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Ductal carcinoma in situ in core needle biopsies and its association with extensive in situ component in the surgical specimen

International Archives of Medicine volume 5, Article number: 19 (2012) Cite this article

Abstract

Background

We evaluated the presence of ductal carcinoma in situ (DCIS) in core needle biopsies (CNB) from invasive ductal lesions.

Methods

Retrospective study, which analyzed 90 cases of invasive ductal carcinoma lesions. The percentage of DCIS was quantified in each specimens obtained from CNB, which were compared to the surgical specimens. CNB and surgical specimens were evaluated by the same pathologist, and the percentage of DCIS in CNB was evaluated (percentage) and divided into categories. We considered the following parameters regarding the amount of DCIS: 1 = 0; 2 = 1 for 5%; 3 = 6 for 24%; 4 = 25 for 50%; 5 = 51 for 75% and 6 = 76 for 99%. The number of fragments and the histological pattern of DCIS was found.

Results

We found the following results regarding the distribution of the percentage of DCIS in the CNB: 1 = 63.3%; 2 = 12.2%; 3 = 12.2%; 4 = 5.6%; 5 = 1.1% and 6 = 5.6%. The logistic regression analysis showed that CNB percentages above 45% reflected the presence of DCIS in the surgical specimen in 100% of the cases (p < 0.001), with a specificity of 100%, accuracy of 83.3% and false positive rate of 0% (p <0.001).

Conclusion

There is direct relationship between extensive intraductal component in the surgical specimen when the core biopsy shows 45% or more of the DCI or microinvasive in the material examined.

Background

Currently, the core needle biopsy (CNB) is a widely used technique which provides better results when compared to needle biopsy [1–5]. Based on a positive diagnosis, this procedure represents a high sensitivity (85% to 98%) and specificity close to 100% with final accuracy of 86% to 97% [6–9]. Moreover, when compared to thinner needle punction, it may distinguish benign and malignant tumors and in situ or invasive forms, mainly due to its ability to obtain malignant histological diagnosis. This method is able to provide important information as prognostic and predictive breast cancer such as histological type, nuclear grade and presence of lymphatic vascular embolization as well as information regarding the biological behavior of tumors where important prognostic factors and treatment are essential, such as the status of estrogen receptors, progesterone receptors, c-erbB-2 markers and also to new therapeutic targets (EGFR, Ki67, etc..), which may be analyzed with the diagnosis, hence, providing a better planning with respect to the therapy to be used [6, 10–12].

An important issue in the use of CNB is the possibility of identifying ductal carcinoma in situ (DCIS) associated with invasive lesions. Because the presence of extensive intraductal component (EIC) in breast carcinomas have been associated with increased risk of recurrence in patients treated with conservative surgery in combination with radiation therapy, which would assist in surgical planning [13–19].

Extensive ductal carcinoma in situ (EDCIS) was defined by Schnitt et al [20] when 25% or more of DCIS is present along the invasive lesion. According to Jimenez et al [19], EDCIS in invasive breast carcinomas is associated with increased risk of recurrence in patients treated with conservative surgery and radiotherapy. According to some authors, the status of margins in these cases may represent the greatest predictor of importance for local recurrence. Boyages et al [9] reported a rate of recurrence in the breast of 26% for tumors exhibiting EIC in five years compared to 7% recurrence in negative EIC carcinomas.

In view of the above consideration, this investigation was undertaken to evaluate the presence of DCIS in CNB from invasive ductal lesions and to analysis this relationship.

Methods

Retrospective study in which 90 cases of invasive ductal carcinoma were investigated. The study was performed in the Breast Cancer Unit of the Department of Clinical Pathology, Faculdade de Medicina do ABC. The specimens corresponded to NOS (not otherwise specified) invasive ductal carcinomas, which corresponds to approximately 75 to 80% of breast carcinomas [21]. Our procedures were approved by the Ethical Committee in Research of the Faculdade de Medicina do ABC (number 109/08).

Exclusion criteria

We excluded all pure ductal carcinoma in situ or lobular carcinoma in situ (NL3) and invasive lobular neoplasias which exhibited different clinical and radiological features. We also excluded medullary carcinomas which presented in situ component associated [22].

Inclusion criteria

We selected only ductal carcinomas known to present frank invasion or microinvasion.

Data collection

In order to collect the specimens we used biopsy gun and 14G needle. We removed between two and six fragments from each specimen, the specimens were processed in a period not exceeding 24 hours. The slides were prepared according to standardization of the Department of Pathology of our Institution, histological sections were performed with a microtome with calibrated thickness of 5 microns, stained with hematoxylin-eosin (HE) and subjected to histological examination with optical microscope Olympus CBA.

The patients were staged according to standards of the Manual of Standards of histopathology reports of the Brazilian Society of Pathology, 2006 [23].

We evaluated the percentage of in situ component observed in each of the specimens from CNB to invasive component, histological pattern (HP) and number of fragments (NF). When the in situ component presented a percentage equal or higher than 25% of the sample it was designated as extensive (EIC), whether in the products of CNB or surgical specimens [24]. In relation to the specimens obtained from CNB, we subdivided into categories, according to the percentage of DCIS: category 1=0; 2=1 for 5%; 3=6 for 24%; 4=25 for 50%; 5=51 for 75% and 6= 76 for 99%. It was also related to patients’ age and to the clinical stage of them at diagnosis.

The data were compared with the surgical specimens for each patient to verify whether the findings in the products of CNB are reflected in their surgical specimens and to evaluate the relationship between the presence and absence of in situ component in CNB when compared to their surgical specimen. Furthermore, we also evaluated its relationship with the presence of EIC and submitted to statistical analysis (univariate and multivariate analysis/logistic regression and ROC curves). All specimens went through the same evaluation criteria by the same pathologist to relate the findings of individual CNB with the specimen from each patient.

Statistical analysis

Tables were constructed to characterize the findings of the samples. In these tables, categorical variables were presented as absolute frequencies (n) and relative frequencies (%). For analysis of dichotomous or qualitative variables associated with interest group, we used the chi-square or Fisher test. Differences were considered significant when the probability of a Type I error was less than 5% (p < 0.05). Variables with p <0.1 in bivariate analysis were included in multivariate analysis by using logistic regression (forward stepwise). We built a model for the evaluation of the findings in CNB and the surgical specimens and correlated it through development of the ROC curve elaboration. In both groups we studied variables such as age, stage, number of fragments and nominal variables: histological type of DCIS when present and the percentage of DCIS in the samples according to the standards range, which were identified by numbers. Statistical calculations were performed with the Statistical Package for Social Sciences (SPSS) version 18.0 (2009).

Results

The distribution of patients according to age was based on suggested intervals according to the Van Nuys Prognostic Index [24], which is used to assess the risk of recurrence of patients according to age at diagnosis of DCIS, with the following results: among 90 cases two (2.2%) were younger than 40 years old, 57 (63.3%) aged between 40 and 60 years old and 31 (34.5%) aged over 60 years old. The mean age of the patients was 57.7 + 15 years old.

Among the 90 patients evaluated, 33 (36.7%) were in situ component. This component ranged from 0 to 90% (average 10.3 + 22%).

Table 1 shows the distribution of patients according to age (category) of the in situ component, the number of fragments and stage.

Table 1 Frequency distribution of 90 patients, according to the percentage range of the in situ component, the number of fragments and stage
Full size table

We observed in Table 2 that the groups differ with respect to the in situ component in CNB, range and stage. The EIC positive group (23 cases) showed higher percentage of cases with DCIS in CNB compared to the negative group (63 cases). The EIC positive group presented higher percentage of positive cases with the highest percentage of in situ components compared to the negative group. The EIC negative group presented higher percentage of negative cases in T2 and T4, while the EIC positive group presented higher percentage regarding stage, especially in pT1c. We noted that 23 samples of CNB (25.6%) presented EIC in the specimen (Table 2).

Table 2 Comparison of positive and negative groups regarding the extensive in situ component in the specimen
Full size table

The groups differed in relation to histological types (Table 3). The positive group presented higher percentage of positive cases in all histological types compared to the negative group. In relation to the multivariate study we used variables significantly associated with the group: in situ CNB, CNB%, stage and four histological types.

Table 3 Correlation of overlap between the different histologic patterns identified in the CIE BAG and> 45% in the piece
Full size table

In Table 4 we observed the values of the estimated probability, odds ratios and indices of efficiency of logistic regression model.

Table 4 Values of the estimated probability, odds ratios and indices of efficiency of logistic regression model
Full size table

Figure 1 and Figure 2 present data regarding statistical analysis. We reported logistic curve and ROC curve for the% of DCIS found in the specimen.

Figure 1
figure 1

Logistic curve. Log (p/1-p) = -2.019 + 0.101% *Core%. p = probability of the patient to be positive.

Full size image
Figure 2
figure 2

ROC curve for the% of DCIS found in the specimen.

Full size image

Discussion

In this study we evaluated the presence of DCIS in CNB from invasive ductal lesions. Our results demonstrate that there is relationship between DCIS in the surgical specimen and 45% or more of the in situ component in CNB.

Previous studies indicated that EIC in breast carcinomas was associated with an increased risk of recurrence in patients treated with conservative surgery and radiotherapy [13–17]. EIC was identified as a risk factor for local recurrence following lumpectomy since 1984 [20]. Based on our report, the risk of local recurrence for high-grade invasive tumors was 4% to 39% when EIC was present.

Although the 12-gauge CNB presents a tissue volume about five times larger than the 14-gauge (this form would present higher chances to represent the tumor profile besides its relatively cheap price), some information regarding the tumor size is sometimes compromised. It leads some authors to prefer the 14-gauge needle biopsy, which is standardized in our department. Thus, we used 14-gauge needles, as recommended by the literature. On the other hand, we found no correlation with the number of fragments provided for diagnosis, because approximately 65 cases (72.2%) were composed of 3–4 fragments, compared with 15 cases (20% of the sample), which were sent 5–6 fragments per specimen for analysis, opposite to the results found by Parker et al [2], Liberman et al [21], Abreu-e-Lima et al [25] and Abreu-e-Lima et al [26].

CNB analysis in which we did not identify DCIS was associated with a higher likelihood of clear margins (15% versus 24%). Some studies tried to demonstrate the relationship between DCIS in CNB and the presence of the in situ component in extensive surgical specimens in order to prevent the deterioration of margins in conservative surgery. Mai et al [18] evaluated 78 CNB and compared it to surgical specimens in an attempt to predict the presence of EIC in the specimens. They noted that there was good correlation between DCIS and CNB, the CNB showed the presence of at least three foci of low-grade DCIS or at least two foci of high grade DCIS and revealed the presence of compromised margins on products of lumpectomy.

Our investigation was not based on the number of foci identified regarding the presence of DCIS, it was based on an analysis that seemed to be of easy applicability, which was composed by the assessment of the percentage of DCIS found in CNB and its relationship with EIC in the surgical specimen. EIC has been implicated as an independent predictor of recurrence in breast carcinomas treated with conservative surgery and radiotherapy. In 1990, Boyages et al [13], through a study with a follow up of five years showed recurrence in breast tissue in 26% of cases with EIC versus 7% compared to those who did not present this component. Moreover, the presence of EIC in lumpectomy products correlated with extensive residual disease in unresected tissues. Dzierzanowski et al [27] evaluated 95 cases of patients diagnosed with invasive carcinoma and its correlation with extensive in situ component in conservative surgeries. Their selection, however, included cases of pure DCIS and invasive in CNB, where only 34 cases (79%) exhibited CNB associated with the invasive component. In order to avoid a bias towards overestimating the presence of DCIS in CNB compared to the specimen, we selected cases with frank invasion. In this context, Dzierzanowski et al [27] concluded that the presence of pure DCIS in CNB specimens when correlated with the invasive lesion showed a greater risk for positive margins. Nevertheless, the percentage of DCIS in CNB expected for such a conclusion was not well clarified.

In order to evaluate the correlation between DCIS in CNB and the presence of EIC, we assessed whether there would be a percentage that reflects a relationship between the presence of in situ component in the CNB with this finding in surgical specimens. We observed through the logistic regression analysis that the percentages of DCIS in CNB above 45% reflected the presence of the in situ component in the surgical specimen in 100% of cases with a specificity of 100%, accuracy of 83.3% and false positive rate of 0% (p <0.001). Percentage values of DCIS in CNB between 15 and 20% showed a sensitivity of 56.5%, specificity of 97%, accuracy of 86.7% and 13.3% false positive (p <0.001).

With respect to the histological type presented by the DCIS in CNB, it was not relevant based on the presence of EIC in the surgical specimen. It suggests that the histological type of DCIS presented in the CNB, even when dealing with the standard micropapillary, which exhibits high correlation with multifocality in breast lesions, is not associated with the presence of EIC in the surgical specimen.

EIC has been implicated as an independent predictor of recurrence in breast carcinomas treated with conservative surgery and radiotherapy. In patients with invasive carcinoma, the risk of metastatic disease is already present at diagnosis and many failures can occur without evidence of local recurrence, but in DCIS the risk of metastases at diagnosis is negligible. Therefore, an invasive local recurrence brings the possibility of death from breast cancer, especially when conservative surgery for treatment is used [28, 29].

In our study, stage related to higher percentage of positivity for EIC corresponded to PT1C. This fact leads us to suggest that invasive tumors that measured between 1 and 2 cm exhibit a higher probability to be associated with intraductal component, unlike lesions in more advanced stages, i.e., stage pT4, where the component has already acquired earlier in situ invasive profile and is less often found in these lesions.

In a study of Holland et al [17], 71% of cases with positive EIC in the diagnosis of CNB showed residual DCIS in subsequent mastectomy product compared to 28% of cases with negative EIC. Similarly, Schnitt et al [20] reported that 88% of DCIS cases showed residual positive EIC re-excision in cases when compared with negative EIC. It suggests that the distribution of EIC associated with tumors has been underestimated in their contribution to surgical planning. It has been demonstrated in the conservative treatment for breast cancer with EIC, where there is high recurrence rate which is likely due to the presence of residual lesion of DCIS [13]. Holland et al [17] showed that invasive breast tumors with positive CIE have a greater likelihood to present residual DCIS compared to negative EIC tumors. EIC was found in 30% - 40% of all invasive breast tumors. Due to the fact that margin status corresponds to the strongest predictor of local recurrence, such information seems to be an important predictive value when adopting techniques of conservative treatment, and the anticipation of this information whenever possible is a important tool for appropriate surgical planning.

This study was undertaken to characterize in a less invasive diagnostic technique (CNB) the predictive ability in relation to the presence of EIC in the surgical specimens, warning prior to the possible involvement of surgical margins in conservative surgery, showing, if possible, the best parameter to be adopted in these specimens for the characterization of EIC. Therefore, proposing a cutoff for the truly significant presence that helps the surgical approach with lower risk of recurrence. Through this study we suggest the percentage of DCIS in the CNB to be mentioned in reports of pathology, thereby allowing better surgical planning. Furthermore, tumors are a clinical condition worth to be investigated [30–33].

Our study present a point that should be addressed, one may argue that the diagnostic enthusiasm for the high specificity may be moderated by the fact that CNBs was obtained from excised specimens and not from patients. We evaluated only invasive carcinoma and the presence of intraductal invasion in these cases is very frequent. Nonetheless, we may consider excided specimen as a consistent method, because a previous report indicated the importance of complete excision in the prevention of local recurrence of ductal carcinoma in situ [17].

Conclusion

There is a direct relationship between the percentage of DCIS present in DCI or microinvasive obtained by CNB and EIC in the surgical specimen.

Abbreviations

CNB:

Core needle biopsy

DCIS:

Ductal carcinoma in situ

EIC:

Extensive intraductal component

EDCIS:

Extensive ductal carcinoma in situ

HE:

Hematoxylin-eosin

HP:

Histological pattern

NF:

Number of fragments

S:

Sensitivity (S)

E:

Specificity

FP:

False positive

FN:

False negatives.

References

  1. Melo ALKO, Barra MFC, Silva AV, Oliveira MK, Scandiuzzi D, Menezes AC: Prospective study of 100 cases of core biopsy guided by ultrasound and review of literature. Radiol Bras 2003, 36:339–344.

    Google Scholar 

  2. Angelucci A, Pace G, Sanità P, Vicentini C, Bologna M: Tissue print of prostate biopsy: a novel tool in the diagnostic procedure of prostate cancer. Diagn Pathol 2011, 6:34.

    Article  PubMed  Google Scholar 

  3. Kuo YL, Chang TW: Can concurrent core biopsy and fine needle aspiration biopsy improve the false negative rate of sonographically detectable breast lesions? BMC Cancer 2010, 10:371.

    Article  PubMed  Google Scholar 

  4. Brunner AH, Sagmeister T, Kremer J, Riss P, Brustmann H: The accuracy of frozen section analysis in ultrasound- guided core needle biopsy of breast lesions. BMC Cancer 2009, 9:341.

    Article  PubMed  Google Scholar 

  5. Schiffhauer LM, Boger JN, Bonfiglio TA, Zavislan JM, Zuley M, Fox CA: Confocal microscopy of unfixed breast needle core biopsies: a comparison to fixed and stained sections. BMC Cancer 2009, 9:265.

    Article  PubMed  Google Scholar 

  6. Parker SH, Lovin JD, Jobe WE, Luethke JM, Hopper KD, Yakes WF: Stereotactic breast biopsy with a biopsy gun. Radiology 1990, 176:741–747.

    PubMed  CAS  Google Scholar 

  7. Centeno AD, Koch RS, Freurd L, Koch HA: Anatomoradiological correlation of breast alterations by means of core biopsy and fine-needle aspiration cytology. Rev Bras Radiol 2004,2004(14):21–27.

    Google Scholar 

  8. Sauer G, Deissler H, Strunz K, Helms G, Remmel E, Koretz K, Terinde R, Kreienberg R: Ultrasound-guided large-core needle biopsies of breast lesions: analysis of 962 cases to determine the number of samples for reliable tumor classification. Br J Cancer 2005, 92:231–235.

    PubMed  CAS  Google Scholar 

  9. Ciatto S, Houssami N, Ambrogetti D, Bianchi S, Bonardi R, Brancato B, Catarzi S, Risso GG: Accuracy and underestimation of malignancy of breast core needle biopsy: Florence experience of over 4000 consecutive biopsies. Breast Cancer Res Treat 2007, 101:291–297.

    Article  PubMed  Google Scholar 

  10. Litherland J: The role of needle biopsy in the diagnosis of breast lesions. Breast 2001, 10:383–387.

    Article  PubMed  CAS  Google Scholar 

  11. Berner A, Davidson B, Sigstad E, Risberg B: Fine-needle aspiration cytology vs. core biopsy in the diagnosis of breast lesions. Diagn Cytopathol 2003, 29:344–348.

    Article  PubMed  Google Scholar 

  12. El-Sayed ME, Rakha EA, Reed J, Lee AH, Evans AJ, Ellis IO: Predictive value of needle core biopsy diagnoses of lesions of uncertain malignant potential (B3) in abnormalities detected by mammography escreening. Histopathology 2008, 53:650–657.

    Article  PubMed  CAS  Google Scholar 

  13. Boyages J, Recht A, Connolly JL, Schnitt SJ, Gelman R, Kooy H, Love S, Osteen RT, Cady B, Silver B: Early breast cancer: predictors of breast recurrence for patients treated with conservative surgery and radiation therapy. Radiother Oncol 1990, 19:29–41.

    Article  PubMed  CAS  Google Scholar 

  14. Chan LW, Rabban J, Hwang ES, Bevan A, Alvarado M, Ewing C, Esserman L, Fowble B: Is radiation indicated in patients with ductal carcinoma in situ and close or positive mastectomy margins? Int J Radiat Oncol Biol Phys 2011, 1:25–30.

    Article  Google Scholar 

  15. Schouten VA, van Vugt R, Van Dijck J: Local recurrence after different strategies for ductal carcinoma in situ of the breast: A study in the East Netherlands. Int J Radiat Oncol Biol Phys 2007, 69:703–710.

    Article  Google Scholar 

  16. Connolly JL, Boyages J, Nixon AJ, Peiró G, Gage I, Silver B, Recht A, Harris JR, Schnitt SJ: Predictors of breast recurrence after conservative surgery and radiation therapy for invasive breast cancer. Mod Pathol 1998, 11:134–139.

    PubMed  CAS  Google Scholar 

  17. Holland PA, Gandhi A, Knox WF, Wilson M, Baildam AD, Bundred NJ: The importance of complete excision in the prevention of local recurrence of ductal carcinoma in situ. Br J Cancer 1998, 77:110–114.

    Article  PubMed  CAS  Google Scholar 

  18. Mai KT, Yazdi HM, Ford JC, Matzinger FR: Predictive value of extent and grade of ductal carcinoma in situ radiologically guided core biopsy for the status of margins in lumpectomy. Eur J Surg Oncol 2000, 26:646–651.

    Article  PubMed  CAS  Google Scholar 

  19. Jimenez RE, Bongers S, Bouwman D, Segel M, Visscher DW: Clinicopathologic significance of ductal carcinoma in situ in breast core needle biopsies with invasive cancer. Am J Surg Pathol 2000, 24:123–128.

    Article  PubMed  CAS  Google Scholar 

  20. Schnitt SJ, Abner A, Gelman R, Connolly JL, Recht A, Duda RB, Eberlein TJ, Mayzel K, Silver B, Harris JR: The relationship between microscopic margins of resection and the risk of local recurrence in patients with breast cancer treated with breast- conserving surgery and radiation therapy. Cancer 1994, 74:1746–1751.

    Article  PubMed  CAS  Google Scholar 

  21. Liberman L, Dershaw DD, Rosen PP, Giess CS, Cohen MA, Abramson AF, Hann LE: Stereotaxic core biopsy of breast carcinoma: accuracy at predicting invasion. Radiology 1995, 194:379–381.

    PubMed  CAS  Google Scholar 

  22. Tavassoli FA: Pathology of the Breast: Lobular Neoplasia. 2nd edition. Common and familiar special types, Infiltrating Carcinoma; 1999:p461-p468.

    Google Scholar 

  23. Manual de Padronização de Laudos Histopatológicos. 3edth edition. Reichmann & Autores Editores, São Paulo; 2005.

  24. Silverstein MJ, Poller DN, Waisman JR, Colburn WJ, Barth A, Gierson ED, Lewinsky B, Gamagami P, Slamon DJ: Prognostic classification of breast ductal carcinoma in situ. Lancet 1995, 345:1154–1157.

    Article  PubMed  CAS  Google Scholar 

  25. Abreu-e-Lima MC, Maranhão N, Costa I, Acreu-e-Lima M, Abru-e-Lima P, Carvalho ARL: Sensitivity and specificity of stereotactic core biopsy in histological diagnosis of nonpalpable breast lesions. Rev Assoc Med Bras 1999, 45:290–294.

    Article  PubMed  Google Scholar 

  26. Abreu-e-Lima MC, Maranhão N, Almeida V, Melo CB, Araújo E, Abreu-e-Lima M, Carvalho ARL: Comparison of fragments obtained with 14 gauge needle and 12 “core biopsy” Stereotactic of nonpalpable breast lesions: differences between fragment size and frequency of injuries diagnosed. Radiol Bras 2001, 34:255–260.

    Article  Google Scholar 

  27. Dzierzanowski M, Melville KA, Barnes PJ, MacIntosh RF, Caines JS, Porter GA: Ductal carcinoma in situ in core biopsies containing invasive breast cancer: correlation with extensive intraductal component and lumpectomy margins. J Surg Oncol 2005, 90:71–76.

    Article  PubMed  Google Scholar 

  28. Morrow M, Strom EA, Bassett LW, Dershaw DD, Fowble B, Harris JR, O’Malley F, Schnitt SJ, Singletary SE, Winchester DP, American College of Surgeons, College of American Pathology, Society of Surgical Oncology, American College of Radiology: Standard for the Management of Ductal Carcinoma In Situ of the breast (DCIS). CA Cancer J Clin 2002, 52:256–276.

    Article  PubMed  Google Scholar 

  29. Separovi V, Sarevic B, Separovi R, Oresic V, Nola N, Vrdoljak M, Krulin B: Prognostic value of prominent DCIS component in the breast-conserving therapy of stage I and II invasive ductal breast cancer. Breast 1999, 8:72–76.

    Article  Google Scholar 

  30. Maximous DW, Abdel-Wanis ME, El-Sayed MI, Abd-Elsayed AA: Preoperative gemcitabine based chemo-radiotherapy in locally advanced non metastatic pancreatic adenocarcinoma. Int Arch Med 2009, 2:7.

    Article  PubMed  Google Scholar 

  31. Upile T, Jerjes W, Kafas P, Harini S, Singh SU, Guyer M, Bentley M, Sudhoff H, Hopper C: Salivary VEGF: a non-invasive angiogenic and lymphangiogenic proxy in head and neck cancer prognostication. Int Arch Med 2009, 2:12.

    Article  PubMed  Google Scholar 

  32. Bosch-Barrera J, Espinós J: Hepatic breast cancer dissemination after an iatrogenic hepatic laceration during talc pleurodesis: a case report. Int Arch Med 2010, 3:6.

    Article  PubMed  Google Scholar 

  33. El-Sayed MI, Ali AM, Sayed HA, Zaky EM: Treatment results and prognostic factors of pediatric neuroblastoma: a retrospective study. Int Arch Med 2010, 3:37.

    Article  PubMed  Google Scholar 

  34. Rosen PP: Rosen’s Breast Pathology, Volume chapter 11. 3rd edition. Lippincott Williams &Wilkins, Philadelphia; 2009:285–350.

    Google Scholar 

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Acknowledgements

This study received financial support from Núcleo de Estudos, Pesquisas e Assessoria à Saúde da Faculdade de Medicina do ABC (NEPAS-FMABC).

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Authors and Affiliations

  1. Departamento de Mastologia, Faculdade de Medicina do ABC, Avenida Príncipe de Gales, 821, Santo André, SP, 09060-650, Brazil

    Guerino Barbalaco Neto

  2. Departamento de Anatomia Patológica, Faculdade de Medicina do ABC, Avenida Príncipe de Gales, 821, Santo André, SP, 09060-650, Brazil

    Claudia Rossetti

  3. Departamento de Hematologia e Oncologia, Faculdade de Medicina do ABC, Avenida Príncipe de Gales, 821, Santo André, SP, 09060-650, Brazil

    Fernando LA Fonseca

  4. Laboratório de Escrita Científica, Departamento de Morfologia e Fisiologia, Faculdade de Medicina do ABC, Avenida Príncipe de Gales, 821, Santo André, SP, 09060-650, Brazil

    Vitor E Valenti

  5. Departamento de Fonoaudiologia, Faculdade de Filosofia e Ciências, Universidade Estadual Paulista, Avenida Hygino Muzzi Filho, 747, Marília, SP, 17525-900, Brazil

    Vitor E Valenti & Luiz Carlos de Abreu

  6. Departamento de Morfologia e Fisiologia, Faculdade de Medicina do ABC, Av. Príncipe de Gales, 821, Santo André, SP, 09060-650, Brazil

    Luiz Carlos de Abreu

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  1. Guerino Barbalaco Neto
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Correspondence to Luiz Carlos de Abreu.

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We declare no conflict of interest.

Authors’ contribution

All authors participated in the acquisition of data and revision of the manuscript. GBN, CR, FLAF, VEV and LCA conceived of the study, determined the design, performed the statistical analysis, interpreted the data and drafted the manuscript. All authors read and gave final approval for the version submitted for publication.

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Barbalaco Neto, G., Rossetti, C., Fonseca, F.L. et al. Ductal carcinoma in situ in core needle biopsies and its association with extensive in situ component in the surgical specimen. Int Arch Med 5, 19 (2012). https://doi.org/10.1186/1755-7682-5-19

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