Zheng Jinfeng, Mo Haiying, Ma Shufang, Wang Zhenzheng
Department of Pathology, The General Hospital, Jinan Military Command Jinan 250031, China.
Department of Pathology, Zaozhuang Hospital of Zaozhuang Mining Group Zaozhuang 277100, China.
Int J Clin Exp Pathol. 2014 Sep 15;7(10):7230-5. eCollection 2014.
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.
我们研究了原发性食管恶性黑色素瘤的影像学和组织病理学特征,以探讨其临床病理特征、诊断、鉴别诊断及治疗方法。采用组织学和免疫组织化学技术对6例食管恶性黑色素瘤进行免疫标记。结合相关文献,观察并分析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织化学特征、治疗及预后。6例原发性食管恶性黑色素瘤患者均为男性,平均年龄63.4岁。所有患者均有进食差的表现,且症状呈进行性加重。内镜下见深褐色及黑色结节状和息肉样病变,累及1/4 - 1/2管腔。肿瘤组织病理学显示以下特征:肿瘤细胞呈巢状、片状和条索状排列,圆形或多边形,细胞质丰富且呈红色染色,细胞质内有黑色素颗粒,核大小不均,核居中或偏位,核仁清晰可辨,病理核分裂明显。免疫表型如下:肿瘤细胞HMB45、Melan A和S100呈弥漫性表达。细胞角蛋白(CK)阴性,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、食管肉瘤样癌、食管淋巴瘤及其他肿瘤。