Page 404 - Read Online
P. 404

Shah et al.                                                                                                                                            Breast metastasis mimicking as second primary cancer






























           Figure 6: Immunohistochemistry markers results in our patient. CK: cytokeratin; mCEA: carcinoembryonic antigen; ER: estrogen receptor;
           MUC2: mucin2; CDX2: Caudal type homeobox2
           breast they lack an in situ component. Lymphovascular   indicates a poor prognosis. Metastases to the breast
           space invasion may be prominent. This type of unusual   are rare in themselves, and such metastasis occurring
           histopathology  in breast with previous  history of   secondary to a previous anorectal carcinoma makes
           malignancy are suggestive of metastasis. But the final   this case very unusual. The liver, lungs and bone are the
           diagnosis is established after studying the cytokeratin   usual sites of spread from colorectal cancers. Breast
           pattern. IHC when performed, tends to be positive for   metastases with sparing of these organs is unlikely but
           colorectal markers like caudal type homeobox-2 (CDX-  possible. Our patient presented with an isolated breast
           2), cytokeratin (CK20), and  CEA, and  negative  for   lump and without any other complaints. She was
           breast markers CK7, estrogen receptor, progesterone   managed considering the lesion to be second primary
           receptor, human  epidermal  growth factor receptor-2,   cancer of the breast but post operative histopathology
           and  gross  cystic  disease  fluid  protein-15. [14,15]    with IHC showed it to be metastases. On the basis of
           Expression of CK7 and CK20 is considered to be most   histopathology  showing  adenocarcinoma  and history
           helpful in identifying the origin of adenocarcinomas.  of previous malignancy alone, the diagnosis of lesion
                                                              being metastasis to breast should not be arrived upon
           Most importantly, the great majority of primary breast   and in such patients the importance of IHC to exclude
           tumors are CK7-positive and CK20-negative, while   the diagnosis  of primary  breast lesion  cannot  be
           colorectal  carcinomas  are usually  CK7-negative  and   undermined.
           CK20-positive. [16,17]  IHC markers used in our case were
           consistent with these findings as shown in Table 1. The   Financial support and sponsorship
           strong nuclear positivity with CDX-2 is highly sensitive   Nil.
           and specific for colonic cancers.  In addition, estrogen
                                       [18]
           and progesterone  receptors are usually negative in   Conflicts of interest
           metastatic breast cancers. A patchy reaction for CK5/6   There are no conflicts of interest.
           and comedo like necrosis can mimic ductal carcinoma
           in situ disease. Histological features such as epithelial   Patient consent
           stratification,  high  nuclear  atypia,  significant  mitotic   Obtained.
           activity, and positive reactions for CK20 and CDX-2 can
           help to overcome this difficulty. Metastatic carcinomas   Ethics approval
           in the breast are associated with a poor prognosis with   Ethics approval  was obtained  prior to the
           a survival rate of less than 12 months from the time of   commencement of the study.
           breast tumor diagnosis. [16,19,20]
                                                              REFERENCES
           Metastatic disease in the breast is a marker for
           disseminated metastatic  spread, and therefore     1.   Hajdu SI, Urban JA. Cancers  metastatic  to the breast.  Cancer
            394                                                             Journal of Cancer Metastasis and Treatment ¦ Volume 2 ¦ September 30, 2016
   399   400   401   402   403   404   405   406   407   408   409