Objective: To report a patient with neurobrucellosis mimicking primary CNS vasculitis (PCNSV) diagnosed by CSF metagenomic next-generation sequencing (mNGS).
Methods: A 32-year-old male patient with a prior stroke developed headache, dizziness, fever, and memory complaints in the past 30 days. Physical examination was unremarkable except for slight apathy. He was investigated with brain MRI, cerebral digital angiography, CSF analysis with mNGS, and brain biopsy.
Results: An examination of the brain MRI showed a left nucleocapsular gliosis compatible with prior stroke; MR angiogram showed circular enhancement of distal branches of the middle cerebral arteries. Digital angiogram revealed stenosis of intracranial carotid arteries and the left middle cerebral artery. The CSF disclosed 42 cells/mm, 46 mg/dL of glucose, and 82 mg/dL of protein. Brain biopsy showed a chronic leptomeningeal inflammatory process, not fulfilling criteria for PCNSV. mNGS revealed the presence of sp. genetic material. He was treated with antibiotics with full remission of systemic and neurologic symptoms.
Discussion: Brucellosis is an endemic disease in developing countries and may mimic PCNSV. Our patient fulfilled the criteria for possible PCNSV; however, brain biopsy was inconsistent with PCNSV, and CSF mNGS disclosed neurobrucellosis. This case illustrates the importance of CSF mNGS in the differential diagnosis of CNS vasculitis.
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http://dx.doi.org/10.1212/CPJ.0000000000200167 | DOI Listing |
Am J Trop Med Hyg
October 2024
Marmara University School of Medicine, Department of Pediatric Infectious Diseases, Istanbul, Turkey.
Neurobrucellosis is rare in children, presenting with a variety of clinical manifestations, including meningitis, meningoencephalitis, cranial neuropathies, and intracranial mass-like lesions. We present a case of a 17-year-old girl admitted to the hospital in Istanbul for headache. Lumbar puncture showed elevated intracranial pressure, monocytic pleocytosis, elevated total protein, and hypoglycorrhachia.
View Article and Find Full Text PDFRadiol Case Rep
June 2024
Department of Radiology, Isfahan University of Medical Sciences, Isfahan, Iran.
Brucellosis is a zoonotic disease caused by small intracellular aerobic Gram-negative bacilli The literature has frequently documented instances of the gastrointestinal, hepatobiliary, and skeletal systems being involved. In 3%-5% of brucellosis patients, neurobrucellosis has been identified. Guillain-Barré syndrome (GBS) is a disorder of the peripheral nervous system.
View Article and Find Full Text PDFNeurol Clin Pract
August 2023
Hospital Israelita Albert Einstein (MBM, FGM, GBPF, VRP, GSS, AAB, ACPDO, CEB, LAD), São Paulo; Department of Neurology and Neurosurgery (GSS), Universidade Federal de São Paulo, UNIFESP; Neurology Section (PB-N), Department of Clinical Medicine, Faculty of Medicine; and Center of Health Sciences (PB-N), Universidade Estadual Do Ceará, Fortaleza, Brazil.
J Trop Pediatr
December 2022
Department of Neurology, National Institute of Mental Health and Neurosciences (NIMAHNS), Bangalore, Karnataka 560029, India.
Pediatric neurobrucellosis represents a common anthropozoonosis in endemic areas but only anecdotal reports are available till date. Using appropriate search terms in the database platforms of MEDLINE, SCOPUS and Web of Sciences, we performed a systematic review of all the cases of pediatric neurobrucellosis published in the medical literature till date, in the light of a case report. The protocol was registered under PROSPERO (CRD42022333907).
View Article and Find Full Text PDFJ Med Case Rep
January 2023
Department of Pediatrics, Tishreen University Hospital, Lattakia, Syria.
Background: Brucellosis is a zoonotic disease caused by Gram-negative bacteria. It has variable manifestations (gastrointestinal, hepatobiliary, skeletal). Neurobrucellosis may develop at any stage of the disease (acute, subacute, and chronic phases) and affects the central and peripheral nervous systems.
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