该杂志已扩大到涵盖儿科神经科学的各个方面，涉及神经系统及其覆盖物的发育和获得性异常、功能障碍、癫痫、痉挛、基础和临床神经肿瘤学、康复和创伤。全球儿科神经外科是另一个感兴趣的领域，将考虑在该期刊上发表。

The journal 'Child's Nervous System' covers all aspects of pediatric neuroscience, including developmental and acquired abnormalities of the nervous system and its coverings, dysfunctions, epilepsy, spasms, basic and clinical neuro-oncology, rehabilitation, and trauma. Global pediatric neurosurgery is another area of interest, and relevant research will be considered for publication in this journal.

《Child's Nervous System》杂志涵盖了儿科神经科学的各个方面，包括神经系统及其覆盖物的发育和获得性异常、功能障碍、癫痫、痉挛、基础和临床神经肿瘤学、康复和创伤。此外，全球儿科神经外科也是一个重要的研究领域，相关的研究成果将被考虑在该期刊上发表。

Child's Nervous System

Nonmissile intracranial penetrating injury (IPI) in pediatric population is rare. Here, we report the exceedingly rare case of a 5-month-old infant sustained by a metallic clothes fork penetrating into his left forehead. The little baby was identified to carry a traumatic hemorrhagic shock, and a multidisciplinary team (MDT) was immediately established response for whole-course evaluation and decision-making. Computed tomography revealed that the clothes fork had impaled into the left frontal bone and brain parenchyma with about 3.2 cm inside the cranial vault. The infant underwent emergency surgery, and the clothes fork was removed jointly by MDT members under general anesthesia in the retrograde direction. His recovery was uneventful and was followed up 2 years without growth and developmental abnormality. As an extremely rare entity with distinct age-related characteristics, a MDT approach is a best choice and effective strategy to manage infant nonmissile IPI, including preoperative management, surgical treatment, and even following rehabilitation.

Boyu Sun

Jiahui Zhao

Shiyang Zhang

Guozhu Sun

Zongmao Zhao

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery

Childs Nerv Syst

Intracranial penetrating injury by clothes fork in an infant: case report and review of the literature.

婴儿颅内穿透伤：衣物叉子致伤案例报告及文献综述。

Dural arteriovenous fistulas (DAVFs) are rare in pediatrics. A case of DAVF diagnosed because of a slight conjunctival hyperemia and endovascular coil embolization at 2 years old is reported.

Lei Guo

Ting Liu

Xianli Lv

Endovascular embolization of dural arteriovenous fistula in a child presented with slight conjunctival hyperemia.

儿童硬脑膜动静脉瘘的血管内栓塞治疗：伴有轻微结膜充血的病例报告。

Abnormalities in notochordal development can cause a range of developmental malformations, including the split notochord syndrome and split cord malformations. We describe two cases that appear related to unusual notochordal malformations, in a female and a male infant diagnosed in the early postnatal and prenatal periods, which were treated at our institution. These cases were unusual from prior cases given a shared constellation of an anterior cervicothoracic meningocele with a prominent "neural stalk," which coursed ventrally from the spinal cord into the thorax in proximity to a foregut duplication cyst.

Jason A Chen

Joshua D Bernstock

Walid Ibn Essayed

Woo Do

Farokh R Demehri

Mark Proctor

Benjamin C Warf

Syndrome of anterior neural stalk, vertebral abnormality, enteric duplication cyst, and diaphragmatic hernia related to persistent ventral neurenteric canal: report of two cases.

前神经管、椎体异常、肠重复囊肿及膈疝综合征与持续性腹侧神经肠管相关：两例报告。

Ewing sarcoma typically arises in bone and is unrelated to intraparenchymal small blue cell embryonal central nervous system (CNS) tumors previously designated primitive neuroectodermal tumors (PNETs). When the CNS is impacted, it is usually secondary to local extension from either the epidural space, skull, or intracranial or spinal metastases. Primary examples within the cranial vault are rare, usually dural-based, and are largely case reports in the literature. We detail four pediatric patients with solitary, primary intracranial Ewing sarcoma, all manifesting the archetypal EWRS1 gene rearrangement that confirms diagnosis.Neurosurgical Department records, spanning 21 years (1995-2016), were reviewed to identify patients. Demographics, clinical history, pathological/genetic features, and clinical course were retrieved from the medical record and personal files of the authors.Four patients, one male and three females, age 5 to 16 years, were identified. One presented in extremis from a large lesion, two with soft tissue masses, and the fourth as an incidental finding after being involved in a motor vehicle collision. Three had clear bony involvement: a 10-year-old girl with a large left temporal lesion had clear origin in the skull, with spiculated calcified striations throughout the mass; a 9-year-old girl presented with a bony left petrous apex mass; and a 16-year-old girl presented with a left temporal mass with extension to the dura and underlying bone erosion. Only the 5-year-old boy had a large left frontoparietal mass traversing the falx with no bony contact. All four tumors manifested the diagnostic EWSR1 mutation and were treated with an Ewing sarcoma regimen. Outcomes were variable, with one patient showing progressive metastatic disease and death 3 years after presentation, one patient with disease-free survival 10.5 years after completion of therapy, and one alive and well at the completion of therapy 1 year after diagnosis. One patient completed therapy recently with post-therapy scans showing no evidence of disease.Testing for the EWSR1 mutation confirms the diagnosis of Ewing sarcoma and excludes other types of embryonal CNS tumors. Long-term disease-free survival is possible with adherence to the appropriate therapeutic regimen after gross surgical resection.

Michael J. Yang

Ros Whelan

Jennifer Madden

Jean M. Mulcahy Levy

B. K. Kleinschmidt-DeMasters

Todd C. Hankinson

Nicholas K. Foreman

Michael H. Handler

Child s Nervous System

Intracranial Ewing sarcoma: four pediatric examples

颅内尤文肉瘤：四个儿科病例

The purpose is to highlight the primary intracranial (meningeal-based) occurrence of Ewing sarcoma/primitive neuroectodermal tumor (ES/PNET).

Gauri Deshpande

Sridhar Epari

Chhavi Gupta

Omshree Shetty

Mamta Gurav

Girish Chinnaswamy

Aliasagar Moiyadi

Tejpal Gupta

Primary intracranial Ewing sarcoma/ peripheral primitive neuroectodermal tumor, an entity of unacquaintance: a series of 8 cases.

原发性颅内尤文肉瘤/外周原始神经外胚层肿瘤：一种未被充分认识的实体：8例系列报道。

Paya Yazdan Panah

Feride Un Candan

Aaron E.L. Warren

Irfan Ali

Ian Mutchnick

Cemal Karakas

Comparative efficacy and safety of mid-neck vs. supraclavicular vagus nerve stimulation in pediatric drug-resistant epilepsy

中颈与锁骨上迷走神经刺激治疗儿童药物难治性癫痫的疗效与安全性比较

William M. McDevitt

Fardad T. Afshari

Pasquale Gallo

Laura Quinn

Darren Martin-Lamb

Joshua Pepper

William B. Lo

Desiderio Rodrigues

Guirish A. Solanki

Intraoperative neuromonitoring and mapping during spinal cord untethering surgery; a single-centre paediatric neurosurgery unit experience

脊髓松解手术中的术中神经监测与映射；一家儿科神经外科中心的经验

Prolonged seizures cause cytotoxic edema and increase intracranial pressure. Optic nerve sheath diameter (ONSD) and its ratio to eyeball transverse diameter (ONSD/ETD) offer a noninvasive method for monitoring intracranial pressure changes. We calculated the ONSD and ONSD/ETD ratio of postictal children using computed tomography and evaluated the relationship between those values and seizure duration.

İpek Dokurel Çetin

Nihan Şık

Evaluation of optic nerve sheath diameter measurements in postictal pediatric patients

儿童癫痫发作后视神经鞘直径测量的评估

To evaluate the clinical efficacy of external ventricular drainage (EVD) in the treatment of neonatal intraventricular hemorrhage (IVH).

Yi Yuan

Zhi Hu Li

Zong Jian An

Fei Gao

WeiLi Xu

Yong Sun

Advancing the management of neonatal hemorrhages: clinical evaluation of external ventricular drainage efficacy

推进新生儿出血管理：外引流临床疗效评估

Adjuvant radiotherapy has been a standard of care for craniopharyngioma. Nevertheless, it is a rare disease with multiple presentations, and results with conservative surgery followed by radiotherapy (RT) can vary. We compared treatment results for both adult and pediatric patients.

Geovanne Pedro Mauro

Leila Maria Da Róz

Vinicius de Carvalho Gico

Eduardo Weltman

Evandro César de Souza

Rosangela Correa Villar

Hamilton Matushita

Carlos Gilberto Carlotti

Impact of stereotactic radiotherapy for craniopharyngioma: a large, academic hospital cohort

立体定向放射治疗对颅咽管瘤的影响：一家大型学术医院的队列研究

Abbreviation	Childs Nerv Syst
Journal Impact	1.34
Quartiles(Global)	SURGERY(Q3)

ISSN	0256-7040, 1433-0350
h-index	97

Publication Information	Publisher: Springer Verlag，Publishing cycle: Monthly，Journal Type: journal，Open Access Journals: No
Basic data	Year of publication: 1985，Proportion of original research papers: 72.14%，Self Citation Rate:15.40%， Gold OA Rate: 15.82%
Average review cycle	网友分享经验：平均3月
Average recruitment ratio	网友分享经验：约50%

Child's Nervous System

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