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1.
Journal of the Korean Society of Neonatology ; : 181-185, 2000.
Article in Korean | WPRIM | ID: wpr-49080

ABSTRACT

We hereby report on a newborn infant with a lipomeningomyelocele present with hydrosyringomyelia. MR scans disclosed a low-lying spinal cord to be continuous dorsally with the neural placode, the nerve roots crossed the subarachnoid space and the lipoma lied outside the dura and contiguous with subcutaneous fat. And hydrosyringomyelia was noted on lower spinal cord. She had no neurologic signs at birth and she got operation at 4 months of age before any neurologic signs accompanied and she is doing well not presenting any neorologic or orthopedic complications until 8 months of age.


Subject(s)
Humans , Infant, Newborn , Lipoma , Neurologic Manifestations , Orthopedics , Parturition , Spinal Cord , Subarachnoid Space , Subcutaneous Fat , Syringomyelia
2.
Journal of Korean Neurosurgical Society ; : 221-227, 1999.
Article in Korean | WPRIM | ID: wpr-96730

ABSTRACT

Lipomeningomyelocele(LMMC) is one of the most common forms of occult spinal dysraphism seen in clinical practice. It is now widely accepted that prophylactic surgery is indicated in most cases, but areas of controversies were remained. From January 1986 to December 1996, long term data are available for 57 patients who underwent surgery for LMMC repair. The most common presenting symptom of these patients were mass on back which was followed by weakness of lower extremities and bladder-bowel symptoms. Transitional type was most common(53%) and followed by caudal(28%) and dorsal type(19%). Surgical repair was performed at age of 1 month to 40 years(mean age: 48months old, median 5 months old). Follow up for these patients ranged from 10 to 130 months(mean 50.3 months). None of the patients who underwent surgery before deficits had occured had ever developed new neurological deficits at the end of the follow up. However, 8 of 57 patients(14%) had aggravation of thier initial neurologic status by history preoperatively. Those progressive symptoms were somewhat reversed or stabilized in all of them postoperatively. In addition, surgical correction in infancy provides a degree of reversibility but do not in older children. We concluded that early diagnosis and treatment should be taken to prevent these progression and permanency of neurological changes.


Subject(s)
Child , Humans , Early Diagnosis , Follow-Up Studies , Lower Extremity , Neural Tube Defects , Spinal Dysraphism
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