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Year : 2018  |  Volume : 17  |  Issue : 3  |  Page : 117-124  

Role of high resolution ultrasound complementary to digital mammography

Department of Radiodiagnosis, Dayanand Medical College and Hospital, Ludhiana, Punjab, India

Date of Web Publication31-Aug-2018

Correspondence Address:
Dr. Kamini Gupta
Department of Radiodiagnosis, Dayanand Medical College and Hospital, Ludhiana - 141 001, Punjab
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/aam.aam_36_17

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Background: Breast carcinoma is a major cause of mortality among women worldwide. Early detection and cure is the key to reduce the mortality of the disease. This article studied the role of high resolution ultrasound in detection and characterization of lesions to complement mammographic diagnosis and improve patient management. Aims and Objectives: To evaluate the role of complementary high resolution ultrasound, BIRADS scoring and to correlate it with histological diagnosis. Results and Observations: HRUS is excellent in detecting microcalcifications, malignant features of solid masses, differentiating focal asymmetry from masses, differentiating between solid and cystic lesions, simple and complex cysts and detecting satellite lesions and mammographically inaccessible areas for which special views can be done. Conclusions: Every case referred for digital mammography should undergo ultrasound irrespective of the age, symptoms and density of the breast parenchyma and a combined final BIRADS grading should be done. Ultrasound is an excellent imaging modality for breast lesions in expert hands.

   Abstract in French 

Contexte: Le cancer du sein est une cause majeure de mortalité chez les femmes du monde entier. La détection précoce et la guérison sont la clé pour réduire la mortalité de la maladie. Cet article a étudié le rôle de l'échographie à haute résolution dans la détection et la caractérisation des lésions pour compléter le diagnostic mammographique et améliorer la prise en charge des patients. Buts et objectifs: Évaluer le rôle de l'échographie à haute résolution complémentaire, notation de BIRADS et la corréler avec le diagnostic histologique. Résultats et observations: Le HRUS est excellent pour détecter les microcalcifications, les malignités des masses solides, différencier l'asymétrie focale des masses, différencier les lésions solides et kystiques, les kystes simples et complexes et détecter les lésions satellites et les zones mammographiquement inaccessibles. Conclusions: Chaque cas référé pour la mammographie numérique devrait subir une échographie indépendamment de l'âge, des symptômes et de la densité du parenchyme mammaire et un classement final combiné de BIRADS devrait être fait. L'échographie est une excellente modalité d'imagerie pour les lésions mammaires chez les mains expertes.

Keywords: Carcinoma, digital mammography, high resolution, intraductal, microcalcifications, ultrasound

How to cite this article:
Gupta K, Sandhu P, Arora S, Bedi G. Role of high resolution ultrasound complementary to digital mammography. Ann Afr Med 2018;17:117-24

How to cite this URL:
Gupta K, Sandhu P, Arora S, Bedi G. Role of high resolution ultrasound complementary to digital mammography. Ann Afr Med [serial online] 2018 [cited 2023 Sep 24];17:117-24. Available from:

   Introduction Top

Ultrasonography (USG) of breast is a useful adjuvant modality to X-ray mammography. Its role is well established in differentiating solid from cystic lesions. It also characterizes whether a cyst is simple or complex. Ultrasound (US) is also the modality of choice to characterize palpable lumps in radiographically dense breasts.[1] Recently, there is a focus on the advantages of combining high-resolution US imaging findings with those of X-ray mammography in characterization of breast lesions. Every case whether symptomatic or asymptomatic referred for digital mammography (DM) should also undergo USG. Radiologists should complement the diagnosis of one modality with other so as not to miss any lesion suspicious or diagnostic of breast cancer.

Breast cancer is the most common malignancy of women worldwide and is a leading cause of death.[2] To reduce the cancer-related mortality, early diagnosis and treatment is a must. Five-year survival of early localized breast cancer can be up to 99%. If the cancer spreads to distant organs, 5-year survival rate drops to 24%.[3] High-resolution US (HRUS) is an efficient modality to detect microcalcifications with a sensitivity of 95%.[4] It can also pinpoint an intraductal lesion in the hands of an experienced and skilled radiologist.

In the present study, findings of USG of breasts when combined with those of DM led to better characterization of lesions as benign or malignant and provided a more accurate imaging diagnosis and Breast Imaging-Reporting and Data System (BIRADS) grade. USG also guided the radiologist to choose an appropriate lesion for biopsy in multicentric and multifocal lesions.

Aims and objectives

  1. To perform HRUS of each patient referred for DM
  2. To analyze US findings and to correlate them with mammographic findings so as to provide a final combined BIRADS score
  3. To evaluate additional advantages of HRUS over DM
  4. To compare imaging diagnosis with final biopsy diagnosis, wherever available.

   Materials and Methods Top

Technique of imaging the breast

In all patients, DM was carried out on M/S Wipro GE Healthcare Pvt. Ltd machine – Alpha RT (Model 2013) in the Department of Radiodiagnosis and Imaging, Dayanand Medical College and Hospital, Ludhiana. It was followed by HRUS on (Philips IU22, Model 2011) US machine using linear probe (5–12MHz).

DM is an outpatient procedure preferably done after 1 week of start of menstrual period. During mammography, a qualified radiotechnician positioned the breast in the mammography unit. Breast was placed on a special platform and compressed with a clear plastic paddle. Mediolateral oblique and craniocaudal images were acquired. Supplementary views were taken, whenever necessary.

HRUS was done with 5–12 MHz linear transducer, which has high sensitivity for superficial tissues. Minimum compression was given while performing the procedure. Whole of the breast parenchyma was scanned meticulously in a complete circle starting from 12 o'clock position. Axilla was also scanned in all the patients for any lymphadenopathy.

Patient preparation

Before starting the study, proper history was taken. The procedure was explained to the patient in her vernacular language to allay the fear and anxiety.

Case histories

Case 1

DM of 47-year-old multiparous female showed a high-density irregular lesion causing architectural distortion with microcalcifications in the retroareolar and medial aspect of breast [Figure 1]. It was a BIRADS grade 5 lesion. Complementary US confirmed microcalcifications [Figure 2]a and [Figure 2]b (magnified view), arrow] and provided additional signs of malignancy such as marked hypoechogenicity and microlobulations of the lesion. A core biopsy was performed in the same setting, which confirmed the lesion to be an invasive ductal carcinoma (IDC). In addition, dilated anechoic ducts were noted in retroareolar region [Figure 2]c. No satellite lesions or axillary lymph nodes were detected [Figure 2]d.
Figure 1: Digital mammography in a case of intraductal carcinoma shows a high-density irregular lesion with microcalcifications causing architectural distortion in the retroareolar and medial aspect of breast (craniocaudal view view)

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Figure 2: High-resolution ultrasound shows an irregular, hypoechoic mass with microcalcifications (a and b) and peripheral hyperechogenicity confirming the malignant nature of the mass. In addition, dilated anechoic ducts are seen in retroareolar region (c). No satellite lesions or axillary lymph nodes are noted (d)

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Case 2

A female presented with blood stained nipple discharge and had a family history of breast cancer. Her right breast DM revealed a lobulated tortuous high-density lesion in the outer and upper quadrant. Few discrete foci of calcifications were also noted [Figure 3]a and [Figure 3]b. No clusters of microcalcifications were seen. It was BIRADS 4c (highly suspicious of malignancy; in view of positive family and clinical history along with a unifocal dilated duct). HRUS revealed a dilated tortuous duct with an intraductal solid mass containing microcalcifications [Figure 3]c and was categorized as grade 5 lesion.
Figure 3: Digital mammography in a patient of ductal carcinoma in situ showing a lobulated tortuous high-density lesion in the outer and upper quadrant of right breast. Few discrete foci of calcifications are noted (a and b). High-resolution ultrasound reveals a dilated tortuous duct with an intraductal solid mass having microcalcifications (c)

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Case 3

A 58-year-old woman came for routine screening mammography. Her DM showed predominantly fatty breasts with focal high-density asymmetrical areas. Her left breast had a few irregular periareolar high-density areas [Figure 4]. No microcalcifications were noted. A lymph node with fatty hilum was seen in axilla in the mediolateral oblique view. It was given BIRADS grade 4a. HRUS showed a high-density angulated and spiculated lesion measuring 1.0 cm × 0.8 cm with peripheral increased echogenicity in the upper medial quadrant of left breast [Figure 5]a. Few retroareolar ducts were just prominent [Figure 5]b. It was diagnosed BIRADS 4c. Biopsy revealed a lobular carcinoma.
Figure 4: Digital mammography of left breast shows few irregular periareolar small high density areas. No microcalcifications are seen. A lymph node with fatty hilum is seen in axilla

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Figure 5: High-resolution ultrasound shows a high-density angulated lesion measuring 1.1 cm × 0.8 cm with peripheral spiculations and increased echogenicity in the upper medial quadrant of left breast (a). Few retroareolar ducts are just prominent (b) diagnosis confirmed as lobular carcinoma

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Case 4

A 36-year-old female came for screening mammography. Her DM revealed predominantly fatty breasts with coarse benign scattered calcifications. A smooth marginated oval to round lesion was seen in the upper and outer quadrant [Figure 6]. No microcalcifications or architectural distortion was noted. It was BIRADS grade 0.
Figure 6: Digital mammography shows a smooth marginated oval to round lesion in the upper and outer quadrant (a). No microcalcifications or architectural distortion noted. Repeat MLO view confirms the superficial nature of the lesion (b)

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As a routine protocol, HRUS was performed, and a mole was seen on the breast skin [Figure 7]a. The mole was limited to skin and subcutaneous fat only [Figure 7]b. DM was repeated keeping the skin lesion along the surface, and the superficial nature of lesion was confirmed [Figure 6]b.
Figure 7: The sonologist could see a mole on the breast skin (a). High-resolution ultrasound shows it to be limited to skin and subcutaneous fat only (b)

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Case 5

A 37-year-old female came with complaint of diffuse cyclical mastalgia. Her mammogram revealed high-density breasts without any focal lesion, asymmetry, or architectural distortion [Figure 8]. It was BIRADS grade 0. HRUS revealed extensive ductal prominence with caliber varying from 2.4 to 3.5 mm [Figure 9]a. Few ducts showed focal solid lesions [Figure 9]b, arrow] and microcalcifications. Twinkling star artifact could be demonstrated in these microcalcifications [Figure 9]c and [Figure 9]d. It was reported grade 5, and surgical biopsy confirmed the diagnosis of IDC.
Figure 8: Digital mammography of a 37-year-old uniparous female reveals high-density breasts without any focal lesion, asymmetry or architectural distortion

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Figure 9: High-resolution ultrasound shows extensive ductal prominence (a) with a few of the ducts showing focal solid masses (b, arrow) as well as microcalcifications. Twinkling star artifact can be seen in these microcalcifications (c and d); Diagnosis confirmed as ductal carcinoma in situ

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Case 6

A 52-year-old female presented with a hard breast mass. DM revealed a well-defined, smooth marginated, round high-density lesion in periareolar location [Figure 10]. It was graded as BIRADS 3. HRUS revealed a thick-walled cystic lesion with an eccentric, solid, polypoidal, and avascular component [Figure 11]. It was upgraded to BIRADS 4c. Needle aspiration revealed lobular carcinoma.
Figure 10: Digital mammography in a case of lobular carcinoma reveals a well-defined, smooth marginated, round high-density lesion in the periareolar location

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Figure 11: High-resolution ultrasound reveals it to be a thick-walled cystic lesion with an eccentric solid polypoidal component

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Case 7

A 34-year-old woman had predominantly dense breasts with mixed fibroglandular tissue. A well-defined macrolobulated/angular lesion was seen in the upper medial quadrant on DM. No microcalcifications were noted [Figure 12]. It was labeled grade 3. On US, it was an anechoic, thin-walled cyst with distal acoustic enhancement [Figure 13] and thus downgraded to BIRADS grade 2.
Figure 12: Digital mammography in a 34-year-old female with positive family history shows a well-defined macrolobulated/angular lesion in the upper medial quadrant. No microcalcifications are noted

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Figure 13: On ultrasound, it is a clean, anechoic, thin-walled cyst with distal acoustic enhancement confirming it to be a simple benign cyst

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Case 8

An already operated case of carcinoma breast presented with diffuse skin thickening. Her mammogram revealed diffuse thickening of skin and nipple retraction without any focal lesion [Figure 14]. On US, skin and subcutaneous fat were echogenic and thickened [Figure 15]a with dilated subcutaneous veins [Figure 15]b. On increasing depth resolution, there was an ill-defined hypoechoic lesion [Figure 15]c. Further examination with convex probe revealed multiple enlarged, hypoechoic, lobulated axillary lymph nodes [Figure 15]d causing vascular compression. Repeat mammogram focusing the axilla revealed enlarged lymph nodes [Figure 16]. Metastatic deposits were confirmed on lymph node biopsy.
Figure 14: Digital mammography of an operated and treated case of carcinoma breast showing diffuse thickening of skin and nipple retraction without any focal lesion

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Figure 15: Ultrasound shows thickening and increased echogenicity of skin and subcutaneous fat (a). Dilated subcutaneous veins are seen (b). On increasing depth, there is an ill-defined hypoechoic lesion (c). Image taken with convex probe reveals multiple enlarged hypoechoic lobulated axillary lymph nodes (d)

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Figure 16: Repeat mammogram focusing the axilla shows enlarged nodes indicating metastases

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   Results and Observations Top

A series of eight cases referred to the Department of Radiodiagnosis for DM with breast-related symptoms or for routine screening were analyzed. Out of which, five were multiparous women of age more than 40 years and three were uniparous and <40 years of age. US contributed to the characterization of breast lesions, and a combined sonographic and mammographic BIRADS score was found to be more accurate in diagnosing and labeling a lesion either benign or malignant. US BIRADS grade confirmed the mammographic grade in 1 case, downgraded in 2 cases, and upgraded in 5 cases. Core biopsy of the lesions could be done under US guidance. Certain mammographically inaccessible areas could be examined on sonography. It added to the staging of disease. [Table 1] and [Table 2] show the clinical details and diagnostic workup along with final diagnosis of the cases discussed.
Table 1: Age distribution, Clinical symptoms and History data of patients referred for digital mammography (n=8)

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Table 2: Digital mammography, High resolution ultrasound and Final biopsy findings of patients (n=8)

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   Discussion Top

US is an adjuvant imaging modality to DM. It is easily available, radiation-free, inexpensive, needs no contrast injection, and patient friendly. The only limitation is that it is operator dependent and requires skill and experience for interpretation.

In the last decade, continuous advances in the US technology such as tissue harmonic imaging and frequency compounding made significant improvement in the image quality. Resolution of details has revolutionized sonography. The precursor lesions of breast carcinoma such as ductal carcinoma in situ (DCIS) is the center of attention nowadays. The various sonographic signs of DCIS have been described such as attenuation of echo of the normal breast adipose tissue and horizontal spread in the form of dilated ducts and architectural distortion. The signs of malignant masses are posterior acoustic shadowing and echogenic halo in addition to microcalcifications.

Yang et al. in 2014 demonstrated that considering DM as the gold standard; US could achieve a sensitivity of 95%, specificity of 87.8%, and accuracy of 91% in the detection of microcalcifications. Histopathology had a sensitivity of 80%, specificity of 71.4%, and accuracy of 75.3%. They highlighted that US was more sensitive in the detection of microcalcification in breast cancer cases, especially when it is within a mass lesion and is a reliable diagnostic sign of carcinoma.[4] Similarly, in the present study, HRUS confirmed the malignant nature of breast masses, and a tissue diagnosis from the most suspicious area could be obtained by taking a biopsy in the same setting under US guidance. HRUS could directly visualize the intraductal mass and detect occult microcalcifications. This helped in upgrading the BIRAD score of a lesion in an appropriate clinical setting.

Nagashima et al. in 2005 concluded that US examination is an effective method to identify and localize breast microcalcifications, especially when present within the mass and can be used as an alternative to stereotactic localization in the selected patients with early breast cancer.[5]

Samardar et al. in 2002 described that invasive lobular carcinoma is thought to arise from the terminal ductules and invades the normal breast parenchyma in a single “Indian-file” pattern. Because of this pattern, the tumor manifests as a subtle area of distortion or asymmetry. If such lesions are detected at DM, a supplementary breast imaging with additional views and US can be key to diagnosis.[6] It was also observed in this study that HRUS helped in differentiating focal asymmetry from a mass lesion in a clinically asymptomatic female.

Berg et al. opined that over 90% of cancers seen only on US were found in females with more than 50% dense breast tissue, suggesting that women with other risk factors may also benefit from screening USG. Thus, the addition of single screening USG to mammography for women with higher risk of breast cancer results in increased detection of breast cancers that are predominantly small in size.[7]

US in one of the case in present series which led to the evaluation of an extramammary benign soft-tissue lesion. There is only an occasional case reported in the scientific literature, in which multiple cutaneous neurofibromas were identified, and on mammography, a few projected over the parenchyma. In such cases, a proper clinical examination and USG helped.[8]

Okello et al. concluded that breast US resulted in a significant incremental breast cancer detection rate (of 27%) among symptomatic women with mammographically dense breast tissue. They also recommended that US should routinely be performed in mammographically dense breasts and in lesions with BIRADS score 3 and 4.[9]

Mujagić et al. concluded that in women younger than 50 with dense breasts, the sensitivity of US was significantly higher (33.3%) than mammography, while in women over 50 years with predominantly fatty beasts, this difference was only 4.7%.[10]

It is observed that DM is not the modality of choice for dense breasts as subtle lesions can be missed. US is the modality to accurately characterize lesions in dense breasts.

It has been shown by Berg and Gilbreath that US provides a more accurate measurement of the size of a mass than mammography or clinical examination.[11] Masciadri and Ferranti described the US features of simple and complex cysts and opined that US is the modality to differentiate between solid and cystic lesions and can diagnose simple cyst (BIRADS Grade 2) with high accuracy and sensitivity. Complex cysts require cytological correlation.[12] Fornage B also opined that US examination is an adjunct to mammography, as it can measure the primary breast tumor, detect and pathologically confirm additional lesions in a multicentric disease. It can also detect lymph nodal metastasis to axilla, supraclavicular or intramammary region and contralateral axilla in approximately 90% cases of breast cancer.[13] In the present study, it was observed that US can scan mammographically inaccessible areas.

It is observed that combined use of mammography and USG is appropriate in most instances to characterize various lesions and to avoid unnecessary interventions in cases in which imaging findings are unequivocally benign. Negative findings on combined mammography and sonography are highly reassuring to the patient. US is also an important modality to determine whether a clinically or mammographically apparent lesion is real or artifactual.

   Conclusions Top

This study concludes that mammographic screening for breast cancer is important, and its role cannot be underestimated. The role of high-resolution US in certain situations such as dense breasts, differentiation of focal asymmetry from a true lesion, differentiation between solid and cystic lesion, characterization of simple and complex cyst, screening of mammographically inaccessible areas, different lymph node stations, and of course direct visualization of intraductal mass with microcalcifications for guided biopsy is uncomparable to any other modality. It is highly efficient, cost-effective, and quick imaging technique for evaluating breast lesions.

Therefore, every case referred for DM should undergo US irrespective of the age, symptoms, and density of the breast parenchyma, and a combined BIRADS grading should be offered.


We would like to thank Department of Gynae and Surgery for referral of cases.

Financial support and sponsorship


Conflicts of interest

There are no conflicts of interest.

   References Top

Jackson VP. The role of US in breast imaging. Radiology 1990;177:305-11.  Back to cited text no. 1
Jemal A, Siegel R, Ward E, Hao Y, Xu J, Thun MJ, et al. Cancer statistics, 2009. CA Cancer J Clin 2009;59:225-49.  Back to cited text no. 2
American Cancer Society. Breast Cancer Facts & Figures 2013-2014. Atlanta: American Cancer Society, Inc. 2013.  Back to cited text no. 3
Yang WT, Suen M, Ahuja A, Metreweli C.In vivo demonstration of microcalcification in breast cancer using high resolution ultrasound. Br J Radiol 1997;70:685-90.  Back to cited text no. 4
Nagashima T, Hashimoto H, Oshida K, Nakano S, Tanabe N, Nikaido T, et al. Ultrasound demonstration of mammographically detected microcalcifications in patients with ductal carcinoma in situ of the breast. Breast Cancer 2005;12:216-20.  Back to cited text no. 5
Samardar P, de Paredes ES, Grimes MM, Wilson JD. Focal asymmetric densities seen at mammography: US and pathologic correlation. Radiographics 2002;22:19-33.  Back to cited text no. 6
Berg WA, Blume JD, Cormack JB, Mendelson EB, Lehrer D, Böhm-Vélez M, et al. Combined screening with ultrasound and mammography vs. mammography alone in women at elevated risk of breast cancer. JAMA 2008;299:2151-63.  Back to cited text no. 7
Cao MM, Hoyt AC, Bassett LW. Mammographic signs of systemic disease. Radiographics 2011;31:1085-100.  Back to cited text no. 8
Okello J, Kisembo H, Bugeza S, Galukande M. Breast cancer detection using sonography in women with mammographically dense breasts. BMC Med Imaging 2014;14:41.  Back to cited text no. 9
Mujagić S, Burina M, Mustedanagić-Mujanović J, Šarkanović G. The importance of combining of ultrasound and mammography in breast cancer diagnosis. Acta Med Acad 2011;40:27-33.  Back to cited text no. 10
Berg WA, Gilbreath PL. Multicentric and multifocal cancer: Whole-breast US in preoperative evaluation. Radiology 2000;214:59-66.  Back to cited text no. 11
Masciadri N, Ferranti C. Benign breast lesions: Ultrasound. J Ultrasound 2011;14:55-65.  Back to cited text no. 12
Fornage BD. Local and regional staging of invasive breast cancer with sonography: 25 years of practice at MD Anderson cancer center. Oncologist 2014;19:5-15.  Back to cited text no. 13


  [Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6], [Figure 7], [Figure 8], [Figure 9], [Figure 10], [Figure 11], [Figure 12], [Figure 13], [Figure 14], [Figure 15], [Figure 16]

  [Table 1], [Table 2]

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