Biomedical subjects

Sheila Timp

Publications and source records attributed to Sheila Timp.

4 recordsLinked to original sources

PubMed2006

Finding corresponding regions of interest in mediolateral oblique and craniocaudal mammographic views.

In this paper we present a method to link potentially suspicious mass regions detected by a Computer-Aided Detection (CAD) scheme in mediolateral oblique (MLO) and craniocaudal (CC) mammographic views of the breast. For all possible combinations of mass candidate regions, a number of features are determined. These features include the difference in the radial distance from the candidate regions to the nipple, the gray scale correlation between both regions, and the mass likelihood of the regions determined by the single view CAD scheme. Linear Discriminant Analysis (LDA) is used to discriminate between correct and incorrect links. The method was tested on a set of 412 cancer cases. In each case a malignant mass, architectural distortion, or asymmetry was annotated. In 92% of these cases the candidate mass detections by CAD included the cancer regions in both views. It was found that in 82% of the cases a correct link between the true positive regions in both views could be established by our method. Possible applications of the method may be found in multiple view analysis to improve CAD results, and for the presentation of CAD results to the radiologist on a mammography workstation.

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PubMed2005

Interval change analysis to improve computer aided detection in mammography.

We are developing computer aided diagnosis (CAD) techniques to study interval changes between two consecutive mammographic screening rounds. We have previously developed methods for the detection of malignant masses based on features extracted from single mammographic views. The goal of the present work was to improve our detection method by including temporal information in the CAD program. Toward this goal, we have developed a regional registration technique. This technique links a suspicious location on the current mammogram with a corresponding location on the prior mammogram. The novelty of our method is that the search for correspondence is done in feature space. This has the advantage that very small lesions and architectural distortions may be found as well. Following the linking process several features are calculated for the current and prior region. Temporal features are obtained by combining the feature values from both regions. We evaluated the detection performance with and without the use of temporal features on a data set containing 2873 temporal film pairs from 938 patients. There were 589 cases in which the current mammogram contained exactly one malignant mass. Cross validation was used to partition the data set into a train set and a test set. The train set was used for feature selection and classifier training, the test set for classifier evaluation. FROC (free response operating characteristic) analysis showed an improvement in detection performance with the use of temporal features.

Aged↗

PubMed2005

A regional registration method to find corresponding mass lesions in temporal mammogram pairs.

In this paper we develop an automatic regional registration method to find corresponding masses on prior and current mammograms. The method contains three steps. In the first, we globally align both images. Then, for each mass lesion on the current view, we define a search area on the prior view, which is likely to contain the same mass lesion. Third, at each location in this search area we calculate a registration measure to quantify how well this location matches the mass lesion on the current view. Finally we select the best location. To determine the performance of our method we compare it to several other registration methods. On a dataset of 389 temporal mass pairs our method correctly links 82% of prior and current mass lesions, whereas other methods achieve at most 72%.

Algorithms↗

PubMed2004

A new 2D segmentation method based on dynamic programming applied to computer aided detection in mammography.

Mass segmentation plays a crucial role in computer-aided diagnosis (CAD) systems for classification of suspicious regions as normal, benign, or malignant. In this article we present a robust and automated segmentation technique--based on dynamic programming--to segment mass lesions from surrounding tissue. In addition, we propose an efficient algorithm to guarantee resulting contours to be closed. The segmentation method based on dynamic programming was quantitatively compared with two other automated segmentation methods (region growing and the discrete contour model) on a dataset of 1210 masses. For each mass an overlap criterion was calculated to determine the similarity with manual segmentation. The mean overlap percentage for dynamic programming was 0.69, for the other two methods 0.60 and 0.59, respectively. The difference in overlap percentage was statistically significant. To study the influence of the segmentation method on the performance of a CAD system two additional experiments were carried out. The first experiment studied the detection performance of the CAD system for the different segmentation methods. Free-response receiver operating characteristics analysis showed that the detection performance was nearly identical for the three segmentation methods. In the second experiment the ability of the classifier to discriminate between malignant and benign lesions was studied. For region based evaluation the area Az under the receiver operating characteristics curve was 0.74 for dynamic programming, 0.72 for the discrete contour model, and 0.67 for region growing. The difference in Az values obtained by the dynamic programming method and region growing was statistically significant. The differences between other methods were not significant.

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