Mammary Carcinoma Arising in Microglandular Adenosis: A Report of Five Cases

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Abstract

CASE REPORT

By searching the electronic database, we found five cases of MGACA (including an in situ lesion). The clinical characteristics of these five are summarized in Table 1. The median age of the patients at the time of the diagnosis was 47 years (range, 40 to 60 years). All patients underwent breast conserving surgery. Two patients had lymph node metastasis on pathologic examination and four received adjuvant chemo-radiation therapy. During follow-up, one patient (case 1) developed recurrence in the ipsilateral breast and axillary lymph nodes 1 year after the surgery. The rest of the patients had no evidence of disease and are being regularly followed up. This study was approved by the Institutional Review Board of Seoul National University Bundang Hospital (protocol # B-1609-364-701), and informed consent was waived.

Table 1.

Clinical characteristics of the five cases of MGACA

The pathologic findings and the results of the immunohistochemical studies are shown in the Table 2. One patient (case 5) was diagnosed as ductal carcinoma in situ (DCIS) and the rest of the cases were all invasive carcinomas. The lesions in these five cases displayed the histologic spectrum ranging from MGA to AMGA and finally to MGACA (Fig. 1). The MGA areas had the typical structure: groups of small round glands infiltrating the stroma of the breast and adipose tissue. Glands were single layered and lined by an intact basement membrane, which can be highlighted by periodic acid–Schiff (PAS) and reticulin stains. However, myoepithelium was absent, as revealed by the absence of immunohistochemical reactivity for calponin. In the lumens of the glands, eosinophilic secretions were common.

Table 2.

Pathologic and immunohistochemical features of the five cases of MGACA

Fig. 1.

Representative histologic features of the five cases. (A, C, E, G, I) Microglandular adenosis (MGA) or atypical MGA component. (B, D, F, H, J) Carcinoma component arising in MGA in each case. (H) Histologic features of matrix forming metaplastic carcinoma. (J) Ductal carcinoma in situ (A, B, case 1; C, D, case 2; E, F, case 3; G, H, case 4; I, J, case 5).

In areas diagnosed as AMGA, glands became irregular in shape and cytologically, the nuclear pleomorphism or atypism increased as the amount of eosinophilic secretions decreased. Furthermore, the proliferating atypical cells filled the lumens completely to form carcinoma in situ lesions and finally grew to break the basement membrane to invade the stroma which can be visualized as interrupted and discontinued strands of fibers on PAS and reticulin stains.

Even though this histological spectrum occurred in all four cases of the invasive cancers, the invasive components of some cases had unique morphologic features to be sub-classified separately. Cases 2 and 3 had some characteristic features in the glands, which were similar to those of the pancreas or of the salivary gland. These specific glands tend to make acinar structures with abundant eosinophilic cytoplasmic granules. Case 5, the DCIS lesion, also showed acinic cell differentiation. The acinic cell differentiation in these three cases was confirmed by the immunohistochemical staining for α1-antitrypsin and chymotrypsin (Table 2, Fig. 2). Case 4 was diagnosed as metaplastic carcinoma, specifically a matrix-producing carcinoma showing an abrupt transition from the typical invasive carcinoma to spindle cell carcinoma with chondromyxoid matrix.

Fig. 2.

Acinic cell differentiation in case 3. Tumor cells have eosinophilic granular cytoplasm (A) and show immunoreactivity to α1-antitrypsin (B).

All tumor cells of MGACA in our cases were negative to estrogen receptor, progesterone receptor, and human epidermal growth factor receptor 2, that is, triple-negative. For the immunohistochemical study with S-100 protein, which is the most well-known immunohistochemical marker for MGA lesions, we used a polyclonal antibody which is mainly reactive to S-100b subunit. The reactivity gradually decreased as the lesions progressed from MGA to AMGA and MGACA, showing near negativity in some areas of invasive carcinoma (Fig. 3). On the other hand, Ki-67 index increased form MGA to AMGA and finally to MGACA, as expected. p53 reactivity was negative in four cases except for case 4. For cytokeratin 5/6, four cases including one DCIS case demonstrated at least focal positivity (Table 2).

Fig. 3.

S-100 protein and p53 expression in case 4. (A, B) Atypical microglandular adenosis (AMGA) shows diffuse strong positivity to S-100 protein (A), while carcinoma arising in microglandular adenosis (MGACA) shows decreased expression to S-100 protein (B). (C, D) p53 staining is evident in MGACA (D), but not in AMGA (C).

DISCUSSION

The MGA differs substantially from other adenosis lesions in many aspects including the immunohistochemical properties. The myoepithelial linings, which disappear in MGA, resulted in negative reactivity to the myoepithelial markers such as calponin and p63. In our case, calponin was all negative in the MGA lesions as well as in the associated carcinoma. The PAS and reticulin staining instead revealed the intact and regular linings of the basement membranes of MGA. These staining patterns therefore could be used to distinguish the invasive portion from the DCIS or other AMGA lesions. The invasive cancers showed the irregular and discontinuous stromal fibers around tumor cell nests.

Through the immunohistochemical studies, we could detect some phenotypic changes from MGA to MGACA. Ki-67 index increased in a stepwise manner as the diseases progressed. Especially in case 4, p53 overexpression gradually increased during transition from AMGA to MGACA. In contrast, the positivity of S-100 protein, the most unique immunohistochemical property of MGA, diminished gradually as the disease progressed to MGACA.

However, some studies reported positive results with S-100 protein in carcinoma portions as strong as in the pure MGA lesions [5,6]. This discordance may have resulted from the use of different members of S-100 protein, which is known to have at least 21 types currently [7]. In a study of MGACA, Koenig et al. [3] used two separate antibodies of S-100 protein, S-100a and S-100b for immunohistochemical characterization of MGACA, and reported that S-100b protein showed decreased reactivity, which is similar to our result. They suggested that this finding might be derived from the different localizations of the S-100a and S-100b, which are ductal cytoplasm and myoepithelium, respectively [3]. However, as MGA shows immunoreactivity to S-100b, it is plausible that epithelial cells of MGA pose myoepithelial cell features and this characteristic may be lost during the progression from MGA to MGACA.

The various histologic and immunohistochemical features of MGACA in our cases have some points of interest. Among the various molecular subtypes of the triple-negative breast cancer [8], the metaplastic carcinoma case resembles mainly the mesenchymal subtype because it had chondromyxoid and spindle cell areas and was highly proliferative (Ki-67 index, 80%). Several MGACAs of our cases demonstrated acinic cell differentiation. Interestingly, two invasive cancers with acinic cell differentiation were all positive for α1-antitrypsin and totally negative for chymotrypsin. The DCIS case with acinic cell differentiation showed weak positivity for α1-antitrypsin. These findings are reminiscent of acinic cell carcinoma of the salivary gland rather than that of the pancreas, which is usually positive for chymotrypsin and α1-antichymotrypsin and almost always negative for α1-antitrypsin. It is also consistent with the fact that the traditional acinic cell carcinomas of the breast look similar to that of the salivary gland. Large proportions of the acinic cell carcinomas of the breast reported in articles share many aspects in common with our cases both histologically and immunohistochemically; this suggests that most acinic cell carcinomas originated in breast may arise from MGA lesions.

The molecular characteristics of MGA and MGACA are currently being investigated [9-12] and one study reported some shared genetic mutations between MGA and MGACA in four out of 12 cases [11]. The overlapped sequences included recurrent gains on 1q, 2q, and 8q and losses in 14q. They suggested that MGA might be a non-obligate precursor to a specific subgroup of high grade triple-negative breast carcinomas [11].

As the histologic spectrum of the MGA associated lesions (from the MGA to AMGA and MGACA) becomes a frequent finding, some researchers suggested a new term, “microglandular adenoma” instead of “microglandular adenosis” for its potential to become a cancer [9]. According to their opinions, MGA seems to be more similar to the adenoma of the gastrointestinal tract rather than other adenosis lesions of the breast in terms of the possibility to progress to malignancies.

In conclusion, MGACA is one of the rare breast cancers and has many unique features that are worth classifying. Further studies will be needed to find the association between the genetic backgrounds and the characteristics of the lesions.

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