Pneumocephalus

气胸
  • 文章类型: Case Reports
    小儿神经外科在脑积水的治疗中面临着重大的困难,一种以脑脊髓液(CSF)异常积聚为特征的疾病。它的患病率在全球每1000名活产儿中有0.5到0.8个不等,不同的病因,包括先天性异常和获得性疾病。其好处包括降低感染风险和避免由于分流引起的问题,在某些情况下,内镜第三脑室造瘘术(ETV)已成为一种有益的手术技术。绕过阻塞的心室通道,ETV为脑脊液引流创造了新的通道。尽管有效,对潜在疾病和解剖学变量进行彻底检查对于患者选择的阳性结果是必要的.给病人,最好的照顾,本文试图总结脑积水的患病率以及ETV在管理脑积水中所起的作用。它还强调了定制手术技术的重要性。了解脑积水的发生率和可用的治疗选择对于提高婴儿的生活质量和长期预后至关重要。
    Pediatric neurosurgery faces a major difficulty in the treatment of hydrocephalus, a condition marked by an abnormal build-up of cerebrospinal fluid (CSF) in the brain. Its prevalence varies between 0.5 and 0.8 per 1,000 live births worldwide, with different etiologies, including congenital abnormalities and acquired diseases. With benefits including a lower risk of infection and avoiding issues due to the shunt, endoscopic third ventriculostomy (ETV) has become a beneficial surgical technique in certain instances. Bypassing clogged ventricular channels, ETV creates a new channel for CSF drainage. Despite its effectiveness, a thorough examination of underlying disease and anatomical variables is necessary for positive outcomes in patient selection. To give patients, the best possible care, this article attempts to summarize the prevalence of hydrocephalus and the part that ETV plays in managing it. It also emphasizes the significance of customized surgical techniques. It is critical to comprehend the incidence of hydrocephalus and available treatment choices to enhance the infant\'s quality of life and long-term outcomes.
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  • 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: Journal Article
    一名没有明显病史的69岁妇女前往急诊科评估和管理精神状态改变以及上呼吸道感染症状恶化的10天病史。两天前,她在紧急护理中心接受了评估,她报告了生产性咳嗽和颈部疼痛。急诊科的评估引起了对脓毒症和脑膜炎的怀疑,和头部的计算机断层扫描显示非创伤性脑外伤,有证据表明窦骨侵蚀进入大脑。培养结果显示播散的肺炎链球菌。继发于脑膜炎的脑血管病变导致大脑区域的双侧急性缺血性中风,有可能导致严重残疾。
    A 69-year-old woman without significant medical history presented to an emergency department for evaluation and management of altered mental status and a 10-day history of worsening symptoms of upper respiratory infection. Two days previously, she had been evaluated at an urgent care center, where she reported productive cough and neck pain. Evaluation in the emergency department aroused suspicions of sepsis and meningitis, and computed tomography of the head revealed nontraumatic pneumocephalus with evidence of bony erosion of the sinus into the brain. Culture results revealed disseminated Streptococcus pneumoniae. Cerebral vasculopathy secondary to the meningitis caused bilateral acute ischemic strokes in areas of the brain, with the potential to lead to significant disability.
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  • 文章类型: Case Reports
    这里,我们描述了起源于额筛窦内翻性乳头状瘤(IP)的气颅的独特病例。一名71岁的糖尿病患者出现头痛和意识改变。影像学检查显示,左额窦出现了气颅和骨骼破坏。他使用ORBEYE外镜同时接受了鼻内镜和经颅手术。肿瘤的病理诊断证实IP。手术后,气颅明显消退,鳞状细胞癌抗原水平,被抬高了,decreased.此病例强调了多学科方法和创新手术方法在治疗复杂的鼻窦病变中的重要性。
    Here, we describe the unique case of a pneumocephalus originating from an inverted papilloma (IP) in the frontoethmoidal sinus. A 71-year-old man with diabetes presented with headaches and altered consciousness. Imaging revealed the pneumocephalus together with bone destruction in the left frontal sinus. He underwent simultaneous endoscopic endonasal and transcranial surgery using an ORBEYE exoscope. Pathological diagnosis of the tumor confirmed IP. Post-surgery, the pneumocephalus was significantly resolved and the squamous cell carcinoma antigen level, which had been elevated, decreased. This case underscores the importance of a multidisciplinary approach and innovative surgical methods in treating complex sinonasal pathologies.
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  • 文章类型: Case Reports
    纤维发育不良是一种良性纤维骨病变,正常骨被未成熟的发育不良编织骨和纤维组织所取代。纤维发育不良有可能在罕见的情况下累及颅面区域的多个骨骼。应仔细评估这种参与类型的管理。
    这里,我们报告了一名52岁男性患者,患有进行性和双侧额叶头痛.放射/病理诊断显示鼻旁窦纤维发育不良,前颅底延伸和脑气。病人做了开颅手术,手术后两周,症状缓解,无任何并发症。
    在纤维发育不良的情况下,新发病和/或症状轻微的患者可能在多个颅面骨骼中有广泛的病变。
    UNASSIGNED: Fibrous dysplasia is a benign fibro-osseous lesion where normal bone is replaced with immature dysplastic woven bone and fibrous tissue. Fibrous dysplasia has the potential to involve multiple bones of the craniofacial area in a rare condition. Management of this involvement type should be assessed carefully.
    UNASSIGNED: Here, we report a 52-year-old man with progressive and bilateral frontal headache. The radio/pathologic diagnosis revealed fibrous dysplasia of paranasal sinuses with anterior skull-base extension and pneumocephalus. The patient underwent a craniotomy, and 2 weeks after the procedure, the symptoms were alleviated without any complications.
    UNASSIGNED: in case of fibrous dysplasia, patients with new onset and/or mild symptoms may have extensive lesions in multiple craniofacial bones.
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  • 文章类型: Case Reports
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  • 文章类型: Case Reports
    我们在这里报告了非常罕见的自发性心室内张力性气颅病例。该病例涉及一名40岁的患者,该患者有松果体区肿瘤病史,并通过多脑室腹膜分流术治疗继发性脑积水。他因为不寻常的头痛出现在急诊室,恶心,和视觉损失。此外,他报告了几个星期的轻微鼻漏。最初的脑部CT扫描显示自发性脑室内张力性气血。没有近期头部外伤的病史,也没有分流系统断开的迹象。补充的放射学评估包括薄层骨CT扫描和放射性同位素池造影,该造影显示骨缺损和同位素渗漏在鼓膜和左颞骨鳞状部分之间的交界处。进行了中颅窝手术以修复骨膜破裂。
    Here, we report a very rare case of spontaneous intraventricular tension pneumocephalus. This case concerns a 40-year-old patient with medical history of a tumor of the pineal region and a secondary hydrocephalus treated by multiple ventriculoperitoneal shunts. He presented in the emergency room because of unusual headaches, nausea, and visual loss. In addition, he reported slight rhinorrhea in the past few weeks. The initial brain computed tomography scan revealed a spontaneous intraventricular tension pneumocephalus. There was no history of recent head trauma and no sign of disconnection of the shunt system. A complementary radiologic assessment including a thin-slice bone computed tomography scan and a radioisotope cisternography revealed an osseous defect and an isotope leakage at the junction between the tegmen tympani and the squamous part of the left temporal bone. A middle cranial fossa surgery was performed to repair the osteo-meningeal breach.
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  • 文章类型: Case Reports
    具有孤立精神病表现的慢性硬膜下血肿(CSDH)很少见。在本文中,我们报道了一例77岁女性患者,该患者在重复性头部创伤后出现精神病性抑郁症,但没有任何神经系统症状.脑磁共振成像显示右额顶区域硬膜下血肿为20mm,左额区域硬膜下血肿为7mm。精神症状在撤离后的第一周内得到改善,但随着右侧气颅的发生而复发。在后续行动中,随着气颅的消失,精神症状有所改善。应该记住,由于硬膜下血肿可以看到孤立的精神症状,血肿的清除对改善精神症状具有重要作用。
    Chronic subdural hematomas (CSDH) with isolated psychiatric presentation are rare. In this paper, we report a case of 77-year-old-female patient who had psychotic depression after repetitive head trauma without any neurological symptoms. The brain magnetic resonance imaging revealed an 20 mm subdural hematoma in the right frontoparietal region and a 7 mm subdural hematoma in the left frontal region. The psychiatric symptoms improved within the first week after evacuation but relapsed with the occurrence of right sided pneumocephalus. In the follow up, with the disappearance of the pneumocephalus, the psychiatric symptoms improved. It should be kept in mind that isolated psychiatric symptoms can be seen due to subdural hematoma and evacuation of the hematoma has an important role in improving the psychiatric symptoms.
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  • 文章类型: Journal Article
    背景:伽玛刀立体定向放射外科(GKRS)是公认的安全有效的脑转移治疗方法;然而,一些并发症可能带来重大的临床挑战.该病例报告强调了GKRS后罕见的脑脊液(CSF)渗漏和颅内积气,强调需要意识和及时管理这些并发症。
    方法:2017年对一名35岁男性患者进行了GKRS治疗,该患者于2015年有唇部恶性肿瘤病史,恶性肿瘤经神经周围扩散至左侧海绵窦。患者因持续头痛和头晕在出院后39天紧急入院。
    方法:脑计算机断层扫描(CT)显示弥漫性双侧气颅,同时观察到脑脊液渗漏。
    方法:进行了包括左额颞部开颅术的外科手术,以切除残留的颅底肿瘤并修复硬脑膜,由导航仪系统引导。最终的病理评估显示存在鳞状细胞癌标志物。
    结果:患者对整个手术表现出良好的耐受性,并经历了迅速而平稳的恢复过程。手术后,症状缓解,脑脊液漏停止。随访图像显示气颅消退。
    结论:由于GKRS后早期引起的尘骨并不常见。肿瘤的快速缩小和脑转移通过硬脑膜扩散的时机可能导致CSF渗漏和颅内积气。我们回顾了当前的治疗方案,并介绍了成功的基于开颅手术的硬脑膜修复病例。
    BACKGROUND: Gamma knife stereotactic radiosurgery (GKRS) is a recognized safe and effective treatment for brain metastasis; however, some complications can present significant clinical challenges. This case report highlights a rare occurrence of cerebrospinal fluid (CSF) leakage and pneumocranium following GKRS, emphasizing the need for awareness and prompt management of these complications.
    METHODS: A 35-year-old male with a history of malignant neoplasm of the lip in 2015 and perineural spread of malignancy into the left cavernous sinus was treated with GKRS in 2017. The patient was admitted emergently 39 days after discharge due to persistent headache and dizziness.
    METHODS: Brain computed tomography (CT) revealed diffuse bilateral pneumocranium alongside an observation of CSF leakage.
    METHODS: A surgical procedure involving a left frontal-temporal craniotomy was performed to excise a residual skull base tumor and repair the dura, guided by a navigator system. The conclusive pathological assessment revealed the presence of squamous cell carcinoma markers.
    RESULTS: The patient exhibited excellent tolerance to the entire procedure and experienced a prompt and uneventful recovery process. After surgery, the symptoms alleviated and CSF leak stopped. The follow-up image showed the pneumocranium resolved.
    CONCLUSIONS: Pneumocranium due to early-stage post-GKRS is uncommon. The rapid tumor shrinkage and timing of brain metastasis spreading through the dura can lead to CSF leak and pneumocranium. We reviewed current treatment options and presented a successful craniotomy-based dura repair case.
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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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