Pediatric neurosurgery
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Pediatric neurosurgery · Nov 2005
The retrograde ventriculo-sinus shunt (El Shafei RVS shunt). Rationale, evolution, surgical technique and long-term results.
Since 1990, 110 retrograde ventriculo-sinus (RVS) shunts were implanted; 98 patients (89.1%) benefited - 1 of them (0.9%) after shunt revision. The manifestations of high intra cranial pressure (ICP) disappeared, there were no problems related to improper cerebrospinal fluid (CSF) drainage, and the transcranial Doppler (TCD) resistive index (RI) measurements decreased to within normal ranges. Radiologically, the ventriculomegaly showed no regression in patients with open craniums and variable degrees of mild regression in patients with rigid craniums. Complications that needed shunt removal or revision occurred in 13 patients (11.8%); 1 patient (0.9%) died before shunt revision; they were all due to technical errors committed during the stages of evolution of the surgical technique for shunt implantation. The follow-up ranged between 4 months and 11 years (mean 3.42 years). ⋯ the RVS shunt is a simple, minimally invasive, physiological procedure for treatment of hydrocephalus and is suitable for all ages.
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Pediatric neurosurgery · Sep 2005
Review Case ReportsAsymptomatic syringomyelia in the course of medulloblastoma.
Syringomyelia is frequently associated with Chiari malformation or one of many other pathological conditions. Its co-occurrence with medulloblastoma is rare, and to our knowledge, only 4 patients have been reported, although some reports have documented on syringomyelia associated with intracranial processes or intramedullary tumor. The authors describe an unusual case of asymptomatic thoracic syringomyelia complicated by an intrasyringal hemorrhage in a child with medulloblastoma. This report illustrates that, although unusual, syringomyelia is a potential complication in the natural history of medulloblastoma, and the authors consider the possible pathogenesis of syrinx enlargement.
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Pediatric neurosurgery · Sep 2005
Case ReportsSuperior sagittal sinus thrombosis associated with raised intracranial pressure in closed head injury with depressed skull fracture.
A case of delayed signs of intracranial hypertension following closed head injury with a depressed cranial fracture and superior sagittal sinus thrombosis is reported. Conservative treatment of intracranial hypertension, including just repeated lumbar puncture and oral acetazolamide, was performed. Spontaneous recanalization of the superior sagittal sinus was observed. Pathogenesis and different modalities of treatment are discussed.
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Pediatric neurosurgery · Jul 2005
Ventriculosubgaleal shunts for posthemorrhagic hydrocephalus in premature infants.
The early management of posthemorrhagic hydrocephalus in premature infants is challenging and controversial. These infants need a temporary cerebrospinal fluid (CSF) diversion procedure until they gain adequate weight, and the blood and protein levels in CSF are reasonably low before permanent shunt can be placed. Various options are available with their associated advantages and disadvantages. Ventriculosubgaleal shunts have been recommended as a more physiologic and less invasive means of achieving this goal. We have performed this procedure in 6 premature infants to evaluate their effectiveness and complications. ⋯ Placement of ventriculosubgaleal shunts for interim CSF diversion in neonates with posthemorrhagic hydrocephalus is effective as a temporary method of CSF diversion. However, our experience has shown that it is associated with a unacceptably high CSF infection rate. A potential cause for infection is CSF stasis just beneath the extremely thin skin of the premature infants, promoting colonization by skin flora. CSF sampling before conversion to a permanent shunt and replacement of the proximal hardware, which has been in situ for a prolonged period, may decrease the infection rates. At present, the procedure is no longer performed at our institution.
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Pediatric neurosurgery · Jul 2005
Case ReportsParadoxical intracranial tuberculoma requiring surgical treatment.
Paradoxical enlargement of intracranial tuberculomas or development of new ones during adequate antituberculous chemotherapy is an uncommon event. Treatment of such cases is controversial. Steroid therapy is usually advocated without change in the antituberculous drug program. ⋯ While her pulmonary lesions and intracranial tuberculomas except one were healed with chemotherapy, one tuberculoma increased in size 1 month after starting chemotherapy. She was followed with dexamethasone treatment in addition to antituberculous therapy for 2 months. Then, the lesion was removed because it had increased in size in spite of appropriate chemotherapy.