DocumentCode
303887
Title
Morphological analysis of mammary biopsy images
Author
Marroquin, E.M. ; Santamaria, E. ; Jove, X. ; Socoró, J.C.
Author_Institution
Dept. of Commun. & Signal Theory, Univ. Ramon Llull, Barcelona, Spain
Volume
2
fYear
1996
fDate
13-16 May 1996
Firstpage
1067
Abstract
The authors present an automatic system to analyse a cell nucleus in a given biopsy of mammary tissue which is cancerous. Identification and characterization of the cell nucleus provides enough information to diagnose a high or low grade cancer. This is a high interest differentiation for the pathologist to apply the correct therapy. Performing these measures by human observation is a hard, imprecise and subjective task. The algorithm they present processes the image in order to identify the cell nucleus over the rest of the tissue. Images are enhanced and segmented using morphological transformations. An ultimate erosion is used in two steps to separate cell nuclei in contact. It is based in a combination of symmetrical ultimate erosion with directional ultimate erosion
Keywords
biological techniques; cellular biophysics; feature extraction; image classification; image segmentation; mathematical morphology; medical image processing; optical microscopy; automatic system; cancer diagnosis; cancerous mammary tissue; cell nucleus analysis; cell nucleus characterization; cell nucleus identification; directional ultimate erosion; high resolution optical microscopy; image enhancement; image processing; image segmentation; mammary biopsy images; morphological analysis; morphological transformations; pathologist; symmetrical ultimate erosion; therapy; Biomedical measurements; Biopsy; Cancer; Humans; Image analysis; Nuclear measurements; Optical microscopy; Shape measurement; Signal analysis; Uniform resource locators;
fLanguage
English
Publisher
ieee
Conference_Titel
Electrotechnical Conference, 1996. MELECON '96., 8th Mediterranean
Conference_Location
Bari
Print_ISBN
0-7803-3109-5
Type
conf
DOI
10.1109/MELCON.1996.551392
Filename
551392
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