CASE REPORT

An 18-year-old female presented with a palpable mass in the upper outer quadrant of the right breast. She had no relevant past medical or family history. Ultrasonographic examination revealed that the mass had increased in size from 1.5 × 1.3 cm to 3.4 × 2.7 cm within a seven-month period. The patient visited Samsung Medical Center in Seoul, Korea, following a biopsy in another hospital, where she was diagnosed with PEComa. Wide excision was performed.

The gross examination showed a well-encapsulated, 4 × 3.2-cm–sized mass, and the cut surface was homogeneously solid and brown. Microscopic findings revealed a thick fibrous capsule wherein epithelioid cells were arranged in a nested architecture surrounded by branching thin-walled vessels (Fig. 1A). The individual epithelioid cells had clear to granular cytoplasm (Fig. 1B). Spindle cells were not observed. The nuclei of the tumor cells were uniform and round, and showed mild atypia. Occasional melanin pigments were noted in the cytoplasm of the tumor cells (Fig. 1C). Necrosis was not identified, and mitoses were counted at up to 3 per 10 high-power fields (HPFs). The tumor showed diffuse strong positivity to HMB45 (1:80, mouse clone HMB45, Dako Corporation, Carpinteria, CA, USA) (Fig. 2A) and TFE3 (1:20, rabbit clone MRQ-37, Cell Marque, Rocklin, CA, USA) (Fig. 2B). TSC2 (1:200, rabbit clone D93F12, Cell Signaling Technology, Danvers, MA, USA) was also positive. Melan A (1:80, mouse clone A103, Dako Corporation), smooth muscle actin (1:100, mouse clone 1A4, Dako Corporation), S100 protein (1:2,000, rabbit polyclonal, Dako Corporation), and cytokeratin (1:500, mouse clone AE1/AE3, Dako Corporation) were not expressed. Moreover, progesterone receptor (PR; 1:800, mouse clone 16, Novocastra Laboratories Ltd., Newcastle upon Tyne, UK) was positive (Fig. 2C), while estrogen receptor (ER; 1:400, mouse clone 6F11, Novocastra Laboratories Ltd.) was negative.

The histologic and immunohistochemical findings were most consistent with PEComa with TFE3 expression.

Ten months after resection, the patient remained healthy with no evidence of recurrence or other unusual findings. This study was approved by the Institutional Review Board of Samsung Medical Center, and the need for informed consent was waived (2018-06-045).

DISCUSSION

PEComa is a tumor composed of PECs. PECs were first described by Apitz in 1943, who recognized unusual “abnormal myoblasts” in an angiomyolipoma, clear cell sugar tumor (CCST), and lymphangioleiomyomatosis [7]. Later, these cells were revealed to be immunoreactive for HMB45. The World Health Organization defines PEComa as a “mesenchymal tumor composed of histologically and immunohistochemically distinctive perivascular epithelioid cells.” [1]

The most common sites of PEComas are the retroperitoneum, abdominopelvic region, uterus, and gastrointestinal tract [1]. The typical histologic findings demonstrate a nested architecture of epithelioid and spindle cells with abundant granular eosinophilic or clear cytoplasm. The epithelioid component of these tumors characteristically expresses melanocytic markers, while the spindle cell component occasionally expresses myogenic markers. PEComas occur more commonly in young and middle-aged patients, and the female to male ratio is greater than 6:1.

In the current report, we present a very rare case of PEComa in the breast. The single known previously reported case was that of an extrapulmonary CCST in the breast of a 16-year-old female, which showed strong immunohistochemical reactivity to HMB45, melan A, and PR [4].

In our case, the tumor was positive for HMB45 and PR (Fig. 2A, C) and negative for melan A. Interestingly, this case showed diffuse strong expression of TFE3 (Fig. 2B) with preserved TSC2 staining. The strong positivity of TFE3 was notable. Conventional PEComas, both sporadic and syndromic, frequently shows inactivation of TSC2 or TSC1 and loss of expression in immunohistochemistry [8]. Recently, Argani et al. [3] suggested that there may be a “distinct subset of PEComa” that harbors TFE3 gene fusions. They concluded that such cases tend to present in a “young age group [and] have no association with tuberous sclerosis, with predominant alveolar architecture and epithelioid cytology [and] minimal immunoreactivity for muscle markers,” [3] a description that conforms to our case. Schoolmeester et al. [6] also reported the distinct morphology and immunohistochemical features of TFE3-rearranged PEComas in the gynecologic tract. TFE3-rearranged PEComas do not share the TSC2/TSC1 genetic abnormalities of conventional PEComas, and retain their protein expressions on immunohistochemistry [7]. Our case showed strong TFE3 expression and the preservation of TSC2 expression. These two sets of genes (TFE3, and TSC2/TSC1) have been suggested to be mutually exclusive and crucial in the pathogenesis of PEComas [5].

The TFE3 gene is located on the short arm of the X chromosome and normally encodes a transcription factor that binds one of the E-box sequences (present in the immunoglobulin enhancer) in the promoter sequences [9]. Downstream of transforming growth factor beta signaling, TFE3 is promoted by encoded transcription factors. Xp11-associated renal cell carcinoma (now reclassified as the MiT family translocation renal cell carcinoma) and alveolar soft part sarcoma (ASPS) are associated with this translocation. TFE3 translocations may play regulatory roles in the epithelioid morphology of tumors arising from different origins [6].

PR immunoreactivity in PEComa has also been described in a previous study [2]. It has been suggested that female hormones play a role in the development of these tumors, considering their female predominance and the frequent involvement of gynecological organs. PEComa of the uterus described by Armah and Parwani [2] showed strong positivity to PR and stronger positivity to ER. However, our case demonstrated PR positivity coupled with ER negativity. The significance of this finding has yet to be determined.

The malignancy criteria of PEComas have not been established because only extremely rare cases have metastasized or recurred. In one study of 26 PEComas, Folpe et al. [10] suggested that tumor size greater than 8 cm, more than one mitosis per 50 HPFs, and presence of necrosis were strongly associated with malignant behavior. In another, Schoolmeester et al. [11] suggested malignancy criteria intended only for gynecologic organs including tumor size greater than 5 cm, high-grade nuclear features, necrosis, vascular invasion, and a mitotic rate greater than 1/50 HPFs.

Although PEComas show a distinct morphology, other entities in the breast presenting an alveolar architecture of epithelioid cells should be considered in determining the identity. The differential diagnosis should include metastatic renal clear cell carcinoma, clear cell glycogen rich carcinoma, and ASPS as per histologic findings. Pancytokeratin negativity excludes the two carcinomas. While epithelioid nested architecture and TFE3 positivity are common histologic features of ASPS, HMB45 positivity excludes this diagnosis.

When pathologists encounter an unusual epithelioid tumor of the breast, PEComa should be considered in the differential diagnosis. In addition to HMB45, other immunohistochemical data such as those of TFE3 and TSC2/TSC1 may be informative.

The accumulation of more data for PEComa and rigorous studies on relevant topics including genetic background may be helpful for determining the origin, prognosis, and treatment options for the rare cases of PEComa.

Fig. 1.

Microscopic findings of the TFE3-expressing breast perivascular epithelioid cell tumor. (A) Epithelioid cells were arranged in a nested architecture with surrounding branching thin-walled vessels. (B) The individual epithelioid cells show clear to granular cytoplasm. (C) Occasional melanin pigments are noted.

Fig. 2.

The immunohistochemical findings of the TFE3-expressing breast perivascular epithelioid cell tumor. The tumor is diffusely positive for human melanoma black 45 (A) and shows nuclear positivity for TFE3 (B) and progesterone receptor (C).

REFERENCES

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Figure & Data

References

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