Cerebrospinal fluid leak

脑脊液漏
  • 文章类型: Case Reports
    据报道,颈椎的整脊脊柱操纵疗法(CSMT)会引起机械硬脑膜损伤,导致脑脊液(CSF)泄漏。我们介绍了一例孤立的胸腔CSMT后有症状的颅内低血压。初始成像无法明确定位CSF泄漏,但是动态成像能够更好地识别缺陷。尝试了多个硬膜外血贴,包括图像引导方法和纤维蛋白密封剂,但最终需要手术修复.我们的案例说明了在最近的CSMT环境中硬膜撕裂的风险以及管理这种伤害的挑战。
    Chiropractic spinal manipulation therapy (CSMT) of the cervical spine has been reported to cause mechanical dural injuries that result in cerebrospinal fluid (CSF) leaks. We present a case of symptomatic intracranial hypotension after isolated thoracic CSMT. Initial imaging was unable to definitively localize the CSF leak, but dynamic imaging was able to better identify the defect. Multiple epidural blood patches were attempted, including image-guided approaches and with fibrin sealant, but surgical repair was ultimately required. Our case illustrates the risk of dural tear in the setting of recent CSMT and the challenges of managing such an injury.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    在过去的二十年里,鼻内镜颅底手术(EESBS)通过使切除脑膜瘤等重要病理的机会最少,彻底改变了颅底肿瘤的治疗。垂体腺瘤,和脊索瘤.尽管它的功效,并发症,如脑脊液(CSF)泄漏构成重大挑战,EESBS后的平均发病率为8.9%。因此,我们的研究目的是调查在采用内镜经鼻入路颅底手术后与术后脑脊液漏相关的危险因素,专注于在吉达的阿卜杜勒-阿齐兹国王医疗城和麦加的阿卜杜拉国王医疗城接受治疗的患者,沙特阿拉伯。
    对2016年1月至2022年12月期间接受内镜经鼻入路切除硬膜内颅底病变的患者进行回顾性回顾,共51例患者。收集了基本的人口统计数据,伴随着患者的合并症,出现症状,肿瘤病理学,肿瘤部位,切除的程度,和结果。
    对51名参与者进行了分析,平均年龄43.41岁.男性参与者(58.8%),头痛是最常见的症状(74.5%),其次是视觉障碍(51.0%)。非分泌性肿瘤占优势,主要位于鞍区和鞍上区域(58.8%)。大体全切除术占大多数(56.9%),术后脑脊液漏发生率为9.8%。值得注意的是,所有4例脑脊液漏患者都经历了术前头痛.高血压在病例1和4中普遍存在,病例4有神经系统疾病和放射治疗史。前颅底肿瘤在病例3和4中最常见。
    本研究中手术后脑脊液漏的发生率与先前报道的相似。值得注意的是,重复手术可能会增加术后脑脊液漏的风险。因此,仔细评估肿瘤切除和颅底重建的手术方法很重要,考虑到肿瘤的特点和患者的整体状况。
    UNASSIGNED: Over the past two decades, endoscopic endonasal skull base surgery (EESBS) has revolutionized the treatment of skull base tumors by enabling minimal access to resect significant pathologies such as meningiomas, pituitary adenomas, and chordomas. Despite its efficacy, complications such as cerebrospinal fluid (CSF) leak pose significant challenges, with an average incidence of 8.9% following EESBS. Therefore, our study aims to investigate the risk factors associated with postoperative CSF leak after employing an endoscopic endonasal approach for skull base surgery, focusing on patients treated at King Abdul-Aziz Medical City in Jeddah and King Abdullah Medical City in Makkah, Saudi Arabia.
    UNASSIGNED: A retrospective review of patients who underwent an endoscopic endonasal approach for the resection of intradural skull base pathology between January 2016 and December 2022 was performed with a total of 51 patients. Basic demographic data were collected, along with patient comorbidities, presenting symptoms, tumor pathology, tumor site, the extent of resection, and outcomes.
    UNASSIGNED: 51 participants were analyzed, with a mean age of 43.41. Male participants comprised (58.8%), while headaches were the most common symptom (74.5%), followed by visual disturbances (51.0%). Nonsecretory tumors predominated, primarily located in the sellar and suprasellar regions (58.8%). Gross total resection was performed in the majority (56.9%), with a 9.8% incidence of postoperative CSF leak. Notably, all four patients with CSF leak experienced preoperative headaches. Hypertension was prevalent in Cases 1 and 4, with Case 4 having a history of neurological disease and radiation therapy. Anterior skull base tumors were most frequent in Cases 3 and 4.
    UNASSIGNED: The incidence of CSF leakage after surgery in this study was similar to that previously reported. It is worth noting that repeated surgeries may increase the risk of postoperative CSF leakage. Therefore, it is important to carefully evaluate the surgical approach for tumor removal and skull base reconstruction, considering the tumor characteristics and the patient\'s overall condition.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    目的:提高对硬膜穿刺后持续性头痛患者的认识,以评估自发性脑脊液(CSF)漏。
    背景:脊髓脑脊液漏引起的自发性颅内低血压(SIH)可能发生在或多或少的轻微创伤事件之后。我们报告了我们在经皮或开放性脊柱手术后发生的自发性脊髓脑脊液漏的经验。诊断混乱的潜在来源。
    方法:在一项回顾性队列研究中,使用前瞻性维护的SIH患者数据库,我们确定了所有在2022年1月1日至2023年6月30日期间接受评估的新患者,这些患者被转诊以评估医源性脊髓CSF漏,但被发现患有自发性脊髓CSF漏.
    结果:248例SIH患者中有9例(4%)最初被转诊用于评估医源性脊髓脑脊液漏。脊柱手术包括硬膜外类固醇注射,椎板切除术,硬膜外麻醉,还有腰椎穿刺.脑磁共振成像(MRI)显示9例患者中有7例(78%)颅内低血压的变化。在所有患者中,自发性CSF泄漏至少从脊柱手术中清除了五个级别。
    结论:脊柱手术后顽固性直立性头痛患者应怀疑自发性脊髓脑脊液漏。即使在脊柱手术后数小时内出现渗漏症状,尤其是脑MRI异常。
    OBJECTIVE: To raise awareness that patients with persistent post-dural puncture headache should be considered for evaluation of spontaneous cerebrospinal fluid (CSF) leak.
    BACKGROUND: Spontaneous intracranial hypotension (SIH) due to a spinal CSF leak may occur following more-or-less trivial traumatic events. We report our experience with spontaneous spinal CSF leaks that occur following percutaneous or open spine procedures, a potential source of diagnostic confusion.
    METHODS: In a retrospective cohort study, using a prospectively maintained database of patients with SIH, we identified all new patients evaluated between January 1, 2022, and June 30, 2023, who were referred for evaluation of an iatrogenic spinal CSF leak but were found to have a spontaneous spinal CSF leak.
    RESULTS: Nine (4%) of the 248 patients with SIH were originally referred for evaluation of an iatrogenic spinal CSF leak. The spinal procedures included epidural steroid injections, laminectomies, epidural anesthesia, and lumbar puncture. Brain magnetic resonance imaging (MRI) showed changes in intracranial hypotension in seven of the nine patients (78%). The spontaneous CSF leak was found to be at least five levels removed from the spinal procedure in all patients.
    CONCLUSIONS: A spontaneous spinal CSF leak should be suspected in patients with recalcitrant orthostatic headaches following a spinal procedure, even if symptoms of the leak occur within hours of the spinal procedure and especially if brain MRI is abnormal.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    脑脊液(CSF)渗漏是与内镜经鼻颅底手术(EESBS)相关的常见并发症。术后动员相关的姿势变化被认为会导致CSF泄漏。然而,没有研究表明姿势变化与CSF渗漏之间存在密切的关系.我们使用直立计算机断层扫描(CT)来阐明姿势变化对EESBS后重建颅底(RSB)的影响。前瞻性纳入了在我们机构接受EESBS的30名患者,并比较它们的直立和仰卧CT以测量RSB的形态变化。还从医疗图表和手术视频中收集了患者的临床数据,并评估了它们与形态变化的关系。在直立CT中,RSB颅内平均移位0.94(0.0-2.9)mm。在病变延伸至蝶窦的病例中,这种移位更大,硬脑膜缺损,术中RSB的搏动,和大的骨头窗户。由于坐姿的颅内压降低,因此变化的方向与重力驱动的直观运动相反。因此,这些移位可直接与术后重建材料移位引起的脑脊液漏有关。考虑到这些形态变化的颅底重建和术后姿势管理对于防止CSF泄漏可能是必要的。
    Cerebrospinal fluid (CSF) leakage is a common complication associated with endoscopic endonasal skull-base surgery (EESBS). Postoperative mobilization-associated postural changes are considered to cause CSF leakage. However, no study has demonstrated a robust relationship between postural changes and CSF leakage. We used upright computed tomography (CT) to clarify the effects of postural changes on the reconstructed skull base (RSB) after EESBS. Thirty patients who underwent EESBS at our institution were prospectively included, and their upright and supine CTs were compared to measure morphological changes in the RSB. Patient clinical data were also collected from medical charts and surgical videos, and their relationships with morphological changes were assessed. In upright CTs, the RSB shifted intracranially by 0.94 (0.0-2.9) mm on average. This shift was larger in cases with lesions extending to the sphenoid sinus, dural defects, intraoperative pulsation of the RSB, and large bone windows. The direction of the change was opposite to intuitive movement driven by gravity because of reduced intracranial pressure in the sitting position. Thus, these shifts can be directly associated with postoperative CSF leakage caused by reconstruction material displacement. Skull-base reconstruction and postoperative postural management accounting for these morphological changes may be necessary for preventing CSF leakage.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Case Reports
    我们报告了一例罕见的基底神经节实质内出血,并在腰椎手术后发生脑室内扩展。一名65岁的女性接受了L4-L5腰椎椎板切除术和后路脊柱固定术。她的最初手术因硬脑膜合成移植物修复的脑脊液(CSF)泄漏而变得复杂。她立即的术后过程因延迟出现而变得复杂,令人大开眼界的失用症,左侧偏瘫和随后的头部计算机断层扫描(CT)显示右侧基底神经节实质内出血(IPH)伴有脑室内扩展。头部CT血管造影未见明显。她被带回手术室,接受右侧减压性半切除术和脑室外引流(EVD)治疗脑积水。她的EVD在出血后第13天停止,她在出血后第14天出院到长期护理机构,改良的Rankin量表(mRS)评分为6。六个月后她回来做了颅骨成形术,在她9个月的最后一次随访中,mRS为4,持续混乱和严重的左侧偏瘫,但能够形成简单的句子。总之,颅内出血是脊柱手术的罕见并发症,发生在一小部分人口中。脊柱手术后的LobarIPH是一种罕见的并发症,并且被假设是在硬体切开术期间过度CSF损失的结果。
    We report on a rare case of basal ganglia intraparenchymal hemorrhage with intraventricular extension occurring after a lumbar spinal surgery. A 65-year-old female presented for an elective L4-L5 lumbar laminectomy and posterior spinal fixation. Her initial operation was complicated by a cerebrospinal fluid (CSF) leak repaired with a dural synthetic graft. Her immediate post-operative course was complicated by delayed emergence, eye-opening apraxia, and left-sided hemiplegia and subsequent computed tomography (CT) of the head demonstrated a right-sided basal ganglia intraparenchymal hemorrhage (IPH) with intraventricular extension. CT angiogram of the head was unremarkable. She was taken back to the operating room for right-sided decompressive hemicraniectomy and external ventricular drainage (EVD) for hydrocephalus. Her EVD was discontinued on post-bleed day 13 and she was discharged on post-bleed day 14 to a long-term care facility with a modified Rankin scale (mRS) score of 6. She returned for a cranioplasty six months later, and on her last follow-up at nine months, had a mRS of 4 with persistent confusion and severe left-sided hemiparesis but was able to form simple sentences. In summary, intracranial hemorrhage is a rare complication of spine surgery, occurring in a small percentage of the population. Lobar IPH following spinal surgery is a rare complication, and has been hypothesized to be a result of excessive CSF loss during durotomy.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Case Reports
    颅内低血压可能由于代偿性充血和静脉充血而导致脑垂体增大。自发性颅内低血压(SIH)通常与结缔组织疾病有关,使患者容易发生硬脑膜减弱,包括硬脑膜扩张和脑膜憩室。SIH的症状通常包括姿势性头痛,头晕和耳鸣。我们介绍了一个20多岁的女性,患有马凡氏综合征和垂体腺瘤病史,报告顽固性姿势性头痛的人。荷尔蒙检查没有发现异常,而脑MRI显示颅内低血压后遗症。进一步的MRI研究显示,胸腰椎脑膜憩室在L4-S2水平伴有明显的硬膜囊扩张。脊髓造影证实了许多腰椎憩室,在L5和S1右神经根有脑脊液漏。患者在渗漏水平接受了血液贴片给药,症状得到改善。
    Intracranial hypotension may result in pituitary gland enlargement due to compensatory hyperaemia and venous engorgement. Spontaneous intracranial hypotension (SIH) is frequently associated with connective tissue disorders predisposing patients to dural weakening including dural ectasia and meningeal diverticula. Symptoms of SIH typically include postural headache, dizziness and tinnitus. We present a case of a female in her 20s with Marfan syndrome and a history of pituitary adenoma, who reported intractable postural headaches. Hormonal workup revealed no abnormalities, whereas brain MRI showed sequelae of intracranial hypotension. Further MRI studies revealed thoracic and lumbar meningeal diverticula with significant dural sac ectasia at the L4-S2 level. Myelogram confirmed numerous lumbar spine diverticula with cerebrospinal fluid leak at the L5 and S1 right nerve roots. The patient underwent blood patch administrations at the level of the leak with improvement of symptoms.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    背景:腰椎硬膜外补血片(EBP)在所有脑脊液(CSF)漏的情况下都不是成功的,特别是在颈胸区域。本研究是对一组接受计算机断层扫描(CT)引导的宫颈EBP治疗因宫颈区域CSF渗漏引起的自发性颅内低血压(SIH)的患者的回顾性分析。
    方法:我们回顾性收集了2009年3月至2020年的数据。我们的纳入标准是(1)与脑脊液漏相关的临床综合征,(2)在采取直立姿势和躺下获得缓解后不久出现头痛,(3)颈部脑脊液漏的CT脊髓造影证据,(4)患者对保守治疗7天没有反应。排除标准为出血素质和感染患者。有六名女性和四名男性。年龄从32岁到57岁不等,平均42岁。在介绍时,所有患者均接受对比增强磁共振成像(MRI)和CT脊髓造影.宫颈EBP在CT扫描引导下进行。在手术前后以10点数字评定量表(NRS)进行头痛评估。结果分为完全缓解,部分缓解,没有救济类别。
    结果:10例患者中有9例完全康复。一名患者部分康复。治疗前平均NRS量表为9.6,在EBP之后变为0.4。未见神经或血管并发症。
    结论:计算机断层扫描引导的宫颈EBP是治疗因宫颈区域渗漏引起的SIH的最佳有效方法。它比腰椎EBP具有更高的成功率。然而,颈椎与腰椎EBP的前瞻性随机对照试验将进一步验证我们的观察结果.
    BACKGROUND: Lumbar epidural blood patch (EBP) is not successful in all cases of cerebrospinal fluid (CSF) leak, particularly in the cervicothoracic region. The present study is a retrospective analysis of a cohort of patients who had undergone computed tomography (CT)-guided cervical EBP for spontaneous intracranial hypotension (SIH) due to CSF leak in the cervical region.
    METHODS: We retrospectively collected data from March 2009 to 2020. Our inclusion criteria were (1) clinical syndrome associated with CSF leak, (2) headache coming on shortly after assuming the erect position and relief achieved by lying down, (3) CT myelography evidence of CSF leak in the cervical region, and (4) patient not responding to conservative management for 7 days. Exclusion criteria were patients with bleeding diathesis and infection. There were six females and four males. Ages ranged from 32 to 57, with an average of 42 years. On presentation, all patients underwent contrast-enhanced magnetic resonance imaging (MRI) and CT myelography. Cervical EBP was done under CT scan guidance. Assessment of headache was done on a 10-point numerical rating scale (NRS) before and after the procedure. Results are categorized into complete relief, partial relief, and no relief categories.
    RESULTS: Nine out of 10 patients were completely recovered. One patient was partially recovered. The average NRS scale was 9.6 before treatment, which became 0.4 after EBP. No neurological or vascular complications were seen.
    CONCLUSIONS: Computed tomography-guided cervical EBP is an optimum and effective way of treating SIH due to a leak in the cervical region. It has a higher success rate than lumbar EBP. However, prospective randomized controlled trials of cervical vs lumbar EBP will further validate our observation.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Case Reports
    本报告描述了一名61岁男性在腰椎融合手术后不久表现出非典型神经系统恶化的复杂诊断过程和治疗难题,表现出提示假性缺氧性脑病的临床和放射学特征,一种实体,其特征是在没有明显的缺氧损伤的情况下模仿脑缺氧的症状。在从精心的脊柱手术中最初平淡无奇的恢复之后,患者的术后状况被令人困惑的意识下降所困扰,对常规治疗干预无反应,标准神经影像学缺乏明确的病因指标。随后的诊断性奥德赛揭示了脑脊液漏作为推定原因,提出了一种微妙的临床范式,其中脑脊液漏产生了一种模仿假性缺氧性脑肿胀的状态。该报告强调了临床挑战,并强调需要对患有无法解释的神经系统症状的术后患者采取精明的诊断方法,主张进行全面评估以识别潜在的脑脊液漏并减轻潜在的发病率。
    This report delineates the intricate diagnostic journey and therapeutic conundrum presented by a 61-year-old male who exhibited atypical neurological deterioration shortly after lumbar fusion surgery, manifesting clinical and radiological features suggestive of pseudohypoxic encephalopathy, an entity characterized by symptoms mimicking cerebral hypoxia in the absence of a discernible hypoxic insult. Following an initially unremarkable recovery from an elaborate spinal surgery, the patient\'s postoperative condition was confounded by a perplexing decline in consciousness, unresponsive to conventional therapeutic interventions and devoid of clear etiological indicators on standard neuroimaging. The subsequent diagnostic odyssey unraveled a cerebrospinal fluid leak as the putative reason, positing a nuanced clinical paradigm wherein the cerebrospinal fluid leak engendered a state mimicking pseudohypoxic brain swelling. This report underscores the clinical challenges and emphasizes the need for an astute diagnostic approach in postoperative patients with unexplained neurological symptoms advocating for a comprehensive evaluation to identify underlying cerebrospinal fluid leaks and mitigate potential morbidity.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    脊髓膜膨出是一种常见的先天性疾病,其重建对外科医生构成了挑战。肋间背侧动脉(DICA)皮瓣提供了一步无张力闭合,效果良好。这项研究,从2019年1月到2022年9月,分析了9个DICA皮瓣用于脑膜脊髓膨出重建的结果,其中DICA皮瓣的平均尺寸为6.8x4.6cm,平均缺损为6.33x4cm。值得注意的是,术后不需要输血,除1例脓毒性休克相关死亡外,无任何并发症发生.两人术后脑脊液(CSF)渗漏,修复主要用一个需要VP分流。根据我们的经验,DICA皮瓣,具有一致的解剖结构,是重建脑膜脊髓膨出缺损的可靠选择。
    Meningomyelocele is a common congenital condition and its reconstruction poses a challenge for surgeons. The dorsal intercostal artery (DICA) flap offers a one-stage tension-free closure with adequate results. This study, spanning from January 2019 to September 2022, analyses the outcome of nine DICA flaps for meningomyelocele reconstruction, where the average size of the DICA flap was 6.8 x 4.6 cm for an average defect of 6.33 x 4 cm. Notably, no post-operative blood transfusion was required, nor any complications occurred except for one patient\'s septic shock-related death. Two had post-operative cerebrospinal fluid (CSF) leak, repaired primarily with one requiring VP shunt. Based on our experience, the DICA flap, with its consistent anatomy, is a reliable option for the reconstruction of meningomyelocele defects.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    暂无摘要。
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

公众号