Evaluation of the Appearance Characteristics of Suspicious Microcalcifications Detected by Ultrasonography

Yasemin Kayadibi; Deniz Esin Tekcan Şanlı; Neşe Uçar; Emine Yıldırım; Ahmet Necati Şanlı

doi:10.4274/jarem.galenos.2021.18291

ABSTRACT

Objective:

To investigate the imaging properties of mammographically suspicious microcalcifications (MC) that can be detected by ultrasonography (USG).

Methods:

Cases with suspected MC in categories 4 and 5 according to the Breast Imaging-Reporting and Data System (BI-RADS) in screening mammography between June 2019 and January 2021 were included in the study. The patients were scanned with USG. USG guided core needle biopsy was performed for those whose MC area could be detected by USG and evaluated histopathologically. Mammographic features of MCs [morphological type (fine pleomorphic, amorphic, coarse heterogeneous, fine linear pleomorphic branching)], distribution (clustered, regional, segmental, diffuse, linear) and BI-RADS (4A, 4B, 4C, 5) category was determined. Other findings accompanying MC areas on mammography and USG were recorded.

Results:

The mean age of 43 patients included in the study was 45.27±8.58 (30-84). 48.8% (n=21) of the calcifications were fine pleomorphic, 30% (n=13) amorphous, 16% (n=7) coarse heterogeneous, 4.6% (n=2) fine pleomorphic branching type. While 70% (n=30) of the patients had asymmetrical density accompanying MCs on mammography, parenchymal distortion was found in 12% (n=5); on USG, hypoechoic area was found in 58% (n=25) of the patients, irregular ductal ectasia in 19% (n=8), parenchymal distortion in 9% (n=4), and 10% (n=4) microcyst cluster were accompanying pathologies. As a result of the histopathological evaluation, 42% of the patients had benign histopathology (n=18), 16% had ductal carcinoma in situ (n=7), and 42% (n=18) had invasive ductal cancer.

Conclusion:

In our study, the distinctive features of BI-RADS 4 and 5 MCs that can be followed by USG were evaluated. Although MCs that can be detected on USG are more likely to be malignant than benign ones, fine pleomorphic MC areas can be observed most frequently. Knowing the features of mammographic suspected MCs on USG will be helpful in daily radiology practice and biopsy planning.

Keywords:

Microcalcification, mammography, ultrasonography, ultrasound guided biopsy

INTRODUCTION

Mammography is the gold standard imaging method for detecting and characterizing microcalcifications (MC) (1). Ductal carcinoma in situ (DCIS) constitutes 25% of suspected MC on mammography (2,3). 90% of DCIS cases are detected through mammography, which is classified as category 4 or 5 according to the Breast Imaging-Reporting and Data System (BI-RADS) and through mammograms recommended histopathological evaluation (4-7). Ultrasonography (USG) has an important role in the characterization of breast lesions detected by mammography (8). However, the diagnostic power of USG is limited in the detection of MCs that may not be accompanied by a mass, which may be a sign of malignancy (9,10). The detection of MCs with USG becomes easier thanks to the new technological algorithms such as use of high-frequency probes, the development of artifact removal software, tissue harmonic and compound imaging and MicroPure imaging (9,11,12). This situation has raised the question of whether USG guided biopsy can be applied in the histopathological diagnosis of MCs. Although stereotaxic biopsy is the most reliable method for sampling MCs, it has some disadvantages such as prolonged compression, radiation exposure and expensive equipment requirement. In addition, it is difficult to access the pathological area in cases where it is not available in all health centers, the breast volume is very small, and close to the chest wall or axilla (5-7,13). Compared to stereotaxic biopsy, USG guided biopsy is a less painful, faster, more comfortable, cheaper, radiation-free, real-time method that allows manipulation (6,12). The disadvantage of USG-guided biopsy is that it is difficult to detect MCs without a mass, and this rate varies between 24% and 93% according to publications in the literature (9,11,12,14,15). Our aim in this study was to investigate the sonographic features of MCs that can be detected by USG, are not accompanied by a mammographic mass, and classified as category BI-RADS 4 or 5.

GİRİŞ

Mamografi, mikrokalsifikasyonları (MK) saptama ve karakterize etmede altın standart görüntüleme yöntemidir (1). Mamografide şüpheli MK’lerin %25’ini duktal karsinoma in situ (DKİS) oluşturmaktadır (2,3). DKİS olgularının %90’ı, Meme Görüntüleme-Raporlama ve Veri Sistemi’ne (Breast Imaging-Reporting and Data System, BI-RADS) göre kategori 4 veya 5 olarak sınıflandırılan ve histopatolojik değerlendirme önerilen mamografiler aracılığıyla tespit edilmektedir (4-7). Mamografik olarak saptanan meme lezyonlarının karakterizasyonunda ultrasonografinin (USG) önemli bir yeri vardır (8). Bununla birlikte bir kitlenin eşlik etmediği malignite habercisi olabilecek MK’lerin tespitinde USG’nin tanısal gücü sınırlıdır (9,10). Yüksek frekanslı probların kullanımı, artefakt giderici yazılımların geliştirilmesi, doku harmonik ve compound görüntüleme, MikroPure görüntüleme gibi yeni teknolojik algoritmalar sayesinde USG ile MK’lerin tespiti kolaylaşmaktadır (9,11,12). Bu durum; MK’lerin histopatolojik tanısında, “USG eşliğinde biyopsi uygulanabilir mi?” sorusunu gündeme getirmiştir. MK’lerin örneklenmesinde en güvenilir yöntem stereotaksik biyopsi olmakla birlikte uzamış kompresyon, radyasyon maruziyeti ve pahalı ekipman gereksinimi gibi bazı dezavantajları vardır. Ayrıca tüm sağlık merkezlerinde mevcut olmaması, meme hacminin çok küçük ve göğüs duvarına veya aksillaya yakın olduğu durumlarda patolojik alana erişim zordur (5-7,13). Stereotaksik biyopsi ile karşılaştırıldığında, USG kılavuzluğunda biyopsi daha az ağrılı, daha hızlı, daha rahat, daha ucuz, radyasyon içermeyen, gerçek zamanlı ve manipülasyona olanak sağlayan bir yöntemdir (6,12). USG eşliğinde biyopsinin dezavantajı ise kitle eşlik etmeyen MK’lerin tespitinin zor olmasıdır, bu oran literatürdeki yayınlara göre %24 ile %93 arasında değişmektedir (9,11,12,14,15). Bu çalışmadaki amacımız USG ile saptanabilen, mamografik açıdan kitle eşlik etmeyen, kategori BI-RADS 4 veya 5 olarak sınıflandırılmış MK’lerin sonografik görünüm özelliklerini araştırmaktı.

METHODS

Patient Group

After the approval of the local hospital ethics committee (approval number 252 dated 14/04/2021), patients with BIRADS 4 or 5 microcalcifications were screened between 2019-2021. Patients whose non-mass microcalcifications could be observed under USG and who underwent USG-guided core needle biopsy were included in the study. Patients who had undergone previous breast surgery, treated for breast cancer, and were in the ongoing pregnancy or breastfeeding period were excluded from the study. In addition, a signed informed consent form was obtained from all patients.

Imaging Method and Image Analysis

Images of all patients were taken in standardized mediolateral oblique and craniocaudal positions with our hospital mammography device (Giotto Image MC, IMS, Italy). Mammography images of the patients were reviewed retrospectively from the hospital Picture Archiving and Communication System (PACS). According to BI-RADS 5^th edition (2013), patients were evaluated for mammographic breast density (type A-B-C-D), type of MC (amorphous, fine pleomorphic, coarse heterogeneous, fine linear and fine pleomorphic branching), distribution pattern (clustered, regional, segmental, diffuse, linear) and the BI-RADS category (4A, 4B, 4C, 5) was determined (4). Other accompanying findings (asymmetrical density increase, parenchymal distortion) on mammography were recorded. Then, USG examination was performed on these patients. All sonographic examinations were performed with the Toshiba Aplio 500 machine (software version 6.0, Toshiba Medical Systems, Tokyo, Japan). First, routine breast USG was performed on both breasts. Then, the region containing the MC was tried to be localized according to the clock dial, its depth from the skin, its distance from the nipple, chest wall and intramammary lymph nodes. Sonographic findings (hypoechoic area, irregularly dilated ducts, microcyst cluster, parenchymal distortion) accompanying MC areas that could be detected as echogenic focus on USG were evaluated. The USG images of the patients were retrieved retrospectively from the PACS system and evaluated by a consensus of two radiologists (YK and NU) experienced in breast radiology.

Biopsy Technique

Sampling of mammographic MCs that could be detected by USG was performed under local anesthesia with a 14-gauge fully automatic core needle (Geotek, Ankara, Turkey). At least 5 samples were taken from each lesion. Whether the samples taken contained MC was evaluated with the X-ray of the specimen, and if it did not contain MC, the biopsy procedure was repeated. All biopsy procedures were performed under sterile conditions and the samples were sent to the pathology laboratory in sterile boxes.

Histopathological Evaluation

The histological type and grade of the samples (according to the Scarff-Bloom-Richardson grading system), estrogen receptor, progesterone receptor status and human epidermal growth factor receptor (HER)-2 positivity were examined.

Statistical Analysis

Data were evaluated numerically and as a percentage. Since the overall number of cases was relatively small, inferential statistical analysis was not performed.

YÖNTEMLER

Hasta Grubu

Retrospektif olarak tasarlanan bu çalışmada, hastanemizin bağlı bulunduğu Gaziosmanpaşa Eğitim ve Araştırma Hastanesi Etik Kurul Komitesi’nden 14/04/2021 tarihli, 252 numaralı etik kurul onayının alınmasının ardından, Haziran 2019-Ocak 2021 tarihleri arasında, bölümümüzde BI-RADS 4 veya 5 şüpheli MK saptanan ve USG eşliğinde kalın iğne biyopsisi uygulanan hastalar değerlendirildi. MK alanı USG ile tespit edilebilen ve kitle eşlik etmeyen hastalar çalışmaya dahil edildi. Daha önce meme ameliyatı geçirmiş, meme kanseri tedavisi görmüş, devam eden hamilelik veya emzirme dönemindeki hastalar çalışmadan dışlandı. Ayrıca tüm hastalardan imzalı bilgilendirilmiş onam formu da alındı.

Görüntüleme Metodu ve Görüntü Analizi

Tüm hastaların hastanemiz mamografi cihazı (Giotto Image MC, IMS, Italy) ile standardize mediolateral oblik ve kraniokaudal pozisyonlarda görüntüleri alındı. Hastalara ait mamografi görüntüleri hastane Görüntü Arşivleme ve İletişim Sistemi’nden (PACS) retrospektif olarak çağırılarak incelendi. Hastalar BI-RADS 5. edisyona (2013) göre mamografik meme dansitesi (Tip A-B-C-D), MK tipi (amorf, ince pleomorfik, kaba heterojen, ince lineer ve ince pleomorfik dallanan), dağılım paternine (kümeleşmiş, bölgesel, segmental, diffüz, lineer) göre değerlendirildi ve BI-RADS kategorisi (4A, 4B, 4C, 5) belirlendi (4). Mamografide eşlik eden diğer bulgular (asimetrik dansite artışı, parankimal distorsiyon) kaydedildi. Hastalar USG ile değerlendirildi. Tüm sonografik incelemeler Toshiba Aplio 500 (yazılım sürümü 6.0, Toshiba Medikal Sistemleri, Tokyo, Japonya) cihazı ile yapıldı. Öncelikle her iki memeye rutin meme USG, ardından MK içeren bölge, saat kadranı, deriden derinliği, meme başı, göğüs duvarı ve meme içi lenf nodlarına uzaklığına göre lokalize edilmeye çalışıldı. USG’de ekojenik fokus olarak saptanabilen MK alanlarına eşlik eden sonografik bulgular (hipoekoik alan, düzensiz dilate duktuslar, mikrokist kümesi, parankimal distorsiyon) değerlendirildi. Hastaların alınan USG görüntüleri retrospektif olarak PACS sisteminden çağırılarak, meme radyolojisi konusunda deneyimli iki radyolog tarafından (Y.K. ve N.U.) oluşan ortak bir konsensüs ile değerlendirildi.

Biyopsi Tekniği

USG ile saptanabilen mamografik MK’lerin örneklemesi lokal anestezi altında 14-gauge tam otomatik kalın iğne (Geotek, Ankara, Türkiye) ile yapıldı. Her lezyondan en az 5 örnek alındı. Alınan örneklerin MK içerip içermediği spesmen grafisi ile değerlendirildi, MK içermemesi durumunda biyopsi işlemi tekrarlandı. Tüm biyopsi işlemleri steril şartlarda yapılarak alınan örnekler steril kutularda patoloji laboratuvarına gönderildi.

Histopatolojik Değerlendirme

Alınan örneklerin, histolojik tipi ve derecesi (Scarff-Bloom- Richardson derecelendirme sistemine göre), östrojen reseptörü, progesteron reseptörü durumları ve insan epidermal büyüme faktörü reseptör (HER)-2 pozitifliği, değerlendirildi.

İstatistiksel Analiz

Veriler numerik ve yüzde olarak değerlendirildi. Genel olgu sayısı nispeten küçük olduğundan, çıkarımsal istatistiksel analiz yapılmadı.

RESULTS

Between June 2019 and January 2021, BI-RADS 4-5 MC were detected without accompanying mass in 50 of 9468 cases (0.7%) who underwent mammography in our hospital, and MCs could be detected by USG in 43 (83%) of these cases and core needle biopsy was performed under USG guidance. Seven patients with suspected MCs that were seen with mammography but could not be detected by USG were sent for excisional biopsy by mammography-guided wire marking (Figure 1). The mean age of the patients participating in the study was 45.27±8.58 (30-84). While 39 patients were detected by normal routine breast screening, 4 patients under the age of 40 with a family history applied with palpable stiffness. While mammographic breast density was type C in 63% (n=27) of the patients, type D in 23% (n=10) and type B in 14% (n=6), no patients were found in type A category. 48.8% (n=21) of the calcifications were fine pleomorphic, 30% (n=13) amorphous, 16% (7) coarse heterogeneous, 4.6% (2) fine pleomorphic branching type. The mean mammographic MC area was 35.60±19.24 mm (7-90). While 70% (n=30) of the patients had asymmetrical density accompanying MCs on mammography, parenchymal distortion was found in 12% (n=5); on USG, hypoechoic area was found in 56% (n=24) of the patients, irregular ductal ectasia in 19% (n=8), parenchymal distortion in 9% (n=4) and microcyst cluster was the accompanying pathology in 10% (n=4).

As a result of histopathological evaluation, benign pathology was found in 42% of patients (n=18). In the benign group, 10 patients had non-proliferative fibrocystic change (NPFC) [fibrosis (n=3), apocrine change (n=1), mild ductal hyperplasia (n=2), and NPFC (n=4)]; 8 patients were diagnosed with PFC [usual ductal hyperplasia without atypia (n=3), fluoride type hyperplasia without atypia (n=1), columnar cell hyperplasia without atypia (n=1), sclerosing adenosis (n=2), and complex sclerosing lesion (n=1)]. An accompanying invasive component in the absolute pathology was detected in 10 patients who were diagnosed and marked with DCIS by core needle biopsy and referred for surgical operation. In total, 16% (n=7) of patients had DCIS [cribriform (n=5), comedo (n=2)] and 42% of patients (n=18) had malignant [invasive ductal carcinoma with in situ component (IDC+DCIS) (n=10); pure IDC (n=7); invasive lobular carcinoma (n=1)] diagnosis. According to nuclear grading, 6 of DCIS were low grade (grade 1) and luminal A subtype, 1 was high grade (grade 2) and HER-2 (+). Rest of the malignant lesions were high grade grade 2-3) [8 luminal A, 3 luminal B, 7 HER-2 (+)] except one.

While the most common type of MC was fine pleomorphic in the benign group, the most common type of MC was amorphous MC in the PFC group and fine pleomorphic MC in the NPFC group. While the most common accompanying USG finding was a hypoechoic background in the malignant group (n=17) and NPFC group (n=6), the most common accompanying finding in the PFC group (n=3) was ductal ectasia. In the malignant group, while ductal ectasia was observed in the DCIS group (pure DCIS and DCIS with IDC), it was a finding that was not observed in pure invasive cancers. While microcyst clusters were observed in the PFC group (n=2) and DCIS group (n=2), no microcyst clusters were found in the NPFC group and invasive ductal carcinoma group. The findings are summarized in Table 1. Case examples are shared in Figure 2-6.

DISCUSSION

Mammography is the most reliable imaging method used to detect and characterize MCs (13). BI-RADS was developed by the American College of Radiology in order to use a common language by making a standardized assessment (16). As stated in the BI-RADS mammography edition; skin and vascular calcifications, coarse or popcorn type, round, rim, dystrophic, tea-cut, suture calcifications are ate typically benign calcifications; amorphous, coarsely heterogeneous, fine pleomorphic and fine pleomorphic branching MCs are considered suspicious (17). In addition, the distribution of MCs is also important in terms of predicting malignancy; MCs with linear and segmental distribution are the riskiest distribution pattern in terms of malignancy (13,16,18). Those with bilateral diffuse distribution are MCs that generally develop on the basis of fibrocystic disease (4,16). The estimated value of BI-RADS for malignant MCs (BI-RADS 4-5) varies between 13% and 70% (16). Although stereotaxic biopsy is the most reliable method in the evaluation of suspicious patients, USG-guided biopsy is more advantageous compared to stereotaxic biopsy due to the above-mentioned features (12,19). The disadvantage is that not all MCs without an accompanied mass can be detected by USG. While MCs in the 50-100 micron range can be observed on mammography, those in the 200-500 micron range can be observed on USG (20). Benign MCs that do not accompany the mass can usually be overlooked due to mottling artifact in the echogenic breast tissue, while malignant MC areas can be observed more easily with USG due to the hypoechoic pathological background (10,12). In our study, we were able to detect 83% of suspicious and non-mass MCs with USG, and this rate is within the limits of the literature (6,9,11,15,18,21). The malignancy risk of suspected MCs that can be detected by USG is higher than those detected only by mammography (12,22,23). In our study, the majority of MCs detected by USG were malignant. In our study, the most common accompanying finding on USG in the malignant group was hypoechoic background, while in the benign group, the MC area was mostly observed on an isoechoic background. This finding is consistent with the literature (10). In USG, MCs can be seen as an echogenic focus alone, or they can be associated with irregular ductal ectasia with thickened walls, microcyst clusters, parenchymal distortion areas, heterogeneous hypoechoic areas or mass formation (10-12). These findings can be observed in both benign fibrocystic diseases and malignancy (12,14). In our study, ductal ectasia and microcyst clusters are observed in PFCs, in DCIS with accompanying pure DCIS and invasive component, and they were not observed in the group with pure invasive cancer. The MCs that we could detect with USG were the MCs that clustered most frequently, followed by segmental and regional distribution. When the MC area was evaluated, except for two of the cases (7 mm and 8 mm, both were invasive ductal carcinoma), the largest diameter of all was more than 1 cm. While 62% of breasts with MC that can be observed by USG were category BI-RADS type “C”, no type “A” breasts were observed.

Fine pleomorphic type was the most commonly detected among MCs that could be observed by USG in both the malignant and benign groups, and the least common was the fine pleomorphic branching type. There are literature studies showing that the fine pleomorphic type is observed more frequently with USG (15,21,24). The low number of thin pleomorphic branching type can be explained by the exclusion of lesions accompanying the mass from the study. In the benign group, 8 had a cystic component and 6 had ductal ectasia. 6 of these patients had amorphous MC on mammography, 1 had coarse heterogeneous MC and 2 had fine pleomorphic MC. The majority of benign MCs without an accompanying cysts or dilated ducts were observed as echogenic spots on an isoechoic background, and the mammographic MC shape was amorphous and fine pleomorphic type.

The gold standard imaging method in the evaluation of MCs is mammography (5). The reason for investigating this area with USG is that the mass component, which is the marker of the possible invasive area, can be determined by USG and it allows biopsy to be performed from this solid area. Our study showed that USG is a useful method in the evaluation and biopsy of MCs without a mass. According to our results, we observed that hypoechoic background is a helpful finding in malign lesions and microcystic structures in lesions containing more in situ components, but it is not typical and can be observed in benign lesions as well. Prospective studies with larger number of patients are needed to reveal the importance of these accompanying findings in the prediction of malignancy and invasiveness.

Study Limitations

The most important limitation of our study is the small number of patients. Another limitation of ours is the lack of long-term follow-up of patients who had benign results with core biopsy. In our study, MCs occupying less than 0.7 cm could not be evaluated because they could not be observed by USG. In addition, another limitation of our study is that USG is operator dependent and researchers may have dissensus.

TARTIŞMA

Mamografi, MK’leri saptamak ve karakterize etmek için kullanılan en güvenilir görüntüleme yöntemidir (13). Standardize bir değerlendirme yaparak ortak dil kullanmak amacıyla Amerikan Radyoloji Koleji tarafından BI-RADS geliştirilmiştir (16). BI-RADS mamografi edisyonunda belirtildiği üzere; deri ve damar kalsifikasyonları, kaba ya da popcorn tipi, yuvarlak, rim, distrofik, kalsiyum sütü, sütür kalsifikasyonları tipik benign kalsifikasyonlar; amorf, kaba heterojen, ince pleomorfik ve ince pleomorfik dallanan MK’ler ise şüpheli olarak değerlendirilmektedir (17). Ayrıca MK’lerin dağılım şekli de maligniteyi öngörme açısından önemli olup; lineer ve segmental dağılım gösteren MK’ler malignite açısından en riskli dağılım paternidir (13,16,18). Bilateral diffüz dağılım gösterenler ise genellikle fibrokistik hastalık zemininde gelişen MK’lerdir (4,16). Malign MK’ler (BI-RADS 4-5) için BI-RADS’nin tahmini değeri %13 ile %70 arasında değişmektedir (16). Stereotaksik biyopsi şüpheli olanların değerlendirilmesinde en güvenilir yöntem olmakla birlikte stereotaksik biyopsi ile karşılaştırıldığında, USG rehberliğinde biyopsi yukarıda bahsedilen özellikleri nedeniyle daha avantajlıdır (12,19). Dezavantajı ise kitle eşlik etmeyen MK’lerin hepsinin USG ile saptanamamasıdır. Mamografide 50-100 mikron aralığındaki MK’ler izlenebilirken, USG’de 200-500 mikron aralığındakiler izlenebilmektedir (20). Kitleye eşlik etmeyen benign MK’ler genellikle ekojenik meme dokusunda beneklenme artefaktı nedeniyle gözden kaçabilirken, malign MK alanları patolojik hipoekoik patolojik zemin nedeniyle USG ile daha kolay izlenebilmektedir (10,12). Çalışmamızda USG ile şüpheli ve kitle eşlik etmeyen MK’lerin %83’ünü saptayabilmiş olup bu oran literatür sınırları içerisindedir (6,9,11,15,18,21). USG ile saptanabilen şüpheli MK’lerin malignite riski yalnızca mamografi ile saptananlara oranla daha yüksektir (12,22,23). Bizim çalışmamızda da USG ile saptanabilen MK’lerin çoğunluğu malign tipteydi. Çalışmamızda malign grupta USG’de en sık eşlik eden bulgu hipoekoik zemindi, benign grupta ise MK alanı daha çok izoekoik bir zeminde izlenmekteydi. Bu bulgu literatür ile uyumludur (10). USG’de MK’ler tek başlarına ekojenik fokus olarak görülebildikleri gibi, duvarı kalınlaşmış düzensiz duktal ektaziler, mikrokist kümeleri, parankimal distorsiyon alanları, heterojen hipoekoik alanlar ya da kitle formasyonu ile birliktelik gösterebilirler (10-12). Söz konusu bu bulgular; hem benign fibrokistik hastalıklarda hem de malignitede izlenebilmektedir (12,14). Çalışmamızda duktal ektazi ve mikrokist kümeleri PFKD’de, saf DKİS ve invaziv komponentin eşlik ettiği DKİS’lerde izlenmekte olup saf invaziv kanser saptanan grupta izlenmemiştir. USG ile saptayabildiğimiz MK’ler en sık küme yapmış, sonrasında segmenter ve bölgesel dağılım gösteren MK’lerdi. MK alanı değerlendirildiğinde olguların ikisi hariç (7 mm ve 8 mm, ikisi de invaziv duktal karsinom idi) hepsinin en geniş çapı 1 cm’den fazlaydı. USG ile izlenebilen MK içeren memelerin %62’si kategori BI-RADS tip “C” olup tip “A” meme izlenmedi.

Hem malign hem benign grupta USG ile izlenebilen MK’ler en çok ince pleomorfik tip olup en az ince pleomorfik dallanan tipti. İnce pleomorfik tipin USG ile daha sık izlendiğine dair literatür çalışmaları mevcuttur (15,21,24). İnce pleomorfik dallanan tipin ise az sayıda olması ise kitle eşlik eden lezyonların çalışmadan dışlanması ile açıklanabilir. Benign grubun 8’inde kistik komponent, 6’sında duktal ektazi mevcuttu. Bu hastaların 6’sında mamografide amorf MK, birinde kaba heterojen ikisinde de ince pleomorfik MK mevcuttu. Kist veya dilate duktus eşlik etmeyen benign MK’lerin ise çoğunluğu izoekoik zeminde ekojenik noktalar şeklinde izlendi. Mamografide ise bu kalsifikasyonlar o amorf ve ince pleomorfik tipteydi.

MK’lerin değerlendirilmesinde altın standart görüntüleme yöntemi mamografidir (5). USG ile bu alanın araştırılmasının sebebi ise muhtemel invaziv alanın belirteci olan kitlesel komponentin USG ile belirlenebilmesi ve biyopsinin bu solid alandan yapılmasına olanak tanımasıdır. Çalışmamız göstermiştir ki kitle eşlik etmeyen MK’lerin değerlendirilmesinde ve biyopsi yapılmasında USG işe yarayabilen bir yöntemdir. Sonuçlarımıza göre, hipoekoik zeminin daha çok malign lezyonlarda, mikrokistik yapıların ise daha çok in situ komponent içeren lezyonlarda yardımcı olabilecek bir eşlikçi bulgu olduğu ancak tipik olmadığını, benign lezyonlarda da izlenebileceğini gözlemledik. Malignite ve invazivlik tahmininde bu eşlik eden bulguların önemini ortaya koymada daha fazla hasta sayısı ile yapılacak prospektif çalışmalara ihtiyaç vardır.

Çalışmanın Kısıtlılıkları

Çalışmamızın en önemli limitasyonu hasta sayımızın az olmasıdır. Bir başka limitasyonumuz ise kalın iğne biyopsi sonucu benign olarak sonuçlanan hastaların uzun süreli takiplerinin yapılmamış olmasıdır. Çalışmamızda 0,7 cm’den az yer kaplayan MK’ler USG ile seçilemediği için değerlendirilememiştir. Ayrıca USG’nin operatör bağımlı olduğu ve araştırmacıların görüş ayrılığı olabileceği de çalışmamızın bir başka sınırlayıcı yanıdır.

CONCLUSION

Although USG is a limited imaging method in the evaluation of MCs, it is a technique that can help radiologists to increase the specificity of mammography especially in the evaluation of MC clusters larger than 1 cm, determine the indication and priority of biopsy, and guide the biopsy procedure.

Ethics Committee Approval: This retrospective study was conducted following Gaziosmanpaşa Training and Research Hospital Ethics Committee approval (approval number: 252, approval date: 14/04/2021).

Informed Consent: Informed consents was obtained in order to use the recorded data of the patients.

Peer-review: Externally peer-reviewed.

Author Contributions: Surgical and Medical Practices - E.Y., A.N.Ş.; Concept - Y.K., N.U.; Design - Y.K.; Data Collection and/or Processing - Y.K., N.U.; Analysis and/or Interpretation - Y.K., D.E.T.Ş.; Literature Search - D.E.T.Ş.; Writing - Y.K., D.E.T.Ş.

Conflict of Interest: The authors have no conflict of interest to declare.

Financial Disclosure: The authors declared that this study has received no financial support.

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