Reis-Filho J S, Faoro L N, Gasparetto E L, Totsugui J T, Schmitt F C
Institute of Molecular Pathology and Immunology of University of Porto, Portugal.
Int J Surg Pathol. 2001 Oct;9(4):331-4. doi: 10.1177/106689690100900413.
Myofibroblastoma of the breast is a rare benign neoplasm, which has rarely been reported in association with gynecomastia. We report a case of a 25-year-old male patient with an epithelioid myofibroblastoma arising in a context of bilateral gynecomastia. The lesion was composed of nests and cords of epithelioid cells, with round to oval nuclei, granular chromatin, and distinct nucleoli dispersed in a myxoid to collagenous stroma with marked vascular proliferation. Immunohistochemical profile showed diffuse positivity for vimentin and focal immunoreactivity for desmin, whereas cytokeratins (CAM5.2 and AE1/AE3), EMA, alpha smooth muscle actin, actin HHF35, CEA, S100, factor VIII, neuron-specific enolase, CD31, and CD34 were all negative. We emphasize that this diagnosis is difficult to establish, owing to the rarity of this variant and clinical presentation.
乳腺肌成纤维细胞瘤是一种罕见的良性肿瘤,很少有与男性乳房发育相关的报道。我们报告一例25岁男性患者,双侧男性乳房发育背景下发生上皮样肌成纤维细胞瘤。病变由上皮样细胞巢和索组成,细胞核圆形至椭圆形,染色质颗粒状,明显的核仁散在于黏液样至胶原性基质中,伴有明显的血管增生。免疫组织化学特征显示波形蛋白弥漫阳性,结蛋白局灶性免疫反应阳性,而细胞角蛋白(CAM5.2和AE1/AE3)、上皮膜抗原、α平滑肌肌动蛋白、HHF35肌动蛋白、癌胚抗原、S100、因子VIII、神经元特异性烯醇化酶、CD31和CD34均为阴性。我们强调,由于这种变异型罕见且临床表现不典型,该诊断难以确立。