Chiari I malformations and hydromyelia--complications.

abstract：BACKGROUND:Lateral meningocele syndrome (LMS) is an exceedingly rare connective tissue disease with phenotypic anomalies similar to those seen in Marfan syndrome, Ehler-Danlos syndrome, and Loeys-Dietz syndrome. However, this syndrome is invariably associated with the presence of multiple lateral thoracolumbar spinal m...

journal_title：Pediatric neurosurgery

authors： Cuoco JA,Klein BJ,Busch CM,Gosnell HL,Kar A,Marvin EA,Apfel LS

更新日期：2020-01-01 00:00:00

abstract：:Cystoperitoneal (CP) shunting is minimally invasive and achieves a high rate of resolution on neuroimaging. However, in the absence of definite symptoms, shunting should be reconsidered, because some patients can experience shunt dependency after CP shunting. In this study, the risk of shunt dependency in patients wit...

journal_title：Pediatric neurosurgery

authors： Kim SK,Cho BK,Chung YN,Kim HS,Wang KC

更新日期：2002-10-01 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：PURPOSE:Over 170 years ago, traumatic spondylolisthesis of the axis or hangman's fracture was described. Most descriptions of this entity have focused on adult presentations. METHODS:We review the literature on pediatric cases of hangman's fracture emphasizing the embryological as well as presentation aspects. RESULT...

journal_title：Pediatric neurosurgery

authors： Montalbano M,Fisahn C,Loukas M,Oskouian RJ,Chapman JR,Tubbs RS

更新日期：2017-01-01 00:00:00

abstract：:Intracranial congenital arachnoid cysts are benign intra-arachnoidal fluid collections with a wall composed of arachnoid cells encompassing a cavity containing a fluid similar to cerebrospinal fluid. This cavity frequently communicates with the subarachnoid space. Arachnoid cysts are reported to account for about 1% o...

journal_title：Pediatric neurosurgery

authors： Kabil MS,Shahinian HK

更新日期：2007-01-01 00:00:00

abstract：:Cerebral sparganosis in childhood is very rare. Until 1996, 2 cases in children up to 15 years of age had been described. We report a case of cerebral sparganosis in a 6-year-old girl who presented with seizures. Sequential brain magnetic resonance imaging scans spaced over 4 months showed a lesion which migrated from...

journal_title：Pediatric neurosurgery

authors： Kim CY,Cho BK,Kim IO,Hwang YS,Wang KC

更新日期：1997-02-01 00:00:00

abstract：BACKGROUND:An 11-month-old boy with autosomal recessive infantile osteopetrosis presented, 7 months after bone marrow transplantation, with normal ventricular size and life-threatening intracranial hypertension due to pansynostosis. METHODS:The cranial vault was expanded by using jackscrew distracters to upwardly adva...

journal_title：Pediatric neurosurgery

authors： Dowlati D,Winston KR,Ketch LL,Quinones R,Giller R,Frattini A,van Hove J

更新日期：2007-01-01 00:00:00

abstract：:Changes in spinal curvature, scoliosis, kyphosis and lordosis are associated with the growth of patients with myelomeningocele. Previous investigators have stated that progressive developmental scoliosis is related to tethered spinal cord. In order to investigate the relationship of tethered spinal cord release to pro...

journal_title：Pediatric neurosurgery

authors： Reigel DH,Tchernoukha K,Bazmi B,Kortyna R,Rotenstein D

更新日期：1994-01-01 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：OBJECT:The evolution and severity of hydrocephalus in animal models varies in the species and mode of induction. This makes comparisons of the physiological system under investigation difficult between models. We noted that injection of kaolin into neonatal rats results in a dichotomous outcome into either an acute or ...

journal_title：Pediatric neurosurgery

authors： Ishizaki R,Tashiro Y,Inomoto T,Hashimoto N

更新日期：2000-12-01 00:00:00

abstract：:Posterior plagiocephaly secondary to lambdoid suture stenosis requires surgical release and repair to prevent progressive deformational changes associated with a suture stenosis. A surgical technique is described for release of the stenosed lambdoid suture and asterion region, followed by occipital reconstruction. Thi...

journal_title：Pediatric neurosurgery

authors： Jimenez DF,Barone CM

更新日期：1995-01-01 00:00:00

abstract：:An intradural, intramedullary lipoma originating within the upper cervical cord with significant extension into the posterior fossa is reported in an infant. Two additional lipomas were found in the lumbar region. This constellation of findings represents the first description of multiple intradural, intramedullary sp...

journal_title：Pediatric neurosurgery

authors： Wilson JT,Shapiro RH,Wald SL

更新日期：1996-01-01 00:00:00

abstract：:Spondylolysis and spondylolisthesis can be associated with significant low back pain, especially in physically active adolescents. Non-operative management is usually successful in improving symptoms, but surgical intervention is occasionally required for those that fail reduction of activity and bracing. In a subpopu...

journal_title：Pediatric neurosurgery

authors： Lundin DA,Wiseman D,Ellenbogen RG,Shaffrey CI

更新日期：2003-10-01 00:00:00

abstract：:Extraventricular neurocytomas mimic central neurocytomas histologically but are located outside the lateral and/or third ventricles. Pontine neurocytomas represent an extremely rare subset of extraventricular neurocytomas, and reports are limited to 2 adults followed under 28 months. The authors present the case of a ...

journal_title：Pediatric neurosurgery

authors： Hawasli AH,Haydon DH,Dahiya S,Smyth MD

更新日期：2012-01-01 00:00:00

abstract：:We present a case report of a 21-month-old female patient to highlight magnetic resonance (MR) imaging findings associated with papilledema in a pediatric patient with an intracranial tumor. The MR findings included optic disc elevation, dilated perioptic subarachnoid spaces, optic nerve tortuosity and restricted diff...

journal_title：Pediatric neurosurgery

authors： Pakzad-Vaezi K,Cochrane D,Sargent M,Singhal A

更新日期：2009-01-01 00:00:00

abstract：:There are several treatment modalities for Langerhans' cell histiocytosis (LCH) of bone, formerly usually referred to as eosinophilic granuloma, including surgery, radiotherapy and chemotherapy. In spinal lesions, surgery is not recommended generally, because of the potential for reconstitution of vertebral height. We...

journal_title：Pediatric neurosurgery

authors： Karagoz Guzey F,Bas NS,Emel E,Alatas I,Kebudi R

更新日期：2003-04-01 00:00:00

abstract：OBJECTIVE:The Delta valve is a pressure differential valve with a siphon control device. The valve mechanism is normally closed, but is designed to open in response to positive ventricular pressure, thereby avoiding overdrainage of cerebrospinal fluid (CSF). As a result, the incidence of subdural fluid collections as w...

journal_title：Pediatric neurosurgery

authors： Davis SE,Levy ML,McComb JG,Sposto R

更新日期：2000-08-01 00:00:00

abstract：:Anaplastic gangliogliomas with an oligodendroglial component are exceedingly rare tumors of uncertain growth potential. We report a 17-year-old female with a massive ganglioglioma containing anaplastic oligodendroglioma apparently arising from the thalamus. Two weeks after partial resection, she was started on a regim...

journal_title：Pediatric neurosurgery

authors： Johnson MD,Jennings MT,Toms ST

更新日期：2001-06-01 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：:A 3-year-old boy presented with headaches, vomiting, lethargy and papilledema. Communicating hydrocephalus along with transependymal fluid absorption and meningeal contrast enhancement was identified on CT. The enhancement was initially thought to be the result of a partially treated meningitis (child was previously o...

journal_title：Pediatric neurosurgery

authors： Vassilyadi M,Michaud J

更新日期：2005-01-01 00:00:00

abstract：:A 16-year-old male presented with obstructive hydrocephalus secondary to pineal germinoma. There have been many reported cases of abdominal metastasis of pineal germinoma after ventriculoperitoneal shunting. Endoscopic ventriculostomy was preferred in our case, thus avoiding iatrogenic peritoneal seeding, but spinal m...

journal_title：Pediatric neurosurgery

authors： Ho CL,Deruytter MJ

更新日期：2006-01-01 00:00:00

abstract：OBJECTIVE AND IMPORTANCE:Gorham-Stout disease is a rare entity characterized by vascular proliferation causing local destruction of bone tissue. Owing to its low incidence and variable clinical presentation, the diagnosis requires a high degree of awareness by the clinician. CLINICAL PRESENTATION:We present the case o...

journal_title：Pediatric neurosurgery

authors： Hernández-Marqués C,Serrano González A,Cordobés Ortega F,Alvarez-Coca J,Sirvent Cerda S,Carceller Lechón F,Azorín Cuadrillero D

更新日期：2011-01-01 00:00:00

abstract：:Cyanotic breath-holding spell is a benign and self-limiting disease of young children but occasionally associated with sudden, unexpected death. The authors report a rare case in a 2-year-old girl with a severe form that started after radical resection of a cervicomedullary ganglioglioma. She was admitted to our hospi...

journal_title：Pediatric neurosurgery

authors： Fujisawa H,Yoshida Y,Niida Y,Hasegawa M,Yamashita J

更新日期：2005-03-01 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：:We evaluated the prevalence of pathological visually evoked potentials (VEP) before the appearance of papilledema or other signs of elevated intracranial pressure in children suffering from craniosynostosis. In 52 children (19 girls, 33 boys, median age 7.6 months, mean age 7.6 months, range from 3 to 34 months) preop...

journal_title：Pediatric neurosurgery

authors： Mursch K,Brockmann K,Lang JK,Markakis E,Behnke-Mursch J

更新日期：1998-12-01 00:00:00

abstract：:Molecular genetic analysis of several common cancers has yielded information concerning their etiology and prognosis. Restriction fragment length polymorphism (RFLP) studies showing consistent loss of specific DNA sequences in tumor tissue have identified genes, known as tumor suppressors, associated with the etiology...

journal_title：Pediatric neurosurgery

authors： Cogen PH

更新日期：1991-01-01 00:00:00

abstract：:Primary spinal primitive neuroectodermal tumor (PSPNET) is extremely rare and only 25 cases have been reported in the world literature so far. Three patients of 8, 9 and 18 years of age, who presented with variable grades of neurological deficit were diagnosed as having a dorsal intramedullary lesion, a holocord lesio...

journal_title：Pediatric neurosurgery

authors： Kumar R,Reddy SJ,Wani AA,Pal L

更新日期：2007-01-01 00:00:00

abstract：:Optimal treatment for hydrocephalus related to Dandy-Walker syndrome (DWS) remains elusive. Patients with DWS-related hydrocephalus often require combinations of shunting systems to effectively drain both the supratentorial ventricles and posterior fossa cyst. We describe an endoscopic technique, whereby a frontally p...

journal_title：Pediatric neurosurgery

authors： Sikorski CW,Curry DJ

更新日期：2005-09-01 00:00:00

abstract：:It is essential that various factors be considered when determining the differential diagnosis of congenital scalp lesions, including lesion size, appearance, intracranial extension, underlying medical condition and the embryological germ layer involved. We present the case of a newborn diagnosed as having a sebaceous...

journal_title：Pediatric neurosurgery

authors： Saedi T,Cetas J,Chang R,Krol A,Selden NR

更新日期：2008-01-01 00:00:00

abstract：:Tumors of the pineal region in children often belong to 2 categories, namely germ cell tumors and pineal parenchymal tumors. Very rare pathologies have previously been reported in this region. Most of these tumors may be similar radiologically, while their management differs. The present series reports 2 children with...

journal_title：Pediatric neurosurgery

authors： Maiti TK,Arimappamagan A,Mahadevan A,Yasha TC,Pandey P,Santosh V

更新日期：2015-01-01 00:00:00