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# Mammographic images segmentation based on chaotic map clustering algorithm

- Marius Iacomi
^{1, 2}, - Donato Cascio
^{1}Email author, - Francesco Fauci
^{1}and - Giuseppe Raso
^{1}

**14**:12

https://doi.org/10.1186/1471-2342-14-12

© Iacomi et al.; licensee BioMed Central Ltd. 2014

**Received: **8 November 2013

**Accepted: **14 March 2014

**Published: **25 March 2014

## Abstract

### Background

This work investigates the applicability of a novel clustering approach to the segmentation of mammographic digital images. The chaotic map clustering algorithm is used to group together similar subsets of image pixels resulting in a medically meaningful partition of the mammography.

### Methods

The image is divided into pixels subsets characterized by a set of conveniently chosen features and each of the corresponding points in the feature space is associated to a map. A mutual coupling strength between the maps depending on the associated distance between feature space points is subsequently introduced. On the system of maps, the simulated evolution through chaotic dynamics leads to its natural partitioning, which corresponds to a particular segmentation scheme of the initial mammographic image.

### Results

The system provides a high recognition rate for small mass lesions (about 94% correctly segmented inside the breast) and the reproduction of the shape of regions with denser micro-calcifications in about 2/3 of the cases, while being less effective on identification of larger mass lesions.

### Conclusions

We can summarize our analysis by asserting that due to the particularities of the mammographic images, the chaotic map clustering algorithm should not be used as the sole method of segmentation. It is rather the joint use of this method along with other segmentation techniques that could be successfully used for increasing the segmentation performance and for providing extra information for the subsequent analysis stages such as the classification of the segmented ROI.

## Keywords

## Background

At present, breast cancer is the most common cancer among women, after cancers of the skin, and the second leading cause of cancer death in women after lung cancer [1–3]. The most widely used method for detecting breast cancer in its early stages is the mammography, a technique which has lately taken advantage of the supplementary features offered by the digital format [1]. During the last decades, the automatic detection of pathologies in the mammographic images has became a widespread auxiliary technique in radiology and the CAD (Computer Aided Detection) systems have proven their effectiveness mostly as a “second reader” (see [4–6]). The partitioning of the image in medically meaningful components (homogeneous with respect to one or several appropriately chosen characteristics) is a compulsory step in the process of automatic searching of pathologies in the images [7–11]. This phase plays a crucial role [12]: any non segmented lesion at this stage will be irremediably lost for any further analysis. While a wide variety of segmentation approaches have been proposed, there is no standard algorithm that can ensure high levels of accuracy for all imaging applications [13–15]. Furthermore, many segmentation methods rely on specific testing on an actual database [16] and the performance depends on database specificities. In particular, the segmentation of mass lesions in mammographies remains a challenging task since the masses are usually embedded and obscured by surrounding normal breast parenchyma [1, 17]. The segmentation methods proposed in mammography and more generally in medical imaging span a broad range of techniques, see e.g. [18] for a recent review and [19, 20] for particular examples. One of the generic segmentation approaches proposed more than three decades ago is the feature-based clustering method [21], which associates to each pixel or group of pixels from the image a set of appropriately chosen numerical parameters and transforms the primary segmentation task in a derived clustering problem in the associated feature space. Within this approach, the process of feature clustering becomes the crucial part of the segmentation algorithm. The main advantage of this approach is that the method does not require the use of a training set [15]. Towards the end of the last century, a new promising nonparametric method of clustering relying on the physical properties of the inhomogeneous Potts model has been proposed by Blatt, Wiseman and Domany [22]; a similar approach was proposed in terms of coupled chaotic dynamical networks by Manrubia and Mikhalkov [23] and has been further refined and restated with coupled chaotic maps by L. Angelini et al. [24]. During the last decade, a series of successful applications of this clustering method has emerged in the literature, such as landmine detection [25], EEG signals analysis in medicine [26] or financial analysis (stock markets [27], financial time series [28]). On the other hand, the chaotic map based algorithms have been proposed in many other contexts such as analysis of matrix metalloproteinases [29] or the medical image encryption technology [30]. The wide applicability of the feature clustering with coupled chaotic maps inspired us to investigate its effectiveness in the case of mammographic images with their specific characteristics. This paper focuses on the application of the chaotic maps clustering method for the segmentation of digital mammographic medical images. The results of this application are subsequently presented.

## Methods

In the initialization phase, the mammographic image to be analyzed is divided into elementary units of pixels (squares) and a feature vector is computed for each elementary unit. A dynamical variable is also associated with each unit and initialized at random. Finally, an “interaction coefficient” is computed for each pair of units.

_{ i }}, one defines a real dynamical variable

*x*

_{i}∈ [−1,1] (

*i*labels the data points). For two points

*i*and

*j*, the “interaction” matrix element is defined as

*a*is a local scale parameter. The iterative evolution law is given by

is the usual logistic map which is at the origin of the chaotic dynamics of the system. The local length scale *a* is estimated as average distance of the *K*-nearest neighbors (KNN), where *K* is the only free parameter of the algorithm.

*S*

_{ i }(

*t*) of the sign bits corresponding to the map

*x*

_{ i }(

*t*) as

*S*

_{ i }(

*t*) = 1 if

*x*

_{ i }(

*t*) > 0 and

*S*

_{ i }(

*t*) = 0 otherwise, and one computes on this basis the value of the mutual information as:

where *H*
_{
i
} is the Boltzmann entropy for the *i*-th map sequence and *H*
_{
i j
} is the joint entropy of the maps *i* and *j*. The mutual information provides a good measure of the synchronism [31], and it ranges between 0 for completely non-correlated maps and *ln* 2 for exactly synchronized maps. All the pairs of maps for which the mutual information exceeds a threshold θ are considered connected and the corresponding points in the feature space are assumed to belong to a same cluster. Thus, each value of the threshold θ defines a clustering of the data points. The number of clusters monotonically increases with the threshold and their hierarchy is naturally obtained from the graph’s increasing connectivity. For θ = 0 all data points belong to a single cluster while for θ = *ln* 2 the partitioning will consist in one cluster for each point. Between these extreme values lays the “best” partitioning scheme whose optimality is identified by its maximal stability when varying θ. The stability conditions can be imposed on the number of clusters and on the size of the biggest clusters. These conditions are strong indications that the clustering scheme obtained through application of the algorithm is not a spurious artifact of meaningless numerical output but it rather reflects some deeper similarity property of the input data.

The method has been implemented in order to take as input the data points corresponding to the digital mammographic images to be segmented. The computation begins with the partition of the image into squares small enough to match the typical dimensionality of the smallest objects of interest for the radiologist and rich enough in pixels in order to enable the computation of relevant associated features. In our experiments the side of the square usually ranged around 20 pixels. For each square a vector of features is computed leading to an associated data point in the feature space. Due to the fixed geometry of the initial partitioning, no geometrical or form-based feature can be taken into account at this stage. The position of the square in the image has a definite importance: any segmented lesion should be a contiguous region composed of one or several groups of pixels, therefore any medically meaningful clusters of points in the feature space have to correspond to spatially connected groups of neighbor squares in the image. Hence, it results necessary to treat separately the positional feature (the *x* and *y* of a data point) as a compulsory check. Other features used are the usual statistical central moments (mean pixel gray value, variance, kurtosis, skewness) and several autocorrelation values (such as energy, entropy, contrast) accounting for the texture (see [32–34] for other generic texture features and [35–38] for mammographic specific features).

The values of features have been linearly normalized to zero mean and unit variance over the whole image set of points as in [39]. Furthermore, a Karhunen-Loève transformation has been subsequently used in order to eliminate redundancies and focus the analysis on the main independent components of the feature vectors.

In order to make a more meaningful evaluation of the eventual gains of applying the chaotic maps method, the clusters have been also obtained in an alternative manner, by using the simple Euclidean distance in the feature space between the pairs of squares rather than the mutual information.

The clusters obtained on this basis are visualized as different gray-level regions on the image. Due to the border effects, the contour of the breast usually introduces a series of spurious clusters with no real meaning. In our analysis, we have chosen to cut-off these artifacts by default assigning a strip of border pixel squares to the unique border cluster; the choice has the advantage that the breast shape contour is immediately visible on the segmented image (in white), while exhibiting low probability to cut-off also eventual pathologies, usually found more in depth.

The mammographic image database used for this study consists of a group of 149 selected cases for a total of 298 images. More specifically, we operated on three distinct datasets: a first set of 24 digitally acquired cases on a GE Senograph 2000D containing 98 images (characteristics: size 1914×2294 pixels, pixel size 0.094 mm, spatial resolution ~5 lp/mm, log pixel-intensity relationship), a second set of 22 digitalized cases on a Lorad Selenia Full Field Digital Mammograph containing 97 images (characteristics: size 3328×4096 pixels, pixel size 0.070 mm, spatial resolution ~7 lp/mm, linear pixel-intensity relationship); and a third set of 103 anonymized individual images containing micro-calcifications clusters digitally acquired on a Fuji CR mammograph (characteristics: size 1770×2370 pixels, pixel size 0.101 mm, spatial resolution ~5 lp/mm, linear pixel-intensity relationship). The combined first two sets contained a number of 10 cases with small (typical dimension ≤ 2 mm) mass lesions showing up in 20 images (10 images for each set) and 28 cases with large sized (typical dimension > 2 mm) mass lesions showing up in 56 images (30 images for the first set and 26 images for the second). The third set contained 73 cases/images with micro-calcifications clusters and 30 reference healthy images. The digital images were all intended for presentation and had a 12-bit greyscale depth. All the digitally acquired images were subsequently stored on a PACS system. The pathologies have been diagnosed and classified by two expeThe mammographic image database used for this study consists of a group of 149 selected cases for a total of 298 images. More specifically, we operated on three distinct datasets: a first set of 24 digitally acquired cases on a GE Senograph 2000D containing 98 images (characteristics: size 1914×2294 pixels, pixel size 0.094 mm, spatial resolution ~5 lp/mm, log pixel-intensity relationship), a second set of 22 digitalized cases on a Lorad Selenia Full Field Digital Mammograph containing 97 images (characteristics: size 3328×4096 pixels, pixel size 0.070 mm, spatial resolution ~7 lp/mm, linear pixel-intensity relationship) ; and a third set of 103 anonymized individual images containing micro-calcifications clusters digitally acquired on a Fuji CR mammograph (characteristics: size 1770×2370 pixels, pixel size 0.101 mm, spatial resolution ~5 lp/mm, linear pixel-intensity relationship). The combined first two sets contained a number of 10 cases with small (typical dimension ≤ 2 mm) mass lesions showing up in 20 images (10 images for each set) and 28 cases with large sized (typical dimension > 2 mm) mass lesions showing up in 56 images (30 images for the first set and 26 images for the second). The third set contained 73 cases/images with micro-calcifications clusters and 30 reference healthy images. The digital images were all intended for presentation and had a 12-bit greyscale depth. rt senior radiologists; all diagnosed pathologies have been further confirmed by histological examination.

The procedure was tested on images belonging to a private anonymous database collected in the Policlinic Hospital of Palermo. Policlinic Hospital is a hospital firm of University of Palermo in which formation, scientific research and health service are well integrated. Policlinic Hospital attests that all research involving humans is carried out in compliance with the Helsinki Declaration and involves appropriate patient consent.

## Results and discussion

*k*(from the KNN) and

*a*(the scale parameter), there appears to be no automatic “best clustering” criterion since the number of clusters exhibits no obvious stationarity when varying θ. The typical dependence of the number of clusters as a function of the threshold θ is depicted in Figure 2. If the clustering is to identify one or a few medically significant regions in the image, it is expected that the corresponding clusters present a minimum of stability also in the number of internal points. The most important clusters in the image actually do exhibit some stability at the varying of the threshold (the internal number of points remains approximately constant on several θ ranges, see e.g. also [26]), but this behavior remains less typical since in a large number of cases, there is no obvious stability subrange or there is no meaningful cluster in the image. In Figure 3 we have represented a typical behavior of the number of points (pixel squares) contained in the two biggest meaningful clusters (other than the three default ones – image background, border pixels and normal internal breast points).

The segmentation algorithm described above displays a fair number of findings in the images containing mass lesions. The “cluster noise” is very large: in fact, at higher threshold levels, most clusters contain actually just one pixel square and show up in internal breast areas characterized by rapid variation of luminosity, typically not far from the breast contour.

As a general characteristic, the small mass lesions with dimensions of the same order as the size of the pixel square (that is between 1–2 mm), are well identified by the algorithm: practically all of them (15 out of 16, about 94% within this category) show up as isolated point clusters in the segmented image for all but the first threshold values. This behavior may be linked with the important differences in the feature characterization of healthy tissue and small lesions. The meaningfulness of the segmented ROI clusters is ensured by their lack of suspicious clusterized neighboring pixel squares rather than by the variational technique used in the original form of the algorithm’s implementation: the isolation criterion shows no false positive for cluster groups up to four pixel squares immersed in an uniform (healthy tissue) background, not too close to the border of the breast. If one includes also those small clusters connected with the breast border, the correct recognition rate diminishes accordingly and some false positives show up near the border; it’s worthwhile mentioning that in this case the isolation criterion is less operational since all the interesting points cannot be satisfactorily resolved from the spurious pixel squares near the border. No isolated small cluster appears in healthy images.

**Segmentation of images with pathologic and non-pathologic small mass lesions**

Only internal isolated ROI, actual diagnosis | Including breast border isolated ROI, actual diagnosis | ||
---|---|---|---|

Pathologic | Non-pathologic | Pathologic | Non-pathologic |

15 TP | 0 (FP) | 16 TP | 3 (FP) |

1 FN | 4 (TN) | 4 FN | 5 (TN) |

For large-sized mass lesions extending over an area corresponding to more pixel squares (with typical linear diameters ranging from 3 mm up to about 30 mm), the corresponding segmentation clusters rarely match the shape of the lesion due to the usual non-uniformity of the features over ROI area. About 10% of these lesions (5 out of 56) are matched with an overlap of about 80% by the corresponding segmented clusters; the other large lesions either exhibit overlaps under 30% with their segmented cluster counterparts (33 out of 56), or have no meaningful corresponding cluster associated with them (18 out of 56). On the other hand, in the segmented images, the algorithm introduces often bigger-sized cluster artifacts associated with breast borders or non-pathological denser areas in 32 of the cases, and it is difficult to establish an unambiguous automatic decisional criterion for the degree of meaningfulness of these clusters.

**Segmentation of large-sized mass lesions (negative images included)**

Large mass lesions | |
---|---|

Pathologic | Non-pathologic/absent |

38 (= 5 + 33) TP (partial match) | 32 (FP) |

18 FN | 87 (TN) |

^{a}. This result is not surprising due to the well-known reliability of the micro-calcifications characterization through the local features on the image. The overlap of the segmented cluster with the micro-calcifications area varies in the range 10-90% with the peak in the range 30-50%. The agreement is better for denser distributed micro-calcifications.

Due to the distinction naturally arising between small and large/sized mass lesions, one can define an accuracy for each class as *acc*
_{i} = (TP_{i} + TN_{i})/( TP_{i} + TN_{i} + FP_{i} + FN_{i} ) where i labels the mass lesion class and the “true/false” are given with respect to the small or large mass lesions. We find thus for small mass lesions an accuracy *acc*
_{SMALL MASS} = (195-3-4)/195 ~ 96% (considering also the isolated clusters near the border) and for large mass lesions an accuracy *acc*
_{LARGE MASS} = (87 + 38)/195 ~ 64%, in agreement with our previous observations. Of some interest is also the overall accuracy *acc*
_{MASS} = 118/195 ~ 60.5% for discriminating between images with generic mass lesions and non-pathological/healthy.

The performance of the method doesn’t exhibit a significant dependence on the database: the accuracy results restricted to the first set are *acc*
_{SMALL MASS} = 95/98 ~ 97% and *acc*
_{LARGE MASS} = 61/98 ~ 62%, while on the second set one has *acc*
_{SMALL MASS} = 93/97 ~ 96% and *acc*
_{LARGE MASS} = 64/97 ~ 66%.

Concerning the 103 images in the micro-calcifications dataset, 3 of the healthy images present an internal contiguous cluster similar to the one underlying a part of the positives. The remaining 73 positive ones do exhibit internal “big” clusters distributed according to the following overlaps:

If the overlap in the segmented image with micro-calcifications is enough consistent (our tests show that an overlap of at least 30% with the denser micro-calcification area constitutes already a safe indication) to trigger a further analysis in an automatic system, the internal segmentation cluster will contain most of the micro-calcifications and may be used as a relevant investigation starting point. It should be mentioned at this point that the feature-only based approach produces an essentially similar segmentation pattern. Therefore, the chaotic map clustering of the mammographic images containing micro-calcifications brings no extra information with respect to this alternative method.

*acc*

_{MICRO}= (103-23-3)/103 ~ 75%.

**Overlap of the cluster with the ROI for micro-calcifications images**

Overlap range | 0-5% | 5-15% | 15-25% | 25-35% | 35-45% | 45-55% | 55-65% | 65-75% | 75-85% | 85-95% |

# of images | 11 | 4 | 8 | 12 | 12 | 9 | 2 | 4 | 6 | 5 |

## Conclusion

The non-parametric chaotic map clustering of the mammographic images has been considered here as stand-alone segmentation approach, mainly from an applicability point of view. The ultimate goal of applying such a segmentation method to the medical mammographic images is the potential performance improvement of an automatic detection system based on it. As discussed, the specific aspect of mammographic segmentation which remains a non-trivial challenge is the segmentation of mass lesions, while the identification of micro-calcifications with this new algorithm hardly could lead to any spectacular breakthrough advance (micro-calcifications detection rates of about 94% with 6.25% of false positives and 2% false negatives were already reported more than a decade ago, see [40]).

At this stage of the analysis, the results obtained do allow some general conclusions concerning the valuable applicability of the chaotic map algorithm for the segmentation of mammographic images, in an efficient automatic work-flow, in comparison with the results obtained by alternative methods as those used by present day commercial CAD systems. While many (about 90%) of the mass lesions are either lost or appear with wrong sizes, shapes and as neighboring independent clusters (see Figures 5 & 6 above), most of the smaller ones show up conveniently as internal clusters in the segmented images. Indeed, about 94% of the small lesions more than 6 mm away from the border were correctly segmented by the algorithm; the true positive rate decreases to 80% if the smaller mass lesions near the breast border are included. This fact looks especially important when considering that the small lesions are usually less easily identifiepathologic cases cod than the extended ones, and the support of an automatic CAD system is more useful in their case. On the other hand, one has to keep in mind that the important number of “parasite” clusters with no medical significance adds a further complication in correctly evaluating the output of the segmentation algorithm which the stability analysis cannot eliminate.

Concerning the micro-calcifications, the chaotic maps segmentation process gives interesting and peculiar results. In about 2/3 of the pathologic cases considered here, the algorithm provides an useful shape of the region with denser micro-calcifications. While these results are still not significantly edging the ones derived from simple feature analysis, the algorithm may be used as alternative check in a more complex workflow.

Due to the particularities of the mammographic images, we conclude that the chaotic map clustering algorithm should not be used as unique stand-alone method of segmentation. It is rather the joint use of this method along with other segmentation techniques that could be successfully used for increasing segmentation performance and providing extra information for subsequent analysis stages such as the classification of the segmented ROI.

## Endnote

^{a}The CAD tool used for computing the position of micro-calcifications is CyclopusCAD Mammo® produced by CyclopusCAD srl.

## Declarations

### Acknowledgements

Authors thank Policlinic Hospital of Palermo and in particular Dr. Raffaele Ienzi for providing the images.

## Authors’ Affiliations

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- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2342/14/12/prepub

### Pre-publication history

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