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Introduction: Stroke can lead to neurological changes beyond the initial lesion site, including post-stroke crossed-cerebellar degeneration. While traditional methods typically rely on total lesion volume to assess remote effects, the spatial distribution of lesions may more accurately predict cerebellar atrophy and associated functional deficits. This study investigated whether anatomically specific cortical lesions contribute to cerebellar gray matter volume loss, expanding on the hypothesis that cerebellar atrophy may reflect more than global brain injury severity, and instead result from targeted disruption of cortico-cerebellar pathways.
Methods: Data from 142 chronic left hemisphere stroke participants (57 females, 85 males; M = 61 years) were analyzed using voxel-based lesion-symptom mapping (VLSM) and region of interest (ROI) analyses. High-resolution structural MRI scans were processed to quantify cerebellar gray matter volume (GMV) across 28 spatially distinct regions, with lesions manually delineated and mapped.
Results: Significant associations were found between lesion load in specific white matter tracts and cerebellar GMV atrophy. Lesions in the posterior limb of the internal capsule, retrolenticular part of the internal capsule, fornix/stria terminalis and superior corona radiata were strongly linked to GMV reductions in right cerebellar lobules and vermis. Notably, cortical lesions primarily impacted the right cerebellar regions, supporting the concept of post-stroke crossed cerebellar diaschisis. In a complementary analysis, voxel-based lesion-symptom mapping using Apraxia of Speech (AOS) severity scores revealed overlapping lesion predictors with those driving cerebellar degeneration, particularly within the superior corona radiata and retrolenticular part of the internal capsule. This overlap suggests that damage to these tracts may contribute jointly to speech-motor impairment and remote cerebellar atrophy.
Conclusion: The spatial distribution of cortical lesions, rather than total lesion volume, plays a crucial role in predicting cerebellar degeneration. These findings suggest the importance of considering lesion location in stroke rehabilitation, and provide further insights into the functional connections between the cerebrum and cerebellum.
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http://dx.doi.org/10.1016/j.nicl.2025.103875 | DOI Listing |
Int J Gen Med
September 2025
Department of Neurology, Aerospace Center Hospital, Beijing, 100049, People's Republic of China.
Acute vestibular syndrome (AVS) is characterized by the sudden onset of dizziness or vertigo, accompanied by nausea, vomiting, gait instability, and nystagmus, lasting for more than 24 hours and often persisting for several days to weeks. Central AVS primarily involves central vestibular structures, such as the brainstem and cerebellum, and is most commonly caused by ischemic stroke in the posterior circulation. When acute posterior circulation infarction presents solely with isolated dizziness or vertigo, without other symptoms of central nervous system damage, it is often misdiagnosed as a peripheral vestibular disorder, this can lead to serious consequences.
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August 2025
Pediatrics Department, Kazan State Medical University of the Ministry of Health of the Russian Federation, Kazan, Russia.
Background: Acid sphingomyelinase deficiency (ASMD) type A/B, a rare lysosomal storage disorder caused by biallelic mutations in the SMPD1 gene, presents with variable visceral and neurological manifestations. Arnold-Chiari malformation is a structural defect of the cerebellum and brainstem with distinct pathogenesis and clinical course. To our knowledge, the coexistence of these two conditions has not been previously reported.
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August 2025
Department of Pediatrics, Affiliated Hospital of Inner Mongolia Medical University, Hohhot, Inner Mongolia, China.
Background And Objective: This study aims to analyze the clinical characteristics of anti-GABAR encephalitis in pediatric patients. Due to its rarity and diagnostic challenges in children, we compare clinical features between adult and pediatric cases.
Materials And Methods: Using the key words "anti-GABAR encephalitis, children, autoimmune encephalitis, limbic encephalitis", we conduct a comprehensive literature review of all studies related to anti-GABAR encephalitis published from January 2010 to January 2024.
Surg Case Rep
September 2025
Department of Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Kyoto, Japan.
Introduction: von Hippel-Lindau (VHL) disease is an autosomal dominant hereditary disorder characterized by the development of tumor-like lesions in multiple organs. While central nervous system hemangioblastomas, pancreatic neuroendocrine tumors, and pancreatic cysts are commonly associated with VHL disease, there have been few reported cases of pancreatic hemangioblastoma in patients with VHL disease.
Case Presentation: A male patient in his 30s had been diagnosed with VHL disease and had been followed for cerebellar and spinal hemangioblastomas, and renal cell carcinoma, for which he had undergone several tumor resections, radiation therapy, and a ventriculoperitoneal shunt.
Cureus
August 2025
Ophthalmology, All India Institute of Medical Sciences, New Delhi, New Delhi, IND.
Dandy-Walker syndrome (DWS), also referred to as Dandy-Walker malformation, is a rare congenital developmental anomaly characterized by enlargement of the posterior fossa, dilatation of the fourth ventricle, and cerebellar hypoplasia with upward rotation. Retinoblastoma is the most common primary intraocular malignancy in children and typically presents in the pediatric age group, with leukocoria and strabismus being common early signs. Although DWS and retinoblastoma are individually rare, their simultaneous occurrence is exceptionally uncommon.
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