6,313 research outputs found
A Survey on MRI Brain Image Segmentation Technique
One of the most dangerous disease occurring these days i.e. brain tumor can be detected by MRI images. Biomedical imaging and medical image processing that plays a vital role for MRI images has now become the most challenging field in engineering and technology. A detailed information about the anatomy can be showed through MRI images, that helps in monitoring the disease and is beneficial for the diagnosis as it consists of a high tissue contrast and have fewer artifacts. For tracking the disease and to proceed its treatment, MRI images plays a key role. It is having several advantages over other imaging techniques and is an important step for post-processing of medical images. However, having a large amount of data for manual analysis can sometimes proved to be an obstacle in the way of its effective use. In this paper, the introduction of image processing and the details of image segmentation techniques such as image preprocessing, feature extraction, image enhancement and classification of tumor processes, and how image segmentation can be applied to all Other available imaging modalities that are different from one another. This paper provides the survey on various methods used for image segmentation that have been applied for MRI images, that detects the tumor by segmenting the brain images into constituent parts. Also the advantages and disadvantages of Image segmentation is discussed using the various approaches of image segmentation of MRI brain images
The Brain Tumor Segmentation (BraTS) Challenge 2023: Brain MR Image Synthesis for Tumor Segmentation (BraSyn)
Automated brain tumor segmentation methods have become well-established and
reached performance levels offering clear clinical utility. These methods
typically rely on four input magnetic resonance imaging (MRI) modalities:
T1-weighted images with and without contrast enhancement, T2-weighted images,
and FLAIR images. However, some sequences are often missing in clinical
practice due to time constraints or image artifacts, such as patient motion.
Consequently, the ability to substitute missing modalities and gain
segmentation performance is highly desirable and necessary for the broader
adoption of these algorithms in the clinical routine. In this work, we present
the establishment of the Brain MR Image Synthesis Benchmark (BraSyn) in
conjunction with the Medical Image Computing and Computer-Assisted Intervention
(MICCAI) 2023. The primary objective of this challenge is to evaluate image
synthesis methods that can realistically generate missing MRI modalities when
multiple available images are provided. The ultimate aim is to facilitate
automated brain tumor segmentation pipelines. The image dataset used in the
benchmark is diverse and multi-modal, created through collaboration with
various hospitals and research institutions.Comment: Technical report of BraSy
Simulation of brain tumors in MR images for evaluation of segmentation efficacy
Obtaining validation data and comparison metrics for segmentation of magnetic resonance images (MRI) are difficult tasks due to the lack of reliable ground truth. This problem is even more evident for images presenting pathology, which can both alter tissue appearance through infiltration and cause geometric distortions. Systems for generating synthetic images with user-defined degradation by noise and intensity inhomogeneity offer the possibility for testing and comparison of segmentation methods. Such systems do not yet offer simulation of sufficiently realistic looking pathology. This paper presents a system that combines physical and statistical modeling to generate synthetic multi-modal 3D brain MRI with tumor and edema, along with the underlying anatomical ground truth, Main emphasis is placed on simulation of the major effects known for tumor MRI, such as contrast enhancement, local distortion of healthy tissue, infiltrating edema adjacent to tumors, destruction and deformation of fiber tracts, and multi-modal MRI contrast of healthy tissue and pathology. The new method synthesizes pathology in multi-modal MRI and diffusion tensor imaging (DTI) by simulating mass effect, warping and destruction of white matter fibers, and infiltration of brain tissues by tumor cells. We generate synthetic contrast enhanced MR images by simulating the accumulation of contrast agent within the brain. The appearance of the the brain tissue and tumor in MRI is simulated by synthesizing texture images from real MR images. The proposed method is able to generate synthetic ground truth and synthesized MR images with tumor and edema that exhibit comparable segmentation challenges to real tumor MRI. Such image data sets will find use in segmentation reliability studies, comparison and validation of different segmentation methods, training and teaching, or even in evaluating standards for tumor size like the RECIST (Response Evaluation Criteria in Solid Tumors) criteria
Multiscale, multimodal analysis of tumor heterogeneity in IDH1 mutant vs wild-type diffuse gliomas.
Glioma is recognized to be a highly heterogeneous CNS malignancy, whose diverse cellular composition and cellular interactions have not been well characterized. To gain new clinical- and biological-insights into the genetically-bifurcated IDH1 mutant (mt) vs wildtype (wt) forms of glioma, we integrated data from protein, genomic and MR imaging from 20 treatment-naïve glioma cases and 16 recurrent GBM cases. Multiplexed immunofluorescence (MxIF) was used to generate single cell data for 43 protein markers representing all cancer hallmarks, Genomic sequencing (exome and RNA (normal and tumor) and magnetic resonance imaging (MRI) quantitative features (protocols were T1-post, FLAIR and ADC) from whole tumor, peritumoral edema and enhancing core vs equivalent normal region were also collected from patients. Based on MxIF analysis, 85,767 cells (glioma cases) and 56,304 cells (GBM cases) were used to generate cell-level data for 24 biomarkers. K-means clustering was used to generate 7 distinct groups of cells with divergent biomarker profiles and deconvolution was used to assign RNA data into three classes. Spatial and molecular heterogeneity metrics were generated for the cell data. All features were compared between IDH mt and IDHwt patients and were finally combined to provide a holistic/integrated comparison. Protein expression by hallmark was generally lower in the IDHmt vs wt patients. Molecular and spatial heterogeneity scores for angiogenesis and cell invasion also differed between IDHmt and wt gliomas irrespective of prior treatment and tumor grade; these differences also persisted in the MR imaging features of peritumoral edema and contrast enhancement volumes. A coherent picture of enhanced angiogenesis in IDHwt tumors was derived from multiple platforms (genomic, proteomic and imaging) and scales from individual proteins to cell clusters and heterogeneity, as well as bulk tumor RNA and imaging features. Longer overall survival for IDH1mt glioma patients may reflect mutation-driven alterations in cellular, molecular, and spatial heterogeneity which manifest in discernable radiological manifestations
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