AQP4 water channels are thought to be the target of autoimmune attack in neuromyelitis optica-spectrum disorders (NMOsd). AQP4 are highly expressed on ventricular ependyma. The objective of this study was to describe a novel pattern of linear, 'pencil-thin' enhancement of ventricular ependyma in NMOsd. We report two NMOsd patients with pencil-thin ependymal enhancement along the frontal and occipital horns of lateral ventricles. Differential diagnosis of ependymal enhancement should include NMOsd alongside with infectious and neoplastic etiologies. Pencil-thin ependymal enhancement may be a helpful radiological marker of NMOsd that can be used to differentiate this condition from multiple sclerosis.

Download full-text PDF

Source
http://dx.doi.org/10.1177/1352458511431730DOI Listing

Publication Analysis

Top Keywords

ependymal enhancement
16
pencil-thin ependymal
12
ventricular ependyma
8
enhancement
5
nmosd
5
enhancement neuromyelitis
4
neuromyelitis optica
4
optica spectrum
4
spectrum disorders
4
disorders aqp4
4

Similar Publications

Objective: Ependymomas, rare neuroglial tumors originating from ependymal cells, can occur in the CNS and typically affect the brain's ventricles or spinal cord. Prognosis is influenced by tumor grade, location, resection extent, and preoperative Karnofsky Performance Status Scale (KPSS) scores. This study evaluates clinical features, treatment outcomes, and factors affecting prognosis in patients with intracranial ependymomas.

View Article and Find Full Text PDF
Article Synopsis
  • Chitosan nanoparticles (NPs) are effective for delivering anticancer drugs by enhancing their solubility, permeability, and bioavailability without surfactants, enabling higher drug concentrations at tumor sites and reducing toxicity.
  • These NPs can be engineered for slow drug release, which improves therapy effectiveness and reduces the need for frequent dosing.
  • Targeting overexpressed folate receptors (FRs) on certain cancer cells with folate-modified chitosan NPs can improve treatment outcomes and predict therapy success, while also enhancing the oral absorption of poorly soluble drugs.
View Article and Find Full Text PDF

Glia in tissue engineering: From biomaterial tools to transplantation.

Acta Biomater

December 2024

Department of Neurobiology, University of Texas Medical Branch, 301 University Boulevard, Galveston, TX 77555-0625, United States; Sealy Institute for Drug Discovery, University of Texas Medical Branch, 105 11th Street Galveston, TX 77555-1110, United States. Electronic address:

Glia are imperative in nearly every function of the nervous system, including neurotransmission, neuronal repair, development, immunity, and myelination. Recently, the reparative roles of glia in the central and peripheral nervous systems have been elucidated, suggesting a tremendous potential for these cells as novel treatments to central nervous system disorders. Glial cells often behave as 'double-edged swords' in neuroinflammation, ultimately deciding the life or death of resident cells.

View Article and Find Full Text PDF

After injury, mammalian spinal cords develop scars to confine the lesion and prevent further damage. However, excessive scarring can hinder neural regeneration and functional recovery. These competing actions underscore the importance of developing therapeutic strategies to dynamically modulate scar progression.

View Article and Find Full Text PDF

Introduction Central nervous system (CNS) tumors pose significant diagnostic challenges due to their varied morphological and differentiating characteristics. Modern advancements in immunohistochemistry (IHC) and molecular pathology have greatly enhanced prognostication, screening, and therapeutic management. Gliomas, a type of tumor originating from glial cells in the CNS, can develop from astrocytes, oligodendrocytes, or ependymal cells.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!