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Filter-type Protection Device Retrieval Interfered by Deployed Stent during Subclavian Artery Stenosis Treatment: Case Report and Complication Avoidance Recommendation. 锁骨下动脉狭窄治疗中过滤器式保护装置回收受支架部署干扰:1例报告及避免并发症的建议。
Pub Date : 2023-10-14 eCollection Date: 2023-01-01 DOI: 10.2176/jns-nmc.2023-0146
Nobuyuki Mitsui, Manabu Kinoshita, Junji Nakazawa, Hirokazu Ozaki, Teruo Kimura
Endovascular treatment is a standard procedure for subclavian artery stenosis or obstruction. However, great care should be taken to avoid embolic complications to the vertebral artery, and several methods have previously been reported. Hence, as surgical procedures become increasingly complicated, unintended issues may arise during treatment. Here, the authors report a case where the filter-type protection device was caught in the stent because the patient moved during treatment, leading to open surgery to recover the filter-type protection device. A 78-year-old female suffering from a left subclavian steal syndrome underwent stenting due to subclavian artery stenosis. The stenotic lesion was approached via the transfemoral route, and a filter-type protection device was advanced to the vertebral artery via the transbrachial route to prevent embolic complications. As the procedure was performed under local anesthesia, the patient moved during stent deployment proximally to the left vertebral artery origin, and the stent unintentionally advanced distally, covering the vertebral artery and obstructing the retrieval catheter for the filter-type protection device to advance. Failed attempts in recovering the filter-type protection device required open surgery for retrieval. Fortunately, there was no postoperative neurological and radiographic complication, ameliorating her chief complaint. The retriever catheter for the protection device should be advanced beyond the vertebral artery orifice just proximal to the protection device before stenting to avoid such complications while also thoroughly considering the type of anesthesia during treatment.
血管内治疗是锁骨下动脉狭窄或梗阻的标准治疗方法。然而,应该非常小心,以避免栓塞并发症的椎动脉,并有几种方法已被报道。因此,随着外科手术变得越来越复杂,在治疗过程中可能会出现意想不到的问题。在这里,作者报告了一例由于患者在治疗过程中移动导致过滤器型保护装置卡在支架内,导致开放手术恢复过滤器型保护装置的病例。一位78岁的女性患有左锁骨下窃血综合征,由于锁骨下动脉狭窄,接受了支架植入术。经股动脉入路狭窄病灶,经肱动脉入路椎动脉推进滤过式保护装置,防止栓塞并发症。由于手术是在局部麻醉下进行的,在支架部署过程中,患者向左侧椎动脉起源近端移动,支架不自觉地向远端移动,覆盖椎动脉,阻塞了过滤式保护装置前进的取出导管。试图恢复过滤器式保护装置失败,需要开腹手术进行恢复。幸运的是,术后没有神经学和影像学并发症,改善了她的主诉。在支架置入前,保护装置的取物导管应提前至离保护装置近端的椎动脉口以外,以避免此类并发症的发生,同时在治疗过程中也应充分考虑麻醉的类型。
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引用次数: 0
Neoadjuvant Therapy with Everolimus for Subependymal Giant Cell Astrocytoma: A Case Report. 依维莫司新辅助治疗室管膜下巨细胞星形细胞瘤1例。
Pub Date : 2023-10-14 eCollection Date: 2023-01-01 DOI: 10.2176/jns-nmc.2022-0375
Hiroki Karita, Kyoji Tsuda, Maya Kono, Tetsuya Yamamoto, Satoshi Ihara

Direct surgical resection remains to be the standard treatment for tuberous sclerosis complex (TSC) with subependymal giant cell astrocytoma (SEGA). Medical therapy with everolimus (mammalian target of rapamycin inhibitor or mTOR) serves as a second-line treatment for patients with SEGA who are determined to be ineligible for surgical resection. Some recent studies have reported that neoadjuvant therapy for SEGA may be a useful, novel treatment. In this study, we herein present a case of SEGA and demonstrate the efficacy of preoperative everolimus therapy. We have also examined the utility and safety of neoadjuvant therapy for SEGA and investigated four previously reported cases of preoperative administration of mTOR inhibitors. In these cases, everolimus was administered preoperatively to shrink the tumor although the duration of treatment varied. Afterward, gross total tumor removal was conducted in all the cases. No postoperative complications were reported during the follow-up period. These findings indicate that neoadjuvant therapy with an mTOR inhibitor can be a potential treatment for SEGA. The findings of this present study also suggested that a short administration period of about 2 months may be sufficient to achieve preoperative tumor reduction.

直接手术切除仍然是结节性硬化症(TSC)合并室管膜下巨细胞星形细胞瘤(SEGA)的标准治疗方法。依维莫司(哺乳动物雷帕霉素靶点抑制剂或mTOR)的药物治疗可作为确定不适合手术切除的SEGA患者的二线治疗。最近的一些研究报道了SEGA的新辅助治疗可能是一种有用的新型治疗方法。在本研究中,我们在此报告一例SEGA,并证明术前依维莫司治疗的有效性。我们还研究了SEGA新辅助治疗的有效性和安全性,并调查了先前报道的4例术前使用mTOR抑制剂的病例。在这些病例中,术前给予依维莫司以缩小肿瘤,尽管治疗时间不同。所有病例均行肿瘤全切除。随访期间无术后并发症发生。这些发现表明mTOR抑制剂的新辅助治疗可能是SEGA的潜在治疗方法。本研究的结果还表明,约2个月的短给药期可能足以实现术前肿瘤缩小。
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引用次数: 0
Surgical Treatment for Metastatic Brain Tumor in the Cerebellar Hemisphere from Small-cell Neuroendocrine Carcinoma of the Urinary Bladder: A Case Report and Review of the Literature. 膀胱小细胞神经内分泌癌小脑半球转移性脑肿瘤的外科治疗:一例报告和文献复习。
Pub Date : 2023-09-29 eCollection Date: 2023-01-01 DOI: 10.2176/jns-nmc.2023-0058
Junki Sogano, Satoshi Takahashi, Nobuyuki Tanaka, Hajime Kubo, Hajime Okita, Mototsugu Oya, Masahiro Toda

We performed surgical treatment for cerebellar metastasis of relatively rare small-cell neuroendocrine carcinoma (SCNC) of the urinary bladder. On preoperative imaging, the lesion was solitary, and the edema around the tumor was unremarkable; thus, other differential diagnoses besides a metastatic brain tumor were also considered preoperatively. Intraoperatively, the tumor was soft, and the circumference brain and boundary were indistinct and easily hemorrhagic. The tumor was grossly totally removed, and postoperative radiotherapy was added. The clinical symptoms of the patient were relieved, and he was discharged on foot. Thus far, relatively few reports have described surgical treatment of brain metastases of SCNC of the urinary bladder. We herein report a case of metastatic brain tumor due to SCNC of the urinary bladder that required surgical treatment, along with a review of the previous literature regarding its clinical features and the characteristics of intracranial lesions related to surgery, such as imaging and intraoperative findings.

我们对相对罕见的膀胱小细胞神经内分泌癌(SCNC)的小脑转移进行了手术治疗。术前影像学检查,病灶为孤立性,肿瘤周围水肿不明显;因此,除转移性脑肿瘤外,术前还应考虑其他鉴别诊断。术中肿瘤较软,周围脑及边界模糊,易出血。肿瘤被大致完全切除,并增加了术后放疗。病人的临床症状得到缓解,步行出院。到目前为止,相对较少的报道描述了膀胱SCNC脑转移的手术治疗。我们在此报告了一例因膀胱SCNC而需要手术治疗的转移性脑肿瘤,并回顾了有关其临床特征和与手术相关的颅内病变特征的先前文献,如影像学和术中发现。
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引用次数: 0
Cerebral Venous Sinus Thrombosis Successfully Treated with Mechanical Thrombectomy under Intracranial Pressure Monitoring: A Case Report. 颅内压监测下机械性血栓切除术成功治疗脑静脉窦血栓形成1例报告。
Pub Date : 2023-09-29 eCollection Date: 2023-01-01 DOI: 10.2176/jns-nmc.2023-0076
Tatsuya Hagioka, Takeshi Shimizu, Shingo Toyota, Tomoaki Murakami, Takamune Achiha, Motohide Takahara, Kazuhiro Touhara, Yuhei Hoshikuma, Maki Kobayashi, Haruhiko Kishima

A 54-year-old man with no medical history presented to our hospital with vomiting, left hemiplegia, and seizures. On arrival, he was experiencing generalized tonic-clonic seizures, which required him to be intubated and deeply sedated. Contrast-enhanced computed tomography revealed extensive venous sinus obstruction from the superior sagittal sinus to the bilateral sigmoid sinus and cerebral edema with intracranial hemorrhage. An intracranial pressure (ICP) monitor was immediately placed intracranially, and mechanical thrombectomy (MT) was performed under ICP monitoring. MT was immediately terminated when the venous sinus was partially recanalized enough to decrease the ICP; then, anticoagulation therapy was initiated. Postoperative follow-up angiography revealed that venous sinus obstruction and intracranial venous perfusion improved over time. Although he had intracranial hemorrhage-induced left hemiplegia and sensory deficits, his condition improved with rehabilitation, and the patient was eventually discharged home. The indication criteria and techniques for MT for cerebral venous sinus thrombosis are yet to be established. As in this case, in patients with impaired consciousness due to intracranial hemorrhage or epilepsy, preoperative ICP monitor placement is deemed useful to evaluate venous perfusion during MT and decide the treatment goal.

一名无病史的54岁男子因呕吐、左侧偏瘫和癫痫发作到我们医院就诊。抵达后,他出现全身强直阵挛性癫痫发作,需要插管并服用深度镇静剂。对比增强计算机断层扫描显示从上矢状窦到双侧乙状窦的广泛静脉窦阻塞和脑水肿伴颅内出血。立即在颅内放置颅内压(ICP)监测仪,并在ICP监测下进行机械血栓切除术(MT)。当静脉窦部分再通足以降低ICP时,MT立即终止;然后开始抗凝治疗。术后随访血管造影术显示,静脉窦阻塞和颅内静脉灌注随着时间的推移而改善。尽管他有颅内出血引起的左侧偏瘫和感觉缺陷,但随着康复,他的病情有所改善,患者最终出院回家。MT治疗脑静脉窦血栓形成的适应症标准和技术尚待确定。在这种情况下,对于因颅内出血或癫痫导致意识受损的患者,术前放置ICP监测仪被认为有助于评估MT期间的静脉灌注并决定治疗目标。
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引用次数: 0
Spontaneous Intracranial Hypotension Occurring after Craniotomy for Brain Tumor Biopsy Mimicking Postoperative Bleeding. 模拟术后出血的脑肿瘤活检开颅术后自发性颅内低血压。
Pub Date : 2023-09-29 eCollection Date: 2023-01-01 DOI: 10.2176/jns-nmc.2023-0139
Joji Inamasu, Masashi Fujisawa, Mizuto Sato

In this study, we report on a previously healthy 44-year-old man who underwent an open biopsy under general anesthesia for a tumorous lesion found in his left frontal lobe via a small supratentorial craniotomy. While both postoperative course and brain computed tomography (CT) scans had been considered unremarkable, the patient became stuporous on postoperative day (POD) 4. A brain CT obtained on that day showed a subdural hematoma with marked brain shift which we thought might have been due to postoperative bleeding; he was immediately brought to an operating theater for hematoma removal. However, no bleeding source was found, and the brain remained depressed after hematoma evacuation. Furthermore, the brain shift remained unchanged on postoperative CT. While spontaneous intracranial hypotension (SIH) was considered, imaging studies to search for possible cerebrospinal fluid (CSF) leakage in the spinal column were not performed as the patient's condition has improved. However, he became stuporous again on POD 8, which urged us to perform CT myelogram. The CT myelogram showed a massive CSF leakage at the L1-L2 level. Subsequent autologous blood patch has successfully terminated the CSF leakage, and he became fully oriented shortly after the blood patch therapy. Thus, it should be noted that SIH may occur during postoperative period of intracranial surgery, and it may manifest radiographically as a subdural hematoma indistinguishable from postoperative bleeding. SIH should also be included in a differential diagnosis of postoperative headache, regardless of its characteristics, because headache associated with SIH may not always be orthostatic.

在这项研究中,我们报道了一名先前健康的44岁男子,他在全麻下通过幕上小开颅术对左额叶发现的肿瘤病变进行了开放性活检。虽然术后过程和大脑计算机断层扫描(CT)均被认为不显著,但患者在术后第4天(POD)变得麻木。当天的脑部CT显示,硬膜下血肿伴有明显的脑转移,我们认为这可能是由于术后出血所致;他立即被送到手术室进行血肿清除。然而,没有发现出血源,血肿清除后大脑仍处于抑郁状态。此外,术后CT检查中大脑移位保持不变。虽然考虑了自发性颅内低血压(SIH),但由于患者的病情有所改善,没有进行影像学研究来寻找脊柱中可能的脑脊液(CSF)渗漏。然而,他在POD 8上再次变得麻木,这促使我们进行CT骨髓图检查。CT骨髓图显示L1-L2水平的大量CSF渗漏。随后的自体血液贴剂成功地终止了CSF渗漏,在血液贴剂治疗后不久,他就完全定向了。因此,应该注意的是,SIH可能发生在颅内手术的术后阶段,它可能在放射学上表现为硬膜下血肿,与术后出血难以区分。SIH也应包括在术后头痛的鉴别诊断中,无论其特征如何,因为与SIH相关的头痛可能并不总是直立的。
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引用次数: 0
Hemifacial Spasm Caused by Vascular Compression of the Anterior Inferior Cerebellar Artery-Posterior Inferior Cerebellar Artery Common Trunk Anomaly at the Cisternal Portion of the Facial Nerve: A Case Report. 小脑前下动脉血管压迫引起的面痉挛面神经胸骨部小脑后下动脉总干异常1例。
Pub Date : 2023-09-29 eCollection Date: 2023-01-01 DOI: 10.2176/jns-nmc.2023-0125
Mariya Hokazono, Takafumi Shimogawa, Akira Nakamizo, Koji Yoshimoto

W report the first case of hemifacial spasm (HFS) caused by vascular compression of the anterior inferior cerebellar artery (AICA)-posterior inferior cerebellar artery (PICA) common trunk anomaly at the cisternal portion of cranial nerve VII (CN VII). A 71-year-old female with a typical right HFS was admitted to our hospital. As per her magnetic resonance (MR) imaging results, no offending arteries were noted around the CN VII root exit zone (REZ). Computed tomography angiography revealed an AICA-PICA common trunk anomaly with a dominant PICA, with the rostral branch of the AICA-PICA common trunk anomaly compressing the CN VII at the cisternal portion. The patient underwent microvascular decompression (MVD), and the HFS disappeared after surgery. The amplitude of the abnormal muscle responses (AMR) disappeared immediately after complete transposition of the offending artery. However, the patient experienced mild transient facial palsy 3 days after MVD which was eventually resolved with the administration of vitamin B12. No HFS recurrence was observed during the 1-year follow-up period. The AICA-PICA common trunk anomaly has been found to cause HFS as it compressed the CN VII at the cisternal portion, and not at the REZ. AMR monitoring might be helpful for cases where the unusual vessel particularly compresses the CN VII.

我们报告了第一例由小脑前下动脉(AICA)-小脑后下动脉(PICA)总干在颅神经VII池部分的血管压迫引起的面肌痉挛(HFS)(CN VII)。我们医院收治了一位71岁的女性,患有典型的右侧HFS。根据她的磁共振(MR)成像结果,在CN VII根出口区(REZ)周围没有发现侵犯性动脉。计算机断层扫描血管造影术显示AICA-PICA共同干异常,主要为PICA,AICA-PICA共同干异常的嘴侧支压迫池部的CN VII。患者接受了微血管减压(MVD),术后HFS消失。病变动脉完全移位后,异常肌肉反应(AMR)的振幅立即消失。然而,患者在MVD后3天出现轻度短暂性面瘫,最终通过服用维生素B12解决。在1年的随访期间,没有观察到HFS复发。AICA-PICA共干异常已被发现导致HFS,因为它在脑池部分而不是在REZ压缩了CN VII。AMR监测可能有助于异常血管特别压迫CN VII的情况。
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引用次数: 0
A Case of Ruptured Carotid Traumatic Blood Blister-like Aneurysm. 颈动脉外伤性血泡样动脉瘤破裂1例。
Pub Date : 2023-09-29 eCollection Date: 2023-01-01 DOI: 10.2176/jns-nmc.2023-0088
Yoshiyuki Matsumoto, Ryuta Nakae, Fumihiro Matano, Asami Kubota, Akio Morita, Yasuo Murai, Shoji Yokobori

Ruptured cerebral aneurysms that occur in the anterior wall of the internal carotid artery (ICA) are known as blood blister-like aneurysms (BBAs); they have been reported to account for 0.3% to 1% of all ruptured ICA aneurysms. In this report, we describe the treatment of an unusual traumatic BBA (tBBA) with high-flow bypass using a radial artery graft, which resulted in a favorable outcome. A 59-year-old female suffered from an acute epidural hematoma, traumatic subarachnoid hemorrhage, and traumatic carotid-cavernous sinus fistula (tCCF) after being involved in a motor vehicle accident. Her angiography results showed tCCF and a tBBA on the anterior wall of the right ICA. On the fourth day after injury, we found rebleeding from the tBBA and performed an emergency high-flow bypass using a radial artery graft with lesion trapping as a curative procedure for the tCCF and tBBA. Postoperatively, right abducens nerve palsy appeared, but no other neurological symptoms were noted; the patient was thereafter transferred to a rehabilitation hospital 49 days after injury. Traumatic ICA aneurysms commonly occur close to the anterior clinoid process, form within 1 to 2 weeks of injury, and often rupture around 2 weeks after trauma. This case was considered rare as the ICA was likely injured and bleeding at the time of injury, resulting in a form of tBBA; this allowed early detection and appropriate treatment that resulted in a good outcome.

发生在颈内动脉(ICA)前壁的破裂脑动脉瘤被称为血泡状动脉瘤(BBAs);据报道,它们占所有破裂的ICA动脉瘤的0.3%至1%。在本报告中,我们描述了一种不寻常的创伤性BBA(tBBA)的治疗方法,即使用桡动脉移植物进行高流量搭桥术,取得了良好的结果。一名59岁的女性在一次机动车事故中遭受急性硬膜外血肿、创伤性蛛网膜下腔出血和创伤性颈动脉海绵窦瘘(tCCF)。她的血管造影结果显示右ICA前壁有tCCF和tBBA。在损伤后的第四天,我们发现tBBA再次出血,并使用带病变捕获的桡动脉移植物进行紧急高流量搭桥术,作为tCCF和tBBA的治疗程序。术后出现右侧外展神经麻痹,但未发现其他神经系统症状;患者在受伤49天后被转移到康复医院。外伤性ICA动脉瘤通常发生在前床突附近,在受伤后1至2周内形成,通常在创伤后2周左右破裂。这种情况被认为是罕见的,因为ICA可能在受伤时受伤并出血,导致tBBA的形式;这使得早期发现和适当的治疗能够产生良好的结果。
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