Abstract
Follicular lesions of the thyroid are traditionally difficult and tedious challenges in diagnostic surgical pathology in part due to lack of obvious discriminatory cytological and microarchitectural features. We describe a computerized method to detect and classify follicular adenoma of the thyroid, follicular carcinoma of the thyroid, and normal thyroid based on the nuclear chromatin distribution from digital images of tissue obtained by routine histological methods. Our method is based on determining whether a set of nuclei, obtained from histological images using automated image segmentation, is most similar to sets of nuclei obtained from normal or diseased tissues. This comparison is performed utilizing numerical features, a support vector machine, and a simple voting strategy. We also describe novel methods to identify unique and defining chromatin patterns pertaining to each class. Unlike previous attempts in detecting and classifying these thyroid lesions using computational imaging, our results show that our method can automatically classify the data pertaining to 10 different human cases with 100% accuracy after blind cross validation using at most 43 nuclei randomly selected from each patient. We conclude that nuclear structure alone contains enough information to automatically classify the normal thyroid, follicular carcinoma, and follicular adenoma, as long as groups of nuclei (instead of individual ones) are used. We also conclude that the distribution of nuclear size and chromatin concentration (how tightly packed it is) seem to be discriminating features between nuclei of follicular adenoma, follicular carcinoma, and normal thyroid.
Highlights
Follicular lesions of the thyroid are traditionally difficult and tedious challenges in diagnostic surgical pathology in part due to lack of obvious discriminatory cytological and microarchitectural features
The results of classifying individual nuclei using the Mahalanobis distance nearest neighbors (MNN), support vector machines (SVM)-Quadratic, and SVM-radial basis function (RBF) methods are contained in Tables 1–3, respectively
This is not a trivial problem since in the last year alone at only one hospital within our local health system ~100 thyroidectomies were performed with the diagnosis of follicular adenoma or follicular carcinoma
Summary
Follicular lesions of the thyroid are traditionally difficult and tedious challenges in diagnostic surgical pathology in part due to lack of obvious discriminatory cytological and microarchitectural features. FA may have a fibrous capsule, but lacks capsular and/or vascular invasion These two features are diagnostic because other visual features commonly used by pathologists including microarchitecture and cytological characteristics, notably nuclear and cytoplasmic morphology are virtually indistinguishable between FA and FTC [1]. A proper distinction between FA and FTC can be rendered only after the lesion has been removed surgically (thyroid lobectomy or total thyroidectomy) and the entire lesion has been sampled to determine if capsular and/or vascular invasion is present microscopically. Voting-based strategies for combining the output of several different classifiers have been designed [43,44,45,46,47]
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