Cerebellar, Hippocampal, and Basal Nuclei Transient Edema with Restricted Diffusion (CHANTER) syndrome is a recently recognized distinct clinicoradiographic pattern of neurologic injury occurring most commonly following polysubstance or opioid abuse. Patients present acutely with unresponsiveness or coma. Magnetic resonance (MR) imaging demonstrates key findings, including bilateral diffusion restriction in the cerebellar cortices and hippocampi and variable diffusion restriction in the basal ganglia. Additionally, cerebellar cytotoxic edema can exert a mass effect on the adjacent fourth ventricle, causing obstructive hydrocephalus and requiring emergent intervention to prevent brain herniation and death. Here, we present a 37-year-old male patient who arrived at the Emergency Department with non-responsiveness in the setting of positive toxicology for cannabis, cocaine, and fentanyl. One day following the presentation, an MRI demonstrated restricted diffusion of the bilateral cerebellar hemispheres and bilateral hippocampi and small foci of restricted diffusion involving the basal ganglia. T2 fluid-attenuated inversion recovery (T2 FLAIR) hyperintensities involving the bilateral precentral gyri were also identified. Additional diagnostic workup, including electroencephalogram (EEG), vessel imaging, and viral panels, effectively ruled out alternative diagnoses, making CHANTER most likely. Following medical treatment without surgical intervention, the patient was discharged to an acute rehab facility with symptoms of impaired judgment, difficulty following commands, and difficulty walking. In the following months, the patient improved in cognitive function and gait. MRI at three months demonstrated interval resolution of previous T2 FLAIR hyperintensities, restricted diffusion zones, and development of new T2 FLAIR hyperintensities in the periventricular and subcortical white matter. This case highlights the need for prompt recognition of radiographic features of CHANTER, as affected patients may demonstrate significant recovery of neurologic status in the months following injury, compared to other patterns of hypoxic brain injury. These patients, therefore, merit more aggressive treatment to maximize recovery.
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http://dx.doi.org/10.7759/cureus.73467 | DOI Listing |
Pediatr Nephrol
January 2025
Childhood Chronic Diseases Department, University Hospital of Nantes, 7 Quai Moncousu, 44093, Nantes, France.
Background: Severe respiratory complications following kidney transplantation have been reported, yet remain poorly understood in the pediatric population. This study aimed to document respiratory disease in this population.
Methods: At annual follow-ups, patients completed a respiratory symptoms questionnaire and underwent pulmonary function tests (PFTs).
Nat Med
January 2025
Seattle Children's Therapeutics, Seattle, WA, USA.
Diffuse intrinsic pontine glioma (DIPG) is a fatal central nervous system (CNS) tumor that confers a median survival of 11 months. As B7-H3 is expressed on pediatric CNS tumors, we conducted BrainChild-03, a single-center, dose-escalation phase 1 clinical trial of repetitive intracerebroventricular (ICV) dosing of B7-H3-targeting chimeric antigen receptor T cells (B7-H3 CAR T cells) for children with recurrent or refractory CNS tumors and DIPG. Here we report results from Arm C, restricted to patients with DIPG.
View Article and Find Full Text PDFJ Neuroophthalmol
January 2025
Departments of Ophthalmology and Visual Sciences (HMM, AH, EM), and Radiology (DMM), University of Toronto, Toronto, Canada; Department of Ophthalmology (LD), McMaster University, Hamilton, Canada; Departments of Ophthalmology and Visual Sciences, and Neurology (JDT), University of Michigan, Ann Arbor, Michigan; Department of Neurology (JDT), University of Michigan, Ann Arbor, Michigan; Division of Neurology, Department of Medicine (EM), University of Toronto, Toronto, Canada.
Background: Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (CLIPPERS) is a rare and poorly understood inflammatory disorder of the central nervous system centered on the pons. It has a characteristic imaging appearance with enhancing and T2-hyperintense punctate and curvilinear lesions in the pons. The lesions lack restricted diffusion and have relatively little perilesional edema.
View Article and Find Full Text PDFClin Nucl Med
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Cardiology Department, CHU Orleans, Orleans, France.
Late-stage eosinophilic myocarditis (or Löffler endocarditis) is known to occur in patients with hypereosinophilic syndrome and can cause restrictive cardiomyopathy. Eosinophilic myocarditis is an acute life-threatening inflammatory disease of the heart that can be associated with cancer. We report a case of a 70-year-old White woman, previously treated for diffuse large B-cell lymphoma in remission, admitted for acute dyspnea with a 1-year history of hypereosinophilia.
View Article and Find Full Text PDFClin Nucl Med
February 2025
Cardiology Department, CHU Orleans, Orleans, France.
Late-stage eosinophilic myocarditis (or Löffler endocarditis) is known to occur in patients with hypereosinophilic syndrome and can cause restrictive cardiomyopathy. Eosinophilic myocarditis is an acute life-threatening inflammatory disease of the heart that can be associated with cancer. We report a case of a 70-year-old White woman, previously treated for diffuse large B-cell lymphoma in remission, admitted for acute dyspnea with a 1-year history of hypereosinophilia.
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