Revista do Instituto de Medicina Tropical de São Paulo (Aug 2012)

Optochiasmatic tuberculoma as the sole manifestation of late recurrent tuberculosis

  • Marco A. Lima,
  • Antonio Aversa,
  • Pericles Maranhão-Filho,
  • Gabriela A. Lima,
  • Andre Curi,
  • Carolina A. Schmaltz,
  • Flavia M. Santanna

DOI
https://doi.org/10.1590/S0036-46652012000400008
Journal volume & issue
Vol. 54, no. 4
pp. 229 – 230

Abstract

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Brain tuberculomas account for 10-20% of space occupying brain lesions in developing countries. Most lesions are observed at time of tuberculosis diagnosis or soon after starting treatment. We herein describe a 32 year-old patient with a 14-month history of headache and progressive visual loss. Her past medical history revealed pulmonary tuberculosis treated eight years before. A brain MRI showed a T1- and T2-weighted isointense contrast-enhancing lesion in the optic chiasm. A presumptive diagnosis of optochiasmatic tuberculoma was made and isoniazid, rifampin, pyrazinamide, and ethambutol were started. Despite treatment, the patient evolved to blindness. The prompt recognition of this condition is extremely important since the presence of optochiasmal enhancement is associated with blindness in patients with tuberculosis.

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