Purpose: Information on abnormal diffusion-weighted imaging (DWI) patterns in bacterial meningitis (BM) is limited. This study aimed to investigate the frequency and patterns of DWI abnormalities in BM in patients with culture-positive BM.
Methods: The medical records of 14 consecutive patients with BM with magnetic resonance imaging evaluation, admitted to our hospital over the past 14 years, were reviewed. BM was defined by a cerebrospinal fluid (CSF) culture positive for bacteria, or the combination of CSF pleocytosis and a positive blood culture.
Results: Brain DWI abnormalities were identified in 13 (93 %) of the 14 patients and classified into six patterns: ischaemic stroke (n = 9), ventriculitis (n = 4), sulcal hyperintensity (n = 7), scattered hyperintensities surrounding the cerebral hemispheres (n = 6), middle meningeal arterial sign (n = 5), or abscess (n = 1). The causes of ischaemic stroke included infective endocarditis (n = 4), vasculitis (vasculopathy; n = 2), and unclassified (n = 3).
Conclusion: DWI abnormalities in BM were very frequent. Based on the high frequency and wide spectrum of DWI abnormalities in BM, we suggest performing DWI for all patients with BM.
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http://dx.doi.org/10.1016/j.clineuro.2025.108822 | DOI Listing |
Clin Neurol Neurosurg
March 2025
Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Purpose: Information on abnormal diffusion-weighted imaging (DWI) patterns in bacterial meningitis (BM) is limited. This study aimed to investigate the frequency and patterns of DWI abnormalities in BM in patients with culture-positive BM.
Methods: The medical records of 14 consecutive patients with BM with magnetic resonance imaging evaluation, admitted to our hospital over the past 14 years, were reviewed.
Neuroradiology
March 2025
East Sussex Healthcare NHS Trust, Saint Leonards-on-Sea, UK.
Background And Purpose: The Artery of Percheron (AoP) supplying bilateral paramedian thalami and rostral midbrain is a rare anatomical variant. In the event of occlusion of AoP, a characteristic pattern of ischaemia is seen, presenting as bithalamic signal abnormality on magnetic resonance imaging (MRI). However, this particular imaging finding has significant radiological and clinical overlap with other conditions, necessitating a comprehensive understanding of the imaging characteristics and potential differential diagnosis.
View Article and Find Full Text PDFBMC Med Imaging
March 2025
Department of Radiology, Peking University Third Hospital, Beijing, 100191, China.
Background: Single intrauterine fetal death (sIUFD) will lead to an increased risk of adverse events such as fetal brain abnormalities in the survivor. However, how to detect these anomalies in the early stages remains to be explored.
Objective: To compare apparent diffusion coefficient (ADC) values of fetal brain in cases of single intrauterine fetal death (sIUFD) with twins control and singleton control using diffusion weighted imaging (DWI), and to perform follow-up study to reveal the underlying cerebral microstructure changes.
Epileptic Disord
February 2025
Department of Neurology, Umraniye Training and Research Hospital, University of Health Sciences, Istanbul, Turkey.
Objective: To investigate the role, frequency, and pattern of signal changes in cranial MRI associated with status epilepticus (SE) and their correlation with EEG and clinical findings in patients with large lesions, such as tumors, strokes, or major space-occupying anomalies.
Methods: This retrospective cohort study included 44 patients diagnosed with SE between January 2013 and June 2019. Data on demographic and clinical characteristics, seizure semiology, SE features (type and prognosis), and EEG and MRI findings were collected from hospital records.
J Mol Neurosci
January 2025
Department of Neurology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Science/Peking Union Medical College, Beijing, 100730, China.
CSF1R-related leukoencephalopathy (CSF1R-L) and AARS2-related leukoencephalopathy (AARS2-L) were two disease entities sharing similar phenotype and even pathological changes. Although clinically, radiologically, and pathologically similar, they were caused by mutation of two different genes. As the rarity of the two diseases, the differential diagnosis of them was difficult.
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