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Metaplastic Carcinoma Of The Breast With CD117 Positive Staining. Case Report And Review Of Immunostaining

机译:带有CD117阳性染色的乳腺上皮化生癌。病例报告和免疫染色回顾

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Metaplastic carcinomas of the breast are rare and are reported to comprise less than 1% of all invasive breast tumors. The range of age at diagnosis as well as clinical symptoms does not differ from that of conventional invasive ductal breast cancer. The tumor can be composed of a variety of different cells making it difficult to correctly diagnose this type of growth due to the unknown origin of the cancer. Metaplastic carcinomas can be classified into purely epithelial or mixed epithelial and mesenchymal carcinomas. Features of an adenocarcinoma or squamous cell carcinoma can be seen along with mesenchymal components ranging from chondroid or osseus metaplasia to chondro- or osteosarcoma. (1) In this report we follow a case of metaplastic carcinoma with a immunohistochemistry study that shows positivity for CD117 and the potential consideration for effective treatment in such positivity with a current review of the literature. Report of Case A 52-year-old female presented to the family medicine clinic with a history of weight loss. The patient complained of a breast lump which had been present for 7 months in conjunction with nipple discharge. Local examination showed a 10 X 8 cm lump. The skin above the lump was peau d’orange, the area was ulcerated and inflamed with a blood stained discharge, along with a palpable lymph node at the right axilla. The left breast showed no signs of abnormality. There was no family history of breast cancer. Ultrasound revealed a 6.7 X 4.1 cm cross section diameter, heterogeneous, cystic and calcified mass in the right breast. Left breast by ultrasound was normal. Pathological Findings The mastectomy specimen contained a 14 X 10 X 9 cm mass extended to the maxillary tail and adheres to the upper lateral quadrant with a 9X8cm ulcerating skin surface. Nipple and areola appeared normal. Cut section from the case showed a deeply necrotic myxoid soft heterogeneous mass containing questionable fatty areas with a cystic center. The mass extended closely to the smooth posterior resection margin surrounded by fibrotic tissue. Dissection of the axillary tail revealed 13 small lymph nodes.Multiple sections of the mass (Figure 1) demonstrated vaguely defined high grade fibrosarcoma-like proliferation formed by intersection bundles, whorls and peculiar perivascular formations. Different microscopic forms were seen such as crisscross, herring bone, fascicular, storiform, neuronal and emangiopericitoma pattern. The forms were composed of compact, crowded or loose cells presenting an eosinophillic abundant cytoplasm. The cells had an oval to spindle pleomorphic, hyperchromatic nuclei containing visible small nucleoli. Frequent mitotic figures and scattered mast cells were present.Also rare scattered foci of malignant squamous cells were noted. White areas surrounding the tumor showed breast tissue with fibrocystic changes. All lymph nodes were free of tumor. Immunohistochemistry (Figure 2) showed that tumor cells were reactive for CD 117, epithelial membrane antigen (EMA), Vimentin, Chemotrypsin and partially positive for Pan Cytokeratin. The cells were negative for estrogen receptors, progesterone receptors, Her-2 and CD34. The diagnosis was invasive metaplastic carcinoma with a high grade spindle cell type. No lymphovascular invasion was present. The nipple, areola, resection margins and right axillary lymph nodes were free of tumor.
机译:乳腺的化生癌很少见,据报道占所有浸润性乳腺肿瘤的比例不到1%。诊断时的年龄范围以及临床症状与常规浸润性导管癌没有区别。肿瘤可由各种不同的细胞组成,由于癌症的起源未知,因此很难正确地诊断这种类型的生长。上皮化生癌可以分为纯上皮癌或混合上皮癌和间充质癌。可以看到腺癌或鳞状细胞癌的特征以及间充质成分,从软骨或骨化生到软骨肉瘤或骨肉瘤。 (1)在本报告中,我们通过免疫组织化学研究追踪了一个化生癌病例,该研究显示了CD117的阳性,并在目前的文献综述中显示了对这种阳性的有效治疗的潜在考虑。病例报告一名52岁女性因减肥史被送往家庭医学诊所。该患者抱怨乳房肿块伴有乳头溢液已存在7个月了。局部检查显示有10 X 8 cm肿块。肿块上方的皮肤呈棕褐色,该区域溃疡并发红,并伴有血迹,右腋窝有明显的淋巴结。左乳房无异常迹象。没有乳腺癌家族史。超声检查发现右乳房的横截面直径为6.7 X 4.1 cm,异质性,囊性和钙化肿块。超声检查左乳房正常。病理结果乳房切除术标本包含一个14 X 10 X 9 cm的肿块,该肿块延伸至上颌尾部,并附着于上侧象限,皮肤表面溃疡为9X8cm。乳头和乳晕显得正常。该病例的切面显示出一个严重坏死的粘液样软性异质性肿块,其中包含可疑的脂肪区域和囊性中心。肿块紧密地延伸至平滑的后切除边缘,周围有纤维化组织。腋尾部解剖显示13个小淋巴结,肿块的多个部分(图1)表现出模糊定义的高级别纤维肉瘤样增生,由相交束,螺纹和特殊的血管周围形成。观察到不同的微观形式,例如十字形,鲱鱼形,束状,星形状,神经元状和血管瘤状。形式由紧密,拥挤或疏松的细胞组成,呈现嗜酸性的丰富细胞质。细胞具有从卵形到纺锤状的多形,增色的核,含有可见的小核仁。存在频繁的有丝分裂图和肥大细胞散在,还发现了罕见的恶性鳞状散在灶。肿瘤周围的白色区域显示出乳腺组织的纤维囊变。所有淋巴结均无肿瘤。免疫组织化学(图2)显示,肿瘤细胞对CD 117,上皮膜抗原(EMA),波形蛋白,化学胰蛋白酶具有反应性,而对泛细胞角蛋白则呈部分阳性。这些细胞的雌激素受体,孕激素受体,Her-2和CD34阴性。诊断为浸润性化生性癌,具有高度梭形细胞类型。没有淋巴管浸润。乳头,乳晕,切除切缘和右腋窝淋巴结无肿瘤。

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