Abstract

There are significant differences in microvascular morphological features in diseased tissues, such as cancerous lesions, compared to noncancerous tissue. Quantification of microvessel morphological features could play an important role in disease diagnosis and tumor classification. However, analyzing microvessel morphology in ultrasound Doppler is a challenging task due to limitations associated with this technique. Our main objective is to provide methods for quantifying morphological features of microvasculature obtained by ultrasound Doppler imaging. To achieve this goal, we propose multiple image enhancement techniques and appropriate morphological feature extraction methods that enable quantitative analysis of microvasculature structures. Vessel segments obtained by the skeletonization of the regularized microvasculature images are further analyzed to satisfy other constraints, such as vessel segment diameter and length. Measurements of some morphological metrics, such as tortuosity, depend on preserving large vessel trunks. To address this issue, additional filtering methods are proposed. These methods are tested on in vivo images of breast lesion and thyroid nodule microvasculature, and the outcomes are discussed. Initial results show that using vessel morphological features allows for differentiation between malignant and benign breast lesions (p-value < 0.005) and thyroid nodules (p-value < 0.01). This paper provides a tool for the quantification of microvasculature images obtained by non-contrast ultrasound imaging, which may serve as potential biomarkers for the diagnosis of some diseases.

Highlights

  • Microvasculature architecture is known to be associated with tissue state and pathology

  • We focus on the challenges of vessel quantification for 2-dimensional (D) label-free ultrasound Doppler imaging and propose solutions to overcome such challenges

  • MATERIAL AND METHOD To demonstrate the potential clinical application of contrastfree quantitative ultrasound microvasculature imaging, we performed the technique on a group of patients with suspicious breast lesions or thyroid nodules

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Summary

Introduction

Microvasculature architecture is known to be associated with tissue state and pathology. Various circumstances and diseases can alter such architecture at distinct size scales. Studies have demonstrated that the development of malignant tumors correlates with changes in the vascularity of healthy tissue [1]. Altered mechanical properties in malignant tumors are known to lead to the growth of more permeable and tortuous vessels [2], [3]. Vessel tortuosity has been found to reveal information about some diseases [4], [5].

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