Journal of Biomedical Science and Engineering
Vol. 5  No. 7 (2012) , Article ID: 20531 , 6 pages DOI:10.4236/jbise.2012.57048

A semi-automatic method for segmentation and 3D modeling of glioma tumors from brain MRI

S. Ananda Resmi1, Tessamma Thomas2

1Department of Electronics and Communication Engineering, College of Engineering Perumon, Kollam, India

2Department of Electronics, Cochin University of Science and Technology, Kochi, India

Email: anandaresmi@gmail.com, tess@cusat.ac.in

Received 2 May 2012; revised 1 June 2012; accepted 28 June 2012

Keywords: 3D Modeling; Glioma Tumor; Segmentation; Volumetric Analysis; Brain MRI

ABSTRACT

This work presents an efficient method for volume rendering of glioma tumors from segmented 2D MRI Datasets with user interactive control, by replacing manual segmentation required in the state of art methods. The most common primary brain tumors are gliomas, evolving from the cerebral supportive cells. For clinical follow-up, the evaluation of the preoperative tumor volume is essential. Tumor portions were automatically segmented from 2D MR images using morphological filtering techniques. These segmented tumor slices were propagated and modeled with the software package. The 3D modeled tumor consists of gray level values of the original image with exact tumor boundary. Axial slices of FLAIR and T2 weighted images were used for extracting tumors. Volumetric assessment of tumor volume with manual segmentation of its outlines is a time-consuming process and is prone to error. These defects are overcome in this method. Authors verified the performance of our method on several sets of MRI scans. The 3D modeling was also done using segmented 2D slices with the help of a medical software package called 3D DOCTOR for verification purposes. The results were validated with the ground truth models by the Radiologist.

1. INTRODUCTION

The extraction of 3D objects and its visualization is one of the most important steps in the analysis of the preprocessed medical image data, which can help in performing diagnosis, treatment planning, and treatment delivery. Thus in practice, radiation oncologists spend a substantial portion of their time performing the segmentation task manually, using one of the available visualization and segmentation tools [1]. Also, there may be cases where the automatic methods fail or perform poorly. Another consideration is that medical doctors must always have final control over the segmentation [2].

The most common primary brain tumors are gliomas, wherein 70% are in the group of malignant gliomas (anaplastic astrocytoma World Health Organization (WHO) grade III), glioblastoma multiforme (GBM) WHO grade IV) [3]. The GBM is one of the highest malignant human neoplasms. Due to the biological behavior, gliomas of WHO grade II to IV cannot be cured with surgery alone. The multimodal therapeutical concept involves maximum safe resection followed by radiation and chemotherapy, depending on the patient’s functional impairment scale. The survival rate is still only approximately 15 months, despite new technical and medical accomplishments such as multimodal navigation during microsurgery, stereotactic radiation or the implementation of alkylating substances [4]. The clinical follow-up of tumor volume is essential for an adaptation of the therapeutical concept. Therefore, the exact volume evaluation is fundamental to reveal a recurrent tumor or tumor progress as early as possible.

The driving problem discussed in this paper is the segmentation of 3D brain tumors from magnetic resonance image data. Tumors vary in shape, size, location, and internal texture, and hence tumor segmentation is known to be a very challenging problem [5]. Various promising computer-assisted techniques to extract tumors and blood vessels from 2D MRI have been described in the literature. Of these, Tumor Extraction by Combining k-means Clustering and Perona-Malik Anisotropic Diffusion Model [6], Brain Tumor segmentation from MRI Based on Energy Functionals [7], unsupervised automatic segmentation algorithm using expectation maximization [8] technique, binary mathematical morphology [9,10], Automatic seeded region growing method [11] and Segmentation with Radix4 FFT [12] are some of the examples based on this method. Segmentation using knowledge based techniques [13] are, fuzzy based segmentation [14, 15], segmentation using texture analysis [16], Adaptive template moderated [17], and Atlas based segmentation [18]. Of these, the most popular approaches are based on applying clustering techniques to the features extracted from multiprotocol MR imaging. When manual tracing by a knowledgeable operator is used as ground truth, the overall agreements for the results of automatic methods are ranging from 82% to 94% [19]. For some of these methods, the time required for the computations has been reported to vary from several hours to several tens of hours. Presumably, with modern computing platforms, this time can be reduced to several minutes or several tens of minutes [19]. The 3D segmentation of tumors from 3D image data sets by stacking up a sequence of 2D tumor contours detected by 2D level-sets method in the parallel cross-sectional MRI images [20,21], IARD segmentation techniques [22] which operates efficiently for certain regions of MRI, and hierarchical segmentation method using variational tools that extract bones and blood vessels as two separate 3D objects [23] are some of the 3D segmentation techniques available in literature.

This work highlights an interactive method for brain tumor segmentation, which overcomes some of the above mentioned difficulties. The method consists of automatic segmentation of tumors from 2D MRI slices using morphological methods and these segmented tumor slices are exported to a 3D tool kit in MATLAB. For verification of rendered 3D tumor volume, we used 3D-DOCTOR software package that is usually using by Radiologists. In this work, T2 weighted and T1 FLAIR image was used for extracting tumors from 2D slices.

This Paper is organized as follows. Section II provides a brief overview of image segmentation of tumors from 2D slices and 3D rendering techniques. Section III details results obtained and discussion and finally, a conclusion about the results is presented.

2. METHODS AND MATERIALS

The flow chart for entire procedure of this work is shown in Figure 1. The method involved mainly two parts. The First part is automatic segmentation of tumor from the acquired slices having presence of tumor, in an MRI dataset. The second part involved stacking 2D slices of segmented tumor and perform volumetric rendering using MATLAB tool kit.

2.1. Image Acquisition

In this work, MRI images were collected from the Department of Radiology, Sree Chitra Institute of Medical Sciences and Technology (SCIMST) and Regional Cancer Centre, Thiruvananthapuram, Kerala, India. The images were gray scale images. Axial slices of T2 weighted and T1 FLAIR brain MRI data were considered. In this method, segmentation of Regions of Interest (ROI) was

Figure 1. The flow chart for segmentation of volumetric 3D tumor.

calculated on ten MR image data sets with each set containing 20 slices. For 3D rendering operation, only slices which contain tumor portions are considered. Image database development and validation of the algorithms were based on this MRI database which was already manually identified and segmented by the Radiologist. The selected images were histo-pathologically tested and have confirmed the presence of the disease. The Entire procedure was done using MATLAB and verification of 3D rendered data we used a software package called 3D DOCTOR that is usually used by Radiologists.

2.2. Image Segmentation of Tumor and 3D Rendering

The goal of this work is to extract the tumor and to create 3D models and volume rendering from 2D slice images. T1 FLAIR and T2 weighted images of the same slice used for glioma tumor extraction are given in Figures 2(a) and (b).

As a part of pre processing, skull stripping was performed. Skull stripping is a method of removing the skull and non brain intracranial tissues like fat, muscle, skin etc., that surround the surface of brain cortex and cerebellum in the brain. Brain Extraction was necessary to avoid the misclassifications of the surrounding tissues, skin and scalp as WM or GM. By removing this object, non-brain tissues will be removed and, only soft tissues will remain in the image. Skull stripping was based the on morphological operation known as erosion, using a disc shaped structuring element, which resulted in the removal of thin connections between the brain and non brain portions. Thus a skull stripped brain mask was obtained and this method was automated for every image slice.

Mathematical expression for erosion of A by B is given by:, where “A” is the image being processed, and “B” is a small set of pixels called the structuring element (SE). It is a thinning operation. The level of thinning depends on the structure and shape of the SE chosen. The image obtained after erosion is the skull stripped image “I1”.

Next the brain component “I1” was dilated by a SE, “B1” is slightly smaller in size than the one used in the morphological erosion, this corresponds approximately to restoring the boundaries of the brain component that were distorted in the erosion step.

Dilation of “I1” by “B1” is given by: . It is a thickening operation. For the entire morphological operations in this work, disc shaped structuring element were selected with varying diameter depending upon the nature of structure to be segmented.

Intensity adjustment and thresholding was done to obtain binary thresholded image (Figure 2(d)). Binary image thus obtained was morphologically labeled for obtaining the largest connected component. This lead to obtain a binary mask (Figure 2(e)) of the brain tumor and gray level values were obtained by masking the initial MR image by this mask. In this way, all pixels outside the tumor were set to 0, while the others keep their initial value that was used for further analysis as shown in Figure 2(f).

The 2D segmented slices are stacked before performing rendering operation. In an image data set, out of the twenty two slices only seven or eight slices are useful for segmentation.

The main steps to create 3D models and volume rendering from 2D slice images:

1) Create an empty space for 3D volume.

2) Each image pixel’s x and y coordinate on 2D will be transferred to the empty space. The slice number with respect to the distance between each slice is taken as z coordinate. If a pixel is adjacent to another pixel, the 3D points will be connected together.

3) Repeat the previous 2 steps until all slices are done. All the points in the 3D space will be connected just like in the 2D slices.

4) 3D volume rendering.

(a)(b)(c)(d)(e)(f)

Figure 2. Segmentation procedure for extracting tumors from 2D MRI slices using mathematical morphological operations. (a)-(b) T1 FLAIR and T2 weighted images from which tumors are extracted; (c) Skull stripped and intensity adjusted image after morphological filtering; (d) Thresholded image; (e) Morphological labeled image; (f) Segmented gray level tumor.

For the correct rendering of stacked image slices, since all 2D images are of the same dimension, hence the 3D volume can hold all of them in a rectangular cube. Different degrees of interactive control are provided for 3D tools in MATLAB, for the semi-automatic 3D propagation and rendering. In this way, we can perform a hierarchical volume rendering of the segmented slices.

3D medical imaging software called 3D DOCTOR is used for verification of volume rendered tumor. This package was developed using object-oriented technology and provides efficient tools to process and analyze 3D images, object boundaries, 3D models and other associated data items in an easy-to-use environment.

3. RESULTS AND DISCUSSIONS

This section presents the results obtained from the automatic segmentation using morphological methods on T1 FLAIR and T2 weighted axial MR images of the same slice and the 3D rendered gray level tumor from the segmented image slices. Segmentation is only implemented for tumor-contained slices. These segmented slices were stacked for volume rendering. Segmented slices are shown in Figure 3. The segmented slices were stacked and 3D modelled as shown in Figure 4. The maximum width of this tumor is 1.9 cm, length 2.5 cm and total size of the tumor is 0.68 cm3, it should be noted that the width and height of the tumor is not uniform as shown in the segmented slices.

Usually there are only seven or eight slices which contain tumor in an image data set. The major advantage

(a)(b)(c)(d)(e)(f)(g)(h)

Figure 3. Shows example segmented 2D slices used for volume rendering. Slices from (a)-(h) are segmented output from same image data set.

of this segmented volumetric primary tumors (Glioma) are, preserving the shape and gray level values of the original image for processing. For further texture based analysis and classification gray level intensity images are very essential.

The goal of this semi-automatic interactive segmentation and 3D modeling tool was to make automatic segmentation and 3D modeling of MR images more practical by replacing manual outlining of the tumor by Radiologist, without any loss in accuracy. The 3D modeled tumor volume is verified with the help of 3D DOCTOR software package presently used by Radiologists and medical practitioners. Our validation was done by a Radiologist to determine how closely the segmented images and 3D tumor volume obtained by the above method correlated with the ground truth images (manual) and it was verified to be correct.

4. CONCLUSIONS

A Novel method for the 3D modeling of glioma tumors using 2D segmented slices is presented in this paper. Manual segmentation of 2D slices is more time consuming and is very much prone to error. This interactive 3D modeling method is very accurate and less time consuming than any other method. These volumetric tumors can

(a)(b)(c)

Figure 4. Volumetric tumor rendered using stacked segmented slices shown in Figures 3(a) and (b). Volumetric tumor for different azimuth and elevation angle. (c) Volumetric tumor image by 3D DOCTOR software.

be used for volumetric analysis because it is preserving the gray level values of the original image for processing.

Volumetric tumor representations are suitable for image registration, surgical planning for detection of tumor growth and also for determining prognosis of patients in the case of high grade tumors. It may be noted that, the use of this method is fairly simple when compared to the other frequently used methods. Since it is preserving the gray level values it will be very useful for texture quantification using statistical, structural and spectral approach.

5. ACKNOWLEDGEMENTS

We would like to thank Dr. Bejoy Thomas, MD.; DNB.; PDCC, Additional Professor, Dept. of Imaging Sciences and Interventional Radiology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Kerala, India for his valuable help, suggestions and validation of these results for this work and for providing MR images Radiology department of Sree Chithra Tirunal Institute medical Sciences and Regional Cancer Centre, Trivandrum, Kerala, India

REFERENCES

  1. Robb, R., Hanson, D., Karwoski, R., Larson, A., Workman, E. and Stacy, M. (1989) Analyze: A comprehensive, operator interactive software package for multi-dimensional medical image display and analysis. Computerized Medical Imaging and Graphics, 13, 433-454. doi:10.1016/0895-6111(89)90285-1
  2. Birkbeck, N., Cobzas, D. and Jagersand, M. (2009) An interactive graph cut method for brain tumor segmentation. Proceedings of IEEE Workshop on Applications of Computer Vision (WACV 2009), Snowbird, 7-8 December 2009, 1-7.
  3. Kleihues, P. (2002) The WHO classification of tumors of the nervous system. Journal of Neuropathology & experimental Neurology, 61, 215-229.
  4. Egger, J., Zukic, Dz., Bauer, M.H.A., Kuhnt, D., Carl, B., Freisleben, B., Kolb, A. and Nimsky, Ch. (2010) A comparison of two human brain tumor segmentation methods for MRI data. Proceedings of 6th Russian-Bavarian Conference on Bio-Medical Engineering, Moscow, 8-11 November 2010.
  5. Ho, S., Bullitt, E. and Gerig, G. (2002) Level-set evolution with region competition: Automatic 3-D segmentation of brain tumors. Proceedings of International Conference on Patter Recognition, Quebec, 11-15 August 2002, 532-535.
  6. Masroor A. and Dzulkifli B.M. (2008) Segmentation of brain MR images for tumor extraction by combining Kmeans clustering and Perona-Malik Anisotropic-Diffusion Model. International Journal of Image Processing, 2, 27-34.
  7. Wang, Y., Cao, J.G., Liu, L., Lin, Z.X., Liu, T.D. and Tao, J.P. (2011) An automatic tumor segmentation system of brain tumor from MRI Based on a novel energy functional. Journal of Convergence Information Technology, 6, 59-67. doi:10.4156/jcit.vol6.issue12.8
  8. Constantin, A., Bajcsy, R. and Nelson, S. (2010) Unsupervised segmentation of brain tissue in multivariate MRI. Proceedings of International Symposium on Biomedical Imaging from Nano to Macro, Rotterdam, 14-17 April 2010, 89-92. doi:10.1109/ISBI.2010.5490406
  9. Kapur, T., Eric W. and Grimson, L., et al. (1996) Segmentation of brain tissue from magnetic resonance images: Medical image analysis. Oxford University Press, Oxford, 109-127.
  10. Roy, S., Saha, A. and Bandyopadhyay, S.K. (2011) Brain Tumor segmentation and quantification from MRI of brain. Journal of Global Research in Computer Science, 2, 155-160.
  11. Kumar, M. and Mehta, K. (2011) A modified method to segment sharp and unsharp edged brain tumors in 2D MRI using automatic seeded region growing method. International Journal of Soft Computing and Engineering, 1, 37-40.
  12. Rajeswari, R. and Anandhakumar, P. (2011) Segmentation and identification of brain tumor MRI image with radix4 FFT techniques. European Journal of Scientific Research, 52, 100-109.
  13. Clark, M.C., Hall, L.O., Goldgof, D.B., Velthuizen, R., Murtagh, F.R. and Silbiger, M.S. (1998) Automatic tumor segmentation using knowledge-based techniques. IEEE Transactions on Medical Imaging, 17, 187-201. doi:10.1109/42.700731
  14. Jude Hemanth, D. and Kezi Selva Vijila, C. (2010) Fuzzy based experimental verification of significance of skull tissue removal in brain tumor image segmentation. International Journal of Computer Applications, 1, 56-61.
  15. Shen, S., Sandham, W., Granat, M. and Sterr, A. (2005) MRI fuzzy segmentation of brain tissue using neighborhood attraction with neural-network optimization. IEEE Transactions on Information Technology in Biomedicine, 9, 459-467. doi:10.1109/TITB.2005.847500
  16. Qurat-Ul-Ain, Latif, G., Kazmi, S.B. and Jaffar, M.A. (2010) Classification and segmentation of brain tumor using texture analysis. Proceedings of the 9th WSEAS International Conference on Recent Advances in Artificial Intelligence, Knowledge Engineering and Data Bases, Cambridge, 20-22 February 2010, 147-155.
  17. Kaus, M., Warfield, S.K., Jolesz, F.A. and Kikinis, R. (1999) Adaptive template moderated brain tumor segmentation in MRI. Bildverarbeitung fur die Medizin, 102- 106.
  18. Cuadra, M.B., Pollo, C., Bardera, A., Cuisenaire, O., Villemure, J.-G. and Thiran, J.-P. (2004) Atlas-based segmentation of pathological MR brain images using a model of lesion growth. IEEE Transactions on Medical Imaging, 23, 1301-1314. doi:10.1109/TMI.2004.834618
  19. Moonisa, G., Liub, J.G., Udupab J.K. and Hackneya, D.B. (2002) Estimation of tumor volume with fuzzy-connectedness segmentation of MR images. American Journal of Neuroradiology, 23, 356-363.
  20. Aloui, K. and Naceur, M.S. (2011) 3D tumor segmentation from volumetric brain MR images using level-sets method. Diagnostic Techniques and Surgical Management of Brain, 117-138.
  21. Aloui, K. and Naceur, M.S. (2011) 3D segmentation, compression and wireless transmission of volumetric brain MR images. International Journal of Biological and Life Sciences, 7, 115-120.
  22. Heinonena, T., Dastidarb, P., Freyc, H. and Eskolaa, H. (1999) Applications of MR image segmentation. International Journal of Business and Emerging Markets, 1, 35-46.
  23. Holtzman-Gazit, M., Kimmel, R., Peled, N. and Goldsher, D. (2006) Segmentation of thin structures in volumetric medical images. IEEE Transactions on Image Processing, 15, 354-363. doi:10.1109/TIP.2005.860624