Transrectal real-time tissue elastography - An effective way to distinguish benign and malignant prostate tumors

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Abstract

Background: To investigate the relationship between extracellular matrix parameters and texture of prostatic lesions evaluated by transrectal real-time tissue elastography (TRTE). Methods: 120 patients suspicious for prostate cancer underwent TRTE. Targeted biopsies were carried out after 12-core systematic biopsy. Epithelia were stained with hematoxylin-eosin, and Victoria blue and Ponceau S were used to stain elastic-collagen fibers, and picric acid-sirius red for visualization of collagen type I (Col1) and III (Col3). Smooth muscles were visualized by immunohistochemistry. All image analyses were performed in a blind manner using Image Pro Plus 6.0, and the area ratios of epithelium, elastic fibers, collagen fibers and Col1/Col3 were determined. Results: 42 patients with typical elastograms were included in the final data analysis. Significant differences were detected between the benign and malignant groups in the area ratios of epithelium (P = 0.01), smooth muscles and Col1/Col3 (P = 0.04, P = 0.02, respectively). There were no significant differences in the area ratios of epithelium, smooth muscle and elastic fibers between the stiff and soft lesion groups. The area ratio of Col1 was (0.05±0.03) in the stiff group, and (0.02±0.01) in the soft group (P= 0.00). However, the area ratio of Col3 was (0.03±0.02) in the stiff group, and (0.05±0.04) in the soft group (P = 0.16). Col1/Col3 in the stiff group (1.99±1.59) was greater than in the soft group (0.71±0.64) (P = 0.01). Conclusions: Tissue hardness of prostatic tumors was mainly dependent on the Col1 content, Col1/Col3 being higher in malignant than in benign lesions, so the prostate tissue texture can be used as a target for distinguishing between the two with TRTE.

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Zhang, Y., Tang, J., Liang, H. D., Lv, F. Q., & Song, Z. G. (2014). Transrectal real-time tissue elastography - An effective way to distinguish benign and malignant prostate tumors. Asian Pacific Journal of Cancer Prevention, 15(4), 1831–1835. https://doi.org/10.7314/APJCP.2014.15.4.1831

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