A multi-resolution textural approach to diagnostic neuropathology reporting

被引:7
作者
Fauzi, Mohammad Faizal Ahmad [1 ]
Gokozan, Hamza Numan [2 ]
Elder, Brad [3 ]
Puduvalli, Vinay K. [4 ]
Pierson, Christopher R. [2 ,5 ,6 ]
Otero, Jose Javier [2 ,8 ]
Gurcan, Metin N. [7 ]
机构
[1] Multimedia Univ, Fac Engn, Cyberjaya 63100, Selangor, Malaysia
[2] Ohio State Univ, Dept Pathol, Columbus, OH 43210 USA
[3] Ohio State Univ, Dept Neurol Surg, Columbus, OH 43210 USA
[4] Ohio State Univ, Wexner Med Ctr, Div Neurooncol, Columbus, OH 43210 USA
[5] Nationwide Childrens Hosp, Dept Pathol & Lab Med, Columbus, OH USA
[6] Ohio State Univ, Div Anat, Columbus, OH 43210 USA
[7] Ohio State Univ, Dept Biomed Informat, Columbus, OH 43210 USA
[8] Ohio State Univ, Coll Med, Dept Pathol, Div Neuropathol, Columbus, OH 43210 USA
关键词
Glioblastoma; Metastasis; Intra-operative consultation; Prognostic reporting; Discrete wavelet frames; Texture analysis; FOLLICULAR LYMPHOMA; BREAST-CANCER; P53; CLASSIFICATION; GLIOBLASTOMAS; NEUROBLASTOMA; SEGMENTATION; MUTATIONS; PATTERNS; SYSTEM;
D O I
10.1007/s11060-015-1872-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We present a computer aided diagnostic workflow focusing on two diagnostic branch points in neuropathology (intraoperative consultation and p53 status in tumor biopsy specimens) by means of texture analysis via discrete wavelet frames decomposition. For intraoperative consultation, our methodology is capable of classifying glioblastoma versus metastatic cancer by extracting textural features from the non-nuclei region of cytologic preparations based on the imaging characteristics of glial processes, which appear as anisotropic thin linear structures. For metastasis, these are homogeneous in appearance, thus suitable and extractable texture features distinguish the two tissue types. Experiments on 53 images (29 glioblastomas and 24 metastases) resulted in average accuracy as high as 89.7 % for glioblastoma, 87.5 % for metastasis and 88.7 % overall. For p53 interpretation, we detect and classify p53 status by classifying staining intensity into strong, moderate, weak and negative sub-classes. We achieved this by developing a novel adaptive thresholding for detection, a two-step rule based on weighted color and intensity for the classification of positively and negatively stained nuclei, followed by texture classification to classify the positively stained nuclei into the strong, moderate and weak intensity sub-classes. Our detection method is able to correctly locate and distinguish the four types of cells, at 85 % average precision and 88 % average sensitivity rate. These classification methods on the other hand recorded 81 % accuracy in classifying the positive and negative cells, and 60 % accuracy in further classifying the positive cells into the three intensity groups, which is comparable with neuropathologists' markings.
引用
收藏
页码:393 / 402
页数:10
相关论文
共 52 条
[1]   Content-Based Microscopic Image Retrieval System for Multi-Image Queries [J].
Akakin, Hatice Cinar ;
Gurcan, Metin N. .
IEEE TRANSACTIONS ON INFORMATION TECHNOLOGY IN BIOMEDICINE, 2012, 16 (04) :758-769
[2]  
Barker FG, 1996, CANCER, V77, P1161, DOI 10.1002/(SICI)1097-0142(19960315)77:6<1161::AID-CNCR24>3.0.CO
[3]  
2-Z
[4]  
BARTEK J, 1990, ONCOGENE, V5, P893
[5]   Extraction of color features in the spectral domain to recognize centroblasts in histopathology [J].
Belkacem-Boussaid, Kamel ;
Sertel, Olcay ;
Lozanski, Gerard ;
Shana'aah, Arwa ;
Gurcan, Metin .
2009 ANNUAL INTERNATIONAL CONFERENCE OF THE IEEE ENGINEERING IN MEDICINE AND BIOLOGY SOCIETY, VOLS 1-20, 2009, :3685-+
[6]   MUTATIONAL SPECTRA AND IMMUNOHISTOCHEMICAL ANALYSES OF P53 IN HUMAN CANCERS [J].
BENNETT, WP ;
HOLLSTEIN, MC ;
HSU, IC ;
SIDRANSKY, D ;
LANE, DP ;
VOGELSTEIN, B ;
HARRIS, CC .
CHEST, 1992, 101 (03) :S19-S20
[7]   The Somatic Genomic Landscape of Glioblastoma [J].
Brennan, Cameron W. ;
Verhaak, Roel G. W. ;
McKenna, Aaron ;
Campos, Benito ;
Noushmehr, Houtan ;
Salama, Sofie R. ;
Zheng, Siyuan ;
Chakravarty, Debyani ;
Sanborn, J. Zachary ;
Berman, Samuel H. ;
Beroukhim, Rameen ;
Bernard, Brady ;
Wu, Chang-Jiun ;
Genovese, Giannicola ;
Shmulevich, Ilya ;
Barnholtz-Sloan, Jill ;
Zou, Lihua ;
Vegesna, Rahulsimham ;
Shukla, Sachet A. ;
Ciriello, Giovanni ;
Yung, W. K. ;
Zhang, Wei ;
Sougnez, Carrie ;
Mikkelsen, Tom ;
Aldape, Kenneth ;
Bigner, Darell D. ;
Van Meir, Erwin G. ;
Prados, Michael ;
Sloan, Andrew ;
Black, Keith L. ;
Eschbacher, Jennifer ;
Finocchiaro, Gaetano ;
Friedman, William ;
Andrews, David W. ;
Guha, Abhijit ;
Iacocca, Mary ;
O'Neill, Brian P. ;
Foltz, Greg ;
Myers, Jerome ;
Weisenberger, Daniel J. ;
Penny, Robert ;
Kucherlapati, Raju ;
Perou, Charles M. ;
Hayes, D. Neil ;
Gibbs, Richard ;
Marra, Marco ;
Mills, Gordon B. ;
Lander, Eric ;
Spellman, Paul ;
Wilson, Richard .
CELL, 2013, 155 (02) :462-477
[8]  
BRUNER JM, 1991, MODERN PATHOL, V4, P671
[9]  
BURGER PC, 1989, CANCER-AM CANCER SOC, V63, P2014, DOI 10.1002/1097-0142(19890515)63:10<2014::AID-CNCR2820631025>3.0.CO
[10]  
2-L