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Adenomyoepithelioma A Rare Breast Tumor: Case Studies With Review Of The Literature

机译:子宫腺上皮癌-罕见乳腺肿瘤:病例研究并文献复习

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Introduction : Adenomyoepithelioma is a rare, benign proliferative tumor that can involve the breast tissue. The diagnostic appearance of the lesion can give rise to a difficult differential diagnosis with breast carcinoma. There is the potential for malignant evolution of this lesion. It usually presents as a solitary, unilateral, painless mass at the periphery of the breast. Accurate diagnosis and differentiation from more aggressive tumors is important. Materials and methods :In two cases of breast lumps, fine needle aspiration cytology (FNAC) was done and stained with H & E and Papanicolaou stains. The formalin-fixed tissue sections were stained with hematoxylin and eosin and in one case, immunohistochemistry was performed with smooth muscle actin (SMA).Case 1: A 30-year-old female presented with a firm lump in the upper quadrant of the right breast along with axillary lymphadenopathy since 6 months. On ultrasound it was reported as duct ectasia. FNAC was suggestive of proliferative breast disease with atypia (possibility of duct cell carcinoma). Modified radical mastectomy was done and sent for histopathology. The histopathological diagnosis was adenomyoepithelioma – breast (right), tubular type.Case 2: A 25-year-old female presented with a firm lump in the left breast, occupying all quadrants. On FNAC the aspirates were suggestive of fibroadenoma. Peroperatively it was found to be a cystic swelling occupying the whole breast. The mass was excised and sent for histopathology. The histopathological diagnosis was adenomyeoepithelioma with apocrine metaplasia and cystic degeneration -– breast (left), tubular type.Results : Two cases of breast lump were managed surgically. Both the cases were females with the mean age being 27 years. Both cases were of adenomyoepithelioma (tubular type) with one case showing apocrine metaplasia and cystic change. Conclusion : Prognosis of patients with benign adenomyoepithelioma of the breast is usually good, but it has a potential for local recurrence, especially in the tubular and lobulated variants. Total surgical excision with an adequate margin of uninvolved breast tissue is therefore recommended. Introduction Benign adenomyoepithelioma of the breast is a rare tumor characterized by biphasic proliferation of both an inner layer of epithelial cells and a prominent peripheral layer of myoepithelial cells. It was first described by Hamperl[1] in 1970; more than 60 cases have been reported since then. All cases except 2 occurred in females.[2,3] Benign adenomyoepitheliomas outnumber their malignant counterparts by far. Malignancy may arise either through malignant transformation of 1 of the 2 cellular components or through malignant transformation of both.[4] The difficult differential diagnosis, potential for recurrence and malignant evolution of this lesion merit a careful approach. Materials and methods In two cases of breast lump, FNAC was done and stained with H & E and Papanicolaou stains. The formalin-fixed tissue sections were stained with hematoxylin and eosin, and in one case immunohistochemistry was performed with smooth muscle actin (SMA). Case 1:A 30-year-old female presented with a firm lump in the upper quadrant of the right breast along with axillary lymphadenopathy since 6 months. On ultrasound it was reported as duct ectasia. FNAC was suggestive of proliferative breast disease with atypia (possibility of duct cell carcinoma) (Figure 1, 2).
机译:简介:腺肌上皮瘤是一种罕见的良性增生性肿瘤,可能累及乳房组织。病变的诊断外观可能导致乳腺癌的鉴别诊断困难。该病灶有可能恶变。它通常表现为乳房周围的孤立的,单侧的,无痛的肿块。准确诊断和区分更具侵略性的肿瘤很重要。材料和方法:在2例乳房肿块中,进行了细针穿刺细胞学检查(FNAC),并用H&E和Papanicolaou染色。用福尔马林固定的组织切片用苏木精和曙红染色,在一种情况下,用平滑肌肌动蛋白(SMA)进行免疫组织化学。病例1:一名30岁女性,右上象限有硬块乳房自腋窝淋巴结肿大六个月以来。在超声检查中据报道为导管扩张。 FNAC提示非典型增生性乳腺疾病(可能发生导管细胞癌)。完成改良的根治性乳房切除术并送去进行组织病理学检查。组织病理学诊断为腺肌上皮瘤-乳腺(右),肾小管型。病例2:一名25岁女性,左乳房有硬块,占所有象限。在FNAC上,抽吸物提示纤维腺瘤。围手术期发现这是整个乳房的囊性肿胀。将肿块切除并送去进行组织病理学检查。组织病理学诊断为腺肌上皮瘤伴高教分泌化生和囊性变性-乳腺(左),肾小管型。结果:2例经手术治疗。两例均为女性,平均年龄为27岁。这两例均为腺肌上皮瘤(肾小管型),其中一例显示高教上皮化生和囊性改变。结论:乳腺良性腺肌上皮瘤患者的预后通常良好,但具有局部复发的潜力,尤其是在肾小管和小叶变体中。因此,建议进行充分的手术切除,并留出足够量的未受累的乳房组织。简介乳腺良性腺上皮细胞瘤是一种罕见的肿瘤,其特征是上皮细胞内层和肌上皮细胞的突出外周层双相增殖。 Hamperl [1]于1970年首次描述了它。自那时以来,已报告了60多例。除2例外,其他所有病例均发生在女性中。[2,3]到目前为止,良性腺肌上皮瘤的数量超过了其恶性肿瘤。恶性肿瘤可能是通过2种细胞成分之一的恶性转化或通过两者的恶性转化引起的。[4]该病的鉴别诊断困难,潜在复发和恶性进展,值得认真研究。材料和方法在2例乳腺肿块中,进行了FNAC,并用H&E和Papanicolaou染色。用苏木精和曙红对福尔马林固定的组织切片进行染色,在一种情况下,用平滑肌肌动蛋白(SMA)进行免疫组织化学。病例1:自6个月以来,一名30岁的女性右乳房上象限出现硬块并伴有腋窝淋巴结肿大。在超声检查中据报道为导管扩张。 FNAC提示非典型增生性乳腺疾病(可能发生导管细胞癌)(图1、2)。

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