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Parinaud syndrome due to cofirmed neurotuberculosis in a lupus eritematosis systemic patient
José Wagner Leonel Tavares-Júnior1, José Newton Teles Júnior2, Samir Câmara Magalhães3
1Department of Clinical Medicine, Universidade Federal do Ceará, Fortaleza, CE, Brazil.
Introduction:
This article aims to describe a patient with Parinaud syndrome due to neurotuberculosis confirmed by cerebrospinal fluid analysis.
Case Report:
Initially, patient sought medical care, performed a chest x-ray and later a chest CT scan, with a probable diagnosis of miliary tuberculosis. In addition, she presented binocular diplopia worse at right lateral gaze, paresis of vertical gaze, light near-dissociation and convergent retraction nystagmus and presence of mycobacterium tuberculosis on PCR Xpert MTB/RIF. The treatment of miliary tuberculosis was interrupted due to pharmacodermia, but after diagnosis of neurotuberculosis, it was restarted with isoniazid, pyrazinamide and ethambutol with partial visual symptoms improvement.
Discussion:
This case demonstrates the importance of pursuing diagnosis through more accurate techniques, especially in a patient with previous treatment pharmacoderma, whose absence of proper diagnosis and treatment would be extremely deleterious.
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