Medical image acquisition devices provide a vast amount of anatomical and functional information, which facilitate and improve diagnosis and patient treatment, especially when supported by modern quantitative image analysis methods. However, modality specific image artifacts, such as the phenomena of intensity inhomogeneity in magnetic resonance images (MRI), are still prominent and can adversely affect quantitative image analysis. In this paper, numerous methods that have been developed to reduce or eliminate intensity inhomogeneities in MRI are reviewed. First, the methods are classified according to the inhomogeneity correction strategy. Next, different qualitative and quantitative evaluation approaches are reviewed. Third, 60 relevant publications are categorized according to several features and analyzed so as to reveal major trends, popularity, evaluation strategies and applications. Finally, key evaluation issues and future development of the inhomogeneity correction field, supported by the results of the analysis, are discussed.

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A number of imaging techniques are being used for diagnosis and treatment of vascular pathologies like stenoses, aneurysms, embolisms, malformations and remodelings, which may affect a wide range of anatomical sites. For computer-aided detection and highlighting of potential sites of pathology or to improve visualization and segmentation, angiographic images are often enhanced by Hessian based filters. These filters aim to indicate elongated and/or rounded structures by an enhancement function based on Hessian eigenvalues. However, established enhancement functions generally produce a response, which exhibits deficiencies such as poor and non-uniform response for vessels of different sizes and varying contrast, at bifurcations and aneurysms. This may compromise subsequent analysis of the enhanced images. This paper has three important contributions: i) reviews several established enhancement functions and elaborates their deficiencies, ii) proposes a novel enhancement function, which overcomes the deficiencies of the established functions, and iii) quantitatively evaluates and compares the novel and the established enhancement functions on clinical image datasets of the lung, cerebral and fundus vasculatures.

The aim of this paper is to provide a complete overview of the existing methods for quantitative evaluation of spinal curvature from medical images, and to summarize the relevant publications, which may not only assist in the introduction of other researchers to the field, but also be a valuable resource for studying the existing methods or developing new methods and evaluation strategies. Key evaluation issues and future considerations, supported by the results of the overview, are also discussed.

In this paper, the problem of retrospective correction of intensity inhomogeneity in magnetic resonance (MR) images is addressed. A novel model-based correction method is proposed, based on the assumption that an image corrupted by intensity inhomogeneity contains more information than the corresponding uncorrupted image. The image degradation process is described by a linear model, consisting of a multiplicative and an additive component which are modeled by a combination of smoothly varying basis functions. The degraded image is corrected by the inverse of the image degradation model. The parameters of this model are optimized such that the information of the corrected image is minimized while the global intensity statistic is preserved. The method was quantitatively evaluated and compared to other methods on a number of simulated and real MR images and proved to be effective, reliable, and computationally attractive. The method can be widely applied to different types of MR images because it solely uses the information that is naturally present in an image, without making assumptions on its spatial and intensity distribution. Besides, the method requires no preprocessing, parameter setting, nor user interaction. Consequently, the proposed method may be a valuable tool in MR image analysis.