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Case Reports
. 2012 Oct 10;4(4):e50.
doi: 10.4081/rt.2012.e50. Epub 2012 Dec 17.

Myoepithelioma breast: clinically masquerading as breast carcinoma

Affiliations
Case Reports

Myoepithelioma breast: clinically masquerading as breast carcinoma

Brijesh Thakur et al. Rare Tumors. .

Abstract

Pure myoepithelioma of breast is an extremely rare tumor. Only a few cases have been reported in the literature so far. A 30-year old female presented with a large fungating mass arising from the areolar region of her right breast of six months duration. A clinical diagnosis of breast carcinoma was made and a mastectomy was performed. The specimen measured 23×22×9 cm with attached skin, and showed a large white ulcerated growth with areas of necrosis and hemorrhage. No normal breast tissue, nipple or areolar region was seen. Histopathological examination showed oval to spindle cells arranged in fascicles and bundles with whorling pattern in places showing mild pleomorphism with oval to spindle-shaped vesicular nuclei, prominent eosinophilic nucleoli, eosinophilic cytoplasm and clear cell changes in places, along with perivascular hyalinization and collagenization. Differential diagnosis of pleomorphic hyalinizing angiectatic tumor, solitary fibrous tumor, perivascular epithelioid cell tumor, mammary type myofibroblastic tumor and myoepithelioma were all considered. Immunohistochemistry for vimentin, smooth muscle actin, calponin, caldesmon, p63, epithelial membrane antigen, S-100, CD-31, CD-34, muscle specific antigen, myogenin, desmin, and pancytokeratin was carried out. On the basis of positive staining for vimentin, actin, p63 (nuclear), calponin and caldesmon (focal), a final diagnosis of myoepithelioma was considered; however, cytokeratin negativity was an unusual finding. This case was considered worthy of documentation because of its rarity, and because it highlights the importance of proper clinical examination and radiological examination to prevent misdiagnosis.

Keywords: breast; cytokeratin.; myoepithelioma; p63.

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Conflict of interest statement

Conflict of interests: the authors report no conflicts of interests.

Figures

Figure 1
Figure 1
A) Specimen showing a large white ulcerated growth; B) inferior surface of specimen shows attached skin; C) spindle-shaped cells showing whorling pattern around blood vessels (Haematoxylin and Eosin 100×); D) spindle-shaped cells arranged in fascicles around blood vessels (Haematoxylin and Eosin 100×).
Figure 2
Figure 2
A) Clear cell changes in spindle-shaped cells with prominent nucleoli (Haematoxylin and Eosin 400×); B) spindle-shaped cells showing eosinophilic cytoplasm and prominent nucleoli with clear cell changes at places (Haematoxylin and Eosin 400×); C) focal areas of hyalinization and collagenization (Haematoxylin and Eosin 100×); D) few compressed glands at the margin of tumor (Haematoxylin and Eosin 100×). Inset shows myoepithelial proliferation around a duct (400×).
Figure 3
Figure 3
A) Diffuse cytoplasmic positivity for vimentin (400×); B) cytoplasmic positivity for smooth muscle actin (400×); C) nuclear immunopositivity for p63 (400×); D) focal positivity for calponin (400×); E) focal positivity for caldesmon (400×); F) CD34 positivity in blood vessel lining but negative in tumor cells (400×).

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