Skip to main content
Breast Care logoLink to Breast Care
. 2015 Apr 28;10(3):207–210. doi: 10.1159/000381823

Breast Lesions during Pregnancy – a Diagnostic Challenge: Case Report

Ines Beyer 1,*, Nikola Mutschler 1, Katrin S Blum 1, Svjetlana Mohrmann 1
PMCID: PMC4569211  PMID: 26557826

Summary

Background

Palpable masses of the breast often occur during pregnancy and should be further investigated. The standard diagnostic during pregnancy is an ultrasound combined, if needed, with a core needle biopsy. Most lesions are benign in younger women but, nevertheless, the incidence of pregnancy-associated breast cancer is 1 in 3,000 deliveries and rising.

Case Report

We report the case of a 24-year-old patient diagnosed with a palpable breast lesion at 37 weeks of gestation. An ultrasound was performed and the lesion was rated BI-RADS 4. The initial core needle biopsy showed a ductal carcinoma in situ. After delivery and ablactating, a mammography, breast magnetic resonance imaging and a second ultrasound-guided biopsy was performed. Due to the inconclusive imaging and histological results, a wide excision was performed and a juvenile papillomatosis was confirmed. No further resection was necessary as the initial margins were sufficient.

Conclusion

This case suggests that the diagnosis of masses of the breast during pregnancy and lactation can be quite difficult. Diagnosis should be confirmed by an excision biopsy and by histological examination through an experienced pathologist. As a significant proportion of papillomas contain malignant regions, an argument exists for the complete excision of all papillary tumours.

Keywords: Juvenile papillomatosis, Pregnancy-associated breast lesions, Diagnosis

Established Facts

• Breast lesions often occur during pregnancy and are mostly benign in younger women, but the incidence of pregnancy-associated breast cancer is rising.

Novel Insights

• Complete surgical excision of the breast lesion is advised, even during pregnancy and the lactation period, to confirm the histology to prevent excessive treatment, e.g. treatment with tamoxifen in case of a ductal carcinoma in situ.

Introduction

Palpable masses of the breast often occur during pregnancy and lactation. Masses that remain longer than 2 weeks should be further investigated [1]. Due to changes in the breast during pregnancy, the standard diagnostics may not show reliable results on normal breast tissue. Mammography is not particularly useful in pregnant and lactating women, due to a decreased sensitivity caused by the radio-dense nature of the breast tissue. In addition, foetal radiation levels, even when performed with proper shielding of the foetus, may concern the mother [2,3]. Therefore, the standard diagnostic method during pregnancy is ultrasound, as there is no radiation exposure risk for the foetus and it can distinguish between benign and malignant processes. According to the German S3 guidelines, ultrasound can also be combined with a percutaneous core needle biopsy to confirm the nature of the mass in the case of a suspicious lesion [4]. As a biopsy has a very low rate of complications, it should be performed in all cases, even if the patient is still pregnant, to differentiate benign from malignant masses [5,6,7]. Most lesions in young women are benign; nevertheless, the incidence of pregnancy-associated breast cancer is 1 in 3,000 deliveries and accounts for approximately 1% of all breast cancers [8,9]. In addition, as women delay pregnancy past the age of 30, the number of patients diagnosed with breast cancer during pregnancy increases [10]. With the following case report we show the diagnostic challenges associated with unclear breast lesions during pregnancy.

Case Report

We report here on a 24-year-old Gravida I Para 0 patient with years of known systemic lupus erythematosus. A mass of approximately 4 cm in diameter was detected in the left breast during the 37th week of gestation. The initial ultrasound showed a lesion of 20.1 × 43 × 28 mm, corresponding to a score of 4 according to the Breast Imaging, Reporting and Data System (BI-RADS) analogue the DEGUM criteria (fig. 1) [11]. To determine the nature of the mass, a core needle biopsy and histological analysis were performed, leading to a diagnosis of ductal carcinoma in situ (DCIS). Although a DCIS is a pre-invasive lesion and can be associated with invasive carcinomas, further diagnostics were delayed until after the delivery of the full-term newborn. As the patient was diagnosed at the end of the third trimester, the patient insisted on a normal delivery at 40 weeks of gestation. Subsequent to primary ablactation postpartum, all diagnostic steps were performed or repeated, i.e. mammography, ultrasound, ultrasound-controlled core needle biopsy, and magnetic resonance imaging (MRI). The ultrasound result showed again a BI-RADS 4 lesion, while the mammography revealed a focal asymmetry on the left side with extremely dense breast tissue, American College of Radiology (ACR) category 4, and no sign of calcification (not shown). On MRI, a round lesion with non-mass enhancement was found, resembling a carcinoma, leading to an MRM BI-RADS 6 classification (fig. 2). Based on the preliminary evidence of a malignancy, a second core needle biopsy was performed on the clearest ultrasound-identified mass. The histological result showed a radial scar, which in approximately 30% of cases is associated with malignancy [12]. In addition, to gain a safe diagnosis of the lesion, a wide excision of the tumour was performed. The final report of the histology of the excised lump revealed a juvenile papillomatosis, which was confirmed by a second (external) pathologist. A further resection was not required as the initial resection margins were sufficient and an excellent cosmetic result was attained. As a risk for recurrent tumour development existed, the patient was advised to have a yearly follow-up, which so far has been unremarkable.

Fig. 1.

Fig. 1

An ultrasound image of the breast showing the maximal diameter of the breast tumour. The tumour is of irregular shape, inhomogeneous structure, with no clear borders and a complex echo density. Doppler sonography was not performed.

Fig. 2.

Fig. 2

A breast magnetic resonance image of the patient with the region of the tumour in the upper left breast indicated by the arrow. No clear mass is seen in the coronal STIR (a), or in the axial FSE T2-weighted image (b). Maximum intensity projection of subtracted T1-weighted images after intravenous contrast medium application shows a round enhancement in the upper part of the left breast (c), with a homogenous non-mass enhancement seen in the axial T1-weighted image (d).

Discussion

Diagnosis of masses in the breast during pregnancy and lactation is considerably more difficult due to hormonal changes in the breast tissue that may obscure the mass and delay detection [2]. Changes in the breast tissue may include increased density, size and glandularity. Mammography can be performed during pregnancy with low foetal radiation exposure, but should be avoided. Moreover, the sensitivity of mammography is lower due to the enhanced density of the breast during pregnancy and lactation [13,14]. In younger women, breast MRI is usually performed in addition to ultrasound but, as it requires the use of gadolinium as intravenous contrast medium, it should be restricted to non-pregnant women or only used with strong indication [14]. In the ‘White Paper on Magnetic Resonance Safety’, the American College of Radiology (ACR) recommends the use of MRI scans during pregnancy at any stage if the benefit of the MRI is higher than the risk to the mother and the foetus, and if the required information cannot be obtained by a different imaging method [15]. The main problem concerning a breast MRI during pregnancy is the high background enhancement of the parenchymal tissue, which also occurs during lactation and which may obscure pathologies [16,17]. As the first trimester of pregnancy is the period of organogenesis, it is strongly advised that MRI is avoided during this formative stage of pregnancy [18].

Breast ultrasound is an attractive method in pregnant patients as it is safe for the foetus and sensitive in the detection of malignant breast lesions [19]. Hence, as ultrasound is the most effective method, it can be combined with colour Doppler ultrasound, which reveals the higher vascularity during pregnancy and even more so during lactation [20].

Despite reported complications, e.g. infections, allergy to local anaesthetic, haematoma formation and the development of milk fistula during pregnancy, core needle biopsy remains an established and safe procedure, regardless of the gestational period, and should therefore be used unequivocally to diagnose a breast mass [6,7,21,22,23]. This procedure is less invasive and stressful for the patient and has a very high sensitivity for the detection of malignant breast lesions. However, it is necessary that the pathologist is aware that the biopsy is from a pregnant patient as, due to hormonal influences, an epithelial proliferation in the lobular unit and an increased glandular vascularity will be observed [24.] In case of a disparity between the breast imaging and the histological results, biopsy should be repeated [14]. If this is not conclusive, the diagnosis should be confirmed by an excision biopsy and an experienced pathologist should conduct the histological examination [25,26,27].

The presented patient was diagnosed with a form of ductal hyperplasia, juvenile papillomatosis; also known as ‘Swiss cheese disease’. This is a rare but benign, proliferative tumour in young adolescent women. The histological changes associated with juvenile papillomatosis are considered premalignant in adults, and approximately 10% of patients have an associated breast carcinoma [28]. The general histological criteria for juvenile papillomatosis were defined by Rosen et al. (1985) as: duct papillomatosis with or without a degree of epithelial atypia, apocrine and non-apocrine cysts, papillary apocrine hyperplasia, sclerosing adenosis, and duct stasis [25]. For histological confirmation and prevention of recurrence, due to the uncertain prognosis, complete surgical excision and a yearly clinical follow-up is recommended [29]. To date, however, no link has actually been established between juvenile papillomatosis and pregnancy or lactation. Sabate et al. [30] reported a series of 18 patients with juvenile papillomatosis of which 5 were diagnosed during pregnancy. The microscopic findings, however, showed cystic and ductal hyperplasia with papillary hyperplasia [31].

In conclusion, a complete surgical excision of all papillary tumours is indicated, as a significant proportion of papillomas will contain foci of atypical or overt malignant regions, despite a sometime benign histological result of core biopsies [32]. If the mass is detected in the late third trimester the excision can be postponed until after delivery. It is, however, considered safe to perform a core needle biopsy and, if necessary, an excision, if the mass is detected during the first and second trimester [33]. When a segmental resection is performed, the other milk ducts can be spared and the patient retains the option of breastfeeding [34]. As the final histological result may differ from the initial biopsy, with regard to the cosmetic result, it might be beneficial to utilise closer surgical safety margins initially.

Disclosure Statement

All authors have declare no conflict of interest.

References

  • 1.Loibl S, von Minckwitz G, Gwyn K, et al. Breast carcinoma during pregnancy. Cancer. 2006;106:237–246. doi: 10.1002/cncr.21610. [DOI] [PubMed] [Google Scholar]
  • 2.Nicklas AH, Baker ME. Imaging strategies in the pregnant breast cancer patient. Semin Oncol. 2000;27:623–632. [PubMed] [Google Scholar]
  • 3.Brent RL. The effect of embryonic and fetal exposure to x-ray, microwaves, and ultrasound: Counseling the pregnant and nonpregnant patient about these risks. Semin Oncol. 1989;16:347–368. [PubMed] [Google Scholar]
  • 4.Interdisziplinäre S3-Leitlinie für die Diagnostik, Therapie und Nachsorge des Mammakarzinoms, 2012, AWMF-Register-Nummer 032-045OL.
  • 5.Eedarapalli P, Jain S. Breast cancer in pregnancy. J Obstet Gynaecol. 2006;26:1–4. doi: 10.1080/01443610500363808. [DOI] [PubMed] [Google Scholar]
  • 6.Liberman L, Kaplan JB, Morris EA, et al. To excise or to sample the mammographic target: What is the goal of stereotactic 11-gauge vacuum-assisted breast biopsy? AJR Am J Roentgenol. 2002;179:679–683. doi: 10.2214/ajr.179.3.1790679. [DOI] [PubMed] [Google Scholar]
  • 7.Simon JR, Kalbhen CL, Cooper RA, Flisak ME. Accuracy and complication rates of US-guided vacuum-assisted core breast biopsy: Initial results. Radiology. 2000;215:694–697. doi: 10.1148/radiology.215.3.r00jn37694. [DOI] [PubMed] [Google Scholar]
  • 8.Loibl S, Han SN, Amant F. Being pregnant and diagnosed with breast cancer. Breast Care. 2012;7:204–209. doi: 10.1159/000339674. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Loibl S, Han SN, von Minckwitz G, et al. Treatment of breast cancer during pregnancy: An observational study. Lancet Oncol. 2012;13:887–896. doi: 10.1016/S1470-2045(12)70261-9. [DOI] [PubMed] [Google Scholar]
  • 10.Krishna I, Lindsay M. Breast cancer in pregnancy. Obstet Gynecol Clin North Am. 2013;40:559–571. doi: 10.1016/j.ogc.2013.05.006. [DOI] [PubMed] [Google Scholar]
  • 11.Madjar H, Ohlinger R, Mundinger A, et al. BI-RADS-analogue DEGUM criteria for findings in breast ultrasound-consensus of the DEGUM Committee on Breast Ultrasound. Ultraschall Med. 2006;27:374–379. doi: 10.1055/s-2006-926943. [DOI] [PubMed] [Google Scholar]
  • 12.Kennedy M, Masterson AV, Kerin M, Flanagan F. Pathology and clinical relevance of radial scars: A review. J Clin Pathol. 2003;56:721–724. doi: 10.1136/jcp.56.10.721. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Nicklas AH, Baker ME. Imaging strategies in the pregnant breast cancer patient. Semin Oncol. 2000;27:623–632. [PubMed] [Google Scholar]
  • 14.Litton JK, Theriault RL. Breast cancer and pregnancy: Current concepts in diagnosis and treatment. Oncologist. 2010;15:1238–1247. doi: 10.1634/theoncologist.2010-0262. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Kanal E, Borgstede JP, Barkovich AJ, et al. American College of Radiology White Paper on MR Safety: 2004 update and revisions. AJR Am J Roentgenol. 2004;182:1111–1114. doi: 10.2214/ajr.182.5.1821111. [DOI] [PubMed] [Google Scholar]
  • 16.Talele AC, Slanetz PJ, Edmister WB, et al. The lactating breast: MRI findings and literature review. Breast J. 2003;9:237–240. doi: 10.1046/j.1524-4741.2003.09322.x. [DOI] [PubMed] [Google Scholar]
  • 17.Heywang-Kobrunner S, Schereer I, Dershaw D. Differential diagnosis and diagnostic work up and the young patient. In: Heywang-Kobrunner S, Schereer I, Dershaw D, editors. Diagnostic breast imaging: Mammography, sonography, magnetic resonance imaging and interventional procedures. New York: Thieme; 1997. [Google Scholar]
  • 18.Leyendecker JR, Gorengaut V, Brown JJ. MR imaging of maternal diseases of the abdomen and pelvis during pregnancy and the immediate postpartum period. Radiographics. 2004;24:1301–1316. doi: 10.1148/rg.245045036. [DOI] [PubMed] [Google Scholar]
  • 19.Kim SJ, Chang JM, Cho N, et al. Outcome of breast lesions detected at screening ultrasonography. Eur J Radiol. 2012;81:3229–3233. doi: 10.1016/j.ejrad.2012.04.019. [DOI] [PubMed] [Google Scholar]
  • 20.Ahn BY, Kim HH, Moon WK, et al. Pregnancy- and lactation-associated breast cancer: mammographic and sonographic findings. J Ultrasound Med. 2003;22:491–497. doi: 10.7863/jum.2003.22.5.491. [DOI] [PubMed] [Google Scholar]
  • 21.Collins JC, Liao S, Wile AG. Surgical management of breast masses in pregnant women. J Reprod Med. 1995;40:785–788. [PubMed] [Google Scholar]
  • 22.Kasprowicz N, Bauerschmitz GJ, Schönherr A, et al. Recurrent mastitis after core needle biopsy: Case report of an unusual complication after core needle biopsy of a phyllodes tumor. Breast Care. 2012;7:240–244. doi: 10.1159/000339689. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Schackmuth EM, Harlow CL, Norton LW. Milk fistula: A complication after core breast biopsy. AJR Am J Roentgenol. 1993;161:961–962. doi: 10.2214/ajr.161.5.8273635. [DOI] [PubMed] [Google Scholar]
  • 24.Rosen PP. Anatomic and physiologic morphology. In: Rosen PP, editor. Rosen's breast pathology. 2nd ed. Philadelphia, PA: Lippincott-Raven; 2001. pp. 1–21. [Google Scholar]
  • 25.Rosen PP, Holmes G, Lesser ML, et al. Juvenile papillomatosis and breast carcinoma. Cancer. 1985;55:1345–1352. doi: 10.1002/1097-0142(19850315)55:6<1345::aid-cncr2820550631>3.0.co;2-b. [DOI] [PubMed] [Google Scholar]
  • 26.Ostrzega N. Fine-needle aspiration cytology of juvenile papillomatosis of breast: A case report. Diagn Cytopathol. 1993;9:457–460. doi: 10.1002/dc.2840090417. [DOI] [PubMed] [Google Scholar]
  • 27.Ohlinger R, Schwesinger G, Schimming A, et al. Juvenile papillomatosis (JP) of the female breast (Swiss Cheese Disease) – role of breast ultrasonography. Ultraschall Med. 2005;26:42–45. doi: 10.1055/s-2004-813122. [DOI] [PubMed] [Google Scholar]
  • 28.Gill J, Greenall M. Juvenile papillomatosis and breast cancer. J Surg Educ. 2007;64:234–236. doi: 10.1016/j.jsurg.2007.03.007. [DOI] [PubMed] [Google Scholar]
  • 29.Lad S, Seely J, Elmaadawi M, et al. Juvenile papillomatosis: A case report and literature review. Clin Breast Cancer. 2014;14:e103–105. doi: 10.1016/j.clbc.2014.03.003. [DOI] [PubMed] [Google Scholar]
  • 30.Sabate JM, Clotet M, Torrubia S, et al. Radiologic evaluation of breast disorders related to pregnancy and lactation. Radiographics. 2007;27(Suppl 1):S101–124. doi: 10.1148/rg.27si075505. [DOI] [PubMed] [Google Scholar]
  • 31.Rosen PP. Breast tumors in children. In: Rosen PP, editor. Rosen's breast pathology. 2nd ed. Philadelphia, PA: Lippincott-Raven; 2001. pp. 729–748. [Google Scholar]
  • 32.Brookes MJ, Bourke AG. Radiological appearances of papillary breast lesions. Clin Radiol. 2008;63:1265–1273. doi: 10.1016/j.crad.2008.02.012. [DOI] [PubMed] [Google Scholar]
  • 33.Dominici LS, Kuerer HM, Babiera G, et al. Wound complications from surgery in pregnancy-associated breast cancer (PABC) Breast Dis. 2010;31:1–5. doi: 10.3233/BD-2009-0289. [DOI] [PubMed] [Google Scholar]
  • 34.Gentilini O, Botteri E, Rotmensz N, et al. Breast-conserving surgery in 201 very young patients (<35 years) Breast. 2010;19:55–58. doi: 10.1016/j.breast.2009.11.001. [DOI] [PubMed] [Google Scholar]

Articles from Breast Care are provided here courtesy of Karger Publishers

RESOURCES