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Case Reports in Medicine
Volume 2011, Article ID 738413, 4 pages
Case Report

Primary Colorectal Adenocarcinoma Metastatic to the Breast: Case Report and Review of Nineteen Cases

1Department of Graduate Medical Education, H. Lee Moffitt Cancer Center & Research Institute, 12902 Magnolia Drive, Tampa, FL 33612, USA
2Department of Anatomic Pathology, H. Lee Moffitt Cancer Center & Research Institute, 12902 Magnolia Drive, Tampa, FL 33612, USA
3Department of Women's Oncology, Breast Program, H. Lee Moffitt Cancer Center & Research Institute, 12902 Magnolia Drive, Tampa, FL 33612, USA
4Department of Pathology and Cell Biology, University of South Florida, Tampa, FL 33612, USA
5Department of Oncologic Sciences, University of South Florida, Tampa, FL 33612, USA
6Pathology & Laboratory Services (113), James A Haley VA Hospital, 13000 Bruce B Downs Boulevard, Tampa, FL 33612, USA

Received 4 August 2010; Accepted 20 April 2011

Academic Editor: P. J. K. Kuppen

Copyright © 2011 Rodney E. Shackelford et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Metastases to the breast from extramammary primaries are uncommon and account for 0.5–6% of all breast malignancies (Georgiannos et al., 2001, and Vizcaíno et al., 2001). Malignant melanoma, lymphoma, and lung and gastric carcinomas are the most frequently encountered nonmammary metastases to the breast in adults (Georgiannos et al., 2001, and Chaignaud et al., 1994). Primary colorectal adenocarcinoma (CRC) metastatic to the breast is extremely rare, with the medical literature having only 19 recorded cases. Typically CRC metastatic to the breast is indicative of widely disseminated disease and a poor prognosis. Here we present a case of poorly differentiated colon cancer metastatic to the breast and review the current literature on this rare event.

1. Case Presentation

The following case was evaluated and reported in compliance with the University of South Florida’s Institutional Review Board Policy no. 311.

A 44-year-old Caucasian female was diagnosed with stage 1 (Duke’s stage A) primary colonic adenocarcinoma in 2002 and treated with a colectomy. She did not receive adjuvant therapy, and was disease-free for seven years when she presented with nausea, vomiting, and poor coordination. CT scan revealed a left cerebellar mass, as well as multiple lung masses and mediastinal lymphadenopathy. The patient subsequently underwent resection of the cerebellar mass, which was diagnosed as metastatic CRC. The patient underwent palliative radiotherapy to the brain and chest and FOLFOX chemotherapy. After two chemoradiotherapy courses, she noticed a rapidly enlarging mass in her left breast. Clinical examination of the left breast revealed a mobile 1 1 × 8  cm mass in the upper outer quadrant. Breast ultrasound revealed a solid mass in the 9 and 10 o’clock regions of the left breast, and breast MRI demonstrated diffuse enhancement in the left medial superior breast which extended to the chest wall (Figure 1). The patient underwent core needle biopsy which revealed a poorly differentiated adenocarcinoma (Figure 2) with neither an in situ component nor lymphovascular space invasion. No tumor necrosis or cigar-shaped nuclei were identified to suggest a colonic primary. In light of the patient’s clinical history, a panel of immunohistochemical stains was performed. The tumor was positive for CK20 and CDX-2 (Figure 2), and negative for CK-7, estrogen receptor, progesterone receptor, and HER2/neu by immunohistochemistry and fluorescent in situ hybridization (FISH). A diagnosis of metastatic colonic adenocarcinoma to the breast was thus rendered.

Figure 1: (a, b) Breast MRI demonstrated regional enhancement in the left superior breast extending to the chest wall and diffuse skin thickening.
Figure 2: (a, b) The breast biopsy demonstrated an invasive adenocarcinoma with a focal cribriform pattern, hyperchromatic round to oval nuclei, and brisk mitotic activity (H&E, 100x, 200x). (c) Cytokeratin 20 showed diffuse, positive staining in the tumor (cytokeratin 20, 100x). (d) CDX2, specific for intestinal epithelium, exhibited diffuse nuclear immunoreactivity in the tumor cells (CDX2, 200x).

2. Discussion

CRC metastatic to the breast is extremely rare, with the largest previous study reviewing only 8 cases [7]. Here we report a new case and review of 19 cases based on the current literature (Table 1). CRC with associated synchronous or metachronous breast metastases presents at an average age of 54.3 yrs with a range of 32–86 yrs, which is younger than the United States average of a primary CRC diagnosis at 72 yrs [18]. On average, breast metastasis is reported to appear 21 months following CRC diagnosis, with a range of 0 to 7 yrs, with only 3/20 (15%) cases first presenting as a breast lump, or as a breast lump with concurrent CRC. Three (15%) CRC breast metastases were in men, 15 (75%) in women, and no gender was reported in 2 (10%) cases. In 6 (30%) cases the patients died an average of 11 months after the diagnosis of breast metastasis, and the remaining 14 were either still alive at the time of the published case report or no survival data was reported. Fifteen (75%) cases had nonbreast metastases at the time of diagnosed breast metastasis, four reports did not mention other metastases, and in one case CRC breast metastasis was the only metastasis found. Metastases to the brain, liver, lung, skin, abdominal and axillary lymph nodes, and retroperitoneum were common. In one case, ocular and vertebral metastases were present [5]. The majority of metastases (55%) were to the left breast (often upper outer quadrant), with 6 (30%) to the right breast, and 2 bilateral (10%) [10]. Two of three reported male patients exhibited metastases in the left breast only [14, 15, 17]. CRC metastases to the breast averaged 3.5 cm in size and ranged from 1 to 11 cm. Most metastases were described as rapidly growing, discrete masses. CRC metastases to the breast most often appeared as masses without calcifications on mammography; in spite of the nine cases with reported mammographic findings, two (22%) exhibited microcalcifications (Table 2). Histopathology demonstrated an invasive adenocarcinoma, often with mucinous or signet-ring cell features, lacking an in situ component. Lymphovascular space invasion may be prominent. Finally, immunohistochemistry, when performed, revealed tumor cells to be positive for CDX-2, CK20, and CEA, and negative for CK7, ER, PR, HER2, and GCDFP-15, an immunophenotype typical of colorectal carcinoma [117].

Table 1: Colorectal carcinoma metastatic to the breast: summary of cases.
Table 2: Mammographic appearance of breast metastases.

Only a handful of CRC metastatic to the breast cases have been reported, with the two largest studies presenting two new cases each [13, 17]. After an extensive literature search, we located 19 cases. In light of the previously reported cases, the patient presented in this report exhibited some unusual aspects, having the largest breast metastasis (11 cm) and longest interval time from her initial CRC diagnosis to the diagnosed breast metastasis (7 years).

It is imperative to distinguish metastatic colorectal carcinoma to the breast from a primary mammary carcinoma, as the former requires systemic chemotherapy for colon cancer, while a primary breast cancer necessitates surgical management with or without breast-specific adjuvant therapy. Though histomorphologic clues of a metastatic CRC can be helpful, such as the presence of “dirty” necrosis, metastatic CRC can morphologically mimic a primary, poorly differentiated ductal carcinoma of the breast. Immunohistochemistry will in the vast majority of cases identify the phenotype of the carcinoma, as CRC is positive for cytokeratin 20 and CDX2, and negative for breast markers cytokeratin 7, GCDFP-15, mammaglobin, ER, and PR in greater than 90% of cases.

3. Conclusion

Combined with the case presented, CRC metastatic to the breast commonly (1) favors the left breast, (2) is accompanied by extensive metastatic disease to other organs, (3) exhibits rapid growth, (4) has a poor chemotherapy/radiation response, and (5) carries a poor prognosis secondary to disseminated disease. Radiologic studies of the breast may be misleading, as metastases may be associated with calcifications, and usually do not present as multiple, bilateral masses, thus mimicking a primary mammary carcinoma. Histopathologic clues of metastases include a lack of an in situ component, prominent lymphovascular space invasion, and a “triple-negative” phenotype. However, when histology offers no definitive clues of a metastasis, proper diagnosis of this rare event requires an accurate clinical history, proper immunohistochemical workup and high level of suspicion. This multidisciplinary approach is critical in avoiding unnecessary surgical procedures and pursuing proper subsequent patient management.

Conflict of Interests

The authors declared that there is no conflict of interests.


The authors would like to thank Mr. David Stephen, Miss Sabine S. Ellwanger, and Dr. Ramon Sandin for help in translating the Italian, German, and Spanish manuscripts, respectively. No financial support was required or obtained for the preparation of this paper.


  1. R. L. Lal and J. K. Joffe, “Rectal carcinoma metastatic to the breast,” Clinical Oncology, vol. 11, no. 6, pp. 422–423, 1999. View at Google Scholar
  2. A. H. Ozakyol, T. Saricam, and S. Isiksoy, “Breast metastasis of primary colon cancer,” American Journal of Gastroenterology, vol. 95, no. 8, p. 2149, 2000. View at Publisher · View at Google Scholar
  3. L. D. Sanchez, T. Chelliah, I. Meisher, and S. Niranjan, “Rare case of breast tumor secondary to rectal adenocarcinoma,” Southern Medical Journal, vol. 101, no. 10, pp. 1062–1064, 2008. View at Publisher · View at Google Scholar · View at PubMed
  4. G. B. Meloni, S. Dessole, G. Capobianco, M. P. Becchere, and R. Nonnis, “Metastasis to the breast from cecum carcinoma: case report and review of the literature,” Archives of Gynecology and Obstetrics, vol. 265, no. 4, pp. 216–218, 2001. View at Publisher · View at Google Scholar
  5. R. B. Hisham, H. Thuaibah, and Y. A. Gul, “Mucinous adenocarcinoma of the rectum with breast and ocular metastases,” Asian Journal of Surgery, vol. 29, no. 2, pp. 95–97, 2006. View at Google Scholar
  6. K. S. Bhirangi, D. J. D. T. Pinto, and J. J. Crosbie, “Solitary breast metastasis from carcinoma of colon,” Ulster Medical Journal, vol. 66, no. 2, pp. 138–139, 1997. View at Google Scholar
  7. L. Fernández de Bobadilla Olazábal, A. García Villanueva, M. Collado et al., “Breast metastasis of primary colon cancerMetástasis en mama de carcinoma primario de colon,” Revista Espanola de Enfermedades Digestivas, vol. 96, no. 6, pp. 415–419, 2004. View at Google Scholar · View at Scopus
  8. F. M. Jiménez-Macías, J. De La Santa-López, and J. Aguilar-Reina, “Metastatic breast nodule from primary colon cancer,” Gastroenterologia y Hepatologia, vol. 29, no. 3, pp. 150–151, 2006. View at Publisher · View at Google Scholar
  9. R. Mihai, J. Christie-Brown, and J. Bristol, “Breast metastases from colorectal carcinoma,” Breast, vol. 13, no. 2, pp. 155–158, 2004. View at Publisher · View at Google Scholar · View at PubMed
  10. M. Muttarak, A. Nimmonrat, and B. Chaiwun, “Metastatic carcinoma to the male and female breast,” Australasian Radiology, vol. 42, no. 1, pp. 16–19, 1998. View at Google Scholar
  11. C. Scholz and K. W. Degen, “Breast metastases of a sigmoid carcinomaMetastasierung eines sigmakarzinoms in die brust,” Zentralblatt fur Gynakologie, vol. 120, no. 10, pp. 518–520, 1998. View at Google Scholar
  12. C. Del Prete, S. A. Del Prete, and R. C. Babkowski, “Breast metastasis from colonic primary: a case report and review of the literature,” Connecticut Medicine, vol. 73, no. 7, pp. 399–402, 2009. View at Google Scholar
  13. N. R. Wakeham, K. Satchithananda, W. E. Svensson et al., “Colorectal breast metastases presenting with atypical imaging features,” The British Journal of Radiology, vol. 81, no. 965, pp. e149–e153, 2008. View at Google Scholar
  14. Y. Y. Ho and W. K. Lee, “Metastasis to the breast from an adenocarcinoma of the colon,” Journal of Clinical Ultrasound, vol. 37, no. 4, pp. 239–241, 2009. View at Publisher · View at Google Scholar · View at PubMed
  15. P. A. Lear and F. R. Jackaman, “Carcinoma of the rectum with metastasis in the male breast,” Journal of the Royal College of Surgeons of Edinburgh, vol. 25, no. 4, pp. 246–247, 1980. View at Google Scholar
  16. A. Bruscagnin, “A case of male breast metastasis from adenocarcinoma of the colon,” Radiologia Medica, vol. 93, no. 4, pp. 463–464, 1997. View at Google Scholar
  17. M. Nielsen, J. A. Andersen, and F. W. Henriksen, “Metastases to the breast from extramammary carcinomas,” Acta Pathologica et Microbiologica Scandinavica A, vol. 89, no. 4, pp. 251–256, 1981. View at Google Scholar
  18. E. C. Paulson, N. Mitra, S. Sonnad et al., “National cancer institute designation predicts improved outcomes in colorectal cancer surgery,” Annals of Surgery, vol. 248, no. 4, pp. 675–685, 2008. View at Publisher · View at Google Scholar · View at PubMed