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Case Reports
. 2017 Spring;8(2):119-122.
doi: 10.22088/cjim.8.2.119.

Neurobrucellosis in systemic lupus erythematosus

Affiliations
Case Reports

Neurobrucellosis in systemic lupus erythematosus

Jamshid Vafaeimanesh et al. Caspian J Intern Med. 2017 Spring.

Abstract

Background: Brucellosis is a zoonotic infection which is endemic in many countries. It is a multisystem disease which may present with a broad spectrum of clinical manifestations and complications. Neurobrucellosis is an uncommon complication of brucellosis.

Case presentation: A 25-year-old woman with a history of lupus for 5 months referred to the emergency ward of Shahid Beheshti Hospital of Qom due to vertigo, drop attack and a convulsion episode from the previous day. She was unable to move at initial evaluation, and her upper and lower extremities were spastic. She had blurred vision one day after admission. Based on her past history and suspecting neurological pulmonary presentations, treatment with immunosuppressive drugs was started and brain MRI was performed. According to the MRI mode and endemic area, neurobrucellosis was suspected and 2ME and Wright tests were performed. Wight test was 1.5120 while 2ME test was 1.640 which were strongly positive. So, with neurobrucellosis diagnosis, the patient was treated but unfortunately 4 days later, after respiratory apnea, she was pronounced dead.

Conclusion: In endemic areas for brucellosis, neurobrucellosis should always be kept in mind in the differential diagnosis of neurological and psychiatric cases that are encountered.

Keywords: Neurobrucellosis; Systemic lupus erythematosus.

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Conflict of interest statement

There was no conflict of interest.

Figures

Figure 1
Figure 1
Sagittal T2W. Incidental note is made of maxillary sinusitis. (A), axial fluid-attenuated inversion recovery (FLAIR) Right aspect of corpus callusum (posterior part of body splenium junction) involvement (B), and axial T2W (C). Brain MRI images demonstrate the mild asymmetrical diffuse and dispread bilateral white matter abnormal high signal intensity at periventricular and centrum semiovale area

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