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DOI: 10.1590/0004-282X-anp-2020-0227
Calcified intracranial tuberculomas as sequelae of pediatric neurotuberculosis
Tuberculomas calcificados intracranianos como sequela de neurotuberculose pediátricaA 29-year-old woman with a history of neurotuberculosis at the age of 18 months presented with seizures, abnormal gait, and fluctuations of consciousness level, recovering after anti-tuberculosis treatment. She remained asymptomatic for the next years, except for moderate cognitive impairment. Years later, a brain magnetic resonance imaging (MRI) scan ([Figure 1]) revealed calcified lobulated masses in the brain parenchyma and basal cisterns.
Intracranial tuberculomas occur in 5–24% of pediatric neurotuberculosis[1] and can be secondary to pial vessel inflammation, perivascular abscesses, or septic emboli[2]. Medical history and the characterization of non-enhancing, diffusely calcified brain masses are important clues for diagnosing residual granulomas.
Authors’ contributions:
CMR: study conceptual design, imaging analysis, writing and review of the manuscript. TAV: imaging and clinical data acquisition, review of the manuscript. LTL: imaging analysis, writing and review of the manuscript.
Publication History
Received: 08 June 2020
Accepted: 25 July 2020
Article published online:
04 July 2023
© 2021. Academia Brasileira de Neurologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commecial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
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References
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- 2 Rock RB, Olin M, Baker CA, Molitor TW, Peterson PK. Central nervous system tuberculosis: pathogenesis and clinical aspects. Clin Microbiol Rev. 2008 Apr;21(2):243-61. https://doi.org/10.1128/CMR.00042-07