),下肢力量和张力明显改善。治疗的结果难以预测。以前的病例研究,包括我们的病例,由于严重压迫导致神经功能障碍,在手术减压和ATD方案后恢复良好。结论:此类病例易误诊为肿瘤,导致误治或延误治疗,应高度警惕。
{"title":"Tubercular arachnoiditis: A rare culprit of paraparesis in a young adult - A case report and review of literature.","authors":"Jiwesh Kumar, Kaushik Roy, Abhirup Chakraborty, Ritankar Patra","doi":"10.25259/SNI_598_2024","DOIUrl":"10.25259/SNI_598_2024","url":null,"abstract":"<p><strong>Background: </strong>The prevalence of central nervous system tuberculosis (TB) is about 1-2% of all TB cases. Atypical cases like the present case, being interpreted as leptomeningeal metastasis in magnetic resonance imaging (MRI), can pose a dilemma, delaying or even leading to mistreatment.</p><p><strong>Case description: </strong>A 19-year-old male presented with acute onset paraparesis and bowel bladder involvement presented with an MRI lumbar spine suggesting leptomeningeal metastasis from D11-L5 levels who underwent decompression biopsy which on histopathological examination revealed to be tubercular granulomatous infection. Anti-tubercular drug (ATD) started, and significant improvement was seen in the lower limb power and tone. The outcome of treatment has been unpredictable. Previous case studies having neurological deficits due to severe compression, including ours, show good recovery after surgical decompression and ATD regime.</p><p><strong>Conclusion: </strong>Such cases should be managed with high suspicion as they can be easily misdiagnosed to be tumors, leading to mistreatment or delayed treatment.</p>","PeriodicalId":94217,"journal":{"name":"Surgical neurology international","volume":"15 ","pages":"432"},"PeriodicalIF":0.0,"publicationDate":"2024-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11618825/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142788284","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Increase of primary intracranial sarcoma in children: Clinical manifestations, diagnosis, and management. 儿童原发性颅内肉瘤的增加:临床表现、诊断和治疗。
Pub Date : 2024-11-22 eCollection Date: 2024-01-01 DOI: 10.25259/SNI_202_2024
Jorge Zumaeta, Annel Murga, Noe Santiago Rea, Jose Daniel Flores-Sanchez, Manuel Lazon, Fernando Palacios Santos, Sandro Casavilca Zambrano, Immanuel Olarinde, Jose Valerio

Background: Primary intracranial sarcomas (PISs) are very rare malignant tumors, and there is paucity of data on it, exclusively in patients <18 years old. We report pediatric PIS at a tertiary hospital in Peru, where the incidence of PIS has increased in recent years.

Methods: We retrospectively analyzed data in children diagnosed with PIS based on clinical presentation, imaging studies, and histopathology between January 2020 and December 2023.

Results: Twenty-five cases were identified. The median age was 5 years. There is slight female predominance (56%). On presentation, 68% of patients had features of intracranial hypertension (ICH), others had convulsions or motor deficits. There was radiologic evidence of cerebral hemorrhage in 80% of those with features of ICH and convulsion. All but one case had a supratentorial tumor. Emergency craniotomy was done in 84% of cases, and gross total resection (GTR) was achieved in the first surgery in 72% of cases. We used an adjuvant chemotherapyradiotherapy-chemotherapy (CTX-RT-CTX) regimen in 72% of cases, but 12% started this scheme 2 weeks after surgical resection. The cases followed up for more than a year that were managed with CTX-RT-CTX after GTR had a survival greater than a year, compared to the cases that received complementary treatment after 4 weeks.

Conclusion: PIS among children represents an infrequent pathology that, in the last years, its incidence has increased in Peru. The presence of intracerebral hemorrhage is a very suggestive finding of this diagnosis; therefore, emergent surgical management is an option before an irreversible ICH presents. Adjuvant treatment with the CTX-RT-CTX regimen started 2 weeks after GTR may improve survival in children with PIS.

背景:原发性颅内肉瘤(Primary intracranial sarcoma, PISs)是一种非常罕见的恶性肿瘤,相关资料很少,仅在患者中。方法:我们回顾性分析2020年1月至2023年12月期间根据临床表现、影像学研究和组织病理学诊断为PIS的儿童的资料。结果:共鉴定25例。中位年龄为5岁。有轻微的女性优势(56%)。在就诊时,68%的患者有颅内高压(ICH)的特征,其他患者有抽搐或运动缺陷。放射学证据显示,80%伴有脑出血和抽搐的患者存在脑出血。除一例外,其余均为幕上肿瘤。84%的病例进行了紧急开颅手术,72%的病例在第一次手术中实现了总切除(GTR)。我们在72%的病例中使用了辅助化疗-放疗-化疗(CTX-RT-CTX)方案,但12%的病例在手术切除后2周开始使用该方案。与术后4周接受补充治疗的病例相比,术后接受CTX-RT-CTX治疗的病例随访1年以上,生存期大于1年。结论:PIS在儿童中是一种罕见的病理,在过去几年中,其发病率在秘鲁有所增加。脑出血的出现是这个诊断的一个很有启发性的发现;因此,在出现不可逆转的脑出血之前,紧急手术治疗是一种选择。GTR后2周开始的CTX-RT-CTX方案的辅助治疗可能提高PIS患儿的生存率。
{"title":"Increase of primary intracranial sarcoma in children: Clinical manifestations, diagnosis, and management.","authors":"Jorge Zumaeta, Annel Murga, Noe Santiago Rea, Jose Daniel Flores-Sanchez, Manuel Lazon, Fernando Palacios Santos, Sandro Casavilca Zambrano, Immanuel Olarinde, Jose Valerio","doi":"10.25259/SNI_202_2024","DOIUrl":"10.25259/SNI_202_2024","url":null,"abstract":"<p><strong>Background: </strong>Primary intracranial sarcomas (PISs) are very rare malignant tumors, and there is paucity of data on it, exclusively in patients <18 years old. We report pediatric PIS at a tertiary hospital in Peru, where the incidence of PIS has increased in recent years.</p><p><strong>Methods: </strong>We retrospectively analyzed data in children diagnosed with PIS based on clinical presentation, imaging studies, and histopathology between January 2020 and December 2023.</p><p><strong>Results: </strong>Twenty-five cases were identified. The median age was 5 years. There is slight female predominance (56%). On presentation, 68% of patients had features of intracranial hypertension (ICH), others had convulsions or motor deficits. There was radiologic evidence of cerebral hemorrhage in 80% of those with features of ICH and convulsion. All but one case had a supratentorial tumor. Emergency craniotomy was done in 84% of cases, and gross total resection (GTR) was achieved in the first surgery in 72% of cases. We used an adjuvant chemotherapyradiotherapy-chemotherapy (CTX-RT-CTX) regimen in 72% of cases, but 12% started this scheme 2 weeks after surgical resection. The cases followed up for more than a year that were managed with CTX-RT-CTX after GTR had a survival greater than a year, compared to the cases that received complementary treatment after 4 weeks.</p><p><strong>Conclusion: </strong>PIS among children represents an infrequent pathology that, in the last years, its incidence has increased in Peru. The presence of intracerebral hemorrhage is a very suggestive finding of this diagnosis; therefore, emergent surgical management is an option before an irreversible ICH presents. Adjuvant treatment with the CTX-RT-CTX regimen started 2 weeks after GTR may improve survival in children with PIS.</p>","PeriodicalId":94217,"journal":{"name":"Surgical neurology international","volume":"15 ","pages":"426"},"PeriodicalIF":0.0,"publicationDate":"2024-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11618731/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142788301","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Targeted palliative endovascular embolization of a glomus jugulotympanicum tumor for refractory Jacobson's neuralgia: A case report. 靶向姑息性血管内栓塞治疗难治性雅各布森神经痛1例。
Pub Date : 2024-11-22 eCollection Date: 2024-01-01 DOI: 10.25259/SNI_901_2024
Brendan Wilson, Mithul Vivek, John Na, Andrea De Gregorio, Luke Pater, Ahmed Muthana, Samer S Hoz, Charles J Prestigiacomo

Background: Glomus tumors around the jugular foramen and inner ear can have variable presentations, including lower cranial nerve palsies, tinnitus, hearing loss, or palpable neck mass. In general, these tumors are benign paragangliomas with the definitive treatment consisting of radiosurgery or surgery. Endovascular embolization can be added as a critical adjunctive therapy to reduce the tumor vascularity before surgical resection. We present the first case of a glomus jugulotympanicum presenting with a severe otalgia-dominant form of glossopharyngeal neuralgia, Jacobson's neuralgia, that was resistant to radiosurgery and relieved successfully by targeted endovascular embolization.

Case description: A 51-year-old female presented with worsening right-sided lancinating ear pain radiating into the jaw and neck, exacerbated by brushing her teeth or any pressure on the skin - consistent with glossopharyngeal neuralgia, Jacobson's variant. Imaging revealed a dumbbell-shaped heterogeneously-enhancing mass in the middle ear cavity extending through the jugular foramen consistent with a glomus jugulotympanicum tumor. After treatment with single-fraction stereotactic radiosurgery, the neuralgia continued to worsen despite medical management and significantly impacted the patient's quality of life. After a multidisciplinary discussion, we performed targeted endovascular embolization of the tumor as palliative therapy. The patient subsequently reported complete relief of neuralgia and full resolution of tinnitus after the embolization procedure, remaining pain free at 20 months follow-up.

Conclusion: Targeted endovascular embolization may serve as a safe and potentially palliative option for refractory Jacobson's neuralgia induced by a glomus jugulotympanicum tumor.

背景:颈静脉孔和内耳周围的血管球瘤有多种表现,包括下颅神经麻痹、耳鸣、听力下降或可触及的颈部肿块。一般来说,这些肿瘤是良性副神经节瘤,最终治疗包括放射手术或手术。在手术切除前,血管内栓塞可以作为一种关键的辅助治疗来减少肿瘤血管。我们报告了第一例颈鼓室静脉球,表现为严重的耳痛为主的舌咽神经痛,雅各布森神经痛,对放射手术有抵抗性,并通过靶向血管内栓塞成功缓解。病例描述:一名51岁女性,表现为右侧穿刺性耳痛恶化,并向下颌和颈部放射,刷牙或按压皮肤时加重,符合Jacobson变异型舌咽神经痛。影像学显示中耳腔内一哑铃状非均匀强化肿块,延伸至颈静脉孔,符合颈鼓膜球瘤。在接受单段式立体定向放射治疗后,尽管药物治疗,神经痛仍继续恶化,并显著影响患者的生活质量。经过多学科的讨论,我们对肿瘤进行了靶向血管内栓塞作为姑息治疗。患者随后报告栓塞手术后神经痛完全缓解,耳鸣完全消失,随访20个月无疼痛。结论:有针对性的血管内栓塞可能是一种安全的、潜在的姑息治疗方法,用于治疗颈鼓膜球肿瘤引起的难治性雅各布森神经痛。
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引用次数: 0
Rare histiocytic neoplasm: A case report. 罕见组织细胞肿瘤1例。
Pub Date : 2024-11-22 eCollection Date: 2024-01-01 DOI: 10.25259/SNI_795_2024
Sabrina Maria Genovese, Jakov Tiefenbach, Ravi A Nunna, Andrew Youkilis

Background: Histiocytic neoplasms are defined by too many histiocytes accumulating in various tissues, including the skin, bones, lymph nodes, and central nervous system. They are uncommon blood-related disorders that constitute <1% of cancers found in soft tissues and lymph nodes. Most referred to as Langerhans cell histiocytosis (LCH) or non-LCH, there are over 100 different sub-types that are divided into five groups. Here, a 76-year-old male presented with an intramedullary thoracic LCH.

Case description: A 76-year-old male presented with the month of slowly progressive bilateral lower extremity weakness (i.e., right > left) accompanied by decreased left-sided sensation below the T7 level. The enhanced thoracic magnetic resonance (MR) imaging documented an intradural intramedullary nodule at the T5 level with a syrinx extending from C7 to T10. The patient underwent a T4-T6 laminectomy for complete resection of the lesion. CD163 and CD68 studies highlighted a small, spindled-shaped tumor with occasionally enlarged histiocytes without co-positivity for S100. Pathologically, the lesion was considered an isolated intramedullary thoracic LCH.

Conclusion: A 76-year-old male presented with progressive paraparesis of 1 month's duration attributed to an enhanced MR-documented T5 single intramedullary T5 thoracic LCH that was successfully resected.

背景:组织细胞肿瘤的定义是过多的组织细胞积聚在各种组织中,包括皮肤、骨骼、淋巴结和中枢神经系统。病例描述:一名76岁男性,表现为缓慢进行性双侧下肢无力(即右>左)一个月,伴T7以下左侧感觉下降。增强胸部磁共振(MR)成像显示在T5水平有一个硬膜内髓内结节,从C7延伸到T10。患者接受了T4-T6椎板切除术以完全切除病变。CD163和CD68的研究强调了一个小的纺锤形肿瘤,偶尔有增大的组织细胞,没有S100的共阳性。病理上,病变被认为是一个孤立的髓内胸椎LCH。结论:一名76岁男性表现为持续1个月的进行性麻痹,原因是mr增强记录的T5单发髓内T5胸椎LCH已成功切除。
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引用次数: 0
Dynamic changes of abnormal muscle response during decompression procedures in double compression-type hemifacial spasm. 双压迫型面肌痉挛减压过程中异常肌肉反应的动态变化。
Pub Date : 2024-11-22 eCollection Date: 2024-01-01 DOI: 10.25259/SNI_768_2024
Keita Fujii, Kentaro Mori, Akira Tamase, Hiroshi Shima, Motohiro Nomura, Tetsuya Yamamoto

Background: Hemifacial spasm (HFS) is a neurovascular movement caused by vascular compression of the facial nerve in its root exit zone (REZ). Cases of HFS caused by double compression (DC) in both REZ and the cisternal portion (CP) have been sporadically reported. The nature of DC-type HFS is still not fully understood. Compression in CP is often overlooked, resulting in reoperation in DC-type HFS cases.

Case description: A 48-year-old man with a 3-year history of left HFS was admitted to our department. Magnetic resonance imaging revealed that the vertebral artery (VA) passed around REZ of the facial nerve, and the anterior inferior cerebellar artery (AICA) was in contact with the facial nerve in CP. Microvascular decompression was performed while monitoring any abnormal muscle response (AMR). Although VA was dissected and detached from REZ, AMR showed only a transient decrease and the amplitude of the AMR wave soon recovered and subsequently increased. No other vessels compressing REZ beneath VA were found. AICA attached to the facial nerve in CP and was compressed upward by VA. When AICA was moved from the facial nerve in CP after the transposition of VA, AMR was immediately resolved. After surgery, the patient was completely free from HFS.

Conclusion: In DC-type HFS, precise preoperative diagnosis and intraoperative identification of the culprit vessel are difficult. In DC-type HFS, decompression of one side of a vessel may exacerbate the compression of the other side. In such a case, AMR helps us become aware of compressions in CP that we may preoperatively overlook. AMR is useful for identifying the exact culprit vessels and recognizing any compression changes caused by intraoperative manipulations.

背景:面神经痉挛(HFS)是由于面神经根出口区(REZ)受到血管压迫而引起的神经血管运动。双压缩(DC)引起的HFS在REZ和池部分(CP)已经零星报道。dc型HFS的性质尚不完全清楚。CP受压常被忽视,导致dc型HFS病例再次手术。病例描述:我科收治一名48岁男性,有3年左侧HFS病史。磁共振成像显示椎动脉(VA)绕过面神经REZ,小脑前下动脉(AICA)与面神经接触。在监测异常肌肉反应(AMR)的同时进行微血管减压。虽然VA被解剖并与REZ分离,但AMR仅表现出短暂的下降,AMR波的振幅很快恢复并随后增加。在VA下方没有发现其他压缩REZ的血管。AICA附着于CP面神经上,被VA向上压缩。VA转位后,当AICA移离CP面神经时,AMR立即得到解决。手术后,患者完全摆脱了HFS。结论:dc型HFS术前难准确诊断,术中难准确识别罪魁祸首血管。在dc型HFS中,一侧血管的减压可能加剧另一侧血管的受压。在这种情况下,AMR帮助我们意识到术前可能忽略的CP压迫。AMR对于确定确切的罪魁祸首血管和识别术中操作引起的任何压缩变化是有用的。
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引用次数: 0
期刊
Surgical neurology international
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