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Recurrent Giant Cell Glioblastoma Across Bilateral Lateral Ventricles 双侧侧脑室复发性巨细胞胶质母细胞瘤
Q Medicine Pub Date : 2016-05-01 DOI: 10.1097/WNQ.0000000000000146
Ye-shuai Hu, Jun Yang, Shun-Chang Ma
Giant cell glioblastoma is an extraordinary subtype of glioblastoma that merits mention as a distinct variant of glioblastoma in World Health Organization classification of gliomas. It represents for about 1% of brain tumors and about 5% of glioblastomas in general. It has no preferential region and may occur in various locations of the central nervous system, most commonly in the temporal lobe. To our knowledge, there have been a few cases involved in the unilateral lateral ventricle reported in the literature, but there have been no reports about the recurrent cases involved in bilateral lateral ventricles. We herein present a very rare case of recurrent giant cell glioblastoma that occurred across bilateral lateral ventricles.
巨细胞胶质母细胞瘤是一种特殊的胶质母细胞瘤亚型,在世界卫生组织的胶质瘤分类中,它是胶质母细胞瘤的一种独特变体。它代表了大约1%的脑肿瘤和大约5%的胶质母细胞瘤。它没有优先区,可发生在中枢神经系统的各个部位,最常见于颞叶。据我们所知,文献中已经报道了少数累及单侧侧脑室的病例,但尚未报道累及双侧侧脑室的复发病例。我们在此报告一例罕见的复发性巨细胞胶质母细胞瘤,发生在双侧侧脑室。
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引用次数: 1
Long-term Changes in L5-S1 Disks Under the Fusion Region and the Effect of Sagittal Balance on Degeneration 融合区L5-S1椎间盘的长期变化及矢状面平衡对退变的影响
Q Medicine Pub Date : 2016-05-01 DOI: 10.1097/WNQ.0000000000000154
B. Yılmaz, Baran Kömür, B. Alicioglu, M. Çiftdemir, M. Özcan, C. Çopuroǧlu, E. Yalnız
Background:The aim of this study was to radiologically assess long-term degeneration in the L5-S1 disks under the fusion region and to research its association with clinical signs in patients with degeneration. Methods:This study evaluated 23 patients who underwent spinal fusion between January 1994 and July 2005. Degeneration in the L5-S1 disks was assessed radiologically over a long-term 10-year follow-up period, and those cases that showed degeneration were further assessed using the Japan Orthopedic Association score and visual analog scale (VAS). Results:Seven of the cases had mild osteophyte development according to radiographic findings. A statistically significant decrease was observed in the front and back disk heights between the preoperative and postoperative measurements (P=0.001 and 0.000). A statistically significant decrease was also observed in the anterior and posterior disk height between the preoperative and postoperative measurements (P=0.007 and 0.007). A significant difference was observed in disk degeneration and facet joint degeneration (P=0.000 and 0.000). On evaluation of radiologic assessments, degeneration was observed in 15 cases (65.3%). Clinical assessment of the cases revealed that 6 patients (26.0%) with radiologic degeneration had lumbar pain of varying degrees, 3 of whom also had pain that spread to the legs; 1 of these caused loss of sensation in the leg. Clinical assessment of pain levels using VAS scoring for all cases revealed an average preoperative score of 8.71, an average early postoperative VAS score of 2.14, and an average long-term follow-up score of 3.35. The recovery rate of the patients was found to be 37.5%, according to Japan Orthopedic Association scoring. The pain level of the patients decreased by almost 4-fold in the postoperative early period and 2.5-fold in the long term. Conclusions:Spinal fusion surgery is an effective treatment method in terms of its clinical results, despite the adjacent segment degeneration that may be identified radiologically in the long term.
背景:本研究的目的是影像学评估融合区下L5-S1椎间盘的长期退变,并研究其与退变患者临床体征的关系。方法:本研究评估了1994年1月至2005年7月间接受脊柱融合术的23例患者。在10年的长期随访期间,影像学评估L5-S1椎间盘的退变,那些出现退变的病例使用日本骨科协会评分和视觉模拟量表(VAS)进一步评估。结果:7例患者影像学表现为轻度骨赘发展。前后椎间盘高度在术前和术后测量之间有统计学意义的降低(P=0.001和0.000)。术前和术后测量的前后椎间盘高度也有统计学意义的降低(P=0.007和0.007)。椎间盘退变和小关节退变差异有统计学意义(P=0.000和0.000)。放射学评估显示,退行性变15例(65.3%)。临床评估显示,6例(26.0%)放射学退变患者有不同程度的腰痛,其中3例还伴有腿部疼痛;其中一种导致腿部失去知觉。使用VAS评分对所有病例进行疼痛水平的临床评估,术前平均评分为8.71,术后早期平均评分为2.14,长期随访平均评分为3.35。根据日本骨科协会的评分,患者的康复率为37.5%。术后早期疼痛水平下降近4倍,远期疼痛水平下降2.5倍。结论:脊柱融合手术是一种有效的治疗方法,尽管邻近节段退变可能在长期影像学上被发现。
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引用次数: 0
Upper Lumbar Disk Herniation Presenting as Chronic Abdominal and Scrotal Pain: A Case Report 上腰椎间盘突出表现为慢性腹部和阴囊疼痛1例
Q Medicine Pub Date : 2016-05-01 DOI: 10.1097/WNQ.0000000000000162
L. Asadian, Kaveh Haddadi, Amirhossein Zare
In this study we present a case of a man with chronic lower abdomen and severe periodic scrotal pain. He was evaluated for all usual cause of such pain. Laboratory tests and abdominal and pelvic sonography were normal. Magnetic resonance imaging revealed L1-L2 disk herniation with a cystic component and severe cord compression.
在这项研究中,我们提出了一个病例的男子慢性下腹和严重的周期性阴囊疼痛。他被检查了引起这种疼痛的所有常见原因。实验室检查和腹部及盆腔超声检查均正常。磁共振成像显示L1-L2椎间盘突出伴囊性成分和严重脊髓压迫。
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引用次数: 1
Symptomatic Infratentorial and Supratentorial Subdural Fluid Collection Complicating Foramen Magnum Decompression for Chiari Malformation Type I: 2 Case Reports and Review of the Literature 症状性幕下和幕上硬膜下积液合并大孔减压治疗Chiari畸形I型:2例报告及文献复习
Q Medicine Pub Date : 2016-05-01 DOI: 10.1097/WNQ.0000000000000145
Erhan Çelikoğlu, M. İş, Ayçiçek Ceçen, A. Ramazanoğlu, N. Keser
Subdural cerebrospinal fluid collection and ventricular dilatation occur rarely after foramen magnum decompression. We report 2 cases of symptomatic subdural fluid collection after uncomplicated foramen magnum decompression for Chiari I malformation with syringomyelia. In these cases, postoperative magnetic resonance imaging showed significant shrinkage of the syrinx. The patients subsequently experienced clinical deterioration on days 9 and 13 after discharge, respectively. Repeat magnetic resonance imaging showed bilateral infratentorial subdural fluid collection extending supratentorially, passing through the tentorial notch, and with prominent midline shift. Inferior decent of the cerebellum into the decompression field was also demonstrated. Following evacuation of the subdural fluid by burr-hole and drainage for 3 days, clinical signs did not improve until symptomatic treatment with strict bed rest in the Trendelenburg position was prescribed. In such cases the arachnoid either should not be opened, or should be widely opened and expansile duraplasty performed. It is the authors’ opinion that the latter is the appropriate treatment, followed by conservative therapy including the Trendelenburg position, and restriction of ambulation and effort.
硬膜下脑脊液收集和脑室扩张在枕骨大孔减压后很少发生。我们报告2例无并发症大枕骨孔减压后出现症状性硬膜下积液的病例。在这些病例中,术后磁共振成像显示鼻窦明显萎缩。患者分别在出院后第9天和第13天出现临床恶化。重复磁共振成像显示双侧幕下硬膜下积液延伸至幕上,穿过幕下切迹,中线移位明显。小脑的下体面进入减压野也被证实。经钻孔引流硬膜下液3天后,临床症状未见改善,直至给予Trendelenburg体位严格卧床对症治疗。在这种情况下,不应打开蛛网膜,或应广泛打开并进行扩张硬膜成形术。作者认为后者是合适的治疗方法,其次是保守治疗,包括Trendelenburg体位,限制活动和努力。
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引用次数: 0
Acute Subdural Hematoma With Lentiform Computed Tomography Appearance: A Case Report and Review of the Literature 急性硬膜下血肿伴透镜状ct表现:1例报告及文献复习
Q Medicine Pub Date : 2016-05-01 DOI: 10.1097/WNQ.0000000000000153
B. Gu, Sang-Youl Lee, J. H. Park
Although high-density lentiform appearance which is typical finding for acute epidural hematoma (AEDH) is unusual, several studies previously reported such atypical appearance of acute subdural hematoma (ASDH) on computed tomography (CT) scan. A 78-year-old woman visited our hospital with right-side grade IV weakness and headache that developed 1 day before, without any trauma history. Brain CT scan revealed left-side high-density lentiform hematoma with peripheral crescent changes. On the opposite side, there was simultaneous typical ASDH. During surgery, there was no epidural hematoma and a large amount of dark red–colored hematoma was seen after opening of dura. A clinical history of patient and careful observation of preoperative CT scan allows clinician to differentiate ASDH from AEDH before operation.
尽管高密度透镜状表现是急性硬膜外血肿(AEDH)的典型表现,但以前的一些研究报道了急性硬膜下血肿(ASDH)在计算机断层扫描(CT)上的非典型表现。一名78岁妇女就诊,1天前出现右侧4级无力和头痛,无外伤史。脑部CT显示左侧高密度透镜状血肿伴周围月牙状改变。另一侧同时存在典型ASDH。术中未见硬膜外血肿,打开硬膜后见大量暗红色血肿。患者的临床病史和术前CT扫描的仔细观察可以使临床医生在手术前区分ASDH和AEDH。
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引用次数: 0
An Unusual Giant Subdural Abscess in a Child 儿童罕见的巨大硬膜下脓肿
Q Medicine Pub Date : 2016-05-01 DOI: 10.1097/WNQ.0000000000000161
R. Shrestha, R. Pradhan, C. You
A 12-year-old boy presented with classical triad of fever, headache, and neurological deficit. There was no history of infectious disease before. The patient claimed history of RTA couple of months back. His condition had deteriorated progressively within the 7 days and referral to our hospital. On admission, he was in altered mental status with high body temperature. On neurological examination, right pupil was dilated 5mm and reacting to light. Right lower limb had 3/5 motor strength. Brain computed tomography and magnetic resonance imaging (MRI) revealed massive space-occupying lesion on superior sagittal sinus extending to
一个12岁的男孩表现为发烧,头痛和神经功能障碍的典型三联征。以前没有传染病史。病人几个月前声称有RTA病史。他的病情在7天内逐渐恶化,转诊到我们医院。入院时,他精神状态改变,体温高。神经学检查,右侧瞳孔扩大5mm,对光有反应。右下肢运动强度3/5。脑部电脑断层扫描及核磁共振显示上矢状窦内有大量占位性病变,并延伸至
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引用次数: 0
The Comparison of the Application of Percutaneous Transpedicular and Extrapedicular Vertebroplasty: Which Approach has Better Results? 经皮椎弓根椎体成形术与椎弓根外椎体成形术的比较:哪种方法效果更好?
Q Medicine Pub Date : 2016-05-01 DOI: 10.1097/WNQ.0000000000000140
N. Uçler, Ş. Yucetas, Tuncay Ateş, H. Çakın
Background:Vertebral compression fractures are a common complication of various pathologies. Vertebroplasty is a choice in these fractures, but the approach to the fractured vertebra corpus with this technique is relatively an important issue. Patients and Methods:In this retrospective study, we evaluated and compared 90 patients with vertebral fractures treated with extrapedicular or transpedicular vertebroplasty, with respect to visual analog score (VAS), cement leakage risk, postoperative bed rest time, and postoperative analgesic use. Results:Our retrospective study showed that intraspinal canal and intervertebral cement leakage were lower in the extrapedicular group than in the transpedicular group (1 vs. 3 and 3 vs. 6). In addition, postoperative bed rest time and postoperative anagesic use were higher in the transpedicular group than in the extrapedicular group (24 vs. 15 h and 7 vs. 3 d). When compared, the extrapedicular group had lower cost and first-year VAS than the transpedicular group, despite preoperative VAS being higher in the extrapedicular group. Conclusions:Our comparative retrospective study showed that extrapedicular approach has better results with respect to VAS, cement leakage risk, postoperative bed rest time, and postoperative analgesic use. In addition to these advantages, extrapedicular approach may have some potential complications, but these complications may be prevented from meticulous manipulations.
背景:椎体压缩性骨折是各种病理的常见并发症。椎体成形术是治疗这些骨折的一种选择,但椎体骨折的入路是一个相对重要的问题。患者和方法:在这项回顾性研究中,我们评估和比较了90例椎体骨折经椎弓根外或经椎弓根椎体成形术治疗的患者,包括视觉模拟评分(VAS)、水泥渗漏风险、术后卧床休息时间和术后镇痛药的使用。结果:我们回顾性研究显示脊柱内的运河和椎间水泥泄漏extrapedicular组低于置钉组(1和3和3和6)。此外,术后卧床休息时间和术后anagesic使用高置钉组比extrapedicular组(24比15 h和7比3 d)相比,extrapedicular组较低成本和一年级比置钉组血管,尽管椎弓根外组术前VAS较高。结论:我们的回顾性比较研究表明,椎弓根外入路在VAS、骨水泥渗漏风险、术后卧床休息时间和术后镇痛药使用方面具有更好的效果。除这些优点外,椎弓根外入路可能有一些潜在的并发症,但这些并发症可以通过细致的操作来预防。
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引用次数: 0
Moyamoya Disease Associated With Thyroid Carcinoma: A Case Report and Review of the Literature 烟雾病合并甲状腺癌1例报告及文献复习
Q Medicine Pub Date : 2016-05-01 DOI: 10.1097/WNQ.0000000000000155
Jian-bin Chen, C. You
Thyroid carcinoma associated with Moyamoya disease has not been reported in the literature. We first described a 46-year-old woman of Moyamoya disease after 10 years of thyroidectomy due to papillary adenocarcinoma of thyroid. During the 10-year medicine history, the patient was treated with levothyroxine (100 µg/d), and thyroid antibody tests demonstrated that elevated thyrotropin receptor antibody sustained for long time. After 10 years, the patient was diagnosed with Moyamoya disease according to digital subtraction angiography findings. The case suggested that thyroid autoimmune stimuli of papillary thyroid carcinoma with thyroid-stimulating hormone receptor antibody may be associated with pathogenic mechanism of Moyamoya disease.
甲状腺癌合并烟雾病尚未见文献报道。我们首先报道了一位46岁的女性,因甲状腺乳头状腺癌切除甲状腺10年后患烟雾病。在10年的用药史中,患者给予左旋甲状腺素100µg/d治疗,甲状腺抗体检测显示促甲状腺素受体抗体长期升高。10年后,患者根据数字减影血管造影结果被诊断为烟雾病。提示甲状腺乳头状癌伴促甲状腺激素受体抗体的甲状腺自身免疫刺激可能与烟雾病的发病机制有关。
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引用次数: 1
Autologous Bone for the Reconstruction of Skull Defects 自体骨用于颅骨缺损的重建
Q Medicine Pub Date : 2016-02-01 DOI: 10.1097/WNQ.0000000000000195
Qiujian Zhang, Xuping Tian, Hansheng Shu, Hui Zhang, Shanjing Xuan, Qing Chao
Objective:To restore the normal barriers protecting the intracranial structures and obtain a permanent or very durable reconstruction. Methods:This retrospective study spanning 3 years included 36 patients who underwent reconstruction of skull defects either with autologous bone or with 3-dimensional (3D) titanium mesh. To analyze difference of both, 2 groups (group A 1 group skull defect for reconstruction with 3D titanium mesh, group B the other group with autologous bone) were divided. Results:A favorable surgery outcome was attained in the follow-up without complications in the group B. Osteolysis was not observed from 3D reconstruction of computed tomography (CT) from 3D reconstruction of CT in the group B (P>0.05). Complications was significantly different, comparing with group A (P<0.05). General features (age, follow-up) were not different (P>0.05). Conclusion:Autologous bone for the reconstruction of skull defects seems to be good technique for permanent or very durable reconstruction.
目的:恢复保护颅内结构的正常屏障,获得永久性或非常持久的重建。方法:回顾性研究了36例采用自体骨或三维钛网重建颅骨缺损的患者。为分析两者的差异,将1组颅骨缺损采用3D钛网修复,B组采用自体骨修复。结果:随访B组手术效果良好,无并发症。B组CT三维重建未见骨溶解(P>0.05)。并发症发生率与A组比较差异有统计学意义(P0.05)。结论:自体骨修复颅骨缺损是一种永久性或非常持久的修复方法。
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引用次数: 3
An Asymptomatic Dandy-Walker Malformation—A Case Report and Literature Review 无症状迪迪-沃克畸形1例报告及文献复习
Q Medicine Pub Date : 2016-02-01 DOI: 10.1097/WNQ.0000000000000122
Jianru Li, Q. Hu, F. Yan, Sudeep Shrestha, Gao Chen
This report describes a very rare Dandy-Walker malformation (DWM) and emphasizes the follow-up for asymptomatic DWM. This case reports a man with undiagnosed DWM who was asymptomatic until the age of 59 years when he presented with headache. Computed tomography and magnetic resonance imaging revealed DWM. To our knowledge, this is the first report that describes a patient who was diagnosed with DWM presenting with headache without any other symptoms.
本文报告一例罕见的Dandy-Walker畸形(DWM),并强调对无症状的DWM的随访。本病例报告了一名患有未确诊的DWM的男子,直到59岁时才出现头痛症状。计算机断层扫描和磁共振成像显示DWM。据我们所知,这是第一个描述被诊断为DWM的患者表现为头痛而无其他症状的报告。
{"title":"An Asymptomatic Dandy-Walker Malformation—A Case Report and Literature Review","authors":"Jianru Li, Q. Hu, F. Yan, Sudeep Shrestha, Gao Chen","doi":"10.1097/WNQ.0000000000000122","DOIUrl":"https://doi.org/10.1097/WNQ.0000000000000122","url":null,"abstract":"This report describes a very rare Dandy-Walker malformation (DWM) and emphasizes the follow-up for asymptomatic DWM. This case reports a man with undiagnosed DWM who was asymptomatic until the age of 59 years when he presented with headache. Computed tomography and magnetic resonance imaging revealed DWM. To our knowledge, this is the first report that describes a patient who was diagnosed with DWM presenting with headache without any other symptoms.","PeriodicalId":56275,"journal":{"name":"Neurosurgery Quarterly","volume":"26 1","pages":"87-89"},"PeriodicalIF":0.0,"publicationDate":"2016-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1097/WNQ.0000000000000122","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"61882281","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
期刊
Neurosurgery Quarterly
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