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Table of Contents
ORIGINAL ARTICLE
Year : 2020  |  Volume : 28  |  Issue : 3  |  Page : 169-172

Interacting factors of strain ratio values in fibroadenomas and the contribution of color scale


1 Department of Radiology, Izmir Katip Celebi University Ataturk Training and Research Hospital, Izmir, Turkey
2 Department of Radiology, Dr. Behçet Uz Child Disease and Pediatric Surgery Training and Research Hospital, University of Health Sciences, Izmir, Turkey
3 Department of General Surgery, Izmir Katip Celebi University Ataturk Training and Research Hospital, Izmir, Turkey

Date of Submission23-Nov-2019
Date of Decision27-Dec-2019
Date of Acceptance15-Jan-2020
Date of Web Publication26-Mar-2020

Correspondence Address:
Dr. Gulten Sezgin
Department of Radiology, Izmir Katip Celebi University Ataturk Training and Research Hospital, Izmir 35360
Turkey
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/JMU.JMU_112_19

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  Abstract 


Background: The purpose of this retrospective study is to investigate the association of qualitative and semiquantitative strain elastography (SE) features with factors such as lesion size, skin-to-lesion distance, and patient's age in fibroadenomas and to discuss false-positive results. Methods: A total of 120 lesions that were performed SE with histopathologically confirmed fibroadenoma were included in the study. All images were reviewed from the archiving system with a consensus of two radiologists. Tsukuba elasticity score was used for color scoring (from 1 to 5). Lesions with strain ratio (SR) ≥2.27 and color scale score of 4 or 5 were considered as false positive. The patients were divided into two groups according to the age: <50 and ≥50 years old. Regard of the size, lesions were divided into two groups: <15 mm and ≥15 mm. The distances of the lesions to the skin were also divided into two groups: <5 mm and ≥5 mm. Statistical analysis to identify associations between these groups and SR was carried out with Pearson Chi-square test and Fisher's exact test. The false-positive rates were calculated. Results: There was no statistically significant difference between patients' age, lesion size, skin-to-lesion distance, and SR values. The false-positive rate was 21.66% for SR, while it was 3.33% for color scale. Conclusion: SR values of the fibroadenomas were not affected by factors such as age, lesion size, and depth. In addition, false-positive rates significantly decrease when color scale scores are evaluated for fibroadenomas.

Keywords: Color scale, fibroadenoma, strain elastography, strain ratio


How to cite this article:
Sezgin G, Coskun M, Apaydin M, Keceli M, Cetinoglu K, Tavusbay C. Interacting factors of strain ratio values in fibroadenomas and the contribution of color scale. J Med Ultrasound 2020;28:169-72

How to cite this URL:
Sezgin G, Coskun M, Apaydin M, Keceli M, Cetinoglu K, Tavusbay C. Interacting factors of strain ratio values in fibroadenomas and the contribution of color scale. J Med Ultrasound [serial online] 2020 [cited 2020 Dec 2];28:169-72. Available from: http://www.jmuonline.org/text.asp?2020/28/3/169/281449




  Introduction Top


Fibroadenomas are the most common benign solid breast lesions and seen in one-quarter of women under 35.[1],[2]

Ultrasonography (US) is the most appropriate imaging method for this age group because of its practical usage and lack of radiation, although mammography is used when it is necessary. However, the low specificity of the US may necessitate the use of additional techniques such as elastography.[3] Two methods are defined in strain elastography (SE): one qualitative-color score and one semiquantitative strain ratio (SR). Several studies reported that SE contributed to the grayscale US had a benefit to distinguish benign and malignant breast lesions.[4],[5],[6],[7],[8]

Fibroadenomas tend to be soft lesions, but some could be as stiff as malignant lesions.[9],[10] In the literature, it was stated that large fibroadenomas were stiffer than smaller ones. Similarly, as patients' age increases, it has been reported that hyaline degeneration resulted in stiffness in fibroadenomas. It was also known that lesions close to the skin were evaluated as stiffer due to difficulty in compressing.

The purpose of this study is to investigate factors associated with SE findings in fibroadenomas and to discuss false-positive findings at SE. In previous studies, these factors were analyzed by shear wave elastography (SWE) technique.[7],[8] SE is inexpensive, common, and easily accessible for evaluating tissue elasticity than SWE.[3]


  Patients and Methods Top


Breast lesions that were examined with SE and histopathologically confirmed fibroadenoma were re-evaluated. This retrospective study was approved by our Institutional's Ethics Committee (23.01.2019/752). Due to the retrospective nature of the study, informed consent was not required.

All images were reviewed with picture archiving computer systems by two radiologists who specialized in breast imaging and have 3 to 10 years of experience. The core biopsies were performed by the same radiologists using full-automatic 16 G biopsy needles (Bard Magnum, Covington, Georgia, USA) following US and SE examinations.

Grayscale US and SE examinations were performed (Hitachi Ezu-MT28-S1 model, Hitachi Inc., Japan) with a 13 MHz superficial probe by the same radiologists. On grayscale images, the long axis and the distance to the skin were measured and recorded. After that, SE was done with two consecutive compressions in 1 sec while the probe axis was perpendicular to the lesion. Three elastography images were obtained for each lesion and the images with the highest SR values were recorded. Two separate regions of interest with a diameter of 2–3 mm2 were placed both over the hard part of the lesion and to the tissue adjacent at the equal depth from the skin. SR value was calculated automatically. Tsukuba elasticity score (TES) created by Itoh et al. was used for color scoring from 1 to 5 [Table 1].[10] According to the TES system, scores of 1, 2, and 3 were considered as benign and scores of 4 and 5 were considered as malignant. The color scoring was assessed from the recorded images with a consensus of two radiologists.
Table 1: Tsukuba elasticity scoring system (10)

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Lesions with SR ≥2.27 and TES of 4 or 5 were considered as false positive.[11]

The patients were divided into two groups according to the age: <50 years old and ≥50 years old. Regard of the size, lesions were divided into two groups: small (<15 mm) and large (≥15 mm). On the other hand, the distances of the lesions to the skin were also divided into two groups of <5 mm and ≥5 mm. In determining these parameters, Elseedawy et al.'s study was taken into consideration.[12]

Statistical analysis to identify associations between these groups and SR and color scale was carried out with the Pearson Chi-square test and Fisher's exact test.


  Results Top


One-hundred twenty patients with fibroadenomas were evaluated. Patient ages were ranged between 17 and 83 years, with a mean age of 36.39 ± 13.09 years and a median of 34 years. The mean lesion size was 16.58 ± 6.13 mm (median: 16 [6–38]). The mean skin-to-lesion distance was 4.58 ± 4.1 mm (median: 3 [0–20]. The SR mean and median were 1.76 ± 1.17 and 1.48, respectively (ranged between 0.14 and 7.52). Association between lesion and SR and patient characteristics at SE are shown in [Table 2]. The false-positive rate for SR was 21.66%. According to the TES 11, 94, 11, 4, and 0, cases were seen in the scale from 1 to 5, respectively. Four patients were false positive in color scale and false-positive rate was 3.33% for color scale. Three of four hard lesions belongs to the patients < 50 years of age (3/103, 2.9%) and the last one was belong to the patient above 50 years of age (1/17, 5.9%). The distance from the lesion to the skin was <5 mm in two cases, while ≥5 mm in other two cases. The mean lesion size was 18.54 ± 5.12 mm and the diameter of two lesions was <15 mm, while the diameter of the other two lesions was ≥15 mm. SR values were between 3.55 and 4.57. Since the number of these cases was very small, no analysis was performed.
Table 2: The descriptive findings of all of patients

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There was no statistically significant difference between patients' age, lesion size, skin-to-lesion distance, and SR, and their P values were 1.000, 0.664, and 0.831, respectively.


  Discussion Top


In this study, we showed that qualitative color scale and semiquantitative SR scale SE findings of fibroadenomas were not affected by factors such as patients' age, lesion size, and depth. We also found that the false-positive rates were quite low on the color scale, and TES is a reliable method for fibroadenoma diagnosis than SR.

Sonographical findings are often adequate in the diagnosis of fibroadenomas, while the addition of sonoelastographic findings contributes to more correct diagnosis. There are some differences in the elastographic findings of malignant and benign masses. In color scale, the size of the benign lesion was the same or less than the gray scale, whereas in malign ones, the lesion seemed larger than gray scale because of secondary to the possible desmoplastic reaction.[13] In addition, the absence of score 5, suggesting malignancy, showed that color scale could be sensitive in the differentiation of benign-malignant lesions.

There is not certain cut off value for SR distinguishing benign-malign lesions.[14] SR is ranging between 2.27 and 3.8 for benign breast lesions.[11] We accepted the lowest value of these as the cutoff value. In some reports, the evaluation of SR is superior to the color scale[9],[15] because the interpretation of the color scale is subjective, qualitative, and operator dependent. Furthermore, these studies have performed between benign and malignant solid masses. In our study, we evaluated only benign masses and false positives were very low in color scale (3.33%). Among these cases, the ratio of patients over the age of 50 (5.9%) was higher than the other group in accordance with the literature.[9],[10] False-positive results were significantly higher in SR analysis than those obtained with the color scale. The high false positivity of SR may be secondary to the adoption of the lowest cutoff value that is given in the literature. Furthermore, consensus evaluation may increase sensitivity in color scale [Figure 1].
Figure 1: A 32-year-old with fibroadenoma female patient. Strain elastography and gray scale ultrasound images are seen side by side. The color scale image shows 2 according to Tsukuba elasticity scoring. The strain ratio value is shown as b/a in the left lower corner of images

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In the study of Elseedawy et al. also, no statistically significant difference was found between the patient's age and lesion stiffness, as in our study.[12] In this study, the patient's age has examined as <50 years old (84 patients) and ≥50 years old (28 patients) in two groups too, and the distributions of their groups are more homogeneous than our study (respectively, 103 and 17).

In our study, the false-positive rate was 21.66% (26/120) for SR, while this ratio 26% (39/151) were reported in Elseedawy et al.'s study.[12] In Yoon et al.'s study performed with the SWE technique, the false-positive rates of benign solid lesions were 6.45–36.6%.[16] Lesion's size and depth were related false-positive results in these studies. In our study, false-positive rates were similar with these studies, but there were no factors (size and depth) interacting false-positive rates.

Score 4 which was highly suggestive for malignant masses in Tsukuba classification was defined in four cases in this study [Figure 2]a and b]. The SR values of these cases were above the cutoff value of 2.27. However, the color scale of 116 patients was compatible with a benign lesion (96.66%) and false-positive rate was only 3.33%. We consider this classification more reliable than SR in fibroadenomas. In other words, when SR was high, it would be more accurate to define the lesion as a fibroadenoma if color scores were 1, 2, and 3. This score system was first classification system and the majority of patients were examined with the TES in the literature.[7],[10]
Figure 2: A 45-year-old (a) and a 72-year-old (b) with fibroadenoma female patients. The color scale findings of two false positive fibroadenomas (Score 4). It's seen the strain ratios also are high

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Some grading systems include cyst or postcompression findings; however, in all scoring systems, low scores are soft, while high scores represented hard lesions.[17],[18] In Tsukuba scoring, benign lesions are defined as scores 1, 2, and 3, while malignant ones are 4 and 5. Itoh et al. reached 86.5% sensitivity and 89.8% specificity with this scoring, but in the same study, it has been shown that elastography has the same diagnostic performance with the grayscale US of Breast Imagıng Reported and Data System.[10]

It is known that breast parenchyma is affected by age, hormonal therapy, menstrual cycles, pregnancy, and lactation. Kılıç et al. have shown that the period of the menstrual cycle is an important factor for SE as in magnetic resonance imaging (MRI) and mammography. They recommend performing the elastography examination in the 2nd week of the menstrual cycle, as in MRI.[19] Since we did not take into consideration of hormonal therapy, menstrual cycles, pregnancy, and lactation processes when performing elastographic examinations, we could not evaluate the interaction of the tumor with the surrounding parenchyma.

One of the limitations of this study is a small number of cases and single-center design. Furthermore, there was no equal distribution of age groups among patients because most of the cases were under 50 years of age and the breast parenchyma was not evaluated as a factor influencing SR. Another limitation is that we did not evaluate the interobserver agreement. In addition, although we used the SE technique SWE technical parameters are also taken as reference.


  Conclusion Top


In conclusion, SE findings of the fibroadenomas have not be affected by factors such as patients' age, lesion size, and depth, in this study. In addition, false-positive rates decrease with the utilization of color scale, and TES can contribute more accuracy to the diagnosis of fibroadenoma than SR. If these results are supported by large series, unnecessary biopsies, short follow-ups, additional examinations, and patient anxiety can be reduced.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
  References Top

1.
El-Wakeel H, Umpleby HC. Systematic review of fibroadenoma as a risk factor for breast cancer. Breast 2003;12:302-7.  Back to cited text no. 1
    
2.
Coriaty Nelson Z, Ray RM, Gao DL, Thomas DB. Risk factors for fibroadenoma in a cohort of female textile workers in Shanghai, China. Am J Epidemiol 2002;156:599-605.  Back to cited text no. 2
    
3.
Gultekin S. Ultrasonografide yeni uygulamalar. Trd Sem 2014;2:158-70.  Back to cited text no. 3
    
4.
Stoian D, Timar B, Craina M, Bernad E, Petre I, Craciunescu M. Qualitative strain elastography – Strain ratio evaluation – An important tool in breast cancer diagnostic. Med Ultrason 2016;18:195-200.  Back to cited text no. 4
    
5.
Yerli H, Yilmaz T, Kaskati T, Gulay H. Qualitative and semiquantitative evaluations of solid breast lesions by sonoelastography. J Ultrasound Med 2011;30:179-86.  Back to cited text no. 5
    
6.
Balçık A, Polat AV, Bayrak İK, Polat AK. Efficacy of sonoelastography in distinguishing benign from malignant breast masses. J Breast Health 2016;12:37-43.  Back to cited text no. 6
    
7.
Wojcinski S, Boehme E, Farrokh A, Soergel P, Degenhardt F, Hillemanns P. Ultrasound real-time elastography can predict malignancy in BI-RADS®-US 3 lesions. BMC Cancer 2013;13:159.  Back to cited text no. 7
    
8.
Berg WA, Cosgrove DO, Doré CJ, Schäfer FK, Svensson WE, Hooley RJ, et al. Shear-wave elastography improves the specificity of breast US: The BE1 multinational study of 939 masses. Radiology 2012;262:435-49.  Back to cited text no. 8
    
9.
Chang JM, Moon WK, Cho N, Yi A, Koo HR, Han W, et al. Clinical application of shear wave elastography (SWE) in the diagnosis of benign and malignant breast diseases. Breast Cancer Res Treat 2011;129:89-97.  Back to cited text no. 9
    
10.
Itoh A, Ueno E, Tohno E, Kamma H, Takahashi H, Shiina T, et al. Breast disease: Clinical application of US elastography for diagnosis. Radiology 2006;239:341-50.  Back to cited text no. 10
    
11.
Fischer T, Peisker U, Fiedor S, Slowinski T, Wedemeyer P, Diekmann F, et al. Significant differentiation of focal breast lesions: Raw data-based calculation of strain ratio. Ultraschall Med 2012;33:372-9.  Back to cited text no. 11
    
12.
Elseedawy M, Whelehan P, Vinnicombe S, Thomson K, Evans A. Factors influencing the stiffness of fibroadenomas at shear wave elastography. Clin Radiol 2016;71:92-5.  Back to cited text no. 12
    
13.
Garra BS, Cespedes EI, Ophir J, Spratt SR, Zuurbier RA, Magnant CM, et al. Elastography of breast lesions: Initial clinical results. Radiology 1997;202:79-86.  Back to cited text no. 13
    
14.
Cosgrove D, Piscaglia F, Bamber J, Bojunga J, Correas JM, Gilja OH, et al. EFSUMB guidelines and recommendations on the clinical use of ultrasound elastography. Part 2: Clinical applications. Ultraschall Med 2013;34:238-53.  Back to cited text no. 14
    
15.
Zhi H, Ou B, Luo BM, Feng X, Wen YL, Yang HY. Comparison of ultrasound elastography, mammography, and sonography in the diagnosis of solid breast lesions. J Ultrasound Med 2007;26:807-15.  Back to cited text no. 15
    
16.
Yoon JH, Jung HK, Lee JT, Ko KH. Shear-wave elastography in the diagnosis of solid breast masses: What leads to false-negative or false-positive results? Eur Radiol 2013;23:2432-40.  Back to cited text no. 16
    
17.
Locatelli M, Rizzatto G, Aiani L. Characterizationof Breast Lesions with real-time Sonoelastography: Results from the Italian Multicenter Clinical Trial. Scientific oral Presentation. Vienna, Austria: ECR; 2007.  Back to cited text no. 17
    
18.
Fleury EF, Rinaldi JF, Piato S, Fleury JC, Roveda Junior D. Appearance of breast masses on sonoelastography with special focus on the diagnosis of fibroadenomas. Eur Radiol 2009;19:1337-46.  Back to cited text no. 18
    
19.
Kılıç F, Kayadibi Y, Kocael P, Velidedeoglu M, Bas A, Bakan S, et al. Changes in the elasticity of fibroadenoma during the menstrual cycle determined by real-time sonoelastography. Eur J Radiol 2015;84:1044-8.  Back to cited text no. 19
    


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