Intradural Extramedullary and Subcutaneous Tumors in Neonate : Atypical Myxoid Spindle Cell Neoplasm.
10.3340/jkns.2012.52.4.417
- Author:
Dong Woo YU
1
;
Joon Hyuk CHOI
;
Eun Sil LEE
;
Seong Ho KIM
Author Information
1. Department of Neurosurgery, College of Medicine, Yeungnam University, Daegu, Korea. shkim@med.yu.ac.kr
- Publication Type:Case Report
- Keywords:
Intradural extramedullary spinal cord neoplasm;
Neonate;
Congenital
- MeSH:
Central Nervous System;
Central Nervous System Neoplasms;
Child;
Follow-Up Studies;
Humans;
Infant;
Infant, Newborn;
Magnetic Resonance Imaging;
Male;
Necrosis;
Organothiophosphorus Compounds;
Spinal Canal;
Spinal Cord Neoplasms;
Spine
- From:Journal of Korean Neurosurgical Society
2012;52(4):417-419
- CountryRepublic of Korea
- Language:English
-
Abstract:
Tumors of the central nervous system are common in the pediatric population and constitute the second most prevalent tumor type in children. Within this group, spinal cord tumors are relatively rare and account for 1 to 10% of all pediatric central nervous system tumors. We describe a very rare case of an intradural extramedullary spinal cord tumor with a subcutaneous mass and discuss its clinical presentation, pathogenesis, and treatment. A male infant was delivered normally, with uneventful development. At 16 days post-delivery, his family took him to a pediatrician because of a mass on his upper back. Magnetic resonance imaging of the thoracic spine revealed a well-demarcated soft-tissue mass with central cystic change or necrosis at the subcutaneous layer of the posterior back (T2-7 level). Another mass was found with a fat component at the spinal canal of the T1-3 level, which was intradural extramedullary space. After six weeks, the spinal cord tumor and subcutaneous mass were grossly total resected; pathologic findings indicated an atypical myxoid spindle cell neoplasm, possibly nerve sheath in type. The final diagnosis of the mass was an atypical myxoid spindle cell neoplasm. The postoperative course was uneventful, and the patient was discharged after nine days without any neurological deficit. We report a rare case of an intradural extramedullary spinal tumor with subcutaneous mass in a neonate. It is necessary to monitor the patient's status by examining consecutive radiologic images, and the symptoms and neurological changes should be observed strictly during long-term follow-up.
