gms | German Medical Science

58. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie e. V. (DGNC)

Deutsche Gesellschaft für Neurochirurgie (DGNC) e. V.

26. bis 29.04.2007, Leipzig

Conus medullaris Ependymoma presenting clinically as subarachnoid hemorrhage. Case report and review of literature

Klinische Manifestation eines Conus-medullaris-Ependymoms als Subarachnoidalblutung. Fallbericht und Literaturrecherche

Meeting Abstract

  • corresponding author C.T. Ulrich - Johann-Wolfgang-Goethe-Universität, Klinik für Neurochirurgie, Frankfurt am Main
  • J. Beck - Johann-Wolfgang-Goethe-Universität, Klinik für Neurochirurgie, Frankfurt am Main
  • V. Seifert - Johann-Wolfgang-Goethe-Universität, Klinik für Neurochirurgie, Frankfurt am Main
  • G. Marquardt - Johann-Wolfgang-Goethe-Universität, Klinik für Neurochirurgie, Frankfurt am Main

Deutsche Gesellschaft für Neurochirurgie. 58. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie e.V. (DGNC). Leipzig, 26.-29.04.2007. Düsseldorf: German Medical Science GMS Publishing House; 2007. DocP 039

The electronic version of this article is the complete one and can be found online at: http://www.egms.de/en/meetings/dgnc2007/07dgnc294.shtml

Published: April 11, 2007

© 2007 Ulrich et al.
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc-nd/3.0/deed.en). You are free: to Share – to copy, distribute and transmit the work, provided the original author and source are credited.


Outline

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Objective: Subarachnoid hemorrhage (SAH) due to spinal ependymoma is very rare. We report a 37-year-old man who presented with an acute onset of headache and leg pain.

Methods: This patient presented with typical clinical signs of SAH, and lumbar puncture confirmed SAH. Cerebral angiography was negative and further diagnostic work-up revealed an ependymoma of the conus medullaris as source of the hemorrhage. A comprehensive review of the literature was conducted.

Results: The ependymoma was resected without any sequelae. In the English and German literature, only 17 cases of SAH due to a spinal ependymoma are reported since 1958.

Conclusions: Spinal ependymoma presenting as SAH is very rare. Therefore, in cases of negative diagnostic findings for cerebral aneurysms or malformations this aetiology should be considered and work-up of the spinal axis completed.