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Dear Editor,

We would like to thank Dr Sriwijitalai and Prof Wiwanitkit11. Sriwijitalai S, Wiwanitkit V. Late-onset congenital syphilis: is it another disease? Arq Neuropsiquiatr 2018;76(9):xx-xx. https://doi.org/10.1590/0004-282X20180086
https://doi.org/10.1590/0004-282X2018008...
for their comments and the opportunity to discuss more details about our publication “Late-onset congenital syphilis with unusual brain abnormalities”. Neurosyphilis is very challenging to diagnose due to its variable and complex presentation. This was a case report of a 17-year-old woman who presented with a refractory partial epilepsy since eight years of age and progressive cognitive decline. The patient had no history of sexual intercourse, autoimmune or chronic diseases. Tests for HIV infection, and PCR for herpes simplex were negative, serum VDRL (1:16) and the FTA-ABS test was positive in the cerebrospinal fluid with an increased protein level. False positive treponemal test results, like the FTA-ABS, occur less frequently than false positive anticardiolipin tests (VDRL) and the specificity of the FTA-ABS is high (1% false positive in the general population)22. Nandwani R, Evans DT. Are you sure it's syphilis? A review of falso positive serology. Int J STD AIDS. 1995 Jul-Aug;6(4):241-8.. The magnetic resonance imaging scan of her brain showed T2/FLAIR white matter hyperintensities and atrophy of the anterior temporal and frontal lobes. This image has seldom been reported in the literature in cases of neurosyphilis33. Mignarri A, Arrigucci U, Coleschi P, Bilenchi R, Federico A, Dotti M. Temporal lobe annormalities in neurosyphilis. Pract Neurol. 2014;14(6):449-50. https://doi.org/10.1136/practneurol-2014-000927
https://doi.org/10.1136/practneurol-2014...
,44. Hama K, Ishiguchi H, Tuji T, Miwa H, Kondo T. Neurosyphilis with mesiotemporal magnetic resonance imaging abnormalities. Inter Med. 2008 Feb;47(20):1813-7.. Her mother reported abnormalities in serological tests for syphilis in her prenatal screening. However, she did not receive any treatment. The test was repeated and her mother had VDRL (1:4), IgM-FTA-ABS and IgG-FTA-ABS positives. The patient was treated with intravenous crystalline penicillin, and there was better control of epilepsy.

Due to the evidences presented above, we believe that the diagnosis of late-onset congenital syphilis could be supported.

Yours sincerely,

Rodrigo Alencar e Silva

Camila Campelo

Clecio Godeiro Jr

References

  • 1
    Sriwijitalai S, Wiwanitkit V. Late-onset congenital syphilis: is it another disease? Arq Neuropsiquiatr 2018;76(9):xx-xx. https://doi.org/10.1590/0004-282X20180086
    » https://doi.org/10.1590/0004-282X20180086
  • 2
    Nandwani R, Evans DT. Are you sure it's syphilis? A review of falso positive serology. Int J STD AIDS. 1995 Jul-Aug;6(4):241-8.
  • 3
    Mignarri A, Arrigucci U, Coleschi P, Bilenchi R, Federico A, Dotti M. Temporal lobe annormalities in neurosyphilis. Pract Neurol. 2014;14(6):449-50. https://doi.org/10.1136/practneurol-2014-000927
    » https://doi.org/10.1136/practneurol-2014-000927
  • 4
    Hama K, Ishiguchi H, Tuji T, Miwa H, Kondo T. Neurosyphilis with mesiotemporal magnetic resonance imaging abnormalities. Inter Med. 2008 Feb;47(20):1813-7.

Publication Dates

  • Publication in this collection
    Sept 2018

History

  • Received
    24 Aug 2018
  • Accepted
    30 Aug 2018
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