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Breast cancer imaging: Mammography among women of up to 45 years

Anna Schnejder-Wilk

Department of Diagnostic Radiology, Centre of Oncology, M. Skłodowska-Curie Memorial Institute, Cracow Branch, Poland Author’s address: Anna Schnejder-Wilk, Department of Diagnostic Radiology, Centre of Oncology, M. Skłodowska-Curie Memorial Institute, Cracow Branch, Garncarska 11 Str., 31-115 Cracow, Poland, e-mail: anna.schnejder@interia.pl

Summary

Background:

Among women under the age of 40, screening mammography examinations are not performed routinely. An ultrasonography scan is considered to be a basic breast imaging examination among younger women. The purpose of this study was to analyze mammography images, as well as to evaluate the usefulness and role of mammography in breast cancer diagnostic processes in women of up to 45 years, based on own experience.

Material/Methods:

A retrospective analysis of mammography images, including 144 cases of breast cancer diagnosed in the group of 140 women of 45 years of age. All the patients underwent pre-treatment mammography and surgery procedure. The images were evaluated in accordance to BIRADS criteria. Lesions detectable in mammography were grouped as follows: • spiculated mass; • non- microcalcified oval/round mass; • microcalcified mass (regardless of shape); • microcalcifications;

• architectural distortion; • breast tissue asymmetry.

Results:

The most common mammographic symptom was solid tumor (41%), followed by microcalcified tumors (20.8%). Clusters of microcalcifications constituted 17.4% of mammography findings. In 4.9% of mammography scans, examination did not reveal any pathological lesions.

Conclusions:

Breast cancer mammograms of women aged up to 45 years do not differ from diagnostic pictures of breast cancer in older women.

The diagnostic appearance of breast cancer in 1/3 of the patients involved microcalcifications detectable only on mammograms.

All the women with suspicion of breast cancer should have their mammography examinations performed, irrespective of ultrasonography scans.

Key words: breast cancer • mammography • young women • microcalcifications

PDF fi le: http://www.polradiol.com/fulltxt.php?ICID=878431

Received: 2009.08.27

Accepted: 2009.09.30

Background

One of the major achievements in the fight against breast cancer was the introduction of mammography and the wide acceptance of mammography screening. In most of the countries, screening includes women aged over 50 years. American College of Radiology recommends to carry out mammography at the age of minimum 40 years.

Women under 40 are not subjected to screening mammo- graphic examinations, due to the relatively low incidence of breast cancer in that age group – approx. 12% of breast cancer cases. The risk of developing breast cancer before

the age of 40 years is less than 1%. Thus, it is believed that economic costs of population screening are too high with regard to the number of the diagnosed cases [1,2].

In young women, mammography is not a routine pro- cedure, even with clinical symptoms. Ultrasonography is considered to be a basic imaging procedure in breast examination in women aged up to 35 years. It allows for the diagnosis of a simple cyst and for avoidance of unnec- essary biopsies in case of palpable lesions. However, it is not fully reliable in differentiating benign mass lesions from the malignant ones [3]. Moreover, ultrasonography

O R I G I N A L A R T I C L E

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does not detect microcalcifications – a symptom present in approx. 40% of all infiltrating ductal carcinomas. As much as 75–83% of the intraductal carcinomas are detect- ed on the basis of microcalcifications found in mammo- grams [4].

The aim of the work was to analyze mammograms of breast cancer in women aged up to 45 years and to evalu- ate the usefulness and the role played by mammography in breast cancer diagnostics in women in the age of up to 45 years – based on own experiences.

Material and Methods

The study material included 140 women in the age range of 28–45 years, treated for breast cancer at the Center of Oncology in Cracow in the years 2000–2002. All the patients underwent mammography and surgical procedure, followed by histopathological examination of the lesion.

In the study group, there were 7 patients with bilateral breast cancer. Three of them underwent mammography of one breast cancer only. Thus, the mammographic analysis included 144 examinations.

Most of the patients presented to the doctor, being alarmed with the experienced symptoms. Only a few patients

presented because of their results of prophylactic imaging examinations that revealed breast lesions. The TNM stage of the cancers found in the study material was advanced in most of the cases. Table 1 presents clinical TNM classifica- tion of the analysed cases.

Table 2 shows the applied surgical and adjuvant treatment.

Mammograms of the diagnosed carcinomas were sub- jected to analysis. The images were assessed on the basis of BIRADS criteria (Breast Imaging Reporting and Data System) developed by the American College of Radiology.

Lesions found in mammograms were grouped as follows:

• spiculated mass – with irregular margin, not containing any microcalcifications;

• non-microcalcified oval/round mass;

• microcalcified mass (regardless of shape);

• microcalcifications: linear, branching; polymorphic, coarse-granulated; fine-granulated;

• architectural distortion;

• breast tissue asymmetry.

Results

Table 3 contains lesions detected in mammography and their incidence rate.

The most frequent symptom was the spiculated mass (Figure 1) – with irregular, stellate margins. This lesion accounted for 22.2% of all symptoms. The second most fre- quent symptom was the microcalcified mass, regardless of its shape (Figure 2), and present in 20.8% of the cases.

Round or oval masses, with regular outline (Figure 3) was seen in 18.8% of the cases. Ductal, irregular, branch- ing microcalcifications – forming continuous (Figure 4), as well as fine-granulated and coarse-granualted, clusters of microcalcifications (Figures 5,6) accounted for 17.4% of all mammographic lesions. In 12.5% of the cases, the lesions included breast tissue asymmetry (Figure 7). Architectural distortion of breast tissue stroma (Figure 8) was classi- fied as a separate group only when being the only symp- tom found in mammography – it was present in 3.5% of the cases. In 7 patients (4.9%), mammography did not reveal

TNM

Tis T1 T2 T3 T4

N0 a b c c M

N0 N1 N2 N0 N1 N2 N0 N1 N2 N3

N0 N1

Number of tumors % 2

1.4 1

0.7 13

9.0 22

15.3 2

1.4 47

32.6 24

16.7 2

1.4 6

4.2 5

3.5 1

0.7 3

2.1 7

4.9 1

0.7 0

0 1

0.7 Table 1. TNM classification of analysed cases.

Treatment Tumorectomy BCT Mastectomia

simplex Patey's

operation Chth + op. m.

Patey Operation m.

Halsted

Adjuvant treatment

chth hth rth

Number of cases 1 28 1 93 15 6 116 41 40

Table 2. Implemented treatment in the investigated group.

Mammography image Number of cases %

Spiculated mass 32 22.2

Oval mass 27 18.8

Mass + microcalcifications 30 20.8

Microcalcifications 25 17.4

Architectural distortion 5 3.5

Breast tissue assymetry 18 12.5

No lesions 7 4.9

Table 3. Mammography images of the analysed cases.

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any suspicious lesions. The sensitivity of the mammograph-

ic examination reached 95% in the studied material. The predominant radiological feature was the spiculated or the oval mass, without microcalcifications (41% in total).

Further 20.8% of the lesions revealed microcalcifications.

Figure 1. Spiculated mass. Hist-pat evaluation: Invasive ductal

carcinoma, T2N0. Figure 3. Round mass. Hist-pat evaluation: Invasive ductal carcinoma, T1N0.

Figure 4. Casting-type, branching microcalcifications hist-pat evaluation. Invasive ductal carcinoma, T2N1.

Figure 2. Mass with associated microcalcifications. Hist-pat

evaluation: Invasive ductal carcinoma, T2N1.

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In total, 38.2% of breast cancer cases showed microcalcifi- cations – within the mass lesion or as a separate symptom.

Microcalcifications were the only mammographic feature in all cases of 'in situ' carcinoma, as well as in 36.8% of infiltrating carcinomas with the intraductal component.

Ductal cancers accounted for 114 cases (i.e. 79% of the material), 48 out of which revealed microcalcifications.

Other histological types included 30 cases, with microcal- cifications in 7 cases. The analysis showed a statistically significant correlation between the presence of microcalci- fications and ductal cancers – P-value from the chi-square test for independence amounted to 0.053.

Discussion

Many studies have been trying to explain the interrela- tion between the young age of patients at the moment of

diagnosis and a worse prognosis of their breast cancer.

Authors of the studies underscore that factors connected with the worse prognosis are often seen in younger indi- viduals. These factors include: larger tumor, higher histo- logical grading, involvement of the vessels or lymph nodes, no hormonal receptors, tumors with a high S-phase frac- tion[5–12]. Some studies suggest that age is an indepen- dent prognostic factor of local and distal recurrences [8].

According to a common knowledge, approx. 15–30% of breast cancer cases among women aged under 35, are con- nected with BRCA1 or BRCA2 gene mutation. These lesions are characterized by: more frequent incidence of high his- tological grading, low expression of estrogen receptors and high rate of proliferation [5].

Figure 5. Fine-granulated microcalcifications. Hist-pat evaluation:

Comedo type intraductal carcinoma, clinically undetectable.

A

B

Figure 6. Polymorphic coarse-granulated microcalcifications. Hist-pat evaluation: Comedo type ductal carcinoma with invasive component, T1N0.

Figure 7. Focal asymmetric density. Hist-pat evaluation: Papillary

carcinoma, T3N1.

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The aggressive course of the disease provokes continu- ous discussions on the usefulness of diagnostic modalities in young women. Many countries that introduced screen- ing mammography campaigns, reserved them initially for women over 50 years old. Swedish studies revealed lower mortality due to screening in the age group of 40–49 years. Nowadays, the American College of Radiology rec- ommends covering with screening women from the age of 40. However, there are no uniform recommenda- tions on the diagnostic procedures for younger patients.

Ultrasonography, treated as a basic diagnostic method at that age, enables us to terminate the diagnostic process after finding a simple cyst (in patients with a palpable tumor) but it is not sufficient to evaluate the extent of sus- picious lesions.

I analyzed mammographic findings of breast cancer in women aged up to 45 years, focusing on the incidence of microcalcifications – symptoms of cancer which are detect- able by mammography only. The age limit was set at 45 years – after having assumed that all women at that age are prior to menopause. This limit was also applied by N.

Houssami in his studies, due to the hormonal status of women [13].

Mammographic findings in breast cancer in young women are the same as in the group of older individuals. The most commonly revealed lesion is the mass.

Masses with irregular spikulated margins are typical for cancers with predominant fibrosis and desmoplastic reac- tion of the connective tissue. Such tumors always suggest the presence of malignancy. In my material, spiculated

mass was found in 22.2% of the cases. E. Show de Paredes et al. revealed it in 27% of cases from the group of 89 can- cers in women aged up to 35 years [14].

Round or oval masses, with smooth or polycyclic (lobu- lated) outline, sometimes resembling a conglomerate of a few clustered tumors, may be hard to diagnose, especially in a dense, glandular structure, when the outline becomes invisible. Such tumors, especially the small ones, may be mistaken for benign lesions.

In the cases analysed by me, this kind of lesions could be seen in 18.8%. Similar results were obtained by E. Show de Paredes et al. – 19% [14]. It is worth underscoring that even in young patients, lesion of such kind should not be arbitrarily graded as benign. If the mass seen in mammog- raphy is not properly delineated, it is not surrounded by a 'halo', and it is hypoechogenic in USG, it should be referred for biopsy.

As much as 70.1% of patients from the study group pre- sented to the doctor because of a palpable tumor. It is not always possible to evaluate the type of lesion in a physical examination. Imaging studies in young women with pal- pable tumors aim at visualizing and assessing the type of tumor, as well as referring suspicious lesions for immediate biopsy [14].

In the studied material, microcalcifications were the only symptom of cancer in 17.4% of the evaluated cases. In fur- ther 20.8% of the cases, they could be seen within a vis- ible tumor. Thus, in 38.2% of the cases, microcalcifications indicated to breast malignancy. In the studies by E. Show de Paredes et al., microcalcifications within (or not within) the tumor were present in 38% of cases [14], in the mate- rial analysed by D.O. Jeffries et al. - in 31% [15], and in the paper by M. Muttarak et al. – in 28.7% of all cases [16].

C. Ferranti et al. studied interrelations between the age, mammographic findings and histopathologic characteristics of the tumor in nonpalpable breast cancers [17]. The analy- sis of 982 cases revealed microcalcifications as an indepen- dent symptom in 51% of the cases and microcalcifications connected with tumor or with abnormal tissue structure in the next 15% of the cases – 66% of the cases in total.

Moreover, they found a connection between microcalcifica- tions and non-invasive tumors in 93.6% of the cases – irre- spective of the patients' age. In case of invasive tumors, the incidence of microcalcifications was decreasing with age:

starting from 87.9% in women before 40 years of age and with 21.7% in patients over 70. They explained this inter- relation with the fact that in breasts of younger women – having a dense and inhomogeneous structure – nodular shadows may be invisible, while microcalcifications are always detected. The second explanation was that micro- calcifications are more often connected with non-invasive lesions and with tumors including the intraductal compo- nent – i.e. the lesions which are more common in younger women.

Breast tissue asymmetry and architectural distortion belong to indirect symptoms of breast cancer and are rare- ly seen independently. Breast tissue asymmetry without a

Figure 8. Architectonic distortion. Hist-pat evaluation: Invasive ductal

carcinoma, T2N0.

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visible mass was found in 7–27% of the cases of infiltrat- ing lobular carcinoma. Tumor tissue saturation equal to 85% is comparable to the surrounding normal breast tissue.

Similar lesions are found in approx. 4% of infiltrating duc- tal carcinomas. Tissue densification may be accompanied by 'architectural distortion' – i.e. the distortion of the nor- mal breast tissue structure with a thickening and distor- tion of the structure of fibrous septa.

In a dense, glandular structure, any densification may be hard to distinguish from the surrounding tissue and the only discernible symptom would be then the architectural distortion, sometimes very discreet. Such lesions are hard to detect on mammograms, and they are mostly found in 1/3, in one projection only. In women with palpable lesions, the comparison of the results of the physical examination and of mammography increases the chances of a correct diagnosis [18]. In the study material, architectural dis- tortion was found in 3.5% of the cases, and breast tissue asymmetry in 12.5%. The studies by E. Show de Paredes and by D.O. Jeffries, compared by me, revealed 5% and 8%

of cases of breast tissue asymmetry, respectively [14,15].

Dense, glandular breast tissue may be the reason for mam- mography being unable to detect any lesions, despite the ongoing neoplastic processes. My material included 7

References:

1. Johnson ET: Breast cancer racial differences before age 40 – implications for screening. J Natl Med Assoc, 2002; 94(3): 149–56 2. Dawson AE, Mulford DK, Taylor AS et al: Breast carcinoma detection

in women age 35 years and younger. Cancer, 1998; 84(3): 163–68 3. Bassett LW, Ysrael M, Gold RH et al: Usefulness of mammography

and sonography in women less than 35 years of age. Radiology, 1991;

180: 831–35

4. Dziewulska E, Pietrow D, Wesołowska E et al: Przedinwazyjny przewodowy rak sutka – symptomatologia radiologiczna, korelacja z rozpoznaniem histopatologicznym. Pol J Radiol, 2003; 68(1): 31–38 5. Colleoni M, Rotmensz N, Robertson C et al: Very young women

(<35 years) with operable breast cancer: features of disease at presentation. Ann Oncol, 2002; 13: 273–79

6. Brand IR, Sapherson DA, Brown TS: Breast imaging in women under 35 with symptomatic breast disease. Br J Radiol, 1993; 66: 394–97 7. Gajdos C, Tartter PI, Bleiweiss IJ et al: Stage 0 to stage III breast

cancer in young women. Journal of the American College of Surgeons, 2000; 190(5): 523–29

8. Vrieling C, Collette L, Fourquet A et al: Can patient, treatment- and pathology-related characteristics explain the high local recurrence rate following breast-conserving therapy in young patients? EJC, 2003; 39: 932–44

9. Chung M, Chang HR, Bland KI et al: Younger women with breast carcinoma have a poorer prognosis than older women. Cancer, 1996;

77(1): 97–103

10. Bertheau P, Steiberg SM, Cowan K et al: Breast cancer in young women: clinicopathologic correlation. Seminars in Diagnostic Pathology,1999; 16(3): 248–56

such cases, which accounted for 4.9% of all cases. In the study by E. Show Paredes et al., 11% of mammographies of patients aged up to 35 years showed no lesions – despite lesions found on physical examination. However, authors of that study underscore that among 34 patients (52%) with a very dense structure of their breast tissue, there were 14 cases of microcalcifications, 12 cases of masses with- out calcifications, and 8 cases of no discernible lesions [14]. Similar data, in the age group of up to 35 years, were obtained by D. Jeffries et al. – 86% [15] and JE. Meyer et al. – 90% [19], as well as M. Muttarak et al, but in the group aged up to 40 years – 93% [16].

Conclusions

1. Radiological image of breast cancer in women of up to 45 years does not differ from the radiological findings in case of breast cancer in older women.

2. The symptom of breast cancer in 1/3 of all patients is microcalcifications, visible only on mammography.

3. All women suspected with breast cancer require not only usg, but also mammography.

11. Sidoni A, Cavaliere A, Bellezza G et al: Breast cancer in young women: clinicopathological features and biological specificity.

Breast, 2003; 12(4): 247–50

12. Sundquist M, Thorstenson S, Brudin L et al: Incidence and prognosis in early onset breast cancer. Breast, 2002; 11(1): 30–35

13. Houssami N, Irwig L, Simpson JM et al: Sydney breast imaging accuracy study: comparative sensitivity and specificity of mammography and sonography in young women with symptoms.

AJR, 2003; 180: 935–40

14. Show de Paredes E, Marsteller LP, Eden BV: Breast cancers in women 35 years of age and younger: mammographic findings. Radiology, 1990; 177: 117–19

15. Jeffries DO, Adler DD: Mammographic detection of breast cancer in women under the age of 35. Investigative radiology, 1990; 25: 67–71 16. Muttarak M, Pojchamarnwiputh S, Chaiwun B: Breast cancer in

women under 40 years: preoperative detection by mammography.

Ann Acad Medicine Singapore, 2003; 32(4): 433–37

17. Ferranti C, Coopmans de Yoldi G, Biganzoli E et al: Relationships between age, mammographic features and pathological tumour characteristics in non-palpable breast cancer. Br J Radiol, 2000; 73:

698–705

18. Newstead GM, Baute PB, Toth HK: Invasive lobular and ductal carcinoma: mammographic findings and stage at diagnosis.

Radiology, 1992; 184: 623–27

19. Meyer JE, Kopans DB, Oot M: Breast cancer visualized by mammography in patients under 35. Radiology, 1983; 147: 93–94

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