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ISSN: 2471-8556
Oncology & Cancer Case Reports
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A Rare Case of Metastatic Primary Peritoneal Adenocarcinoma Presenting as Breast Cancer

Watson GA*, Greally M, Murphy DJ, Doyle A, Quinn C and Walshe JM

Department of Medical Oncology and Pathology, St. Vincent’s University Hospital, Elm Park, Ireland

*Corresponding Author:
Watson GA
Department of Medical Oncology and
Pathology, St. Vincent’s University Hospital
Elm Park, Dublin 4, Ireland
Tel: 0035318032990
E-mail: Geoff_watson7@hotmail.com

Received date: August 07, 2016 ; Accepted date: December 15, 2016; Published date: December 20, 2016

Citation: Watson GA, Greally M, Murphy DJ, Doyle A, Quinn C, et al. (2016) A Rare Case of Metastatic Primary Peritoneal Adenocarcinoma Presenting as Breast Cancer. Oncol Cancer Case Rep 2:118. doi:10.4172/2471-8556.1000118

Copyright: © 2016 Watson GA, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Abstract

Metastasis to the breast as a presenting feature of extramammary malignancy is extremely uncommon. Often in this setting, the distinction between primary and secondary breast malignancy can be challenging. Ovarian or primary peritoneal metastasis to the breast is suggestive of disseminated disease and associated with a guarded prognosis, thus accurate differentiation is crucial for early and appropriate intervention. We report the case of a patient presenting with what initially appeared to be locally advanced breast cancer but subsequent review of pathology and imaging confirmed the presence of metastatic primary peritoneal cancer.

Keywords

Peritoneal cancer; Carcinomatosis; Malignancy; Breast metastasis; WT1

Case Report

A 61-year-old female presented to the triple assessment breast clinic with a three day history of left breast pain following minor trauma. Physical examination revealed an enlarged, pale, and edematous left breast with nipple retraction and skin dimpling. Mammogram revealed a heterogeneously dense breast parenchyma without a definite mass. Breast ultrasound demonstrated an ill-defined 2 cm hypoechoic mass in the left breast with an abnormal ipsilateral axillary lymph node, features concerning for locally advanced breast cancer (Figure 1).

oncology-cancer-clinical-Targeted-left-breast

Figure 1: Targeted left breast ultrasound shows a 2 cm hypoechoic mass with irregular margins and posterior acoustic shadowing.

Both the breast mass and axillary lymph node were biopsied, and pathology reported an invasive ductal carcinoma with a nodal metastasis, ER positive, HER2 negative. The breast demonstrated multifocal enhancement in the inferior breast on magnetic resonance imaging (MRI) and multiple abnormal left axillary nodes were noted. A staging CT of thorax, abdomen and pelvis (TAP) revealed paraaortic lymphadenopathy at the level of the renal arteries, measuring up to 1.8cm in short axis (Figure 2). A CT guided biopsy of a para-aortic lymph node was positive for metastatic disease. There were other sites of disease reported.

oncology-cancer-clinical-Axial-abdominal

Figure 2: Axial abdominal CT with oral and IV contrast shows an enlarged left paraaortic retroperitoneal node (arrow).

Thus at this time, the clinical picture was Stage IV breast cancer to para-aortic lymph nodes. As local disease control in the breast was a concern, chemotherapy was administered. The patient received dose dense Adriamycin and Cyclophosphamide followed by Taxol chemotherapy, which she tolerated without complication. During chemotherapy, her breast mass reduced but was still palpable. She was then commenced on anti-hormonal therapy, the aromatase inhibitor anastrozole aiming for ongoing disease control. Follow-up breast imaging after chemotherapy showed stromal thickening in the left breast with abnormal lymph nodes in the left axilla without a focal breast mass, and physical examination revealed resolution of the changes observed at presentation. Restaging CT scan demonstrated reduced retroperitoneal adenopathy; the index para-aortic node reduced in size from 1.8 cm to 0.9 cm (Figure 3).

oncology-cancer-clinical-Partial-disease

Figure 3: Partial disease response. Axial CT with oral and IV contrast shows axial abdominal CT with oral and IV contrast shows an enlarged left paraaortic retroperitoneal node (arrow).

As her disease bulk was low, the role of mastectomy was discussed for local disease control. At that point, her pathology was reviewed by another senior breast pathologist and the possibility of a gynaecological primary, rather than primary breast cancer, was raised. WT-1 testing was completed and found to be positive both in the para-aortic lymph node and breast. Of note, this woman had a hysterectomy with removal of ovaries 12 years previous for abnormal vaginal bleeding. This surgical specimen was reviewed in light of these findings, however no malignancy was identified. Subsequent review of her imaging from the time of diagnosis revealed very subtle thickening in the omentum, suggestive of a primary peritoneal cancer. When we presented these findings to our patient, she stated that on retrospect she had been experiencing right groin pain and abdominal discomfort which had disappeared on her cytotoxic treatment. A positron emission tomography (PET) scan demonstrated low grade FDG uptake in portocaval and proximal right external iliac regions, consistent with findings on CT imaging. Serum CA-125 at this time was elevated at 53.3 u/ml (normal <35 u/ml). She was referred to our surgical gynecology colleagues for assessment regarding debulking surgery, however the patient reported a very low symptom burden and thus declined surgical intervention. She remained on anastrozole for two years from the time of her initial diagnosis with a normal CA-125.

At two years, she was admitted to hospital with acute cholecystitis. A CT Abdomen also revealed the development of multiple peritoneal soft tissue nodules, features consistent with peritoneal carcinomatosis (Figure 4). She underwent laparoscopic cholecystectomy, and pathology revealed metastatic adenocarcinoma with features consistent with a peritoneal primary present in multiple submucosal and subserosal lymphatic spaces. Repeat oestrogen receptor and WT1 testing was performed on this specimen and both were positive (Figure 5). Four years since diagnosis this lady continues to have platinum sensitive peritoneal cancer although the intervals on “break” from therapy have shortened. She was referred for genetic testing although this is very clearly one related process, metastatic peritoneal cancer to breast. She tested BRCA mutation negative. Now four years since diagnosis, our patient remains alive with good quality of life four years since diagnosis of Stage IV primary peritoneal cancer to breast.

oncology-cancer-clinical-curved-arrows

Figure 4: Axial CT abdomen shows multiple peritoneal soft tissue nodules (curved arrows) consistent with peritoneal carcinomatosis.

oncology-cancer-clinical-adenocarcinoma

Figure 5: Peritoneal biopsy showing (A) metastatic adenocarcinoma (B) positive oestrogen receptor stain (C) positive WT1 Stain.

Discussion

Extrahepatic Metastases to the breast are extremely uncommon, accounting for only 0.5% to 1.3% of breast malignancy [1-5]. The most common sites of origin are lymphoma, melanoma, sarcoma and those from the gastrointestinal and genitourinary tracts in men [2,5]. This presentation is usually associated with advanced disease stage [3,4].

There have been isolated reports of ovarian or peritoneal cancer metastasizing to the breast [1]. The first case was described by Sitzenfrey [6]. In a study performed by Hadju and Urban, 4,051 breast cancer patients were identified and the overall incidence of primary gynaecologic cancers metastatic to the breast was 0.17%, with only 0.07% of metastatic disease originating from a primary ovarian tumor [3]. The largest literature review by Baykal et al. described 37 cases [7].

Dissemination of ovarian or peritoneal cancer occurs largely via intraperitoneal implantation, but also through lymphatic and hematogenous spread [8]. The most common sites of distant metastasis are the liver and the lung, but certain factors may increase the susceptibility of metastases to the breast, including the absence of hereditary breast-ovarian cancer [5,8].

While diagnosis may be challenging, it is important to differentiate between metastatic ovarian cancer and primary breast tumours not only to guide therapy, but also to prevent unnecessary surgical intervention. Treatment options for localized primary breast or ovarian cancer include surgery, radiation, and systemic therapy (hormonal therapy and chemotherapy). However, in more advanced disease, surgical intervention is less relevant.

Metastatic lesions to the breast tend to be more superficial and less fixed to surrounding tissues than primary breast lesions. Recent studies have shown that 85% of patients present with a solitary tumor, while only 4% have diffuse involvement [1,6]. The most common location is the upper outer quadrant (62% of patients) [1,9].

While various imaging modalities may aid in achieving a correct diagnosis, breast metastasis from primary ovarian tumours share many morphological features with primary breast cancers. On mammography, metastatic lesions may appear as discrete, well-circumscribed masses while primary breast cancers typically appear spiculated and display architectural distortion that metastases typically do not [1,7,9]. Microcalcifications may rarely be seen in ovarian cancer metastases due to the presence of psammoma bodies [10,11]. Microscopically, both cancers display marked nuclear atypia, brisk mitotic activity, and papillary architectural patterns [2,11].

Immunohistochemistry testing with tissue-specific markers may be helpful in determining the primary site of origin when an extramammary malignancy is suspected. Ovarian carcinoma and breast carcinoma share many immunohistochemical features (e.g. ER, PR, HER2/neu, CA125, CK7, CK20) [11]. However, other candidate markers (e.g. GCDPF-15/BRST2, WT1, PAX8, PAX2, and mammaglobin) may also be useful [11]. WT1 has been identified as a reliable marker in differentiating metastatic ovarian cancer from other primary sites due to its high sensitivity and low potential for aberrant expression [11,12-14]. The most common histologic variant of ovarian cancer associated with metastatic disease to the breast is papillary serous adenocarcinoma [10]. WT1 is expressed in approximately 95% of serous ovarian carcinomas [15].

Secondary breast involvement from an ovarian tumour may be a harbinger of widespread dissemination. 70% of patients presenting with a metastatic breast lesion have widespread metastatic disease at the time of diagnosis [4] and prognosis is generally poor. In previous studies, survival ranged from 13 days to 3.5 years [1,5], with most patients dying within 1 year [15]. Klein et al. suggest inflammatory metastatic disease to the breast conferred a graver prognosis, with a median survival of 6 months after diagnosis of metastasis to the breast [1].

Conclusion

Ovarian or peritoneal metastasis to the breast is rare, and diagnosis may be difficult as metastases share many common features with primary breast cancer. Clinical presentation, imaging and immunohistochemistry may aid in reaching a correct diagnosis. In our study WT1 testing was a vital component in reaching the correct diagnosis. Accurate differentiation is necessary because treatment differs significantly for patients with ovarian metastasis to the breast, as compared with patients with primary breast cancer. These metastases to the breast appear to confer a poor prognosis as patients often have widespread advanced disease. Despite this, our patient is alive four years since diagnosis, perhaps due to her low volume of disease at initial presentation. Physician awareness of this clinical entity is paramount in allowing early recognition and the initiation of appropriate therapy and optimizing patient outcomes.

Consent

Written informed consent was obtained from the patient for publication of this case report and accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal on request.

References

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