Diastematomyelia in Adult: A Case Report.
10.4184/jkss.2012.19.2.68
- Author:
Jin Young LEE
1
;
Joo Sung JO
Author Information
1. Department of Orthopedic Surgery, Kangdong Sacred Heart Hospital, Hallym University School of Medicine, Seoul, Korea. jylee@hallym.or.kr
- Publication Type:Case Report
- Keywords:
L-spine;
Diastematomyelia;
Decompressive laminectomy;
Septum removal;
Posterior instrumentation
- MeSH:
Adult;
Axis, Cervical Vertebra;
Female;
Humans;
Laminectomy;
Neural Tube Defects;
Spinal Cord
- From:Journal of Korean Society of Spine Surgery
2012;19(2):68-71
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
STUDY DESIGN: Case report. OBJECTIVES: We report an adult patient with diastematomyelia. SUMMARY OF LITERATURE REVIEW: Diastematomyelia is an uncommon congenital malformation of the vertebral axis, characterized by a separation of the spinal cord with an interposed bony, cartilaginous or fibrous septum. Most of the patients present this condition in childhood. The cases in adulthood are extremely rare. MATERIALS AND METHODS: The authors experienced a 46-year old female patient with diastematomyelia presenting a gradual onset of neurologic claudication. We treated with decompressive laminectomy, septum removal and posterior instrumentation. RESULTS: We had satisfactory surgical results. CONCLUSIONS: We report an extremely rare case of diastematomyelia in adulthood.