Robot-assisted endoscopic intrauterine myelomeningocele repair: a feasibility study.

abstract：:The case of a child with Apert syndrome is presented in which the development and rupture of an intracranial mycotic aneurysm occurred secondary to multiple infectious complications following craniofacial surgery. An endovascular procedure was utilized in an attempt to embolize the aneurysm and parent vessel. The pati...

journal_title：Pediatric neurosurgery

authors： Uchiyama CM,Brockmeyer DL,Cherny WB,Jacobs JJ,Walker ML

更新日期：2001-08-01 00:00:00

abstract：OBJECTIVE AND IMPORTANCE:Complications arising from the placement of ventriculoperitoneal (VP) shunts are well documented. A case of infertility is presented that was thought to result from factors related to the distal end of a VP shunt residing within a patient's abdomen. CLINICAL PRESENTATION:A 30-year-old female w...

journal_title：Pediatric neurosurgery

authors： White JB,Raffel C,Blackwell RE

更新日期：2007-01-01 00:00:00

abstract：:Although some complications have been reported when using endoscopic techniques, epidural hematoma (EDH) has rarely been caused. The authors report a case of EDH complicating a concomitant endoscopic biopsy procedure with ventricular shunt placement in a young, 14-year-old boy harboring a third ventricle tumor with a ...

journal_title：Pediatric neurosurgery

authors： Hamlat A,Heckly A,Doumbouya N,Seigneuret E,Brassier G

更新日期：2004-09-01 00:00:00

abstract：:Hydrocephalic (n = 19) and normal (n = 20) children in two age groups (averaged at 10 and 14 years old) were asked to learn 5 predetermined timing rhythm interval tasks (including timing duration and relative timing pattern) by pressing keys on a computer keyboard. In the acquisition phase, visual and auditory goal ti...

journal_title：Pediatric neurosurgery

authors： Ding Y,Lai Q,McAllister II JP,Canady AI

更新日期：2001-04-01 00:00:00

abstract：OBJECTIVE:Surgical treatment options are limited for medically and endovascular refractory cerebral venous sinus thrombosis (CVT). We describe the technical feasibility of open, direct sinus thrombectomy in a pediatric patient with medically and endovascular refractory CVT. METHODS:A 15-year-old patient with superior ...

journal_title：Pediatric neurosurgery

authors： Westwick HJ,Obaid S,Bordeleau-Roy F,Truffer E,Weil AG

更新日期：2019-01-01 00:00:00

abstract：:Primary germ cell tumors confined to the optic nerves and chiasm without suprasellar extension are uncommon. These tumors appear similar to chiasmatic gliomas on both computed tomography and magnetic resonance imaging, potentially resulting in treatment errors if the diagnosis is based on radiologic criteria alone. Un...

journal_title：Pediatric neurosurgery

authors： Wilson JT,Wald SL,Aitken PA,Mastromateo J,Vieco PT

更新日期：1995-01-01 00:00:00

abstract：:Prepontine arachnoid cysts are rare developmental anomalies that occur almost exclusively in children. The symptomatic child typically suffers from hydrocephalus, visual impairment, endocrine dysfunction and/or cranial neuropathies. Some cysts, however, are discovered incidentally upon prenatal or postnatal imaging fo...

journal_title：Pediatric neurosurgery

authors： Dodd RL,Barnes PD,Huhn SL

更新日期：2002-09-01 00:00:00

abstract：:Most cerebrospinal fluid (CSF) shunts employed in the treatment of hydrocephalus include in their designs a pump mechanism that has been used in office practice as an indicator of whether the shunt is functioning properly; however, the pumping characteristics of shunts have been shown to correlate poorly with clinical...

journal_title：Pediatric neurosurgery

authors： Piatt JH Jr

更新日期：1996-08-01 00:00:00

abstract：:A 3-year-old boy with chronic papilledema, bilateral coronal synostosis and Pfeiffer syndrome underwent an orbitofrontal advancement. One month postoperatively, his papilledema had resolved, however, his vision progressively deteriorated over the ensuing 3 months to legal blindness. He had no symptoms or signs of incr...

journal_title：Pediatric neurosurgery

authors： Campbell JW,Albright AL,Losken HW,Biglan AW

更新日期：1995-01-01 00:00:00

abstract：:A rare case of a patient with Laurence-Moon-Biedl syndrome associated with hypothalamic hamartoma is described. The English-language literature contains no cases of patients with this association. The clinical manifestations of this syndrome, those of hypothalamic hamartomas, and the appearance of the tumors on magnet...

journal_title：Pediatric neurosurgery

authors： Diaz LL,Grech KF,Prados MD

更新日期：1991-01-01 00:00:00

abstract：:Diffuse pontine tumors are highly lethal and conventional therapy with irradiation provides long-term survival to a very small proportion of the patients. We have reported promising results using high-dose chemotherapy with autologous stem cell rescue in patients with recurrent high-grade astrocytomas in other anatomi...

journal_title：Pediatric neurosurgery

authors： Dunkel IJ,O'Malley B,Finlay JL

更新日期：1996-01-01 00:00:00

abstract：OBJECTIVE:Myxopapillary ependymomas (MPEs) in children are rarely reported low-grade glial tumors; however, MPEs sometimes possess malignant characteristics such as spinal seeding/drop metastasis (SSM). We aimed to present 3 pediatric MPE cases that experienced SSM at 2 neurosurgical centers. MATERIALS AND METHODS:We ...

journal_title：Pediatric neurosurgery

authors： Abdallah A

更新日期：2020-01-01 00:00:00

abstract：:The purpose of this study was to examine the current patterns of head trauma associated with child abuse. We reviewed the records of all patients admitted to our medical center between 1995 and 1997 with a primary diagnosis of head trauma, and analyzed the clinical presentation, mechanism of injury, socioeconomic stat...

journal_title：Pediatric neurosurgery

authors： Dashti SR,Decker DD,Razzaq A,Cohen AR

更新日期：1999-12-01 00:00:00

abstract：:Cavernous malformations (CMs) of the central nervous system are benign, angiographically occult vascular lesions and are diagnosed by magnetic resonance imaging techniques. Giant CMs do not differ from smaller-sized CMs in their clinical, surgical or histopathological presentation but may be radiologically different. ...

journal_title：Pediatric neurosurgery

authors： Ozsoy KM,Oktay K,Gezercan Y,Cetinalp NE,Olguner SK,Erman T

更新日期：2017-01-01 00:00:00

abstract：OBJECTIVE:Cephalocele is a central nervous system (CNS) birth defect. Various CNS and extra-CNS anomalies, as well as prognostic factors have been reported with cephalocele. The aim of this study was to discuss prognostic factors and current possible theories explaining associated anomalies seen in a series of 55 patie...

journal_title：Pediatric neurosurgery

authors： Baradaran N,Nejat F,Baradaran N,El Khashab M

更新日期：2009-01-01 00:00:00

abstract：:We have reviewed 16 children with extradural spinal tumors, both benign and malignant, treated from 1998 to 2006 in Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India. The duration of symptomatology, clinical signs, radiological investigations, surgical approach, outcome and histopathological var...

journal_title：Pediatric neurosurgery

authors： Kumar R,Giri PJ

更新日期：2008-01-01 00:00:00

abstract：:With an incidence of less than 1-3 per million, pediatric aneurysms are rare clinical entities. A traumatic etiology is implicated in a large proportion of these cases, leading to the formation of both 'false' and 'true' aneurysms. These occur most often in the distal circulation, but have also been described in the s...

journal_title：Pediatric neurosurgery

authors： Haji FA,Boulton MR,de Ribaupierre S

更新日期：2011-01-01 00:00:00

abstract：:Meningeal melanocytoma is an infrequent neoplasm of the central nervous system (CNS), especially in childhood and infancy. It was first described as an entity different from pigmented meningiomas and schwannomas in 1972, and few cases have been published so far. In this article, a 5-month-old male patient with meninge...

journal_title：Pediatric neurosurgery

authors： Oruckaptan HH,Soylemezoglu F,Kutluk T,Akalan N

更新日期：2000-05-01 00:00:00

abstract：:This is a report of a prenatal sonographic diagnosis of a lateral ventricle choroid plexus papilloma in an in vitro fertilization (IVF)-induced pregnancy of a 40-year-old woman. The baby was delivered at 35 weeks of gestation and surgery was performed 5 days later with a good outcome. Several cases of malignancies ass...

journal_title：Pediatric neurosurgery

authors： Cohen ZR,Achiron R,Feldman Z

更新日期：2002-11-01 00:00:00

abstract：:Arachnoid cysts are collections of cerebrospinal fluid covered by arachnoidal cells and collagen. They may have a congenital or acquired origin. We present the case of a 7-year-old boy with a cerebellopontine angle arachnoid cyst harbouring a portion of neuroglia. Microscopically, the cyst wall consisted of a delicate...

journal_title：Pediatric neurosurgery

authors： Ariai S,Koerbel A,Bornemann A,Morgala M,Tatagiba M

更新日期：2005-07-01 00:00:00

abstract：:A case of an intracerebral juvenile xanthogranuloma (JXG) producing complex-partial seizures in a 13-year-old boy is presented. Although the child had no history of JXGs or a systemic histiocytic proliferative disorder, the histopathological and immunocytochemical studies of this lesion were identical to that of a cut...

journal_title：Pediatric neurosurgery

authors： Schultz KD Jr,Petronio J,Narad C,Hunter SB

更新日期：1997-06-01 00:00:00

abstract：INTRODUCTION:Our appreciation and understanding of what is now known as the split cord malformation (SCM) have a long history. The oldest known example of SCM is from roughly AD 100. Other isolated examples can be found in the large body of work of the pathologists of the 1800s, where the SCMs were found incidentally d...

journal_title：Pediatric neurosurgery

authors： Saker E,Loukas M,Fisahn C,Oskouian RJ,Tubbs RS

更新日期：2017-01-01 00:00:00

abstract：:Skull defects in children may be congenital or acquired after trauma, infection or tumor. For defects that do not close spontaneously a variety of repair (cranioplasty) materials are available including bone, metals and acrylic. Where possible calvarial autogenous bone is preferred, particularly in younger infants, bu...

journal_title：Pediatric neurosurgery

authors： Hockley AD,Goldin JH,Wake MJ,Iqbal J

更新日期：1990-01-01 00:00:00

abstract：:Congenital dwarfisms can be associated with a variety of vascular anomalies. Here, we describe 2 patients with congenital dwarfisms who presented with moyamoya syndrome and underwent indirect intracranial revascularization. The pathogenesis of moyamoya syndrome in this population is not well understood, but it is a ma...

journal_title：Pediatric neurosurgery

authors： Moftakhar P,Smith ER,Choulakian A,Scott RM,Danielpour M

更新日期：2010-01-01 00:00:00

abstract：:The epidemiology of cerebrospinal fluid (CSF) shunting in the United States is not well known; however, with recent national surveys, the prevalence, incidence, and cost of these procedures can be estimated. The prevalence of CSF shunts in the United States appears to be greater than 125,000, though this is likely an ...

journal_title：Pediatric neurosurgery

authors： Bondurant CP,Jimenez DF

更新日期：1995-01-01 00:00:00

abstract：:Though detected with increasing frequency, intracranial carotid artery dissection remains less common in infancy. We report on 3 otherwise healthy children aged 8, 12 and 15 years who presented with focal headache and stroke secondary to intracranial carotid occlusive disease consistent with arterial dissection. In 2 ...

journal_title：Pediatric neurosurgery

authors： Pozzati E,Galassi E,Godano U,Cordella L

更新日期：1994-01-01 00:00:00

abstract：:Radiotherapy has remained the mainstay of treatment for children with intrinsic, diffuse pontine tumors in spite of over 20 years of clinical trials attempting to validate the additional role of chemotherapy. Conventional phase II clinical trials conducted in patients with recurrent or progressive brainstem gliomas us...

journal_title：Pediatric neurosurgery

authors： Allen JC,Siffert J

更新日期：1996-01-01 00:00:00

abstract：:Malignant tumors arising within dysrhaphic malformations are very rare and are mostly teratomas; so far, only one rhabdomyosarcoma has been reported in this context. We report another case of a girl with lipomyelomeningocele who developed a lumbar rhabdomyosarcoma 2 years after birth and primary closure of the neural ...

journal_title：Pediatric neurosurgery

authors： Wagner W,Koch D

更新日期：2004-11-01 00:00:00

abstract：:Hepatic pseudocyst formation is a rare intra-abdominal complication of ventriculoperitoneal shunts. The presence of an intracranial tumor and a history of central nervous system infection are major risk factors for the development of this complication. Hepatic pseudocysts secondary to ventriculoperitoneal shunts can b...

journal_title：Pediatric neurosurgery

authors： Kaplan M,Ozel SK,Akgun B,Kazez A,Kaplan S

更新日期：2007-01-01 00:00:00

abstract：:Focal intracranial infections due to Salmonella are rare. So far, around 80 cases have been reported in the world literature. The authors present their experience of 6 cases of intracranial Salmonella infections, mainly subdural empyema in 5 and effusion in 1. In 1 case, subdural empyema was bilateral, and in another ...

journal_title：Pediatric neurosurgery

authors： Mahapatra AK,Pawar SJ,Sharma RR

更新日期：2002-01-01 00:00:00