肾嗜酸细胞腺瘤的诊疗(附35例报告)
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  • 英文篇名:Clinical analysis of renal oncocytoma(Report of 35 cases)
  • 作者:邢会武 ; 王军 ; 孟中勤 ; 谢枫 ; 贾占奎 ; 丁亚飞 ; 李松超 ; 杨锦建
  • 英文作者:XING Huiwu;WANG Jun;MENG Zhongqin;XIE Feng;JIA Zhankui;DING Yafei;LI Songchao;YANG Jinjian;Department of Urology,First Affiliated Hospital of Zhengzhou University,Henan Institute of Urology;Department of Pathology,First Affiliated Hospital of Zhengzhou University;
  • 关键词:肾脏 ; 嗜酸细胞腺瘤 ; 诊断 ; 治疗
  • 英文关键词:kidney;;oncocytoma;;diagnosis;;treatment
  • 中文刊名:LCMW
  • 英文刊名:Journal of Clinical Urology
  • 机构:郑州大学第一附属医院泌尿外科河南省泌尿外科研究所;郑州大学第一附属医院病理科;
  • 出版日期:2019-08-06
  • 出版单位:临床泌尿外科杂志
  • 年:2019
  • 期:v.34;No.308
  • 基金:国家自然科学基金(编号81570685)
  • 语种:中文;
  • 页:LCMW201908003
  • 页数:4
  • CN:08
  • ISSN:42-1131/R
  • 分类号:17-20
摘要
目的:探讨肾嗜酸细胞腺瘤(RO)的诊断和治疗。方法:回顾性分析2011年10月~2018年1月我院收治的35例RO患者的临床资料,其中男18例,女17例;年龄28~80岁,平均(53.9±26.1)岁;5例表现为腰痛,1例表现为腰痛合并全程无痛肉眼血尿,29例为体检发现。CT检查肿瘤均为单发实性占位,其中右侧19例,左侧16例;肿瘤最大径1.6~13.0cm,平均(5.4±2.3)cm;表现中央星形瘢痕14例,均未见淋巴结转移。8例行保留肾单位手术(NSS),27例行根治性肾切除术(RN)。结果:35例术后病理诊断均为RO。肉眼见瘤体呈灰褐或灰黄,其中16例可见中央纤维瘢痕;苏木精-伊红(HE)染色后镜下可见瘤细胞多呈巢状排列,胞浆丰富嗜酸性;免疫组化染色细胞角蛋白(CK)、细胞角蛋白8/18(CK8/18)、上皮膜抗原(EMA)、E-钙黏附素(E-cad)、CD117阳性表达率均为100%,Ki-67呈不同程度阳性表达(1%~5%),RCC、S-100阴性表达率均为100%,CK7、CD10、Vimentin大多阴性表达。35例均获随访,随访时间9~83个月,平均(44.5±24.7)个月,均未见肿瘤复发或转移。结论:RO临床较为少见,影像学特征缺乏特异性,病理诊断为目前唯一可靠的诊断方法,手术治疗首选NSS,预后良好,建议术后定期复查。
        Objective:To analyze the diagnosis and treatment of renal oncocytoma(RO).Method:From October 2011 to January 2018,35 RO patients(18 males and 17 females)whose mean age was(53.9±26.1)(range,28-80)years old were retrospectively analyzed.Five cases were presented with lumbago;one case was combined with lumbago and painless gross hematuria;and the others were discovered by examination.CT showed single tumor(19 cases in the right,16 cases in the left),and the maximum diameter of the tumor was 1.6-13.0 cm,with an average of(5.4±2.3)cm.The central star scar was showed in 14 cases.No lymph node metastasis was found.All cases underwent surgery;of which eight underwent nephron-sparing surgery and 27 underwent radical nephrectomy.Result:The 35 cases were diagnosed as RO.The gross specimens were brown tan or yellow.Sixteen cases showed central fibrous scars.HE staining showed that the tumor cells presented solid-nested,the cytoplasm was abundant,red and eosinophilic under the microscope.Immunohistochemical staining was positive in CK,CK8/18,EMA,E-cad,CD117 and Ki-67(1%-5%);negative in RCC and S-100,most negative expression of CK7,CD10 and Vimentin.So far,neither recurrence nor metastasis has been detected for 9-83 months(mean,44.54 months)in all cases.Conclusion:RO is a kind of rare benign tumor.Histopathology remains the only reliable diagnostic modality.Nephron-sparing surgery is the first choice.Recurrence and metastasis are rare after surgery,but patients should be followed up.
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