Letter: Considering Cerebrospinal Fluid Leaks in Ehlers-Danlos Patients: Raising Awareness Amongst Neurosurgeons

Anusha Pasumarthi, An-zhi Luo, Hemali Shah, Ian R Carroll
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Perhaps worst of all, patients with Ehlers Danlos often suffer from chronic pain. The innate ligamentous laxity that riddles all forms of EDS confers substantial risk of chronic multifocal joint, tendon, and spinal pain.1 These other complaints may obscure the clarity of orthostatic headache in a brief clinical interview of EDS patients. There are 2 studies which address the aforementioned concerns. The most recent is by Reinstein et al2 wherein the authors analyzed data obtained from a prospective study that enrolled a group of 50 patients referred for CSF leak consultation. The patients were examined for the presence of connective tissue abnormalities based on echocardiography, eye exam, histopathological skin examination, and dural biopsies, which were then confirmed with genetic testing. A total of 9 patients were identified to have heritable connective tissue disorders, 4 of which were EDS hypermobility type and 2 EDS classic type. The study concluded that patients with spontaneous CSF leaks had higher chances of having an underlying connective tissue abnormality. A prior prospective study conducted by Schievink et al3 examined a group of 18 patients with connective tissue disorders who exhibited spontaneous CSF leaks as well. More specifically, 11% of patients had EDS Type 2, which had not been previously documented to present with spontaneous CSF leaks. The study also reported that the success rate of surgical CSF leak repair remains unchanged regardless of the presence of underlying hereditary connective tissue disorders.3 Nevertheless, further research is warranted to better stratify the associated surgical risks based on the correlation between the type and severity of EDS to the possibility of developing spontaneous CSF leaks. The tenacity needed by a neurosurgeon pursuing a CSF leak in this high risk group should be informed by four evolving understandings that disrupt the classic teachings about CSF leaks: 1) Opening pressure is most often normal in patients with CSF leaks and fails to distinguish between patients with and without CSF leaks visible on spinal imaging4; 2) Pachymeningeal enhancement on brain magnetic resonance imaging (MRI) may be present in only a minority of patients with CSF leaks5; 3) Subtle brainstem measurements such as suprasellar distance, mamillopontine distance, and prepontine distance may be as important as the more classic and obvious pachymeningeal enhancement to predict finding a spinal CSF leak6; and 4) New imaging techniques demonstrate that spinal CSF leak into epidural and paravertebral veins (so-called CSF-venous fistulas) are much more common than previously appreciated and will be missed by conventional MRI, magnetic resonance myelogram, and computed tomography myelogram—with falsely reassuring spine imaging results. These may only become apparent with lateral decubitus digital subtraction myelogram, a technique not yet widely practiced or available.7 Together, these evolving understandings, published after the original reports on EDS, suggest neurosurgeons should: 1) Have a higher index of suspicion for CSF leaks in the EDS population; 2) View with humility our current ability to exclude spinal CSF leaks with opening pressure and imaging; 3) Have a low threshold to expend effort to identify and treat this fixable cause of chronic disability; and 4) Heed the guidance encompassed by the International Classification of Headache Disorders (ICHD-3) which states, “In patients with typical orthostatic headache and no apparent cause, and after exclusion of postural orthostatic tachycardia syndrome, it is reasonable in clinical practice to provide autologous lumbar epidural blood patch”.8 As gatekeepers in the evaluation and treatment of suspected CSF leaks, a neurosurgeon’s clinical decision to vigorously pursue CSF leak in an EDS patient with an orthostatic headache will likely determine the entire clinical course for that patient.","PeriodicalId":93342,"journal":{"name":"Neurosurgery open","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2020-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neurosurgery open","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/neuopn/okaa016","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract

To the Editor: A review of the literature indicates that across the last 7 yr, there is a lack of studies regarding the correlation between cerebrospinal fluid (CSF) leaks and dural laxity in Ehlers-Danlos Syndrome (EDS) patients, possibly because EDS patients are considered high risk surgical candidates. A neurosurgeon may be hesitant to investigate an EDS patient for a leak due to increased risk of impaired wound healing from attenuated and fragile dura. Other factors potentially contributing to the neurosurgeon’s hesitancy include the overlap seen between CSF leak symptoms and other problems common in patients with EDS such as headaches, myelopathy, and cranio-cervical and spinal segmental instability. Perhaps worst of all, patients with Ehlers Danlos often suffer from chronic pain. The innate ligamentous laxity that riddles all forms of EDS confers substantial risk of chronic multifocal joint, tendon, and spinal pain.1 These other complaints may obscure the clarity of orthostatic headache in a brief clinical interview of EDS patients. There are 2 studies which address the aforementioned concerns. The most recent is by Reinstein et al2 wherein the authors analyzed data obtained from a prospective study that enrolled a group of 50 patients referred for CSF leak consultation. The patients were examined for the presence of connective tissue abnormalities based on echocardiography, eye exam, histopathological skin examination, and dural biopsies, which were then confirmed with genetic testing. A total of 9 patients were identified to have heritable connective tissue disorders, 4 of which were EDS hypermobility type and 2 EDS classic type. The study concluded that patients with spontaneous CSF leaks had higher chances of having an underlying connective tissue abnormality. A prior prospective study conducted by Schievink et al3 examined a group of 18 patients with connective tissue disorders who exhibited spontaneous CSF leaks as well. More specifically, 11% of patients had EDS Type 2, which had not been previously documented to present with spontaneous CSF leaks. The study also reported that the success rate of surgical CSF leak repair remains unchanged regardless of the presence of underlying hereditary connective tissue disorders.3 Nevertheless, further research is warranted to better stratify the associated surgical risks based on the correlation between the type and severity of EDS to the possibility of developing spontaneous CSF leaks. The tenacity needed by a neurosurgeon pursuing a CSF leak in this high risk group should be informed by four evolving understandings that disrupt the classic teachings about CSF leaks: 1) Opening pressure is most often normal in patients with CSF leaks and fails to distinguish between patients with and without CSF leaks visible on spinal imaging4; 2) Pachymeningeal enhancement on brain magnetic resonance imaging (MRI) may be present in only a minority of patients with CSF leaks5; 3) Subtle brainstem measurements such as suprasellar distance, mamillopontine distance, and prepontine distance may be as important as the more classic and obvious pachymeningeal enhancement to predict finding a spinal CSF leak6; and 4) New imaging techniques demonstrate that spinal CSF leak into epidural and paravertebral veins (so-called CSF-venous fistulas) are much more common than previously appreciated and will be missed by conventional MRI, magnetic resonance myelogram, and computed tomography myelogram—with falsely reassuring spine imaging results. These may only become apparent with lateral decubitus digital subtraction myelogram, a technique not yet widely practiced or available.7 Together, these evolving understandings, published after the original reports on EDS, suggest neurosurgeons should: 1) Have a higher index of suspicion for CSF leaks in the EDS population; 2) View with humility our current ability to exclude spinal CSF leaks with opening pressure and imaging; 3) Have a low threshold to expend effort to identify and treat this fixable cause of chronic disability; and 4) Heed the guidance encompassed by the International Classification of Headache Disorders (ICHD-3) which states, “In patients with typical orthostatic headache and no apparent cause, and after exclusion of postural orthostatic tachycardia syndrome, it is reasonable in clinical practice to provide autologous lumbar epidural blood patch”.8 As gatekeepers in the evaluation and treatment of suspected CSF leaks, a neurosurgeon’s clinical decision to vigorously pursue CSF leak in an EDS patient with an orthostatic headache will likely determine the entire clinical course for that patient.
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信:考虑埃勒斯-丹洛斯患者的脑脊液泄漏:提高神经外科医生的认识
编者按:对文献的回顾表明,在过去的7年里,缺乏关于埃勒斯-丹洛斯综合征(EDS)患者脑脊液(CSF)渗漏与硬膜松弛之间相关性的研究,这可能是因为EDS患者被认为是高危手术候选人。神经外科医生可能会犹豫是否调查EDS患者的渗漏,因为硬脑膜变薄和脆弱会增加伤口愈合受损的风险。其他可能导致神经外科医生犹豫不决的因素包括CSF渗漏症状与EDS患者常见的其他问题之间的重叠,如头痛、脊髓病、颅颈和脊柱节段不稳定。也许最糟糕的是,埃勒斯-丹洛斯患者经常遭受慢性疼痛。所有形式的EDS都存在先天性韧带松弛,这会带来慢性多灶性关节、肌腱和脊椎疼痛的巨大风险。1在对EDS患者的简短临床访谈中,这些其他症状可能会掩盖直立性头痛的清晰度。有2项研究涉及上述问题。最近的一项是Reinstein等人2的研究,其中作者分析了从一项前瞻性研究中获得的数据,该研究招募了一组50名患者进行脑脊液泄漏咨询。根据超声心动图、眼部检查、组织病理学皮肤检查和硬膜活检检查患者是否存在结缔组织异常,然后通过基因检测进行确认。共有9名患者被确定患有可遗传结缔组织疾病,其中4名为EDS高活动型,2名为EDS经典型。该研究得出结论,自发性脑脊液漏的患者有更高的机会出现潜在的结缔组织异常。Schievink等人3先前进行的一项前瞻性研究对一组18名结缔组织疾病患者进行了检查,这些患者也表现出自发性脑脊液泄漏。更具体地说,11%的患者患有EDS 2型,这在以前没有被记录为自发性CSF渗漏。该研究还报告称,无论是否存在潜在的遗传性结缔组织疾病,手术脑脊液渗漏修复的成功率都保持不变。3然而,有必要进行进一步的研究,根据EDS的类型和严重程度与自发脑脊液渗漏的可能性之间的相关性,更好地对相关的手术风险进行分层。在这一高危人群中,神经外科医生寻求脑脊液泄漏所需的坚韧性应该从四个不断发展的理解中得到启示,这四个理解打破了关于脑脊液泄漏的经典教导:1)脑脊液泄漏患者的开放压力通常是正常的,无法区分脊柱成像中可见的有和没有脑脊液泄漏的患者4;2) 脑磁共振成像(MRI)上的处女膜强化可能仅在少数CSF渗漏患者中存在5;3) 微妙的脑干测量,如鞍上距离、脑桥乳头距离和脑桥前距离,可能与更经典和明显的脑厚增强一样重要,以预测发现脊髓CSF渗漏6;4)新的成像技术表明,脊髓CSF渗漏到硬膜外和椎旁静脉(即所谓的CSF静脉瘘)比以前认识到的要常见得多,传统的MRI、磁共振骨髓图和计算机断层扫描骨髓图都会忽略这一点,而脊柱成像结果却令人不安。这些可能只有在侧卧数字减影骨髓图中才会变得明显,这是一种尚未广泛实践或可用的技术。7总之,在EDS的原始报告之后发表的这些不断发展的理解表明,神经外科医生应该:1)对EDS人群中的CSF泄漏有更高的怀疑指数;2) 谦虚地看待我们目前通过开放压力和成像排除脊髓脑脊液泄漏的能力;3) 有一个较低的阈值来花费精力来识别和治疗慢性残疾的这种可修复的原因;和4)注意国际头痛疾病分类(ICHD-3)所包含的指南,该指南指出,“对于典型的直立性头痛且无明显病因的患者,在排除体位性直立性心动过速综合征后,在临床实践中提供自体腰段硬膜外血液贴剂是合理的”。8作为疑似脑脊液渗漏评估和治疗的看门人,神经外科医生在患有直立性头痛的EDS患者中大力寻求CSF渗漏的临床决定将可能决定该患者的整个临床过程。
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