2015
DOI: 10.1186/s40644-015-0047-z
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Semi-automated segmentation of pre-operative low grade gliomas in magnetic resonance imaging

Abstract: BackgroundSegmentation of pre-operative low-grade gliomas (LGGs) from magnetic resonance imaging is a crucial step for studying imaging biomarkers. However, segmentation of LGGs is particularly challenging because they rarely enhance after gadolinium administration. Like other gliomas, they have irregular tumor shape, heterogeneous composition, ill-defined tumor boundaries, and limited number of image types. To overcome these challenges we propose a semi-automated segmentation method that relies only on T2-wei… Show more

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Cited by 25 publications
(22 citation statements)
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“…We used our semi-automatic LGG segmentation software to segment the tumors in 2D [ 16 ]. First, the user selects the slice where the area of the tumor appears largest, and then draws a region-of-interest (ROI) that completely encloses the tumor and some normal tissue.…”
Section: Methodsmentioning
confidence: 99%
“…We used our semi-automatic LGG segmentation software to segment the tumors in 2D [ 16 ]. First, the user selects the slice where the area of the tumor appears largest, and then draws a region-of-interest (ROI) that completely encloses the tumor and some normal tissue.…”
Section: Methodsmentioning
confidence: 99%
“…One note is that the BRATS dataset contained not just glioblastomas but also anaplastic astrocytomas, which are intermediates between GBMs and lower grade gliomas (LGGs). Given the satisfactory accuracy of segmenting this mixed dataset, this provides encouragement that MITKats could be extended to LGGs, which are typically harder to segment (Akkus et al, 2015). Eventual implementation and validation for LGGs and tumors outside the brain would be useful.…”
Section: Discussionmentioning
confidence: 98%
“…Most automatic and semi-automatic algorithms to date, have only reliably been shown to work in gadolinium enhancing lesions such as GBM [14]. In a study by Akkus et al (2015) of semiautomated segmentation of pLGGs on MRI T1 post-contrast and T2 WI, the intra-operator variability was lower than intra-expert variability and inter-operator variability much smaller than inter-expert variability [28]. While this is encouraging for establishing a standardized method of semi-automated analysis tumor volume in future, such methods need specific software, time for the operator to check the segmentation results and may be more useful for very complex and extensive lesions such as plexiform neurofibromas than relatively small pLGG [29].…”
Section: Discussionmentioning
confidence: 99%