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Microscopy-based Assays for High-throughput Screening of Host Factors Involved in Brucella Infection of Hela Cells
Published on: August 5, 2016
Neuro-brucellosis in children
M S Bessisso1, M F Elsaid, S S Elshazli
1Pediatrics Department, Hamad Medical Corporation, PO Box 3050, Doha, Qatar. Fax. 00 974 392 204. E-mail. mbessisso@hotmail.com.
Abstract:
Brucellosis is an infection caused by gram negative cocobacilli (Brucellae). Presentation is usually non-specific and diagnosis depends on high index of suspicion. Nervous system involvement in children is rare as only 47 cases were reported until 1998. We are reporting two patients with neurobrucellosis. The first case was an 8-year-old boy who presented with papillodeoma, and neck stiffness of one month duration. Cerebrospinal fluid pressure was 360mm/water, protein 0.63gm/dl, and cerebrospinal fluid sugar/serum sugar 0.2/4.7mmol. Brucella titer was high in serum and cerebrospinal fluid. The second case was a 3-year-old girl with congenital hydrocephalus, with history of fever, loss of weight, and abdominal cyst around the distal end of ventriculo-peritoneal shunt tube. Brucella mellitenesis was isolated from cerebrospinal fluid and blood. Both cases were treated successfully by 3 antibiotics for 8-12 week.
Insights
Neurobrucellosis, a rare nervous system infection in children caused by Brucella, requires a high index of suspicion for diagnosis. Successful treatment involves a combination of antibiotics.
Area of Science:
- Infectious Diseases
- Pediatric Neurology
- Microbiology
Background:
- Brucellosis is a bacterial infection caused by gram-negative cocobacilli (Brucellae).
- Nervous system involvement (neurobrucellosis) in children is rare, with limited reported cases.
- Clinical presentation of brucellosis is often non-specific, complicating early diagnosis.
Purpose of the Study:
- To report two pediatric cases of neurobrucellosis.
- To highlight the diagnostic challenges and successful management of neurobrucellosis in children.
Main Methods:
- Case report of two pediatric patients presenting with symptoms suggestive of neurobrucellosis.
- Diagnostic procedures included cerebrospinal fluid analysis (pressure, protein, glucose) and serological testing for Brucella titers.
- Microbiological cultures were performed on cerebrospinal fluid and blood samples.
Main Results:
- The first patient, an 8-year-old boy, presented with papilledema and neck stiffness, exhibiting high Brucella titers in serum and cerebrospinal fluid.
- The second patient, a 3-year-old girl with congenital hydrocephalus, had Brucella melitensis isolated from cerebrospinal fluid and blood.
- Both patients showed successful treatment outcomes.
Conclusions:
- Neurobrucellosis in children, though rare, should be considered in the differential diagnosis of neurological symptoms.
- Prompt diagnosis supported by cerebrospinal fluid analysis and serology, followed by appropriate antibiotic therapy, leads to successful outcomes.
- Combination antibiotic therapy for 8-12 weeks is effective in treating pediatric neurobrucellosis.
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