tension pneumocephalus

  • 文章类型: Case Reports
    背景张力性气颅是一种罕见的术后并发症,通常在开颅手术后表现为精神状态改变或神经迅速下降。我们报告了一例复杂的脑室腹膜(VP)分流术后由移植物缩回引发的张力性气颅。病例史:39岁女性,左三叉神经海绵窦神经鞘瘤复发,先前一次切除后的状态,两种立体定向放射外科治疗,一个疗程的分割放疗,行根治性切除,眼眶切除术和腹部无脂肪移植重建,然后辅助放疗治疗恶性转化。她出现了亚急性脑室扩张,精神状态改变,提示VP分流放置。三周后,她出现了严重的气颅和脑室内空气,左侧蝶骨和上颌骨缺损,脂肪移植物从其中缩回。放置了右额外部心室引流(EVD),导致在高压下立即释放空气。明确的治疗需要用背阔肌游离皮瓣进行颅底重建,对侧鼻中隔皮瓣,抗生素,和VP分流翻修术治疗合并脑脊液(CSF)漏,气颅,脑室炎,还有低压脑积水.在她的最后一次随访中,她恢复到最初的切除后神经基线.结论张力性气颅是一种罕见且危及生命的急症,需要立即进行神经外科手术。我们报告了放疗和CSF转移后移植物回缩引起的张力性气颅的指标。在观察到的地方,由颅底CSF泄漏引起的张力性气颅可能与低压脑积水有关,成功的长期管理需要平衡脑脊液分流的需求与颅底重建的完整性。
    Background  Tension pneumocephalus is a rare postoperative complication, typically presenting with mental status changes or rapid neurological decline after craniotomy. We report a complex case of tension pneumocephalus triggered by graft retraction after ventriculoperitoneal (VP) shunt placement. Case History  A 39-year-old woman with a recurrent left trigeminal cavernous sinus schwannoma, status post one prior resection, two stereotactic radiosurgery treatments, and one course of fractionated radiotherapy, underwent radical resection with orbital exenteration and abdominal fat free graft reconstruction followed by adjuvant radiotherapy for malignant transformation. She developed subacute ventriculomegaly with altered mental status, prompting VP shunt placement. Three weeks later, she presented with profound pneumocephalus and intraventricular air originating from a large, left-sided sphenoid and maxillary defect, from which the fat graft had retracted. A right frontal external ventricular drain (EVD) was placed, resulting in immediate release of air under high pressure. Definitive treatment required skull base reconstruction with a latissimus dorsi free flap, contralateral nasoseptal flap, antibiotics, and VP shunt revision for treatment of combined cerebrospinal fluid (CSF) leak, pneumocephalus, ventriculitis, and low-pressure hydrocephalus. As of her last follow-up, she was restored to her initial postresection neurological baseline. Conclusion  Tension pneumocephalus is a rare and life-threatening emergency that requires immediate neurosurgical intervention. We report the index case of tension pneumocephalus induced by graft retraction following radiotherapy and CSF diversion. Where observed, tension pneumocephalus resulting from a skull base CSF leak may be associated with low-pressure hydrocephalus, and successful long-term management demands balancing the need for CSF diversion against the integrity of the skull base reconstruction.
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  • 文章类型: Case Reports
    此病例报告介绍了一名55岁女性的中表皮样囊肿(IDEC)的独特表现。她出现了由Valsalva动作引发的急性小脑症状。IDECs是一种罕见的颅内表皮样囊肿。它们是良性的,并且具有缓慢的生长模式,可转化为逐渐发展的症状而不是急性症状。症状包括局部畸形,局灶性神经功能缺损,和痛苦。由于乳突骨的侵蚀,该患者出现了急性小脑症状,乳突骨通过乳突空气细胞在咽鼓管和颅内间隙之间形成了一条通路。因此,张力性气颅通过球阀效应出现,在后颅窝引起明显的质量效应。通过恢复颅内外屏障的完整性,IDEC的手术切除和乳突空气细胞的关闭可缓解症状。这种情况突出表明,在充气骨结构附近的IDEC需要更高的警惕性,比如乳突气室和鼻旁窦,提倡采取更积极主动的方法。
    This case report presents a unique presentation of an intradiploic epidermoid cyst (IDEC) in a 55-year-old female. She presented with acute cerebellar symptoms triggered by a Valsalva maneuver. IDECs are a rare type of intracranial epidermoid cysts. They are benign and have a slow growth pattern that translates into progressively developing symptoms instead of acute symptoms. Symptoms include local deformities, focal neurologic deficits, and pain. This patient developed acute cerebellar symptoms due to erosion of the mastoid bone that created a pathway between the eustachian tube and the intracranial space via the mastoid air cells. Consequently, tension pneumocephalus emerged via a ball-valve effect that caused a significant mass effect in the posterior fossa. Surgical resection of the IDEC and closing of the mastoid air cells resulted in symptom relief by restoring the integrity of the intracranial-extracranial barrier. This case highlights that a higher level of vigilance is warranted for an IDEC in the proximity of aerated bone structures, such as the mastoid air cells and the paranasal sinuses, and that a more proactive approach is advocated.
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  • 文章类型: Journal Article
    背景:张力性气颅(PMC)是经鼻内镜(EEA)颅底手术后的一种罕见且令人恐惧的并发症。这是一种神经外科紧急情况,需要紧急减压以避免灾难性的神经系统损伤或死亡。可避免的原因是在EEA患者中应用正压通气(PPV)治疗术后缺氧。为此,我们的机构实施了医院范围的协议,以识别和管理有风险的患者;本文旨在确定该协议是否有效降低PPV继发的PMC张力发生率。
    结果:在协议实施后的3年内,110名患者接受了EEA,从中确定了1例张力PMC(发现不是PPV继发的)。与过去5年中2例PPV继发的张力PMC相比,406例EEA患者。这构成了标准和扩展方法EEA中与PPV相关的张力PMC的可量化降低,标志着协议的有效吸收。
    结论:自实施全机构指南以来,我们未发现本机构EEA颅底手术后PPV出现张力PMC的病例。这强调了我们的简单且具有成本效益的预防方案在减少PPV术后意外应用后的总张力PMC速率方面的实用性。需要进一步的研究来研究EEA后患者中PPV的比较风险和益处,从而为方案的未来迭代提供信息。
    BACKGROUND: Tension pneumocephalus (PMC) is a rare and feared complication following the endonasal endoscopic approach (EEA) to skull base procedures. This is a neurosurgical emergency that requires urgent decompression to avoid catastrophic neurologic damage or death. An avoidable cause is the application of positive pressure ventilation (PPV) in EEA patients for postoperative hypoxia. Our institution implemented a hospital-wide protocol in response to this to identify and manage at-risk patients; this paper aims to identify if this protocol was effective in lowering the rates of tension PMC secondary to PPV.
    RESULTS: In the 3 years following the implementation of the protocol, 110 patients underwent EEAs, from which 1 case of tension PMC (found to be not secondary to PPV) was identified. This is compared with 2 cases of tension PMC secondary to PPV over the preceding 5 years, out of 406 EEA patients. This constitutes a quantifiable reduction in PPV-related tension PMC in both standard and extended approach EEAs, signifying the effective uptake of the protocol.
    CONCLUSIONS: We found no cases of tension PMC after PPV following EEA skull base surgery in our institution since the implementation of an institution-wide guideline. This underscores the utility of our simple and cost-effective preventative protocol in reducing the overall rates of tension PMC following the inadvertent postoperative application of PPV. Further research is needed to study the comparative risks and benefits of PPV in the post-EEA patient and thus inform future iterations of the protocol.
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  • 文章类型: Journal Article
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  • 文章类型: Journal Article
    目的:张力性气颅(TP)是一种罕见的病理,其特征是颅内间隙中不断积聚空气,与疝的风险增加有关,神经系统恶化和死亡。关于神经外科创伤病例,TP主要是在慢性硬膜下血肿清除后遇到的。在这个案例报告中,我们介绍了一例罕见的在开颅手术治疗急性硬膜下血肿(aSDH)后发生的致命性术后TP.病例介绍:一位83岁的先生因意识受损而被送往我院急诊科。初步检查显示Glascow昏迷量表(GCS)3/15,两侧瞳孔3mm,瞳孔光反射受损。CT扫描显示左侧aSDH较大,具有显著的压力现象和中线偏移。通过开颅手术对患者进行血肿的顺利清除,并放置了闭合的重力下引流管。第二天,在他转移到CT扫描仪后,他表现出迅速的神经系统恶化,伴有急性发作性角膜不畅,最后伴有固定和散瞳的瞳孔散大。术后CT扫描显示大量TP,病人被转移到手术室做紧急左骨瓣减压手术,术中没有颅内滞留空气的迹象。最后,他仍然处于严重的临床状态,在术后第八天去世.结论:TP代表罕见但严重的神经外科急症,在急性创伤情况下开颅手术后也可能遇到。相关从业者应该意识到这种潜在的致命并发症,以便进行早期发现和适当管理。
    UNASSIGNED: Tension pneumocephalus (TP) represents a rare pathology characterized by constant accumulation of air in the intracranial space, being associated with increased risk of herniation, neurologic deterioration and death. Regarding neurosurgical trauma cases, TP is majorly encountered after chronic subdural hematoma evacuation. In this case report, we present a rare case of fatal postoperative TP encountered after craniotomy for evacuation of acute subdural hematoma (aSDH).
    UNASSIGNED: An 83-year old gentleman was presented to the emergency department of our hospital with impaired level of consciousness. Initial examination revealed Glascow Coma Scale (GCS) 3/15, with pupils of 3 mm bilaterally and impaired pupillary light reflex. CT scan demonstrated a large left aSDH, with significant pressure phenomena and midline shift. Patient was subjected to an uneventful evacuation of hematoma via craniotomy and a closed subgaleal drain to gravity was placed. The following day and immediately after his transfer to the CT scanner, he presented with rapid neurologic deterioration with acute onset anisocoria and finally mydriasis with fixed and dilated pupils. Postoperative CT scan showed massive TP, and the patient was transferred to the operating room for urgent left decompressive craniectomy, with no intraoperative signs of entrapped air intracranially. Finally, he remained in severe clinical status, passing away on the eighth postoperative day.
    UNASSIGNED: TP represents a rare but severe neurosurgical emergency that may be also encountered after craniotomy in the acute trauma setting. Involved practitioners should be aware of this potentially fatal complication, so that early detection and proper management are conducted.
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  • 文章类型: Journal Article
    目的:描述一种治疗慢性硬膜下血肿(CSDH)的毛刺孔颅骨造口术的简单变化,该方法使用额叶引流系统,以便在发生张力性气颅时及时减压,并且不需要额外的手术。
    方法:我们对20例CSDH患者进行了头孔开颅造口术,以及20例患者进行了相同的手术,同时放置了5fr新生儿饲管作为前颅造口术的备用引流。视情况而定,二级排水沟最长可保持72小时,以便打开并在紧急排水环境中使用,抽吸,或者作为带有水封的单向阀。
    结果:描述了20例接受该手术的患者和20例对照的结果。每组均有一名患者出现张力性气颅。一个患者通过在水封下打开备用排水管以排空气颅而迅速解决,另一个患者不得不重新打开颅骨造口术。
    结论:所描述的毛刺孔颅造口术的变化代表了一种低成本且易于实施的技术,可用于张力性气颅的紧急减压。它还具有降低再手术率和CSDH复发的潜力。需要前瞻性对照研究来进一步验证这种方法。
    OBJECTIVE: To describe a simple variation of burr hole craniostomy for the management of chronic subdural hematoma (CSDH) that uses a frontal drainage system to facilitate timely decompression in the event of tension pneumocephalus and spares the need for additional surgery.
    METHODS: We conducted a retrospective analysis of 20 patients with CSDH who underwent burr hole craniostomy and 20 patients who underwent the same procedure alongside the placement of a 5 Fr neonatal feeding tube as a backup drainage for the anterior craniostomy. Depending on the situation, the secondary drain stayed for a maximum of 72 hours to be opened and used in emergency settings for drainage, aspiration, or as a 1-way valve with a water seal.
    RESULTS: The outcomes of 20 patients who underwent this procedure and 20 controls are described. One patient from each group presented tension pneumocephalus. One was promptly resolved by opening the backup drain under a water seal to evacuate pneumocephalus and the other patient had to undergo a reopening of the craniostomy.
    CONCLUSIONS: The described variation of burr hole craniostomy represents a low-cost and easy-to-implement technique that can be used for emergency decompression of tension pneumocephalus. It also has the potential to reduce reoperation rates and CSDH recurrence. Prospective controlled research is needed to validate this approach further.
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  • 文章类型: Case Reports
    创伤性张力性气颅是创伤性脑损伤的一种罕见且危及生命的并发症,需要及时诊断和神经外科治疗。然而,及时管理阻抗的各种可能性,包括与患者相关的障碍在低收入和中等收入国家通常会遇到。在这里,我们提出了由于最初拒绝紧急手术而导致的创伤性张力性气颅病例的治疗延迟。一名59岁的男性在一次摩托车事故后出现在急诊科,完全警惕,没有神经缺陷。他承认在初次创伤后1小时内流鼻涕明显,但体检时没有出现鼻漏或耳漏。头部CT显示广泛的气颅,有“富士山征”,“前颅底骨折,额窦骨折.由于良好的临床状况和财务恐慌,患者最初拒绝立即进行手术干预。创伤后40小时发生意识的急性下降:GCS为6,两个瞳孔均有轻微扩张(4毫米),瞳孔反射缓慢。急诊双额开颅手术,硬膜下空气引流,术后进行硬脑膜撕裂修复。术后护理顺利,意识迅速改善,随访头颅CT显示硬膜下积液最少,没有残留的气颅。患者在7天后出院,GCS为15,GOS为5,证明了在低收入和中等收入国家克服延迟提供神经创伤护理障碍的重要性。
    Traumatic tension pneumocephalus is a rare and life-threatening complication of traumatic brain injury necessitating prompt diagnosis and neurosurgical treatment. Nevertheless, various possibilities for impedance in timely management, including patient-related barriers are commonly experienced in low-and middle-income countries setting. Here we presented a delay of management in traumatic tension pneumocephalus case due to initial refusal for emergency surgery. A 59-year-old male presented to the emergency department following a motorcycle accident fully alert with no neurological deficit. He acknowledged clear nasal discharge within 1 h after the initial trauma, but no rhinorrhea or otorrhea was present during physical examination. Head CT revealed extensive pneumocephalus with \"Mount Fuji sign,\" anterior skull base fracture, and frontal sinus fracture. The patient initially refused immediate surgical intervention due to excellent clinical condition and financial scare. Acute decrease of consciousness occurred 40 h post-trauma: GCS of 6 with slight dilatation of both pupils (4 mm) and sluggish pupillary reflex. Emergency bifrontal craniotomy, subdural air drainage, and dura mater tear repair were performed afterwards. Postoperative care was uneventful, with rapid improvement of consciousness and follow-up head CT showing minimal subdural fluid collection and absence of remaining pneumocephalus. The patient was discharged from the hospital after 7 days with GCS of 15 and GOS of 5, proving the importance of overcoming barriers for delay in delivering neurotrauma care in low-and middle-income countries.
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  • 文章类型: Journal Article
    颅脑手术后对大脑和颅骨的成像评估是放射科工作流程的常规和重要组成部分。各种正常的预期发现以及早期和晚期并发症与术后颅骨有关。在这篇图片评论中,作者用说明性病例描述了与颅骨手术相关的各种疾病的典型影像学特征.
    对术后头颅影像表现谱的良好了解和理解对于放射科医生准确诊断潜在并发症并将其与正常术后发现区分开来至关重要。改善患者预后并指导进一步治疗。
    Imaging evaluation of the brain and cranium after cranial surgery is a routine and significant part of the workflow of a radiology department. Various normal expected findings and early and late complications are associated with the post-operative cranium. In this pictorial review, the authors describe the typical imaging features of the spectrum of various conditions associated with cranial surgery with illustrative cases.
    UNASSIGNED: A good knowledge and understanding of the spectrum of imaging appearances in the post-operative cranium is vital for the radiologist to accurately diagnose potential complications and distinguish them from normal post-operative findings, improving patient outcomes and guiding further treatment.
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  • 文章类型: Review
    背景:脑室腹膜分流后自发性气颅是一种非常独特的并发症,在少数病人身上看到的。颅内压长期升高会形成小骨缺损,一旦脑室腹膜分流后颅内压降低,这可能会导致肺气肿。
    方法:这里,我们介绍了一例15岁的NF1患者,该患者在分流后10个月出现了气颅,以及我们的治疗策略和对这种情况的文献综述.
    结论:NF1和脑积水可导致颅底侵蚀,在进行VP分流之前需要抬头检查,以避免迟发性气颅。带有LT开口的SOKHA是一种微创方法,适用于同时解决这两个问题。
    BACKGROUND: Spontaneous pneumocephalus following ventriculoperitoneal shunting is a very unique complication, seen in a handful of patients. Small bony defects form as a result of chronically raised intracranial pressure, which can later lead to pneumocephalus once intracranial pressure decreases following ventriculoperitoneal shunting.
    METHODS: Here, we present a case of a 15-year-old girl with NF1 who presented to us with pneumocephalus 10 months following shunting and our management strategy along with a literature review of this condition.
    CONCLUSIONS: NF1 & hydrocephalus can lead to skull base erosion, which needs to be looked up before proceeding with VP shunting to avoid delayed onset pneumocephalus. SOKHA with the opening of LT is a minimally invasive approach suitable to tackle both problems simultaneously.
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  • 文章类型: Case Reports
    脊柱手术后的张力性气颅(TP)非常罕见,英文文献中仅报道了少数病例。大多数TP病例在脊柱手术后迅速发生。传统上,TP使用毛刺孔来缓解颅内压。然而,我们的病例突出了在常规颈椎手术后1个月出现罕见的TP和肺出血延迟表现.据我们所知,这是脊柱手术后使用硬脑膜修复和支持性护理治疗的第一例TP。一名75岁的女性在接受常规宫颈减压和稳定宫颈脊髓病后出现TP。初次手术后一个月,她因伤口漏水和精神状态改变而重新就诊,入院后不久迅速恶化。这个,结合她的影像学特征,影响了紧急探索她手术伤口的决定。她完全康复,住院2周后出院。我们希望强调对脑脊液漏的怀疑指数较高,并且需要较低的阈值才能返回手术室以修复潜在的硬脑膜缺损,并说明脊柱手术后的TP可以成功治疗而没有毛刺孔。
    Tension pneumocephalus (TP) after spinal surgery is very rare with only a few cases reported in the English literature. Most cases of TP occur rapidly after spinal surgery. Traditionally, TP is managed using burr holes to relieve intracranial pressure. However, our case highlights a rare delayed presentation of TP and pneumorrhacis 1 month after routine cervical spine surgery. It is to our knowledge the first case of TP after spinal surgery to be treated using dural repair and supportive care. A 75-year-old woman presented with TP after having routine cervical decompression and stabilisation for cervical myelopathy. She re-presented 1 month after her initial operation with a leaking wound and altered mental status, which deteriorated rapidly shortly after admission. This, in combination with her radiographic features, influenced the decision to explore her surgical wound emergently. She made a full recovery and was discharged after 2 weeks in hospital. We hope to emphasise the need for a high index of suspicion for cerebrospinal fluid leaks and the low threshold to return to theatre to repair a potential dural defect, as well as illustrate that TP after spinal surgery can be treated successfully without burr holes.
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