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首页> 外文期刊>International Journal of Clinical and Experimental Pathology >Clinicopathological findings of primary esophageal malignant melanoma: report of six cases and review of literature
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Clinicopathological findings of primary esophageal malignant melanoma: report of six cases and review of literature

机译:原发性食管恶性黑色素瘤的临床病理表现:六例报告并文献复习

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We studied images and histopathological features of primary esophageal malignant melanoma to explore the clinical pathological features, diagnosis, differential diagnoses, and treatment. Immunolabelling was conducted on six cases of esophageal malignant melanoma using histological and immunohistochemical techniques. Combined with the related literature, the clinical manifestations, imaging, histopathological and immunohistochemical features, treatment, and prognosis of primary esophageal malignant melanoma were observed and analyzed. The six patients with primary esophageal malignant melanoma were all male with an average age of 63.4 years. Poor food intake was observed in all patients, and the symptoms showed progressive aggravation. Endoscopic feed tube revealed dark brown and black nodular and polypoid lesions, 1/4-1/2 loop cavity. Tumor histopathology revealed the following characteristics: tumor cells arranged in nests, sheets and cords, round or polygonal, abundant and red-stained cytoplasm, melanin granules in the cytoplasm, heterogeneous nucleus sizes, centered or deviated nuclei, clearly identifiable nucleoli, and apparent pathological mitosis. The immune phenotype was as follows: tumor cells had diffuse expression of HMB45, Melan A, and S100. The cells were CK negative, and the Ki67-positive cell number was 40%-45%. Primary esophageal malignant melanoma is rare with high malignancy and poor prognosis. Immunohistochemical staining is helpful for diagnosing this tumor. The differential diagnosis includes low differentiated carcinoma, primitive neuroectodermal tumor, esophageal sarcomatoid carcinoma, esophageal lymphoma, and other tumors.
机译:我们研究了原发性食管恶性黑色素瘤的图像和组织病理学特征,以探讨其临床病理特征,诊断,鉴别诊断和治疗。使用组织学和免疫组织化学技术对六例食管恶性黑色素瘤进行了免疫标记。结合相关文献,对原发性食管恶性黑色素瘤的临床表现,影像学,组织病理学和免疫组化特征,治疗方法及预后进行观察和分析。六例原发性食管恶性黑色素瘤患者均为男性,平均年龄为63.4岁。所有患者的食物摄入均较差,症状表现为进行性加重。内窥镜下食管显示黑褐色和黑色结节状和息肉状病变,腔腔为1 / 4-1 / 2。肿瘤组织病理学表现出以下特征:肿瘤细胞排列在巢,片和索中,圆形或多边形,细胞质丰富和染成红色,细胞质中的黑色素颗粒,细胞核大小不均,细胞核居中或偏斜,核仁清晰可辨,并且病理明显有丝分裂。免疫表型如下:肿瘤细胞具有HMB45,Melan A和S100的扩散表达。细胞为CK阴性,且Ki67阳性细胞数为40%-45%。原发性食管恶性黑色素瘤罕见,恶性程度高,预后差。免疫组织化学染色有助于诊断该肿瘤。鉴别诊断包括低分化癌,原始神经外胚层肿瘤,食道肉瘤样癌,食道淋巴瘤和其他肿瘤。

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