Parinaud syndrome due to cofirmed neurotuberculosis in a lupus eritematosis systemic patient

Author:

Tavares-Júnior José Wagner Leonel1ORCID,Teles Júnior José Newton2,Magalhães Samir Câmara3,Cavalcante Thiago Toscano4,Coimbra Pablo Picasso de Araújo5,Luiz Roberta dos Santos Silva6

Affiliation:

1. Department of Clinical Medicine, Universidade Federal do Ceará, Fortaleza, CE, Brazil

2. Medical coordination of the intensive care unit of Hospital Genesis, Fortaleza, CE, Brazil

3. Universidade de Fortaleza - UNIFOR, Fortaleza, CE, Brazil

4. Centro Universitário Christus, Fortaleza, CE, Brazil

5. Uniclinic Diagnóstico por Imagem- UDI Fortaleza, Centro Universitario Chirstus, Fortaleza, CE, Brazil

6. Ministério da Saúde BR, Fortaleza, CE, Brazil

Abstract

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.

Publisher

SAGE Publications

Subject

Ophthalmology,General Medicine

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