J Korean Neurol Assoc.  1998 Feb;16(1):73-76.

Two Cases of Holosyringomyelia with Atypical Clinical Features

Affiliations
  • 1Department of Neurology, College of Medicine, Ewha Womans University.

Abstract

Syringomyelia is a well known clinical syndrome that has typical neurologic manifestations such as sensory dissociation. The authors experienced 2 cases of holosyringomyelia with unusual clinical manifestations. The first case was 26-year-old man complaining of vague sensory symptoms scattered over the trunk but no other neurologic abnormality. At age 14, he suffered from thoracic scoliosis which was corrected with total spine brace. Neurologic examination on admission revealed no sensory dissociation or motor weakness except focal areas of decreased pin-prick on the trunk. Spine MRI scan, surprisingly revealed holosyrinx involving almost entire cord associated with type I Arnold-Chiari malformation. The second case was 38-year-old male who presented with cervical sensory level and absence of position and vibration senses in the lower extremities. The MRI scan revealed syrinx involving entire spinal cord. These cases suggest huge or extensive syringomyelia can be manifested without typical features of syrinx and definite motor weakness and the spine scoliosis associated with vague sensory symptoms may be a sign of syringomyelia.


MeSH Terms

Adult
Arnold-Chiari Malformation
Braces
Humans
Lower Extremity
Magnetic Resonance Imaging
Male
Neurologic Examination
Neurologic Manifestations
Scoliosis
Spinal Cord
Spine
Syringomyelia
Vibration
Full Text Links
  • JKNA
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr