Cervical lipomyelomeningocele: case Illustration
نویسندگان
چکیده
منابع مشابه
Cervical lipomyelomeningocele: case illustration.
Cervical lipomyelomeningocele is a rare congenital spinal pathology. Lipomyelomeningocele is the commonest cause of congenital tethering, which causes neurological deterioration due to the conus medullaris and root ischemia. Early intervention is recommended even in cases with normal neurological examinations in order to prevent deterioration but our patient with cervical lipomyelomeningocele h...
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INTRODUCTION Lipomyelomeningocele is a form of the spina bifida occulta, which show differentiation from spina bifida aperta by pathogenesis. Laterally located thoracal lipomyelomeningocele is very rare congenital spinal pathology. The clinical presentation may be soft tissue mass, sensorial-motor loss and/or bladder dysfunction. CASE PRESENTATION Here we presented a 10-month-old girl patient...
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Sokol, G. M., and Schwartz, M. W. (1973). Archives of Disease in Childhood, 48, 560. Urinary complications oflipomyelomeningocele. A review of22 cases of lipomyelomeningocele was conducted with special reference to the urinary system. 13 patients (60%) had evidence of urinary tract infection. 10 urological x-rays were abnormal. Surgical removal of the lipomyelomeningocele had no effect upon the...
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Spinal cord oligodendrogliomas are rare pathologies of the spinal cord, and their location at conus and/or filum terminale is even rarer. There are only 7 spinal cord oligodendrogliomas reported in the literature. Our case is the eighth spinal cord oligodendrogliomas at this location.
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AIM To summarize clinical presentations and treatment options of spinal gout in the literature from 2000 to 2014, and present theories for possible mechanism of spinal gout formation. METHODS The authors reviewed 68 published cases of spinal gout, which were collected by searching "spinal gout" on PubMed from 2000 to 2014. The data were analyzed for clinical features, anatomical location of s...
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ژورنال
عنوان ژورنال: Neurocirugía
سال: 2007
ISSN: 1130-1473
DOI: 10.4321/s1130-14732007000600007