gms | German Medical Science

56. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie e. V. (DGNC)
3èmes journées françaises de Neurochirurgie (SFNC)

Deutsche Gesellschaft für Neurochirurgie e. V.
Société Française de Neurochirurgie

07. bis 11.05.2005, Strasbourg

Unilateral visual loss related to chiasmal cavernoma

Meeting Abstract

  • C. Bouazza - Neurosurgical Department, Pitié Salpètrière Hospital, Paris, France
  • corresponding author C. Karachi - Neurosurgical Department, Pitié Salpètrière Hospital, Paris, France
  • D. Milea - Ophtalmological Department, Pitié Salpètrière Hospital, Paris, France
  • P. Lehoang - Ophtalmological Department, Pitié Salpètrière Hospital, Paris, France
  • R. van Effenterre - Neurosurgical Department, Pitié Salpètrière Hospital, Paris, France

Deutsche Gesellschaft für Neurochirurgie. Société Française de Neurochirurgie. 56. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie e.V. (DGNC), 3èmes journées françaises de Neurochirurgie (SFNC). Strasbourg, 07.-11.05.2005. Düsseldorf, Köln: German Medical Science; 2005. DocP132

The electronic version of this article is the complete one and can be found online at: http://www.egms.de/en/meetings/dgnc2005/05dgnc0400.shtml

Published: May 4, 2005

© 2005 Bouazza 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

Text

Introduction

Unilateral visual loss with a normal fundus in a young patient is usually related to an inflammatory optic neuropathy. Intrinsic lesions of visual pathways are rare, but include the exceptional differential diagnosis of cavernoma.

Patient

A 29-year-old patient reported a mild unilateral visual loss of rapid onset with ipsilateral right temporal hemianopia, recovering spontaneously in a few days.

Results

The patient relapsed three months later, and an MRI disclosed a chiasmal heterogenous enhancing lesion. Work-up found no evidence for an inflammatory, infectious or metastatic disease and therefore a neuro-surgical approach of the lesion allowed to diagnose a cavernoma, confirmed by pathological examination. Successful resection resulted in partial recovery of the visual field. Post-operative MRI (T2* sequences) ruled out other cavernomatous localization.

Conclusion

Cavernomas located within the visual pathways are rare lesions, their removal being beneficial for the visual outcome.