Granular Cell Tumor of Breast: Rare Tumor Masquerading as Malignancy

S. Hirachan, Y. Singh, A. Jha, U. Manandhar
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Abstract

IntroductionGranular cell tumor (GCT) is a rare soft tissue tumor that arises from the Schwann cells of peripheral nerves. It was first postulated by Abrikossoff in 1926 as Myoblastoma. About 5-15% of these tumors occur in the breast and less than 1% has the potential to be malignant. Here we present a case of 41 years oldpremenopausal woman with Benign GCT of the right breast, having clinically malignant features. The clinical and radiological features of GCT are similar to malignant lump. However, histology showing presence of sheets of polygonal cells with abundant granular eosinophilic cytoplasm with round nuclei and granules with Periodic acid–Schiff (PAS) positive, diastase resistant and S-100 antigen positive are confirmatory. Treatment of Granular cell tumor is wide local excision. There is apparently no role of chemotherapy and radiotherapy. The presence of GCT in the breast is quite rare and clinically as well as radiologicallyit may mimic malignancy, however with histopathology and appropriate immunohistochemistry, proper diagnosis can be made.Keywords: Breast cancer, excision, granular cell tumor
乳腺颗粒细胞瘤:伪装成恶性肿瘤的罕见肿瘤
颗粒细胞瘤(GCT)是一种罕见的软组织肿瘤,起源于周围神经的雪旺细胞。Abrikossoff于1926年首次将其假设为肌母细胞瘤。大约5-15%的肿瘤发生在乳房,不到1%的肿瘤有可能是恶性的。我们在此报告一例41岁的绝经前女性右乳良性GCT,具有临床恶性特征。GCT的临床和影像学表现与恶性肿块相似。然而,组织学显示具有丰富的颗粒状嗜酸性细胞质的多边形细胞片,细胞核圆形,颗粒呈周期性酸希夫(PAS)阳性,淀粉酶耐药和S-100抗原阳性,这是证实性的。颗粒细胞瘤的治疗是广泛的局部切除。化疗和放疗显然没有作用。乳腺GCT的存在是相当罕见的,临床和影像学上它可能模仿恶性肿瘤,但通过组织病理学和适当的免疫组织化学,可以做出正确的诊断。关键词:乳腺癌,切除,颗粒细胞瘤
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