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膀胱肉瘤样癌1例报告及文献复习

The case report about bladder sarcomatoid carcinoma with literature review
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摘要 目的结合文献报告1例膀胱肉瘤样癌病例。方法对1例老年男性膀胱肉瘤样癌病例进行报道并对文献复习。结果病人男,83岁,以无痛性全程肉眼血尿收入院。CT影像学检查示膀胱内混合密度肿物。膀胱镜检示膀胱内多发肿物。予以膀胱部分切除术治疗。术后病理组织镜检示,癌及肉瘤成分共存,两者间分界明显。术后组织免疫组化检查示CK(-),CK7(-),CK20(-),EMA(+),Vimentin(2+),Desmin(-),CD34(-),Myogenin(-),GATA3(+/-),S-100(-),Melanoma(-),Ki-67(+60%)。据此诊断为膀胱肉瘤样癌。术后第3个月复查全腹CT示膀胱内肿瘤复发及膀胱外转移。术后1年后病人死于肿瘤全身转移。结论膀胱肉瘤样癌病例多数同时表达上皮及间质肿瘤标志物。病例病情进展迅速,预后差。需要加强此类病例资料收集。 Objective The clinical observation about a case of bladder sarcomatoid carcinoma is reported by literatures review.Methods A case about an elderly male patient with bladder sarcomatoid carcinoma is represented while reviewing associated literatures.Results A 83-year-old male was admitted into our hospital in complaint of gross hematuria.CT Image examination showed the bladder mass with mixed density.Therefore,we performed a cystoscopy to identify those leision and found multiple tumor widely spreading in bladder.In view of that,the partial bladder resection was performed.The postoperation immunohistochemical examination showed,CK(-),CK7(-),CK20(-),EMA(+),Vimentin(2+),Desmin(-),CD34(-),Myogenin(-),GATA3(+/-),S-100(-),Melanoma(-),Ki-67(+60%)and the diagnosis of sarcomatoid carcinoma in bladder was established.3 mouth after operation,CT examination revealed recurrence in bladder with extra-vesical metastasis.The patient died one year after operation because of multiple metastasis.Conclusion The bladder sarcomatoid carcioma is a rare biphasic tumor that contains epithelial and mesenchymal components.Such disease develop rapidly with poor prognosis.More attention should be paid on the collection of associated clinical data.
作者 肖兆铭 王文瑞 李健 刘汉超 刘屹立 王玥茹 XIAO Zhaoming;WANG Wenrui;LI Jian;LIU Hanchao;LIU Yili;WANG Yueru(Department of Urology,The Fourth Affiliated Hospital of China Medical University,Shenyang,Liaoning 110033,China)
出处 《安徽医药》 CAS 2019年第7期1423-1426,I0003,共5页 Anhui Medical and Pharmaceutical Journal
关键词 膀胱肿瘤 癌肉瘤 病例报告 文献复习 Urinary bladder neoplasms Sarcomatoid cacinoma Case report Literatures review
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