Pub Date : 2024-05-01DOI: 10.17712/nsj.2024.2.20230072
Ameerah K Alsaqobi, Brouj A Miskin, Biju Gopinath, Ghada Elgohary
Bilateral femoral neuropathy is rare, especially that caused by bilateral compressive iliopsoas, psoas, or iliacus muscle hematomas. We present a case of bilateral femoral neuropathy due to spontaneous psoas hematomas developed during COVID-19 critical illness. A 41-year-old patient developed COVID-19 pneumonia, and his condition deteriorated rapidly. A decrease in the hemoglobin level prompted imaging studies during his intensive care unit (ICU) stay. Bilateral psoas hematomas were identified as the source of bleeding. Thereafter, the patient complained of weakness in both upper and lower limbs and numbness in the lower limb. He was considered to have critical illness neuropathy and was referred to rehabilitation. Electrodiagnostic testing suggested bilateral femoral neuropathy because of compression due to hematomas developed during the course of his ICU stay. The consequences of iliopsoas hematomas occurring in the critically ill can be catastrophic, ranging from hemorrhagic shock to severe weakness, highlighting the importance of recognizing this entity.
{"title":"More than what meets the eye in COVID-19 critical illness: A case report of bilateral femoral neuropathy due to psoas hematomas.","authors":"Ameerah K Alsaqobi, Brouj A Miskin, Biju Gopinath, Ghada Elgohary","doi":"10.17712/nsj.2024.2.20230072","DOIUrl":"10.17712/nsj.2024.2.20230072","url":null,"abstract":"<p><p>Bilateral femoral neuropathy is rare, especially that caused by bilateral compressive iliopsoas, psoas, or iliacus muscle hematomas. We present a case of bilateral femoral neuropathy due to spontaneous psoas hematomas developed during COVID-19 critical illness. A 41-year-old patient developed COVID-19 pneumonia, and his condition deteriorated rapidly. A decrease in the hemoglobin level prompted imaging studies during his intensive care unit (ICU) stay. Bilateral psoas hematomas were identified as the source of bleeding. Thereafter, the patient complained of weakness in both upper and lower limbs and numbness in the lower limb. He was considered to have critical illness neuropathy and was referred to rehabilitation. Electrodiagnostic testing suggested bilateral femoral neuropathy because of compression due to hematomas developed during the course of his ICU stay. The consequences of iliopsoas hematomas occurring in the critically ill can be catastrophic, ranging from hemorrhagic shock to severe weakness, highlighting the importance of recognizing this entity.</p>","PeriodicalId":19284,"journal":{"name":"Neurosciences","volume":"29 2","pages":"133-138"},"PeriodicalIF":1.2,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11305369/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140916855","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-05-01DOI: 10.17712/nsj.2024.2.20230061
Mohammed Almuqbil, Waad Aldoohan, Sara Alhinti, Nora Almahmoud, Imad Abdulmajeed, Rayan Alkhodair, Amna Kashgari, Duaa Baarmah, Waleed Altwaijri, Ahmad Alrumayyan
Objectives: To determine the prevalence of tuberous sclerosis complex (TSC) in the paediatric Saudi population and to characterise the range of clinical symptoms, neurocutaneous findings, neuroimaging results, and complications of the disease.
Methods: A total of 61 genetically confirmed TSC patients from the National Guard Health Affairs (NGHA) in Saudi Arabia were the subject of this retrospective descriptive analysis. The data were presented using descriptive measures.
Results: The mean age at diagnosis was found to be 4.9 years. Subependymal nodules (86.9%), numerous cortical tubers and/or radial migration lines (63.9%), and hypomelanotic macules (63.9%) were the 3 most common significant criteria. The vast majority (86.9%) of those diagnosed had epilepsy, of which 50% were considered medically intractable. Nearly half of our subjects underwent genetic testing, which revealed that TSC2 predominated over TSC1. Symptoms of Tuberous Sclerosis Complex-Associated Neuropsychiatric Disorders (TAND) were present in 66.7% of TSC1 patients and 73.9% of TSC2 patients.
Conclusion: The findings of this study demonstrate that the clinical spectrum of TSC among Saudi children is consistent with the body of existing literature. The TSC2 was more prevalent than TSC1. The most frequent signs were cutaneous and neurological. Monitoring TSC patients regularly is crucial to identify any issues as soon as possible.
{"title":"Review of the spectrum of tuberous sclerosis complex: The Saudi Arabian Experience.","authors":"Mohammed Almuqbil, Waad Aldoohan, Sara Alhinti, Nora Almahmoud, Imad Abdulmajeed, Rayan Alkhodair, Amna Kashgari, Duaa Baarmah, Waleed Altwaijri, Ahmad Alrumayyan","doi":"10.17712/nsj.2024.2.20230061","DOIUrl":"10.17712/nsj.2024.2.20230061","url":null,"abstract":"<p><strong>Objectives: </strong>To determine the prevalence of tuberous sclerosis complex (TSC) in the paediatric Saudi population and to characterise the range of clinical symptoms, neurocutaneous findings, neuroimaging results, and complications of the disease.</p><p><strong>Methods: </strong>A total of 61 genetically confirmed TSC patients from the National Guard Health Affairs (NGHA) in Saudi Arabia were the subject of this retrospective descriptive analysis. The data were presented using descriptive measures.</p><p><strong>Results: </strong>The mean age at diagnosis was found to be 4.9 years. Subependymal nodules (86.9%), numerous cortical tubers and/or radial migration lines (63.9%), and hypomelanotic macules (63.9%) were the 3 most common significant criteria. The vast majority (86.9%) of those diagnosed had epilepsy, of which 50% were considered medically intractable. Nearly half of our subjects underwent genetic testing, which revealed that TSC2 predominated over TSC1. Symptoms of Tuberous Sclerosis Complex-Associated Neuropsychiatric Disorders (TAND) were present in 66.7% of TSC1 patients and 73.9% of TSC2 patients.</p><p><strong>Conclusion: </strong>The findings of this study demonstrate that the clinical spectrum of TSC among Saudi children is consistent with the body of existing literature. The TSC2 was more prevalent than TSC1. The most frequent signs were cutaneous and neurological. Monitoring TSC patients regularly is crucial to identify any issues as soon as possible.</p>","PeriodicalId":19284,"journal":{"name":"Neurosciences","volume":"29 2","pages":"113-121"},"PeriodicalIF":1.2,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11305360/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140916907","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-05-01DOI: 10.17712/nsj.2024.2.20230089
Ali H Alassiri, Turki M Alfayea, Tariq I Aljared, Khaled R Alenezi
Subependymal giant cell astrocytoma (SEGA) is a rare circumscribed astrocytic glioma that occurs in approximately 25% of all tuberous sclerosis (TSC) cases. Herein, we discuss an atypical presentation of SEGA, including the genetic alterations, impact on clinical presentation, and the determinants of each medical and surgical treatment option. A 14-year-old girl presented with intermittent headache and a right intraventricular mass originating near the foramen of Monro. The tumor's proximity to critical structures necessitated maximum safe resection, which improved her symptoms. Histological findings indicated SEGA, and genetic sequencing revealed a TSC2 mutation. However, complete clinical and radiological evaluations failed to reveal TSC. Two months later, a new subependymal nodule was incidentally found. She had a recurrent left occipital horn lesion and diffuse smooth leptomeningeal enhancement with no spine drop metastases. She was administered everolimus as the tumor was considered unresectable. Subsequent imaging revealed a reduction in both residual and new lesions.
脐下巨细胞星形细胞瘤(SEGA)是一种罕见的环形星形胶质瘤,约占结节性硬化症(TSC)病例的25%。在此,我们将讨论 SEGA 的一种非典型表现,包括遗传改变、对临床表现的影响以及每种药物和手术治疗方案的决定因素。一名14岁的女孩因间歇性头痛和右侧脑室内肿块(起源于门罗孔附近)而就诊。由于肿瘤靠近重要结构,必须进行最大限度的安全切除,这才改善了她的症状。组织学检查结果显示她患有SEGA,基因测序显示她有TSC2基因突变。然而,完整的临床和放射学评估未能发现 TSC。两个月后,偶然发现了一个新的蝶鞍下结节。她的左枕角病变复发,弥漫性平滑脑膜强化,无脊柱下垂转移。由于肿瘤无法切除,她接受了依维莫司治疗。随后的影像学检查显示,残留病灶和新发病灶均有所减少。
{"title":"Sporadic subependymal giant cell astrocytoma with somatic <i>TSC2</i> mutation: A case report.","authors":"Ali H Alassiri, Turki M Alfayea, Tariq I Aljared, Khaled R Alenezi","doi":"10.17712/nsj.2024.2.20230089","DOIUrl":"10.17712/nsj.2024.2.20230089","url":null,"abstract":"<p><p>Subependymal giant cell astrocytoma (SEGA) is a rare circumscribed astrocytic glioma that occurs in approximately 25% of all tuberous sclerosis (TSC) cases. Herein, we discuss an atypical presentation of SEGA, including the genetic alterations, impact on clinical presentation, and the determinants of each medical and surgical treatment option. A 14-year-old girl presented with intermittent headache and a right intraventricular mass originating near the foramen of Monro. The tumor's proximity to critical structures necessitated maximum safe resection, which improved her symptoms. Histological findings indicated SEGA, and genetic sequencing revealed a <i>TSC2</i> mutation. However, complete clinical and radiological evaluations failed to reveal TSC. Two months later, a new subependymal nodule was incidentally found. She had a recurrent left occipital horn lesion and diffuse smooth leptomeningeal enhancement with no spine drop metastases. She was administered everolimus as the tumor was considered unresectable. Subsequent imaging revealed a reduction in both residual and new lesions.</p>","PeriodicalId":19284,"journal":{"name":"Neurosciences","volume":"29 2","pages":"139-143"},"PeriodicalIF":1.2,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11305366/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140916918","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-05-01DOI: 10.17712/nsj.2024.2.20230060
Rania Magadmi, Sara Nassibi, Fatemah Kamel, Aziza R Al-Rafiah, Duaa Bakhshwin, Maha Jamal, Mohammed Alsieni, Abdulhadi S Burzangi, M A F Zaher, Mohammed Bendary
Objectives: To investigate the fundamental mechanisms of the neuroprotective impact of Astaxanthin (AST) in a mouse model of Alzheimer's disease (AD) induced by scopolamine.
Methods: This research constituted an in vivo animal study encompassing 36 adult male mice, divided into 6 groups: Control, 100 mg/kg AST, 2 mg/kg scopolamine (AD group), 100 mg/kg AST+2 mg/kg scopolamine, 3 mg/kg galantamine+2 mg/kg scopolamine, and 100 mg/kg AST+3 mg/kg galantamine+2 mg/kg scopolamine. After 14 days, the mice's short-term memory, hippocampus tissue, oxidative and inflammatory markers were evaluated.
Results: The AST demonstrated a beneficial influence on short-term memory and a reduction in acetylcholinesterase activity in the brain. It exhibited neuroprotective and anti-amyloidogenic properties, significantly decreased pro-inflammatory markers and oxidative stress, and reversed the decline of the Akt-1 and phosphorylated Akt pathway, a crucial regulator of abnormal tau. Furthermore, AST enhanced the effect of galantamine in reducing inflammation and oxidative stress.
Conclusion: The findings indicate that AST may offer therapeutic benefits against cognitive dysfunction in AD. This is attributed to its ability to reduce oxidative stress, control neuroinflammation, and enhance Akt-1 and pAkt levels, thereby underscoring its potential in AD treatment strategies.
目的研究虾青素(AST)对东莨菪碱诱导的阿尔茨海默病(AD)小鼠模型神经保护作用的基本机制:本研究是一项体内动物研究,包括36只成年雄性小鼠,分为6组:对照组、100毫克/千克AST组、2毫克/千克东莨菪碱组(AD组)、100毫克/千克AST+2毫克/千克东莨菪碱组、3毫克/千克加兰他敏+2毫克/千克东莨菪碱组和100毫克/千克AST+3毫克/千克加兰他敏+2毫克/千克东莨菪碱组。14 天后,对小鼠的短期记忆、海马组织、氧化和炎症指标进行了评估:结果:AST 对小鼠的短期记忆产生了有益的影响,并降低了大脑中乙酰胆碱酯酶的活性。它还具有神经保护和抗淀粉样蛋白生成的特性,显著降低了促炎症标志物和氧化应激,并逆转了 Akt-1 和磷酸化 Akt 通路(异常 tau 的关键调节因子)的衰退。此外,AST还能增强加兰他敏在减少炎症和氧化应激方面的作用:结论:研究结果表明,AST 可为治疗认知功能障碍提供益处。结论:研究结果表明,AST可能对AD患者的认知功能障碍有治疗作用,这归因于它能够减少氧化应激、控制神经炎症、提高Akt-1和pAkt水平,从而突出了它在AD治疗策略中的潜力。
{"title":"The protective effect of Astaxanthin on scopolamine - induced Alzheimer's model in mice.","authors":"Rania Magadmi, Sara Nassibi, Fatemah Kamel, Aziza R Al-Rafiah, Duaa Bakhshwin, Maha Jamal, Mohammed Alsieni, Abdulhadi S Burzangi, M A F Zaher, Mohammed Bendary","doi":"10.17712/nsj.2024.2.20230060","DOIUrl":"10.17712/nsj.2024.2.20230060","url":null,"abstract":"<p><strong>Objectives: </strong>To investigate the fundamental mechanisms of the neuroprotective impact of Astaxanthin (AST) in a mouse model of Alzheimer's disease (AD) induced by scopolamine.</p><p><strong>Methods: </strong>This research constituted an in vivo animal study encompassing 36 adult male mice, divided into 6 groups: Control, 100 mg/kg AST, 2 mg/kg scopolamine (AD group), 100 mg/kg AST+2 mg/kg scopolamine, 3 mg/kg galantamine+2 mg/kg scopolamine, and 100 mg/kg AST+3 mg/kg galantamine+2 mg/kg scopolamine. After 14 days, the mice's short-term memory, hippocampus tissue, oxidative and inflammatory markers were evaluated.</p><p><strong>Results: </strong>The AST demonstrated a beneficial influence on short-term memory and a reduction in acetylcholinesterase activity in the brain. It exhibited neuroprotective and anti-amyloidogenic properties, significantly decreased pro-inflammatory markers and oxidative stress, and reversed the decline of the Akt-1 and phosphorylated Akt pathway, a crucial regulator of abnormal tau. Furthermore, AST enhanced the effect of galantamine in reducing inflammation and oxidative stress.</p><p><strong>Conclusion: </strong>The findings indicate that AST may offer therapeutic benefits against cognitive dysfunction in AD. This is attributed to its ability to reduce oxidative stress, control neuroinflammation, and enhance Akt-1 and pAkt levels, thereby underscoring its potential in AD treatment strategies.</p>","PeriodicalId":19284,"journal":{"name":"Neurosciences","volume":"29 2","pages":"103-112"},"PeriodicalIF":1.2,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11305357/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140916932","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-05-01DOI: 10.17712/nsj.2024.2.20230074
Osama Y Muthaffar, Anas S Alyazidi
Epilepsia partialis continua (EPC) is a rare type of focal motor seizure characterized by continuous, involuntary muscle contractions in a specific part of the body. These contractions usually involve rhythmic, twitching movements and can last for several hours to days. The seizures are usually limited to one part of the body and can be clonic or dystonic. EPC can affect people of all ages but is more common in children and adolescents. The pathophysiology of EPC is complex and depends on the cause. There are several possible causes of EPC including structural brain abnormalities, infections, metabolic and genetic disorders, inflammatory conditions, traumatic brain injury, and vascular causes. The work-up of EPC includes electroencephalography (EEG), magnetic resonance imaging (MRI) of the brain, position emission tomography (PET) scan of the brain, autoimmune antibodies, infection work-up, and metabolic and genetic work-up. The management of EPC can be challenging. Antiseizure medications (ASDs) including benzodiazepines are an integral part of the management of EPC. Immunotherapy trials are recommended in resistant cases. Epilepsy surgery is one of the effective modalities in some surgically amenable cases. This article reviews the topic of EPC and summarizes diagnostic and .treatment recommendations.
{"title":"Epilepsia partialis continua: A review.","authors":"Osama Y Muthaffar, Anas S Alyazidi","doi":"10.17712/nsj.2024.2.20230074","DOIUrl":"10.17712/nsj.2024.2.20230074","url":null,"abstract":"<p><p>Epilepsia partialis continua (EPC) is a rare type of focal motor seizure characterized by continuous, involuntary muscle contractions in a specific part of the body. These contractions usually involve rhythmic, twitching movements and can last for several hours to days. The seizures are usually limited to one part of the body and can be clonic or dystonic. EPC can affect people of all ages but is more common in children and adolescents. The pathophysiology of EPC is complex and depends on the cause. There are several possible causes of EPC including structural brain abnormalities, infections, metabolic and genetic disorders, inflammatory conditions, traumatic brain injury, and vascular causes. The work-up of EPC includes electroencephalography (EEG), magnetic resonance imaging (MRI) of the brain, position emission tomography (PET) scan of the brain, autoimmune antibodies, infection work-up, and metabolic and genetic work-up. The management of EPC can be challenging. Antiseizure medications (ASDs) including benzodiazepines are an integral part of the management of EPC. Immunotherapy trials are recommended in resistant cases. Epilepsy surgery is one of the effective modalities in some surgically amenable cases. This article reviews the topic of EPC and summarizes diagnostic and .treatment recommendations.</p>","PeriodicalId":19284,"journal":{"name":"Neurosciences","volume":"29 2","pages":"71-76"},"PeriodicalIF":1.2,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11305367/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140916843","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-05-01DOI: 10.17712/nsj.2024.2.20230097
Soha A Alomar, Aliaa H Ghoneim
Objectives: To calculate The Evans Index (EI) in normal Individuals. Ventricular enlargement is referred to as hydrocephalus. Computer tomography (CT) scans are commonly used to investigate such intracranial pathologies. The EI is an important parameter for diagnosing hydrocephalus.
Methods: We included all patients who underwent Computer tomography (CT) scan of the brain that was reported as normal. The mean EI was calculated for the whole sample stratified by age, gender, and ethnicity. Patients with an initial report indicating any intracranial pathology, such as hydrocephalus, tumors, hemorrhages, or neurodegenerative disorders, were excluded.
Results: A total of 1,330 brain CT scans carried out at our institution were reviewed retrospectively from August 2021 to December 2021. A total of 423 CT scans were screened after excluding 25 patients with abnormal imaging findings and 14 repeated images for the same patients. A total of 384 patients were included. The mean EI for the entire sample was 0.2550±0.0277. There was a minimal but statistically significant difference based on gender, with a mean EI of 0.2588±0.0274 for males and 0.2517±0.0276 for females (p=0.012). There was no statistically significant difference between Saudi and non-Saudi patients. EI increased progressively with age in both genders.
Conclusion: Our EI values were similar to many of those reported in other countries, which supports the use of the 0.3 cutoff for the diagnosis of hydrocephalus, regardless of gender, age, or ethnicity.
目标: 计算正常人的埃文斯指数(EI):计算正常人的埃文斯指数(EI)。脑室扩大被称为脑积水。计算机断层扫描(CT)通常用于检查此类颅内病变。EI 是诊断脑积水的一个重要参数:方法:我们纳入了所有接受计算机断层扫描(CT)但报告为正常的患者。我们按年龄、性别和种族分层计算了所有样本的平均 EI。初步报告显示有任何颅内病变(如脑积水、肿瘤、出血或神经退行性疾病)的患者不包括在内:回顾性分析了 2021 年 8 月至 2021 年 12 月期间在我院进行的 1,330 次脑部 CT 扫描。在排除了 25 例成像结果异常的患者和 14 例同一患者的重复图像后,共筛选出 423 例 CT 扫描。共纳入 384 例患者。整个样本的平均 EI 为 0.2550±0.0277。男性的平均 EI 为 0.2588±0.0274,女性为 0.2517±0.0276(P=0.012)。沙特籍和非沙特籍患者之间没有明显的统计学差异。男女患者的 EI 均随年龄增长而逐渐增加:我们的 EI 值与许多其他国家报告的 EI 值相似,这支持使用 0.3 临界值诊断脑积水,而不论性别、年龄或种族。
{"title":"Normative parameters of the Evans Index using Computer Tomography in the Saudi population.","authors":"Soha A Alomar, Aliaa H Ghoneim","doi":"10.17712/nsj.2024.2.20230097","DOIUrl":"10.17712/nsj.2024.2.20230097","url":null,"abstract":"<p><strong>Objectives: </strong>To calculate The Evans Index (EI) in normal Individuals. Ventricular enlargement is referred to as hydrocephalus. Computer tomography (CT) scans are commonly used to investigate such intracranial pathologies. The EI is an important parameter for diagnosing hydrocephalus.</p><p><strong>Methods: </strong>We included all patients who underwent Computer tomography (CT) scan of the brain that was reported as normal. The mean EI was calculated for the whole sample stratified by age, gender, and ethnicity. Patients with an initial report indicating any intracranial pathology, such as hydrocephalus, tumors, hemorrhages, or neurodegenerative disorders, were excluded.</p><p><strong>Results: </strong>A total of 1,330 brain CT scans carried out at our institution were reviewed retrospectively from August 2021 to December 2021. A total of 423 CT scans were screened after excluding 25 patients with abnormal imaging findings and 14 repeated images for the same patients. A total of 384 patients were included. The mean EI for the entire sample was 0.2550±0.0277. There was a minimal but statistically significant difference based on gender, with a mean EI of 0.2588±0.0274 for males and 0.2517±0.0276 for females (<i>p</i>=0.012). There was no statistically significant difference between Saudi and non-Saudi patients. EI increased progressively with age in both genders.</p><p><strong>Conclusion: </strong>Our EI values were similar to many of those reported in other countries, which supports the use of the 0.3 cutoff for the diagnosis of hydrocephalus, regardless of gender, age, or ethnicity.</p>","PeriodicalId":19284,"journal":{"name":"Neurosciences","volume":"29 2","pages":"122-127"},"PeriodicalIF":1.2,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11305359/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140916902","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-05-01DOI: 10.17712/nsj.2024.2.20230109
Homoud A Aldahash, Muhammad A Ansary, Hana M Hallak, Meshari R Alhuthayl, Faisal A Alotaibi
Objectives: To determine the effectiveness and safety of Hemopatch® as a primary dural sealant in preventing CSF leakage following cranial surgery. Cerebrospinal fluid (CSF) leaks occur in cranial operations and are associated with significant patient burden and expense. The use of Hemopatch® as a dural sealant in cranial neurosurgical procedures is described and analyzed in this study.
Methods: Data were retrospectively collected from all patients who underwent a craniotomy for various neurosurgical indications where Hemopatch® was used as the primary dural sealant between June 2017 and June 2022. Infection and CSF leak were the main indicators evaluated after surgery.
Results: A total of 119 consecutive patients met our inclusion criteria. The median was age 41.5 years, and 52.5% were female. The mean follow-up period was 2.3 years (7 months to 6 years). There were 110 (92.44%) supratentorial and 9 (7.56%) infratentorial craniotomies. Postoperative CSF leak was reported in 2 patients (1.68%), one in each cohort. Postoperative infection occurred in one patient (0.84%).
Conclusion: The results suggest that using Hemopatch® as a dural sealant in cranial surgery is effective and safe. After supra-/infratentorial craniotomies, the rate of postoperative adverse events in our sample was within the range of known surgical revision rates. Future randomized clinical studies are required to confirm our encouraging findings.
{"title":"Hemopatch<sup>®</sup> as a primary dural sealant in cranial neurosurgery: Technical note and a retrospective study.","authors":"Homoud A Aldahash, Muhammad A Ansary, Hana M Hallak, Meshari R Alhuthayl, Faisal A Alotaibi","doi":"10.17712/nsj.2024.2.20230109","DOIUrl":"10.17712/nsj.2024.2.20230109","url":null,"abstract":"<p><strong>Objectives: </strong>To determine the effectiveness and safety of Hemopatch<sup>®</sup> as a primary dural sealant in preventing CSF leakage following cranial surgery. Cerebrospinal fluid (CSF) leaks occur in cranial operations and are associated with significant patient burden and expense. The use of Hemopatch<sup>®</sup> as a dural sealant in cranial neurosurgical procedures is described and analyzed in this study.</p><p><strong>Methods: </strong>Data were retrospectively collected from all patients who underwent a craniotomy for various neurosurgical indications where Hemopatch<sup>®</sup> was used as the primary dural sealant between June 2017 and June 2022. Infection and CSF leak were the main indicators evaluated after surgery.</p><p><strong>Results: </strong>A total of 119 consecutive patients met our inclusion criteria. The median was age 41.5 years, and 52.5% were female. The mean follow-up period was 2.3 years (7 months to 6 years). There were 110 (92.44%) supratentorial and 9 (7.56%) infratentorial craniotomies. Postoperative CSF leak was reported in 2 patients (1.68%), one in each cohort. Postoperative infection occurred in one patient (0.84%).</p><p><strong>Conclusion: </strong>The results suggest that using Hemopatch<sup>®</sup> as a dural sealant in cranial surgery is effective and safe. After supra-/infratentorial craniotomies, the rate of postoperative adverse events in our sample was within the range of known surgical revision rates. Future randomized clinical studies are required to confirm our encouraging findings.</p>","PeriodicalId":19284,"journal":{"name":"Neurosciences","volume":"29 2","pages":"128-132"},"PeriodicalIF":1.2,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11305368/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140916851","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-05-01DOI: 10.17712/nsj.2024.2.20230127
Tarig Abkur, Zahir Satti, Daniel G Di Luca, Ibrahim Alhashyan, Hanin Algethami
{"title":"Neurophobia: challenges and solutions.","authors":"Tarig Abkur, Zahir Satti, Daniel G Di Luca, Ibrahim Alhashyan, Hanin Algethami","doi":"10.17712/nsj.2024.2.20230127","DOIUrl":"10.17712/nsj.2024.2.20230127","url":null,"abstract":"","PeriodicalId":19284,"journal":{"name":"Neurosciences","volume":"29 2","pages":"144-145"},"PeriodicalIF":1.2,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11305356/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140916858","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-05-01DOI: 10.17712/nsj.2024.2.20230091
Abdulrazag Ajlan, Saif Almeshari, Sarah Basindwah, Majed Aljohani, Yazed Alharbi, Fahad Aldhowaihy, Hisham Alkhaldi, Ashwag Alqurashi
Objectives: To study each atypical feature in atypical meningioma versus other grade 2 meningiomas and its possible relation to recurrence.
Methods: This is a retrospective study of patients with WHO grade 2 meningioma operated in our institution between 01/2008 and 12/2020. The rate of recurrence, reoperation and readmission were recorded during the follow-up period. A statistical analysis was done to determine the significance of each pathological feature in regard to recurrence.
Results: A total of 74 patients were included as WHO grade 2 meningioma with 60 (81%) patients having an AM and 14 (19%) patients with chordoid or clear cell meningioma. The mean age was 51 years±14. The most common location was meningioma abutting the frontal lobe (convexity). Major atypical features were more noted in the AM, however, there was no significant difference between AM and other types of meningioma. Increased Nuclear cytoplasmic ratio and cellularity were found significantly more in AM. The recurrence rate was 16.2%. No specific pathology feature (major or minor) nor the type of Grade 2 meningioma was significantly related to recurrence.
Conclusion: The types of WHO grade 2 meningiomas have similar prognosis and recurrence rates. There is no significant difference between the atypical features in indicating a more aggressive nature or risk of recurrence in grade 2 meningiomas.
{"title":"Atypical meningiomas compared to other WHO Grade 2 meningiomas: Histological features and prognosis.","authors":"Abdulrazag Ajlan, Saif Almeshari, Sarah Basindwah, Majed Aljohani, Yazed Alharbi, Fahad Aldhowaihy, Hisham Alkhaldi, Ashwag Alqurashi","doi":"10.17712/nsj.2024.2.20230091","DOIUrl":"10.17712/nsj.2024.2.20230091","url":null,"abstract":"<p><strong>Objectives: </strong>To study each atypical feature in atypical meningioma versus other grade 2 meningiomas and its possible relation to recurrence.</p><p><strong>Methods: </strong>This is a retrospective study of patients with WHO grade 2 meningioma operated in our institution between 01/2008 and 12/2020. The rate of recurrence, reoperation and readmission were recorded during the follow-up period. A statistical analysis was done to determine the significance of each pathological feature in regard to recurrence.</p><p><strong>Results: </strong>A total of 74 patients were included as WHO grade 2 meningioma with 60 (81%) patients having an AM and 14 (19%) patients with chordoid or clear cell meningioma. The mean age was 51 years±14. The most common location was meningioma abutting the frontal lobe (convexity). Major atypical features were more noted in the AM, however, there was no significant difference between AM and other types of meningioma. Increased Nuclear cytoplasmic ratio and cellularity were found significantly more in AM. The recurrence rate was 16.2%. No specific pathology feature (major or minor) nor the type of Grade 2 meningioma was significantly related to recurrence.</p><p><strong>Conclusion: </strong>The types of WHO grade 2 meningiomas have similar prognosis and recurrence rates. There is no significant difference between the atypical features in indicating a more aggressive nature or risk of recurrence in grade 2 meningiomas.</p>","PeriodicalId":19284,"journal":{"name":"Neurosciences","volume":"29 2","pages":"96-102"},"PeriodicalIF":1.2,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11305365/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140916894","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-05-01DOI: 10.17712/nsj.2024.2.20230126
S Zarrouk, Sounira Mehri, Josef Finsterer
{"title":"Comment on: Diagnosis of autoimmune epilepsy requires documentation of a causal relationship between the immune response and seizures.","authors":"S Zarrouk, Sounira Mehri, Josef Finsterer","doi":"10.17712/nsj.2024.2.20230126","DOIUrl":"10.17712/nsj.2024.2.20230126","url":null,"abstract":"","PeriodicalId":19284,"journal":{"name":"Neurosciences","volume":"29 2","pages":"146-147"},"PeriodicalIF":1.2,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11305370/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140916896","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}