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Preventable cerebral venous sinus thrombosis from diet- and alcohol-induced hyperhomocysteinemia: illustrative case. 饮食和酒精引起的高同型半胱氨酸血症可预防的脑静脉窦血栓形成:说明性病例。
Pub Date : 2026-01-26 DOI: 10.3171/CASE25759
Saaya Maruyama, Kiyoyuki Yanaka, Minami Saura, Toshihide Takahashi, Hitoshi Aiyama, Aiki Marushima, Eiichi Ishikawa

Background: Cerebral venous sinus thrombosis (CVST) is a rare stroke subtype (0.5%-3%) that frequently presents with nonspecific symptoms, delaying diagnosis. Although hyperhomocysteinemia is a known risk factor, acquired cases resulting from severe vitamin B12 and folate deficiencies can be easily overlooked by clinicians in any setting, making this a critical yet preventable cause of life-threatening thrombosis.

Observations: A 44-year-old man with obesity, who adopted a carbohydrate-heavy diet and consumed excessive alcohol (70-140 g/day) following a major life event 3 years prior, presented with worsening headache, somnolence, and right-sided neurological deficits. Imaging confirmed CVST with bilateral parietal venous infarction and left-sided hemorrhage. Severe hyperhomocysteinemia (143.4 nmol/mL) secondary to critically low vitamin B12 and folate levels was identified, likely induced by these lifestyle changes. Anticoagulation therapy, vitamin supplementation, alcohol cessation, and nutritional counseling improved clinical symptoms, with normalization of homocysteine levels within 30 days, despite persistent evidence of brain tissue damage on imaging.

Lessons: This case highlights the serious consequences of severe vitamin deficiencies, triggered by lifestyle changes, in causing significant CVST, regardless of location. It emphasizes the importance of prioritizing detailed history-taking to identify modifiable lifestyle factors, facilitating timely intervention to manage symptoms, normalize homocysteine levels, and prevent recurrence. https://thejns.org/doi/10.3171/CASE25759.

背景:脑静脉窦血栓形成(CVST)是一种罕见的卒中亚型(0.5%-3%),通常表现为非特异性症状,延迟诊断。虽然高同型半胱氨酸血症是一个已知的危险因素,但在任何情况下,由严重维生素B12和叶酸缺乏引起的获得性病例很容易被临床医生忽视,使其成为危及生命的血栓形成的一个关键但可预防的原因。观察:一名44岁的肥胖男性,3年前发生重大生活事件后,采用高碳水化合物饮食并过量饮酒(70-140克/天),表现为头痛加重、嗜睡和右侧神经功能障碍。影像学证实CVST伴双侧顶静脉梗死及左侧出血。严重的高同型半胱氨酸血症(143.4 nmol/mL)继发于维生素B12和叶酸水平极低,可能是由这些生活方式的改变引起的。抗凝治疗、补充维生素、戒酒和营养咨询可改善临床症状,同型半胱氨酸水平在30天内恢复正常,尽管影像学上仍有脑组织损伤的证据。经验教训:该病例强调了由生活方式改变引发的严重维生素缺乏的严重后果,无论在何处,都可能导致严重的CVST。它强调了优先详细记录病史的重要性,以确定可改变的生活方式因素,促进及时干预以控制症状,使同型半胱氨酸水平正常化,并防止复发。https://thejns.org/doi/10.3171/CASE25759。
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引用次数: 0
Pregnancy-related aggressive vertebral hemangioma presenting with radiculopathy: illustrative case. 以神经根病为表现的妊娠相关侵袭性椎体血管瘤:说明性病例。
Pub Date : 2026-01-26 DOI: 10.3171/CASE25860
Cafer Ikbal Gulsever, Serdar Solmaz, Metehan Ozturk

Background: Aggressive vertebral hemangiomas are uncommon vascular spinal lesions that may enlarge during pregnancy due to hormonal and hemodynamic changes. Elevated estrogen and progesterone levels, increased blood volume, and venous congestion can lead to rapid lesion expansion and epidural extension, causing neurological deficits. Although rare, these lesions should be considered in pregnant or postpartum women presenting with back or radicular pain.

Observations: A 30-year-old woman with epilepsy controlled by lamotrigine developed progressive low back and right leg pain during late pregnancy, worsening postpartum. MRI revealed an aggressive L4 vertebral hemangioma with epidural extension compressing the thecal sac and right L4 nerve root. The patient underwent L4 laminectomy, excision of the epidural component, and vertebroplasty. Persistent bleeding after initial posterior cement injection required a second injection through the left pedicle to fill the superior vertebral body, followed by fibrin glue application. She was mobilized on the 1st postoperative day, and her symptoms resolved completely.

Lessons: Pregnancy-related aggressive vertebral hemangioma should be suspected in women with new-onset neurological symptoms during pregnancy or postpartum. Early diagnosis, multidisciplinary planning, and timely decompression with vertebroplasty yield excellent neurological recovery and functional outcomes. https://thejns.org/doi/10.3171/CASE25860.

背景:侵袭性椎体血管瘤是一种罕见的椎管病变,在妊娠期间由于激素和血流动力学的改变而扩大。雌激素和黄体酮水平升高、血容量增加和静脉充血可导致病变迅速扩张和硬膜外延伸,引起神经功能障碍。虽然罕见,但在孕妇或产后出现背痛或神经根性疼痛时应考虑这些病变。观察:一名30岁癫痫患者在妊娠后期出现进行性腰背部和右腿疼痛,产后加重。MRI显示侵袭性L4椎体血管瘤伴硬膜外延伸压迫硬膜囊和右侧L4神经根。患者接受了L4椎板切除术、硬膜外部分切除和椎体成形术。首次后路骨水泥注射后持续出血需要通过左椎弓根第二次注射以填充上椎体,然后应用纤维蛋白胶。术后第1天即可活动,症状完全消失。经验教训:妊娠相关的侵袭性椎体血管瘤应怀疑妇女新发神经系统症状在怀孕期间或产后。早期诊断、多学科规划和及时椎体成形术减压可获得良好的神经恢复和功能预后。https://thejns.org/doi/10.3171/CASE25860。
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引用次数: 0
Posterior hypopharyngeal perforation following two-level anterior cervical discectomy and fusion: illustrative case. 两节段前路颈椎椎间盘切除术和融合术后后下咽穿孔:说明性病例。
Pub Date : 2026-01-26 DOI: 10.3171/CASE25513
Clarence Sumbizi, Orujul Hassan, Ebenezer Hawanga, Edward Kijazi, Allyzain Ismail, Zainab Fidaali, Mahmoud Abdulaal, Athar Ali, Ally Mwanga, Mugisha Clement

Background: Posterior hypopharyngeal perforation is a rare yet serious complication of anterior cervical discectomy and fusion (ACDF), especially at upper cervical levels where anatomical relationships are critical. Prompt recognition and tailored management are key to minimizing morbidity and achieving favorable outcomes.

Observations: The authors report the case of a 54-year-old man who underwent ACDF at C3-5 for cervical disc prolapse. Within hours postoperatively, he developed a sore throat, hypersalivation, subcutaneous emphysema, and anterior neck swelling. Initial imaging showed emphysema without contrast leakage, prompting empiric conservative management with nothing by mouth, intravenous antibiotics, steroids, and proton pump inhibitor. A contrast-enhanced CT study on day 7 revealed a 5.3 × 4.7-mm (length × thickness) posterior hypopharyngeal fistulous tract with contrast leakage but no collection. The patient improved with nonoperative management and close outpatient follow-up, gaining 2 kg over 4 weeks. Follow-up imaging at week 4 confirmed tract resolution, and oral feeding was reintroduced with progressive dietary advancement.

Lessons: Early hypopharyngeal perforation following ACDF may present subtly. High clinical suspicion, even in the absence of early imaging findings, is essential. Contained injuries without systemic deterioration may be successfully treated with conservative therapy, including nutritional support and imaging-guided follow-up. This case underscores the importance of vigilance and individualized management. https://thejns.org/doi/10.3171/CASE25513.

背景:后下咽穿孔是颈前路椎间盘切除术融合术(ACDF)中一种罕见但严重的并发症,特别是在解剖关系至关重要的颈椎上节段。及时识别和量身定制的管理是减少发病率和获得良好结果的关键。观察:作者报告了一例54岁男性因颈椎间盘突出在C3-5行ACDF的病例。术后数小时内,患者出现喉咙痛、唾液分泌过多、皮下肺气肿和颈前肿胀。初步影像学显示肺气肿,无造影剂渗漏,提示经验性保守治疗,不口服,静脉注射抗生素,类固醇和质子泵抑制剂。第7天的CT增强检查显示一个5.3 × 4.7 mm(长×厚)的下咽后瘘道,有造影剂渗漏但未收集。经非手术治疗及密切门诊随访,患者病情有所改善,4周内体重增加2公斤。第4周的随访成像证实了呼吸道的溶解,随着饮食的进展,重新开始口服喂养。经验教训:ACDF后早期下咽穿孔可能不易察觉。即使在没有早期影像学发现的情况下,高度的临床怀疑也是必不可少的。保守治疗包括营养支持和影像学引导下的随访,可成功治疗无全身性恶化的内源性损伤。这个案例强调了警惕和个性化管理的重要性。https://thejns.org/doi/10.3171/CASE25513。
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引用次数: 0
Normal pressure hydrocephalus plus atypical presentation with symptomatic resolution following the restoration of CSF flow: illustrative case. 正常压力脑积水加上不典型的表现,在脑脊液血流恢复后症状消退:说明性病例。
Pub Date : 2026-01-26 DOI: 10.3171/CASE25620
Jordan Hatfield, Kennedy Carpenter, Jordan Komisarow, Allan Friedman, Joel Morgenlander

Background: Normal pressure hydrocephalus (NPH) is a condition characterized by enlarged intracerebral ventricles with normal intracranial pressure. The typical clinical presentation includes cognitive decline, gait disturbances, and urinary incontinence. While the classic triad of symptoms is well documented, atypical presentations, including focal deficits and aphasia, pose significant diagnostic challenges.

Observations: This is the case of a previously healthy 70-year-old patient presenting with rapidly progressive gait disturbances, right hemiplegia, cognitive decline, and mutism. The focal presentation suggested a left hemispheric cerebrovascular insufficiency. A comprehensive diagnostic workup, including serial imaging, lumbar punctures, and electroencephalography, was undertaken given diagnostic uncertainty. Initial evaluations suggested a left hemispheric stroke or neurodegenerative process, ultimately delaying the definitive diagnosis and treatment of NPH. MRI revealed progressive ventriculomegaly and white matter changes prompting a lumbar drain trial. This yielded clinical improvement and ventriculoperitoneal shunt placement. Postoperatively, the patient had complete resolution of symptoms and returned to a normal functional status within 6 weeks.

Lessons: This case demonstrates the diagnostic challenges in differentiating NPH from stroke or neurodegenerative disorders. Recognizing its varied presentations and distinguishing them from other diseases is crucial for initiating appropriate treatment. Early intervention improved this patient's outcome and prevented unnecessary morbidity, demonstrating the significant impact of accurate and timely diagnosis. https://thejns.org/doi/10.3171/CASE25620.

背景:常压脑积水(NPH)是一种以脑室增大而颅内压正常为特征的疾病。典型的临床表现包括认知能力下降、步态障碍和尿失禁。虽然经典的三联症状有很好的记录,但非典型表现,包括局灶性缺陷和失语,构成了重大的诊断挑战。观察:本病例为70岁健康患者,表现为快速进行性步态障碍、右半瘫、认知能力下降和失语。病灶表现提示左半球脑血管功能不全。由于诊断不确定,我们进行了全面的诊断检查,包括连续影像学检查、腰椎穿刺和脑电图检查。最初的评估提示左半球中风或神经退行性过程,最终延迟了NPH的明确诊断和治疗。MRI显示进行性脑室肿大和白质改变,提示腰椎引流试验。这带来了临床改善和脑室腹腔分流安置。术后6周内,患者症状完全缓解,功能恢复正常。经验教训:本病例显示了诊断NPH与中风或神经退行性疾病的鉴别挑战。认识到其不同的表现并将其与其他疾病区分开来,对于开始适当的治疗至关重要。早期干预改善了该患者的预后,防止了不必要的发病率,显示了准确和及时诊断的显著影响。https://thejns.org/doi/10.3171/CASE25620。
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引用次数: 0
Sinking skin flap syndrome masquerading as Chiari malformation: failed syringomyelia treatment rescued by cranioplasty. Illustrative case. 伪装为Chiari畸形的下沉皮瓣综合征:采用颅骨成形术挽救脊髓空洞治疗失败。说明情况。
Pub Date : 2026-01-26 DOI: 10.3171/CASE25763
Jin-Young Kim, Jung-Woo Hur, Jae Taek Hong

Background: Syringomyelia is most often associated with Chiari malformation, for which posterior fossa decompression is the standard treatment. Treatment failure should raise suspicion for alternative mechanisms, particularly in patients with a history of supratentorial craniectomy. In such cases, sinking skin flap syndrome (SSFS) may alter intracranial-extracranial pressure gradients, impair CSF dynamics, and result in an acquired Chiari malformation with secondary syrinx formation.

Observations: A 64-year-old man with a remote supratentorial decompressive craniectomy for intracerebral hemorrhage presented with progressive headache, neck pain, and bilateral arm paresthesia. MRI revealed tonsillar herniation with syringomyelia. Posterior fossa decompression led to initial symptom relief and reduction of the syrinx. Three months later, he developed new bilateral leg sensory deficits, and follow-up MRI showed syrinx recurrence despite adequate decompression and no arachnoid adhesions. Because of prior cranioplasty-related infection, he hesitated to undergo further surgery, but ultimately cranioplasty was performed. Postoperatively, symptoms improved, with sustained clinical recovery and syrinx regression confirmed on serial MRI at 12 and 24 months.

Lessons: Persistent or recurrent syringomyelia after Chiari decompression should prompt evaluation for acquired causes. SSFS may mimic primary Chiari malformation; in such cases, cranioplasty can restore CSF dynamics and achieve durable syrinx resolution. https://thejns.org/doi/10.3171/CASE25763.

背景:脊髓空洞最常与Chiari畸形相关,后窝减压是标准治疗方法。治疗失败应引起对其他机制的怀疑,特别是有幕上颅骨切除术史的患者。在这种情况下,下沉皮瓣综合征(SSFS)可能改变颅内-颅外压力梯度,损害CSF动力学,并导致获得性Chiari畸形伴继发性鼻管形成。观察:一名64岁男性,因脑出血行远端幕上减压颅脑切除术,表现为进行性头痛、颈部疼痛和双侧手臂感觉异常。MRI显示扁桃体疝伴脊髓空洞。后颅窝减压使症状得到缓解,鼻窦复位。3个月后,患者出现新的双侧腿感觉障碍,尽管进行了充分的减压且无蛛网膜粘连,但后续MRI显示鼻窦复发。由于先前的颅骨成形术相关感染,他犹豫是否接受进一步的手术,但最终进行了颅骨成形术。术后症状改善,12个月和24个月的连续MRI证实临床持续恢复和鼻音消退。经验教训:持续性或复发性脊髓空洞后,应及时评估获得性原因。SSFS可能模仿原发性Chiari畸形;在这种情况下,颅骨成形术可以恢复脑脊液动力学并实现持久的鼻窦溶解。https://thejns.org/doi/10.3171/CASE25763。
{"title":"Sinking skin flap syndrome masquerading as Chiari malformation: failed syringomyelia treatment rescued by cranioplasty. Illustrative case.","authors":"Jin-Young Kim, Jung-Woo Hur, Jae Taek Hong","doi":"10.3171/CASE25763","DOIUrl":"10.3171/CASE25763","url":null,"abstract":"<p><strong>Background: </strong>Syringomyelia is most often associated with Chiari malformation, for which posterior fossa decompression is the standard treatment. Treatment failure should raise suspicion for alternative mechanisms, particularly in patients with a history of supratentorial craniectomy. In such cases, sinking skin flap syndrome (SSFS) may alter intracranial-extracranial pressure gradients, impair CSF dynamics, and result in an acquired Chiari malformation with secondary syrinx formation.</p><p><strong>Observations: </strong>A 64-year-old man with a remote supratentorial decompressive craniectomy for intracerebral hemorrhage presented with progressive headache, neck pain, and bilateral arm paresthesia. MRI revealed tonsillar herniation with syringomyelia. Posterior fossa decompression led to initial symptom relief and reduction of the syrinx. Three months later, he developed new bilateral leg sensory deficits, and follow-up MRI showed syrinx recurrence despite adequate decompression and no arachnoid adhesions. Because of prior cranioplasty-related infection, he hesitated to undergo further surgery, but ultimately cranioplasty was performed. Postoperatively, symptoms improved, with sustained clinical recovery and syrinx regression confirmed on serial MRI at 12 and 24 months.</p><p><strong>Lessons: </strong>Persistent or recurrent syringomyelia after Chiari decompression should prompt evaluation for acquired causes. SSFS may mimic primary Chiari malformation; in such cases, cranioplasty can restore CSF dynamics and achieve durable syrinx resolution. https://thejns.org/doi/10.3171/CASE25763.</p>","PeriodicalId":94098,"journal":{"name":"Journal of neurosurgery. Case lessons","volume":"11 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-01-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12839449/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146055799","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
Electrical stimulation properties of carbon fiber versus titanium pedicle screw instrumentation: illustrative case. 碳纤维与钛椎弓根螺钉置入的电刺激特性:说明性案例。
Pub Date : 2026-01-26 DOI: 10.3171/CASE25786
Joseph Dardick, Jawad M Khalifeh, Yuanxuan Xia, Tej D Azad, Nicholas Theodore, Sang Hun Lee, Daniel Lubelski

Background: Carbon fiber (CF) instrumentation is a useful tool for the treatment of spinal oncological disease. CF produces less instrumentation artifact on imaging, facilitating radiation planning and oncological monitoring. CF screws have different physical properties than traditional titanium, leading to decreased manual feedback during placement. Electromyography (EMG) monitoring is an intraoperative adjunct to assist in safe screw placement. While titanium and CF have different electrical properties, there is no literature comparing their responses to intraoperative stimulation.

Observations: The authors present a case of mobile spine chordoma at L1 previously stabilized at an outside hospital. During en bloc resection, asymptomatic titanium screws at L2 were replaced with CF-reinforced PEEK (CFR-PEEK) (Icotec). Stimulation of the CFR-PEEK screws at 2 mA resulted in quadriceps EMG firing. Titanium screws at L3 required 10 mA of stimulation to produce an EMG signal (DePuy Synthes). Intraoperative CT demonstrated optimal screw placement. Postoperatively, the patient was neurologically intact. In ex vivo analysis, the CFR-PEEK screw exhibited increased resistivity and decreased conductivity compared to an analogous titanium screw.

Lessons: Surgeons and intraoperative monitoring teams should be aware of lower EMG stimulation thresholds for CF screws than titanium. Additional adjuncts, such as intraoperative imaging, may be helpful in these cases. https://thejns.org/doi/10.3171/CASE25786.

背景:碳纤维(CF)仪器是治疗脊柱肿瘤疾病的有用工具。CF在成像上产生较少的仪器伪影,有利于放射规划和肿瘤监测。CF螺钉具有与传统钛不同的物理特性,因此在放置过程中减少了人工反馈。肌电图(EMG)监测是术中辅助辅助,以协助安全放置螺钉。虽然钛和CF具有不同的电特性,但没有文献比较它们对术中刺激的反应。观察:作者报告了一例L1的活动脊索瘤,此前在一家外医院稳定。在整体切除期间,将L2无症状钛螺钉替换为cf增强PEEK (CFR-PEEK) (Icotec)。2 mA CFR-PEEK螺钉刺激导致股四头肌肌电图放电。L3处的钛螺钉需要10ma的刺激才能产生肌电图信号(DePuy Synthes)。术中CT显示最佳螺钉放置。术后,患者神经功能完好。在离体分析中,与类似的钛螺钉相比,CFR-PEEK螺钉表现出更高的电阻率和更低的导电性。经验教训:外科医生和术中监护小组应该意识到CF螺钉的肌电刺激阈值低于钛。其他辅助手段,如术中成像,在这些情况下可能会有所帮助。https://thejns.org/doi/10.3171/CASE25786。
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引用次数: 0
Spontaneous regression of a large lateral ventricle cyst: illustrative case. 大侧脑室囊肿自发性消退:说明性病例。
Pub Date : 2026-01-26 DOI: 10.3171/CASE25319
Adrien Lavalley, Andrea Bartoli

Background: Colloid cysts (CCs) are rare benign lesions, typically found in the third ventricle. While most CCs remain asymptomatic, they can occasionally cause significant symptoms such as headaches, visual disturbances, seizures, and, in rare cases, sudden death.

Observations: This article reports a rare case of spontaneous regression of a CC located in the lateral ventricle. After remaining stable for more than 4 years, the cyst underwent spontaneous regression.

Lessons: This case challenges existing ideas regarding the origin and regression mechanisms of CCs. It demonstrates that lateral ventricle CCs can spontaneously regress, highlighting the need to reconsider their embryological origin, their natural history, and the role of surgery. However, the diagnosis of CC has been solely radiological, and other forms of tumor-like cystic lesions, such as neuroepithelial or ependymal cysts, should be taken into consideration. https://thejns.org/doi/10.3171/CASE25319.

背景:胶质囊肿是一种罕见的良性病变,多见于第三脑室。虽然大多数cc没有症状,但它们偶尔会引起明显的症状,如头痛、视觉障碍、癫痫发作,在极少数情况下还会导致猝死。观察:本文报告一例罕见的侧脑室CC自发性消退的病例。在保持稳定4年后,囊肿自然消退。经验教训:本案例挑战了关于CCs起源和回归机制的现有观点。这表明侧脑室cc可以自发退化,强调需要重新考虑其胚胎起源,其自然史和手术的作用。然而,CC的诊断仅仅是影像学上的,其他形式的肿瘤样囊性病变,如神经上皮囊肿或室管膜囊肿,应考虑在内。https://thejns.org/doi/10.3171/CASE25319。
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引用次数: 0
Successful treatment of aneurysmal subarachnoid hemorrhage in polyarteritis nodosa with immunosuppressive therapy: illustrative case. 免疫抑制疗法成功治疗结节性多动脉炎动脉瘤性蛛网膜下腔出血:说明性病例。
Pub Date : 2026-01-26 DOI: 10.3171/CASE25617
Tomoya Yagisawa, Kenji Ibayashi, Rintaro Kuroda, Yasuyuki Kamata, Katsunari Namba, Naoto Kunii, Kensuke Kawai

Background: The incidence of cerebral aneurysms in polyarteritis nodosa (PN) is low, and reports of subarachnoid hemorrhage (SAH) in patients with PN are even rarer. The necessity of head imaging may be underestimated, particularly when the patient is in remission.

Observations: A 20-year-old female with PN, who had been in remission following anti-interleukin-6 receptor antibody therapy, developed SAH and was admitted to the authors' department. Cerebral angiography revealed multiple beaded changes in both carotid and vertebral arterial systems, along with several small aneurysms. These findings posed substantial difficulty in identifying the bleeding source and proceeding with surgical intervention. Therefore, the authors intensified the immunosuppressive therapy targeting the underlying PN. The patient remained free from rebleeding, her headaches and other symptoms resolved, and she was discharged in ambulatory condition. Follow-up MR angiography 3 months after discharge confirmed resolution of the small aneurysms.

Lessons: This case suggests that enhanced immunosuppressive therapy may be effective in treating both extracranial and intracranial vascular lesions in PN. In patients with PN, early and serial head imaging may be beneficial. The appearance of de novo aneurysms in the context of disease progression may indicate the need for more aggressive treatment. https://thejns.org/doi/10.3171/CASE25617.

背景:结节性多动脉炎(PN)中脑动脉瘤的发生率较低,而PN患者蛛网膜下腔出血(SAH)的报道更为罕见。头部成像的必要性可能被低估了,特别是当患者处于缓解期时。观察:一名20岁女性PN患者,在抗白细胞介素-6受体抗体治疗后缓解,发展为SAH,并被送入作者所在科室。脑血管造影显示在颈动脉和椎动脉系统有多个串珠状改变,并伴有几个小动脉瘤。这些发现给确定出血来源和进行手术治疗带来了很大的困难。因此,作者加强了针对潜在PN的免疫抑制治疗。患者无再出血,头痛等症状消失,出院时可走动。出院后3个月随访磁共振血管造影证实小动脉瘤消退。结论:本病例提示强化免疫抑制治疗可能有效治疗PN的颅外和颅内血管病变。对于PN患者,早期和连续的头部成像可能是有益的。在疾病进展的背景下,新动脉瘤的出现可能表明需要更积极的治疗。https://thejns.org/doi/10.3171/CASE25617。
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引用次数: 0
Unilateral biportal endoscopic surgery for intradural lumbar disc herniation: illustrative case. 单侧双门静脉内窥镜手术治疗硬膜内腰椎间盘突出症:说明性病例。
Pub Date : 2026-01-26 DOI: 10.3171/CASE25795
Xuyang Xu, Ayesha Habiba Jamal, Zijie Wang, Jianghu Chen, Xuanming Chang, Jiandong Yang, Zhiqiang Zhang

Background: The authors successfully removed a type B intradural lumbar disc herniation (IDH) using unilateral biportal endoscopic (UBE) technology, without CSF leakage, even though the nerve root sheath was not sutured. This emphasizes the diagnostic and therapeutic role of UBE technology in managing type B IDH.

Observations: An 82-year-old male patient with multilevel lumbar disc herniation underwent endoscopic discectomy and lumbar laminoplasty at the symptomatic level using UBE technology. During surgery, under endoscopic visualization, a white, mass-like protrusion was observed on the surface of the responsible nerve root, consistent with type B IDH. The nerve root sheath was incised, and the herniated nucleus pulposus was successfully removed without CSF leakage. The nerve root sheath was left open without repair.

Lessons: Using UBE technology to treat lumbar disc herniation, if an abnormal bulge or white, mass-like protrusion is observed on the nerve root under endoscopic visualization, clinicians should highly suspect the presence of type B IDH. In such cases, the nerve root sheath can be incised along the direction of the nerve root to safely remove the herniated disc material. Notably, repair of the nerve root sheath is not required, and no CSF leakage occurred in this case. https://thejns.org/doi/10.3171/CASE25795.

背景:作者使用单侧双门静脉内窥镜(UBE)技术成功切除了B型硬膜内腰椎间盘突出症(IDH),即使神经根鞘没有缝合,也没有脑脊液泄漏。这强调了UBE技术在治疗B型IDH中的诊断和治疗作用。观察:一位82岁男性多节段腰椎间盘突出症患者在症状水平采用UBE技术行内镜下腰椎间盘切除术和腰椎板成形术。术中内镜下可见神经根表面白色肿块样突出,符合B型IDH。切开神经根鞘,成功切除髓核突出,无脑脊液渗漏。神经根鞘未修复而保持开放。经验教训:使用UBE技术治疗腰椎间盘突出症,如果在内镜下观察到神经根异常隆起或白色肿块样突出,临床医生应高度怀疑B型IDH的存在。在这种情况下,可以沿着神经根的方向切开神经根鞘,以安全地取出突出的椎间盘。值得注意的是,不需要修复神经根鞘,本病例未发生脑脊液漏。https://thejns.org/doi/10.3171/CASE25795。
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引用次数: 0
Resolution of severe lumbar spinal epidural lipomatosis following tirzepatide-induced weight loss: illustrative case. 替西肽所致体重减轻后严重腰椎硬膜外脂肪增多症的解决:说明性病例。
Pub Date : 2026-01-26 DOI: 10.3171/CASE25886
Masih Tazhibi, David D Liu, Joshua I Chalif, Rohaid Ali, John H Chi

Background: Spinal epidural lipomatosis (SEL) is a rare disorder characterized by pathological accumulation of adipose tissue in the spinal epidural space, leading to signs and symptoms of lumbar stenosis. SEL is increasingly linked to obesity, and treatment requires surgical decompression if conservative measures fail. The role of modern pharmacological weight-loss agents in reversing SEL has not been previously described.

Observations: A 35-year-old man with severe, symptomatic lumbar SEL and class II obesity (BMI 37.8 kg/m) presented with progressive neurogenic claudication and functional decline. MRI revealed multilevel lumbar SEL with severe spinal stenosis. After counseling, the patient initiated tirzepatide therapy and achieved approximately 60 pounds of weight loss within 1 year. This was accompanied by marked symptom resolution and near-complete regression of epidural fat on repeat MRI, negating the need for surgical intervention.

Lessons: This case demonstrates that pharmacological weight loss with agents such as tirzepatide may offer a viable, nonoperative alternative for patients with obesity-related SEL, particularly those who are not ideal surgical candidates. Validation in larger studies is needed to assess long-term efficacy and help guide patient selection for pharmacological versus surgical approaches. https://thejns.org/doi/10.3171/CASE25886.

背景:脊髓硬膜外脂肪增多症(SEL)是一种罕见的疾病,其特征是脂肪组织在脊髓硬膜外间隙的病理性积累,导致腰椎狭窄的体征和症状。SEL与肥胖的关系越来越密切,如果保守措施失败,治疗需要手术减压。现代减肥药在逆转SEL中的作用以前没有被描述过。观察:一名35岁男性,患有严重的症状性腰椎SEL和II级肥胖(BMI 37.8 kg/m),表现为进行性神经源性跛行和功能下降。MRI显示多节段腰椎SEL伴严重椎管狭窄。经咨询,患者开始使用替西帕肽治疗,1年内体重减轻约60磅。这伴有明显的症状缓解和重复MRI显示硬膜外脂肪几乎完全消退,无需手术干预。经验教训:本病例表明,替西帕肽等药物可能为肥胖相关SEL患者提供一种可行的非手术替代方案,特别是那些不适合手术治疗的患者。需要在更大规模的研究中进行验证,以评估长期疗效,并帮助指导患者选择药物治疗还是手术治疗。https://thejns.org/doi/10.3171/CASE25886。
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Journal of neurosurgery. Case lessons
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