Bilateral Parietal Skull Fractures in Infants Attributable to Accidental Falls [0.03%]
婴儿双侧顶骨骨折由意外坠床所致
Aysha AlSahlawi,Gillian Morantz,Caroline Lacroix et al.
Aysha AlSahlawi et al.
Introduction: Multiple skull fractures, including bilateral parietal skull fractures (BPSFs) in infants are considered to be suspicious for abusive head trauma (AHT). The aim of this report is to describe a series of BPSF...
White Cord Syndrome after Thoracic Cord Decompression in a Pediatric Patient [0.03%]
儿科患者胸椎减压术后白索综合征病例报告
Lacey M Carter,Panayiotis E Pelargos,Joanna E Gernsback
Lacey M Carter
Introduction: White cord syndrome (WCS) is a rare phenomenon which causes acute neurologic deterioration after a chronically compressed spinal cord is surgically decompressed, resulting in a T2-hyperintense signal to appe...
Case Reports
Pediatric neurosurgery. 2021;56(5):477-481. DOI:10.1159/000517757 2021
Exclusive Neurogenic Bladder and Fecal Incontinency in an Achondroplasic Child Successfully Treated with Lumbar Foraminal Decompression [0.03%]
一例dandy-walker变异型脑积水并重度肺动脉高压患儿的临床分析
Flavio Giordano,Matteo Lenge,Pierarturo Donati et al.
Flavio Giordano et al.
Introduction: Achondroplasia is a genetic disorder characterized by defects in the development of endochondral bone resulting in skeletal abnormalities like stenosis of the foramen magnum and of the spine, shortened limb ...
Case Reports
Pediatric neurosurgery. 2021;56(5):471-476. DOI:10.1159/000517652 2021
Multiple Tumor-Associated Intracranial Aneurysms Adjacent to a Suprasellar Germ Cell Tumor: Case Report and Review of Literature [0.03%]
与鞍上生殖细胞瘤相邻的多发肿瘤相关颅内动脉瘤一例报告及文献复习
John K Yue,Diana Chang,Taemin Oh et al.
John K Yue et al.
Introduction: Tumor-associated intracranial aneurysms are rare and not well understood. Case presentation: We describe a 4-year-old fem...
Tetrad of Split Cord Malformation I with Neuroenteric Cyst, Dermoid Cyst, and Thickened Filum Terminale in a 2-Year-Old Child: A Case Report [0.03%]
小儿脊髓分裂畸形I型四联征合并神经肠囊肿、畸胎囊肿及终丝增厚1例报告
Ajit Mishra,Mohammed Nadeem,Andiperumal Raj Prabhuraj et al.
Ajit Mishra et al.
Introduction: Split cord malformations (SCMs) are developmental anomalies that are associated with a number of congenital defects. However, a combination of SCM I with a neuroenteric cyst (NEC) is extremely rare, and only...
Case Reports
Pediatric neurosurgery. 2021;56(5):448-454. DOI:10.1159/000514534 2021
GCS-Pupil Score Has a Stronger Association with Mortality and Poor Functional Outcome than GCS Alone in Pediatric Severe Traumatic Brain Injury [0.03%]
儿科重度创伤性脑损伤中，GCS-Pupil评分比单独的GCS与死亡率和不良功能预后的关系更为密切
Binod Balakrishnan,Heather VanDongen-Trimmer,Irene Kim et al.
Binod Balakrishnan et al.
Background: The Glasgow Coma Scale (GCS), used to classify the severity of traumatic brain injury (TBI), is associated with mortality and functional outcomes. However, GCS can be affected by sedation and neuromuscular blo...
Zeferino Demartini,Adriane Cardoso-Demartini,Junio Pereira Pardins et al.
Zeferino Demartini et al.
Case Reports
Pediatric neurosurgery. 2021;56(5):497-500. DOI:10.1159/000517651 2021
Dallas Louis Sheinberg,Jean-Paul Bryant,Roberto J Perez-Roman et al.
Dallas Louis Sheinberg et al.
Introduction: Indeterminate cell histiocytosis is a rare neoplastic disease characterized by proliferation of dendritic cells that share morphologic and immunophenotypic features of Langerhans cells and non-Langerhans his...
Case Reports
Pediatric neurosurgery. 2021;56(5):465-470. DOI:10.1159/000517331 2021
Management of a Persistent Oblique Occipital Sinus with Staged Ligation in a Case of Medulloblastoma: A Case Report [0.03%]
斜坡髓母细胞瘤术后残留髁旁窦的栓塞治疗及随访报道
Gaurav Tyagi,Gyani Jail Singh,Manish Beniwal et al.
Gaurav Tyagi et al.
Introduction: A patent persistent occipital sinus (OS) can be seen in 10% of adults. The presence of such a dominant draining OS can present as a challenge for posterior fossa surgeries. Occlusion or division of the sinus...
Case Reports
Pediatric neurosurgery. 2021;56(5):460-464. DOI:10.1159/000517214 2021
Endovascular Treatment of an Arteriovenous Malformation Associated with a Double Origin of the Posterior Inferior Cerebellar Artery [0.03%]
后下顳动脉双源性动静脉畸形的血管内治疗
Aaron Rodriguez-Calienes,Giancarlo Saal-Zapata,Joselyn De la Cruz
Aaron Rodriguez-Calienes
Introduction: A double origin of the posterior inferior cerebellar artery (DOPICA) is a rare anatomical variant. Posterior fossa arteriovenous malformations (AVMs), especially cerebellar AVMs, are also not common. Consequ...
Case Reports
Pediatric neurosurgery. 2021;56(5):492-496. DOI:10.1159/000517248 2021