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原发性肾脏类癌2例报告并文献复习
引用本文:张进,董柏君,陈奇,陈勇辉,陈海戈,薛蔚,黄翼然.原发性肾脏类癌2例报告并文献复习[J].临床泌尿外科杂志,2011,26(4):280-282.
作者姓名:张进  董柏君  陈奇  陈勇辉  陈海戈  薛蔚  黄翼然
作者单位:上海交通大学医学院附属仁济医院泌尿外科,上海,200127
摘    要:目的:探讨原发性肾脏类癌的临床特征及诊治方法。方法:总结2例原发性肾脏类癌患者的临床资料结合文献复习讨论。例1,女,48岁。因右腰酸痛1个月入院。B超示右肾中上极中等回声占位,边界清楚,内有血流信号。CT示右肾中上极10.0cm×7.5cm实性占位,增强后病灶均匀轻度强化。例2,男,44岁。体检发现左肾占岱40天入院。B超示左肾门处中等回声占位,边界清楚,内有血流信号。CT示左肾中极肾门处3.7cm×3.5cm实性占位,增强后病灶均匀轻度强化;其内伴-钙化点。结果:2例均行根治性肾切除术。病理检查镜下肿瘤细胞形态为多边形,嗜酸性颗粒状细胞质,边界不清,呈柱状或缎带状排列混合有实性巢状排列;细胞核呈园形大小一致,核分裂像难见。免疫组化:突触素、波形蛋白均为阳性。病理诊断为肾脏类癌伴淋巴结转移。例1术后30个月死于肝骨转移;例2术后随访26个月,未见肿瘤复发转移。结论:原发性肾脏类癌临床罕见,易发生淋巴结转移,确诊依靠病理学检查,根治性肾切除应为治疗原发性肾类癌的首选方法。

关 键 词:肾肿瘤  类癌

Primary Carcinoid Tumors of the Kidney (Report of 2 Cases and Review of Literature)
Jin ZHANG,Baijun DONG,Qi CHEN,Yonghui CHEN,Haige CHEN,Wei XUE,Yiran HUANG.Primary Carcinoid Tumors of the Kidney (Report of 2 Cases and Review of Literature)[J].Journal of Clinical Urology,2011,26(4):280-282.
Authors:Jin ZHANG  Baijun DONG  Qi CHEN  Yonghui CHEN  Haige CHEN  Wei XUE  Yiran HUANG
Institution:1 Department of Urology, Renji Hospital, Shanghai J iaotong University Medicine School, Shanghai, 200127, China)
Abstract:Objective:To discuss the diagnosis and treatment of primary renal carcinoid tumor Methods: Two cases of primary renal carcinoid tumor were reported and the relevant literature was reviewed. Case 1, a 48-year-old woman, complained of intermittent right back pain for 1 month. B-ultrasound examination showed large patchs with middle-strong echo, well defined regions in upper pole of the right kidney with blood flow signals. CT scan revealed a 10 cm × 7.5 cm mass with uneven enhancement by contrast in the right kidney. Case 2, a 44-year-old man, presented with a solid mass in the left kidney for 40 days. B-ultrasound and CT scan revealed a 3.7 cm ×3. 5 cm mass with calcification and minimal enhancement by contrast in the mid pole of the left kidney. Results: Radical nephrectomy was performed in two patients. Microscopica 11 y, the tumors consisted of tightly packed cords and trabeculae of polygonal neoplastic cells which showed a trabecular or ribbon-like arrangement admixed with solid nests. Nuclei are round to oval and uniform in size with rare mitotic events. Immunohistochemically, neoplas- tic cells were stained positively for Synaptophysin and Vimentin. The pathological diagnosis for both patients was the renal carcinoid tumor with regional lymph nodes metastases. Case 1 was dead of liver and bone metastases at 30 months after the surgery. Case 2 was alive without disease at 26 months. Conclusions: Primary renal carcinoid tumor is a rare disease and has an aggressive clinical course with lymph node metastases early. Surgical resection of these tumors accompanied by lymph node dissection should be the primary therapy.
Keywords:Kidney neoplasms  carcinoid
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