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Early Adequate Nutrition in ICU Is Associated with Survival Gain : Retrospective Cohort Study in Patient with Traumatic Brain Injury. 重症监护室早期充足营养与存活率提高相关:创伤性脑损伤患者的回顾性队列研究。
IF 1.4 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2025-03-01 Epub Date: 2024-11-08 DOI: 10.3340/jkns.2024.0157
Junseo Oh, Jingyeong Kim, Jihyeon Ahn, Sunghoon Choi, Hyung Min Kim, Jaeim Lee, Hang Joo Cho, Maru Kim

Objective: Patients with traumatic brain injury (TBI) commonly exhibit a poor mental health status and can easily develop aspiration pneumonia. Thus, early proper nutrition through oral or tube feeding is difficult to achieve, leading to malnutrition. However, evidence regarding early nutritional support in the intensive care unit (ICU) is lacking. We aimed to assess the effect of early nutrition in patients with TBI admitted to the ICU.

Methods: Data of adult patients with TBI admitted to the trauma ICU of a regional trauma center in Korea between 2022 and 2023 were retrospectively analyzed. Those with ICU stay <7 days, younger than 18 years, and with underlying diseases that could alter baseline metabolism, were excluded. Nutritional support on day 4 of ICU admission was measured. The patients were classified into mortality and survival groups, and risk factors for mortality were evaluated. Subgroup analyses were performed based on TBI severity.

Results: Overall, 864 patients were diagnosed with acute TBI, of whom 227 were included in this study. The mortality rate in the study population was 15% (n=34). Those in the survival group were younger, had longer hospital stays, had a higher initial Glasglow coma scale (GCS) score, and had a higher intake of calorie supplements than those in the mortality group. In a subgroup analysis of patients with non-severe TBI (GCS >8), total calorie intake (751.4 vs. 434.2 kcal, p=0.029), total protein intake (37.5 vs. 22.1 g, p=0.045), and ratio of supplied to target calories (0.49 vs. 0.30, p=0.047) were higher in the survival group than in the mortality group. Logistic regression analysis revealed that calorie intake (B=-0.002, p=0.040) and initial hemoglobin level (B=-0.394, p=0.005) were risk factors for mortality in patients with non-severe TBI.

Conclusion: More calories were supplied to the survival group than the mortality group among patients with TBI. Additionally, logistic regression analysis showed that increased calorie supply was associated with reduced mortality in patients with non-severe TBI. The mortality group had low protein intake; however, this did not emerge as a risk factor for mortality. Early sufficient nutritional support improves the prognosis of patients with TBI.

目的:创伤性脑损伤(TBI)患者通常精神健康状况较差,且容易发生吸入性肺炎。因此,很难在早期通过口服或管饲获得适当的营养,从而导致营养不良。然而,有关重症监护室(ICU)早期营养支持的证据却很缺乏。我们旨在评估重症监护室收治的创伤性脑损伤患者早期营养的效果:方法:回顾性分析了 2022 年至 2023 年期间入住韩国某地区创伤中心创伤重症监护室的成年创伤性脑损伤患者的数据。结果:共有 864 名患者被诊断为创伤性脑损伤:共有 864 名患者被诊断为急性创伤性脑损伤,其中 227 人被纳入本研究。研究对象的死亡率为 15%(n=34)。与死亡率组相比,存活组患者更年轻,住院时间更长,初始格拉斯哥昏迷量表(GCS)评分更高,摄入的热量补充剂也更多。在对非重度创伤性脑损伤患者(GCS>8)进行的亚组分析中,存活组患者的总热量摄入量(751.4 千卡 vs 434.2 千卡,P=0.029)、总蛋白质摄入量(37.5 克 vs 22.1 克,P=0.045)和供给热量与目标热量之比(0.49 vs 0.30,P=0.047)均高于死亡组患者。逻辑回归分析显示,卡路里摄入量(B=-0.002,P=0.040)和初始血红蛋白水平(B=-0.394,P=0.005)是非重度创伤性脑损伤患者死亡的风险因素:结论:在创伤性脑损伤患者中,生存组比死亡组获得了更多的热量。此外,逻辑回归分析表明,热量供应的增加与非严重创伤性脑损伤患者死亡率的降低有关。死亡组的蛋白质摄入量较低,但这并不是导致死亡的风险因素。早期充足的营养支持可改善创伤性脑损伤患者的预后。
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引用次数: 0
Integration of Palliative Care in Neurosurgical Critical Care : Insights from a Single-Center Perspective. 神经外科重症监护中的姑息治疗整合 :单中心视角的启示。
IF 1.4 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2025-03-01 Epub Date: 2024-09-24 DOI: 10.3340/jkns.2024.0065
Nam Hee Kim, Yejin Kim, Se Yeon Kim, Hyoung Suk Han, Hye Yoon Park, Eun Jin Ha, Shin Hye Yoo

Objective: Palliative care is a specialized approach designed to enhance the quality of life for both patients and their families, offering patient-centered care through comprehensive assessment and care planning. However, the integration of palliative care within neurocritical care settings has been relatively understudied. This descriptive study aims to identify the characteristics, palliative care needs, and outcomes of patients referred to palliative care services during admission to the neurosurgical intensive care unit (NS-ICU).

Methods: A retrospective analysis of adults admitted to the NS-ICU at a referral hospital between December 2019 and December 2021 was conducted. The study focused on those referred to the inpatient palliative care team with diagnoses of non-traumatic brain hemorrhage, traumatic brain injury, or brain neoplasm. Excluded were patients who died before palliative care consultation or lacked sufficient information. The investigation assessed demographic and clinical characteristics at consultation, along with post-consultation hospital outcomes derived from medical records and interview notes.

Results: In this study involving 38 enrolled patients, the median age was 65, with 42.1% females. The most prevalent diagnosis was nontraumatic brain hemorrhage (47.4%). Reasons for palliative care consultation included psychosocial support (95%), goal-of-care discussions (68%), decision-making support (50%), and communication facilitation (39%). The median time from NS-ICU admission to consultation was 3.5 days (interquartile range, 1-8 days), and all interviews involved family members. Key decision topics encompassed mechanical ventilation (23.7%) and tracheostomy (21.1%). Patient preferences for life-sustaining treatment could be estimated in only 47.4% of cases, often resulting in treatment disagreement. Among the 38 patients, 26 (68.4%) died during admission. Before the consultation, full code status, partial code status, and comfort care alone were reported as 32%, 66%, and 2%, respectively; post-consultation, these figures shifted to 11%, 42%, and 47%, respectively.

Conclusion: Palliative care was predominantly sought for psychosocial support and discussions concerning goals of care. Despite challenges in ascertaining patient treatment preferences, palliative care consultations proved invaluable in aiding family members and facilitating treatment decision-making. Our study suggests the potential integration of palliative care within neuro-critical care, contributing to a heightened utilization of comfort care at the end-of-life.

目的:姑息治疗是一种旨在提高患者及其家属生活质量的专业方法,通过综合评估和护理计划提供以患者为中心的护理。然而,在神经重症监护环境中整合姑息关怀的研究相对较少。这项描述性研究旨在确定在神经外科重症监护病房(NS-ICU)住院期间转介至姑息关怀服务的患者的特征、姑息关怀需求和疗效:对一家转诊医院在2019年12月至2021年12月期间入住神经外科重症监护病房(NS-ICU)的成人患者进行了回顾性分析。研究的重点是那些被诊断为非创伤性脑出血、创伤性脑损伤或脑肿瘤并转诊至住院姑息治疗团队的患者。姑息治疗咨询前死亡或缺乏足够信息的患者不在研究范围内。调查评估了就诊时的人口统计学特征和临床特征,以及从医疗记录和访谈记录中得出的就诊后的住院结果:在这项涉及 38 名登记患者的研究中,年龄中位数为 65 岁,女性占 42.1%。最常见的诊断是非创伤性脑出血(47.4%)。姑息治疗咨询的原因包括社会心理支持(95%)、护理目标讨论(68%)、决策支持(50%)和沟通促进(39%)。从NS-ICU入院到咨询的中位时间为3.5天(范围:1-8天),所有访谈均有家属参与。关键决策主题包括机械通气(23.7%)和气管切开术(21.1%)。仅有 47.4% 的病例能估计出患者对维持生命治疗的偏好,这往往导致治疗分歧。38 名患者中有 26 人(68.4%)在入院期间死亡。会诊前,完全代码状态、部分代码状态和单纯舒适护理的比例分别为32%、66%和2%;会诊后,这些数字分别变为11%、42%和47%:姑息关怀主要是为了提供心理支持和讨论护理目标。尽管在确定患者治疗偏好方面存在挑战,但姑息关怀会诊在帮助家庭成员和促进治疗决策方面证明是非常有价值的。我们的研究表明,姑息治疗有可能与神经重症护理相结合,从而提高临终关怀的利用率。
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引用次数: 0
A Parasellar Hydatid Cyst Extending to the Opticocarotid Triangle, Pediatric Case.
IF 1.4 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2025-03-01 Epub Date: 2025-02-03 DOI: 10.3340/jkns.2024.0184
Mustafa Cemil Kilinc, Altan Demirel

The causes of sudden vision loss in one eye include isolated eye diseases, vascular pathologies, and optic nerve compression. This report highlights a case of parasitosis (Echinococcus granulosus) causing sudden vision loss due to optic nerve compression. To our knowledge, this is the first reported case of a hydatid cyst extending into the optic canal through opticocarotid triangle in a pediatric patient. A 12-year-old girl presented to the ophthalmologist with progressive visual deterioration over a period of 1 week. Examination revealed reduced visual acuity in her right eye. No ocular abnormality was detected on examination, cranial imaging revealed a lesion compressing the right optic nerve and the patient was referred to neurosurgery. The bright white lesion with a microscopic appearance resembling an epidermoid tumor was completely excised after aspirating the contents with transcranial access. Pathology was reported as hydatid cyst. Hydatid cysts invading the optic canal should be considered in the differential diagnosis of sudden visual loss in the pediatric age group; however, it continues to be an important health problem in developing countries. Meticulous excision of the cyst capsule without rupture ensures the success of surgical treatment.

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引用次数: 0
Cement-Augmented Pedicle Screw Fixation in Patients with Osteoporosis : Safety, Efficacy and Complications.
IF 1.4 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2025-03-01 Epub Date: 2025-01-23 DOI: 10.3340/jkns.2024.0081
Tomasz Olbrycht, Kajetan Latka, Waldemar Kolodziej, Tomasz Krzeszowiec, Dariusz Latka

Cement-augmented pedicle screw instrumentation is a widely accepted method for managing osteoporotic fractures, but it carries inherent risks, particularly related to cement leakage and embolism. This study aimed to analyze a clinical case of complications following cement fixation and provide a detailed review of relevant literature. A 70-year-old patient underwent transpedicular screw instrumentation from L2-L4 with polymethyl methacrylate augmentation, which resulted in cement leakage into the spinal canal and subsequent pulmonary embolism. After revision surgery and conservative treatment for the embolism, the patient's condition stabilized, demonstrating that conservative measures can be effective in managing cement embolism. To complement this case, a comprehensive literature review was conducted to explore the causes, prevention, and treatment of complications related to cement augmentation. The findings support that while cement-augmented pedicle screw instrumentation remains a leading technique for osteoporotic fractures, the associated risks are manageable with proper treatment protocols. This study holds practical significance for healthcare professionals by highlighting both the risks and solutions associated with cement fixation, thus contributing to improved patient outcomes and the development of standardized treatment guidelines.

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引用次数: 0
Envisioning the Future of the Neurosurgical Operating Room with the Concept of the Medical Metaverse. 用医学元宇宙概念展望神经外科手术室的未来。
IF 1.4 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2025-03-01 Epub Date: 2024-11-04 DOI: 10.3340/jkns.2024.0160
Sun Mo Nam, Yoon Hwan Byun, Yun-Sik Dho, Chul-Kee Park

The medical metaverse can be defined as a virtual spatiotemporal framework wherein higher-dimensional medical information is generated, exchanged, and utilized through communication among medical personnel or patients. This occurs through the integration of cutting-edge technologies such as augmented reality (AR), virtual reality (VR), artificial intelligence (AI), big data, cloud computing, and others. We can envision a future neurosurgical operating room that utilizes such medical metaverse concept such as shared extended reality (AR/VR) of surgical field, AI-powered intraoperative neurophysiological monitoring, and real-time intraoperative tissue diagnosis. The future neurosurgical operation room will evolve into a true medical metaverse where participants of surgery can communicate in overlapping virtual layers of surgery, monitoring, and diagnosis.

医疗元宇宙可定义为一个虚拟的时空框架,通过医务人员或患者之间的交流,生成、交换和利用高维医疗信息。这是通过整合增强现实(AR)、虚拟现实(VR)、人工智能(AI)、大数据、云计算等尖端技术实现的。我们可以设想,未来的神经外科手术室将利用共享扩展现实(AR/VR)手术领域、人工智能驱动的术中神经生理监测和实时术中组织诊断等医疗元宇宙概念。未来的神经外科手术室将发展成为一个真正的医疗元宇宙,手术参与者可以在手术、监测和诊断的重叠虚拟层中进行交流。
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引用次数: 0
Editors' Pick in March 2025.
IF 1.4 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2025-02-24 DOI: 10.3340/jkns.2025.0046
Hee-Jin Yang
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引用次数: 0
Management Strategies of Neurofibromatosis Type 2 in Pediatric Patients : Challenges and Emerging Therapies.
IF 1.4 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2025-02-24 DOI: 10.3340/jkns.2024.0237
Jong Seok Lee

Neurofibromatosis type 2 (NF2) is a rare genetic disorder caused by mutations in the NF2 tumor suppressor gene, characterized by bilateral vestibular schwannomas (VSs) and other central and peripheral nervous system tumors. Pediatric patients often present with more aggressive disease, greater tumor burdens, and increased morbidity compared to adults. Management requires a multidisciplinary approach that balances tumor control with functional preservation. While surgery and radiosurgery remain key treatment options, they carry risks such as hearing loss and malignant transformation of existing tumors. Bevacizumab and emerging therapies like gene therapy show promising therapeutic effects but are limited by variability in efficacy. Comprehensive care, including psychosocial support, is essential to improve clinical outcomes and quality of life for children with NF2.

{"title":"Management Strategies of Neurofibromatosis Type 2 in Pediatric Patients : Challenges and Emerging Therapies.","authors":"Jong Seok Lee","doi":"10.3340/jkns.2024.0237","DOIUrl":"https://doi.org/10.3340/jkns.2024.0237","url":null,"abstract":"<p><p>Neurofibromatosis type 2 (NF2) is a rare genetic disorder caused by mutations in the NF2 tumor suppressor gene, characterized by bilateral vestibular schwannomas (VSs) and other central and peripheral nervous system tumors. Pediatric patients often present with more aggressive disease, greater tumor burdens, and increased morbidity compared to adults. Management requires a multidisciplinary approach that balances tumor control with functional preservation. While surgery and radiosurgery remain key treatment options, they carry risks such as hearing loss and malignant transformation of existing tumors. Bevacizumab and emerging therapies like gene therapy show promising therapeutic effects but are limited by variability in efficacy. Comprehensive care, including psychosocial support, is essential to improve clinical outcomes and quality of life for children with NF2.</p>","PeriodicalId":16283,"journal":{"name":"Journal of Korean Neurosurgical Society","volume":" ","pages":""},"PeriodicalIF":1.4,"publicationDate":"2025-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143483418","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Neurochemical Characterization of A53T-alpha-synuclein and 6-OHDA Rat Models for Parkinson's Disease through Animal PET Imaging Analysis.
IF 1.4 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2025-02-17 DOI: 10.3340/jkns.2024.0109
Junhyung Kim, Hyung Ho Yoon, Jin Hwa Chung, Seok Ho Hong, Sang Ryong Jeon

Objective: In preclinical research of Parkinson's disease, several rodent models, notably the classical 6-hydroxydopamine (6-OHDA) model and the A53T-alpha-synuclein model, have been widely used, yet their distinct neurochemical characteristics in conjunction with behavioral and histopathological changes have been scarcely documented.

Methods: We examined the two rat models of Parkinson's disease and characterized them using [18F]FP-CIT animal PET imaging. The 6-OHDA model (n=10) was induced by unilateral injection of 6-OHDA into the middle forebrain bundle, while the A53T-alpha-synuclein model (n=10) was mediated by the adeno-associated viral vectors injected into the substantia nigra. We hypothesized that these models would present differential neurochemical profiles, which could reflect their behavioral and histopathological features and potentially serve as a supplementary tool for evaluating the outcomes of interventions in animal experiments.

Results: The striatum showed decreased PET uptake on the affected side compared to the unaffected control side, which was highly correlated with the stepping behaviors (R = 0.854 [95% CI, 0.606 to 0.951]). The decrease in striatal PET uptake was more pronounced in the 6-OHDA model than in the A53T-alpha-synuclein model: the 6-OHDA model exhibited a 60% [95% CI, 48% to 65%] decrease in the affected side compared the control side, while the A53T-alpha-synuclein model exhibited a 20% [95% CI, -16% to 47%] decrease. Interestingly, PET uptake in the forebrain cortical region, including the motor cortex, was exclusively decreased in the 6-OHDA model (p = 1.0×10-4 and p = 1.2×10-3, respectively), indicating that 6-OHDA model is affected not only in the nigrostriatal system but also in other cortical regions. Conversely, the A53T-alpha-synuclein model showed no significant alterations in these cortical regions.

Conclusion: Although the A53T-alpha-synuclein model demonstrates less definitive behavioral changes compared to the 6-OHDA model, it presents a more confined pathophysiological representation of Parkinson's disease and may be better suited for evaluating certain therapeutic interventions when utilized with adequate neurochemical characterization.

{"title":"Neurochemical Characterization of A53T-alpha-synuclein and 6-OHDA Rat Models for Parkinson's Disease through Animal PET Imaging Analysis.","authors":"Junhyung Kim, Hyung Ho Yoon, Jin Hwa Chung, Seok Ho Hong, Sang Ryong Jeon","doi":"10.3340/jkns.2024.0109","DOIUrl":"https://doi.org/10.3340/jkns.2024.0109","url":null,"abstract":"<p><strong>Objective: </strong>In preclinical research of Parkinson's disease, several rodent models, notably the classical 6-hydroxydopamine (6-OHDA) model and the A53T-alpha-synuclein model, have been widely used, yet their distinct neurochemical characteristics in conjunction with behavioral and histopathological changes have been scarcely documented.</p><p><strong>Methods: </strong>We examined the two rat models of Parkinson's disease and characterized them using [18F]FP-CIT animal PET imaging. The 6-OHDA model (n=10) was induced by unilateral injection of 6-OHDA into the middle forebrain bundle, while the A53T-alpha-synuclein model (n=10) was mediated by the adeno-associated viral vectors injected into the substantia nigra. We hypothesized that these models would present differential neurochemical profiles, which could reflect their behavioral and histopathological features and potentially serve as a supplementary tool for evaluating the outcomes of interventions in animal experiments.</p><p><strong>Results: </strong>The striatum showed decreased PET uptake on the affected side compared to the unaffected control side, which was highly correlated with the stepping behaviors (R = 0.854 [95% CI, 0.606 to 0.951]). The decrease in striatal PET uptake was more pronounced in the 6-OHDA model than in the A53T-alpha-synuclein model: the 6-OHDA model exhibited a 60% [95% CI, 48% to 65%] decrease in the affected side compared the control side, while the A53T-alpha-synuclein model exhibited a 20% [95% CI, -16% to 47%] decrease. Interestingly, PET uptake in the forebrain cortical region, including the motor cortex, was exclusively decreased in the 6-OHDA model (p = 1.0×10-4 and p = 1.2×10-3, respectively), indicating that 6-OHDA model is affected not only in the nigrostriatal system but also in other cortical regions. Conversely, the A53T-alpha-synuclein model showed no significant alterations in these cortical regions.</p><p><strong>Conclusion: </strong>Although the A53T-alpha-synuclein model demonstrates less definitive behavioral changes compared to the 6-OHDA model, it presents a more confined pathophysiological representation of Parkinson's disease and may be better suited for evaluating certain therapeutic interventions when utilized with adequate neurochemical characterization.</p>","PeriodicalId":16283,"journal":{"name":"Journal of Korean Neurosurgical Society","volume":" ","pages":""},"PeriodicalIF":1.4,"publicationDate":"2025-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143441104","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Germline Variants in Pediatric Cancer : Based on Oncogenic Pathways.
IF 1.4 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2025-02-17 DOI: 10.3340/jkns.2025.0011
Joo Whan Kim

Pathogenic germline variants (PGVs) are increasingly recognized as critical elements in pediatric cancer predisposition. Determining the pathogenicity of germline variants is a dynamic process, with advancements in next-generation sequencing (NGS) and expanding genome databases reshaping our understanding of cancer genomics. This article reviews the role of PGVs in key oncogenic pathways, including RTK/RAS/MAPK, PI3K/AKT, WNT, and Hedgehog signaling, highlighting their associations with specific cancer predisposition syndromes and neurosurgical implications. Most PGVs are inherited in an autosomal dominant pattern and are frequent in tumor suppressor genes, while autosomal recessive conditions like Ataxia-telangiectasia and Fanconi anemia are less common. Germline variants in proto-oncogenes such as PTPN11, KRAS, and HRAS are associated with RASopathies, including Noonan and Costello syndromes, which show variable cancer risks. Similarly, PTEN PGVs, linked to Cowden syndrome, and DICER1 PGVs, responsible for DICER1 syndrome, exemplify the diverse clinical presentations and risks of pediatric cancer predisposition syndromes. Medulloblastoma, a pediatric-specific brain tumor, shows an increasing proportion of PGVs, with approximately 12% of all medulloblastomas harboring PGVs in APC, PTCH1, SUFU, and ELP1 in the WNT-activated and SHH-activated subtypes. Emerging evidence suggests that approximately 8.5-20% of pediatric cancer patients harbor PGVs, with a substantial proportion arising de novo. Routine germline screening for pediatric cancer patients is increasingly recommended, as many PGVs lack family history. Programs like STREAM (Solid Tumor REsearch And Magic) in Korea underscore the importance of comprehensive pediatric genome databases for personalized precision medicine. As neurosurgeons are frequently the first to encounter central nervous system tumor manifestations, a robust understanding of genomic medicine is essential. This review emphasizes the need for international collaboration to develop actionable insights into pediatric cancer genomics, ultimately improving diagnostic, therapeutic, and preventive strategies.

{"title":"Germline Variants in Pediatric Cancer : Based on Oncogenic Pathways.","authors":"Joo Whan Kim","doi":"10.3340/jkns.2025.0011","DOIUrl":"https://doi.org/10.3340/jkns.2025.0011","url":null,"abstract":"<p><p>Pathogenic germline variants (PGVs) are increasingly recognized as critical elements in pediatric cancer predisposition. Determining the pathogenicity of germline variants is a dynamic process, with advancements in next-generation sequencing (NGS) and expanding genome databases reshaping our understanding of cancer genomics. This article reviews the role of PGVs in key oncogenic pathways, including RTK/RAS/MAPK, PI3K/AKT, WNT, and Hedgehog signaling, highlighting their associations with specific cancer predisposition syndromes and neurosurgical implications. Most PGVs are inherited in an autosomal dominant pattern and are frequent in tumor suppressor genes, while autosomal recessive conditions like Ataxia-telangiectasia and Fanconi anemia are less common. Germline variants in proto-oncogenes such as PTPN11, KRAS, and HRAS are associated with RASopathies, including Noonan and Costello syndromes, which show variable cancer risks. Similarly, PTEN PGVs, linked to Cowden syndrome, and DICER1 PGVs, responsible for DICER1 syndrome, exemplify the diverse clinical presentations and risks of pediatric cancer predisposition syndromes. Medulloblastoma, a pediatric-specific brain tumor, shows an increasing proportion of PGVs, with approximately 12% of all medulloblastomas harboring PGVs in APC, PTCH1, SUFU, and ELP1 in the WNT-activated and SHH-activated subtypes. Emerging evidence suggests that approximately 8.5-20% of pediatric cancer patients harbor PGVs, with a substantial proportion arising de novo. Routine germline screening for pediatric cancer patients is increasingly recommended, as many PGVs lack family history. Programs like STREAM (Solid Tumor REsearch And Magic) in Korea underscore the importance of comprehensive pediatric genome databases for personalized precision medicine. As neurosurgeons are frequently the first to encounter central nervous system tumor manifestations, a robust understanding of genomic medicine is essential. This review emphasizes the need for international collaboration to develop actionable insights into pediatric cancer genomics, ultimately improving diagnostic, therapeutic, and preventive strategies.</p>","PeriodicalId":16283,"journal":{"name":"Journal of Korean Neurosurgical Society","volume":" ","pages":""},"PeriodicalIF":1.4,"publicationDate":"2025-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143441090","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Minimizing Hemorrhage Complications in Deep Brain Stimulation Surgery - The Impact of Imaging Modalities and Trajectory Planning.
IF 1.4 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2025-02-17 DOI: 10.3340/jkns.2024.0198
Seung Woo Hong, Dao Duy Phuong, Kyung Won Chang, Hyun Ho Jung, Jin Woo Chang

Objective: This retrospective study aims to analyze hemorrhage complications in patients undergoing deep brain stimulation (DBS) surgery, focusing on the impact of imaging modalities and trajectory planning.

Methods: We conducted a retrospective review of patients who underwent DBS at a single institution from September 2018 to February 2023. Surgical planning data were analyzed using a combination of 1.5 Tesla(T) and 3.0 T Magnetic resonance image (MRI) for trajectory planning. Trajectories were classified into four types (Type 1-4) based on the proximity of vascular structures within 2 mm on preoperative MRI scans, as defined in this study. Hemorrhage presence was evaluated through postoperative computed tomography (CT) scans.

Results: Out of 200 patients analyzed, Type 1 trajectories (no vascular structures within 2 mm on both MRIs) accounted for 72.70% of cases with the lowest hemorrhage rate. Significant differences in hemorrhage rates were observed among the types, with higher risks associated with Type 4 trajectories. Additionally, significant variations in vascular structure types were noted across DBS targets, with STN showing the highest risk.

Conclusion: Meticulous trajectory planning using both 1.5T and 3.0T MRI is crucial in minimizing hemorrhagic complications in DBS. The study underscores the need for precise imaging and planning to enhance patient safety and surgical outcomes.

{"title":"Minimizing Hemorrhage Complications in Deep Brain Stimulation Surgery - The Impact of Imaging Modalities and Trajectory Planning.","authors":"Seung Woo Hong, Dao Duy Phuong, Kyung Won Chang, Hyun Ho Jung, Jin Woo Chang","doi":"10.3340/jkns.2024.0198","DOIUrl":"https://doi.org/10.3340/jkns.2024.0198","url":null,"abstract":"<p><strong>Objective: </strong>This retrospective study aims to analyze hemorrhage complications in patients undergoing deep brain stimulation (DBS) surgery, focusing on the impact of imaging modalities and trajectory planning.</p><p><strong>Methods: </strong>We conducted a retrospective review of patients who underwent DBS at a single institution from September 2018 to February 2023. Surgical planning data were analyzed using a combination of 1.5 Tesla(T) and 3.0 T Magnetic resonance image (MRI) for trajectory planning. Trajectories were classified into four types (Type 1-4) based on the proximity of vascular structures within 2 mm on preoperative MRI scans, as defined in this study. Hemorrhage presence was evaluated through postoperative computed tomography (CT) scans.</p><p><strong>Results: </strong>Out of 200 patients analyzed, Type 1 trajectories (no vascular structures within 2 mm on both MRIs) accounted for 72.70% of cases with the lowest hemorrhage rate. Significant differences in hemorrhage rates were observed among the types, with higher risks associated with Type 4 trajectories. Additionally, significant variations in vascular structure types were noted across DBS targets, with STN showing the highest risk.</p><p><strong>Conclusion: </strong>Meticulous trajectory planning using both 1.5T and 3.0T MRI is crucial in minimizing hemorrhagic complications in DBS. The study underscores the need for precise imaging and planning to enhance patient safety and surgical outcomes.</p>","PeriodicalId":16283,"journal":{"name":"Journal of Korean Neurosurgical Society","volume":" ","pages":""},"PeriodicalIF":1.4,"publicationDate":"2025-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143441100","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Journal of Korean Neurosurgical Society
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