Comparison of Follow-Up Length-Matched Single-Center Myelomeningocele Postnatal Closure Cohort to the Management of Myelomeningocele Study (MOMS) Trial Results [0.03%]
与开放性脊柱裂管理试验结果对比单中心术后随访长度匹配的脊柱裂产后修补队列
Kristin J Weaver,Michael M McDowell,Michael D White et al.
Kristin J Weaver et al.
Objective: We sought to compare our large single-institution cohort of postnatal myelomeningocele closure to the 2 arms of the Management of Myelomeningocele Study (MOMS) trial at the designated trial time points, as well...
Management of Traumatic Epidural Hematoma in Infants Younger than One Year: 50 Cases - Single Center Experience [0.03%]
一岁以下婴儿硬膜外血肿的诊治(50例报告)
Nuri Serdar Baş,Murat Karacan,Ebru Doruk et al.
Nuri Serdar Baş et al.
Aim and background: Traumatic epidural hematoma (EDH) is a rare but possibly fatal complication of head trauma in infants. In this study, infants who were younger than 1 year and followed up and treated for TEDH in our cl...
Prognostic Factors for Pediatric Acute Encephalopathy Associated with Severe Brain Edema [0.03%]
与严重脑水肿相关的儿童急性脑病的预后因素
Goichiro Tamura,Takayuki Inagaki
Goichiro Tamura
Background and objective: Acute encephalopathy is a life-threatening brain dysfunction in children, often associated with a preceding infection and diffuse noninflammatory brain edema. At present, the role of decompressiv...
A Case of Large Aplasia Cutis Congenita with Underlying Skull Defect: Effective Surgical Treatment with Integra® Dermal Regeneration Template [0.03%]
大范围先天性皮肤缺失症合并颅骨缺损的外科手术治疗(应用扩张器及Integra皮肤断层移植物)
Andrea Scotti,Elisa Benanti,Federica Augelli et al.
Andrea Scotti et al.
Introduction: Aplasia cutis congenita (ACC) is a rare congenital abnormality characterized by the absence of a portion of skin at birth which most commonly involves the scalp and can affect the galea, the pericranium, the...
Case Reports
Pediatric neurosurgery. 2021;56(3):268-273. DOI:10.1159/000512022 2021
Knobloch Syndrome, a Rare Cause of Occipital Encephalocele and Seizures: A Case Report [0.03%]
诺卜洛赫综合征——一种罕见的后枕部脑膨出和癫痫原因：一例报告
Bhaskar Madivala Venkateshappa,Bharath Raju,Michael S Rallo et al.
Bhaskar Madivala Venkateshappa et al.
Background: Knobloch syndrome (KS) is a rare autosomal recessive disorder associated with multiple ocular and cranial abnormalities. Occult occipital skull defect or encephalocele should raise suspicion of this disease. I...
Case Reports
Pediatric neurosurgery. 2021;56(3):274-278. DOI:10.1159/000512719 2021
A 3D-Printed Model-Assisted Cervical Spine Instrumentation after Tumor Resection in a 4-Year-Old Child: A Case Report [0.03%]
报道一例4岁患儿肿瘤切除后利用3D打印脊柱模型辅助颈椎内固定手术病例
Marko Jug
Marko Jug
Introduction: In the case of tumor resection in the upper cervical spine, a multilevel laminectomy with instrumented fixation is required to prevent kyphotic deformity and myelopathy. Nevertheless, instrumentation of the ...
Case Reports
Pediatric neurosurgery. 2021;56(3):254-260. DOI:10.1159/000514248 2021
Risk Factors of Persistent Hydrocephalus in Children with Brain Tumor: A Retrospective Analysis [0.03%]
儿童脑肿瘤后交通性脑积水的危险因素分析：回顾性研究
Chiara Pilotto,Ilaria Liguoro,Serena Scaravetti et al.
Chiara Pilotto et al.
Object: Hydrocephalus is one of the main complications of brain tumors in children, being present in about 50% of cases at the time of the tumor diagnosis and persisting up to 10-40% of cases after surgical resection. Thi...
Concurrent Thoracic Spinal Intradural Extramedullary Epidermoid and Neurenteric Cyst in a Spinal Dysraphism Child [0.03%]
脊柱裂儿童胸椎脊髓外硬膜内表皮样囊肿并发神经肠源性囊肿一例报告
Rajeev Sharma,Swati Mahajan,Minakshi Bhardwaj et al.
Rajeev Sharma et al.
Introduction: Intraspinal epidermoid cysts are congenital or acquired in origin; whereas intraspinal neurenteric cysts (NECs) are of congenital origin. Their individual association with spinal dysraphism and vertebral seg...
Case Reports
Pediatric neurosurgery. 2021;56(3):261-267. DOI:10.1159/000511091 2021
Ivethe Pregúntegui-Loayza,Alejandro Apaza-Tintaya,Alberto Ramírez-Espinoza et al.
Ivethe Pregúntegui-Loayza et al.
Introduction: Lhermitte-Duclos disease (LDD), also known as dysplastic cerebellar gangliocytoma, is an uncommon disorder in children, characterized by being a slow-growing lesion of the posterior fossa, which mainly affec...
Case Reports
Pediatric neurosurgery. 2021;56(3):279-285. DOI:10.1159/000514335 2021