A Case of Intramedullary Schwannoma at the Cervicomedullary Junction - A Case Report -

연수와 경수에 발생한 수내 신경초종 - 증 례 보 고 -

  • Lee, Jong-Won (Department of Neurosurgery, College of Medicine, Chung-Ang University) ;
  • Park, Seung-Won (Department of Neurosurgery, College of Medicine, Chung-Ang University) ;
  • Kim, Young-Baeg (Department of Neurosurgery, College of Medicine, Chung-Ang University) ;
  • Hwang, Sung-Nam (Department of Neurosurgery, College of Medicine, Chung-Ang University) ;
  • Choi, Duck-Young (Department of Neurosurgery, College of Medicine, Chung-Ang University)
  • 이종원 (중앙대학교 의과대학 신경외과학교실) ;
  • 박승원 (중앙대학교 의과대학 신경외과학교실) ;
  • 김영백 (중앙대학교 의과대학 신경외과학교실) ;
  • 황성남 (중앙대학교 의과대학 신경외과학교실) ;
  • 최덕영 (중앙대학교 의과대학 신경외과학교실)
  • Received : 1999.09.28
  • Accepted : 1999.10.29
  • Published : 2000.09.28

Abstract

Spinal schwannomas are usually extramedullary intradural tumors and their intramedullary localizations are thought to be extremely rare. A 60-year-old woman complaining spastic quadriparesis, voiding difficulty and dyspnea was admitted. Her cervical MRI revealed an intramedullary mass in the cervicomedullary junction with multiple cyst which extended from lower cervical to C3 spinal cord. The mass showed a low signal on T1WI, high signal on T2WI with an wall enhancement. The patient underwent a suboccipital craniectomy and C1-2 laminectomy and the cystic tumor was totally removed through a midline myelotomy. The tumor was proved as an intramedullary schwannoma by pathologic examination. The Intramedullary presence of a tumor arising from the cells of the nerve sheath is unusual, because the central nervous system fibers do not contain the Schwann cell. There have been several hypotheses, but none has been accepted universally. This rare tumor is considered as a curable benign neoplasm, and an accurate intraoperative diagnosis and surgically total removal are essential.

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