中华病理学杂志
中華病理學雜誌
중화병이학잡지
Chinese Journal of Pathology
2014年
3期
154-157
,共4页
王聪%宋国新%李明娜%朱岩%张炜明%张智弘%范钦和
王聰%宋國新%李明娜%硃巖%張煒明%張智弘%範欽和
왕총%송국신%리명나%주암%장위명%장지홍%범흠화
肾肿瘤%病理学,临床%诊断,鉴别
腎腫瘤%病理學,臨床%診斷,鑒彆
신종류%병이학,림상%진단,감별
Kidney neoplasms%Pathology,clinical%Diagnosis,differential
目的 分析和总结后肾腺瘤的临床、影像学及病理学特征.方法 利用光镜观察及免疫组织化学EnVision法分析8例后肾腺瘤,并结合文献讨论其临床影像学特点、病理诊断、鉴别诊断、治疗和预后.结果 患者女性6例,男性2例,年龄12 ~ 70岁,平均年龄43.6岁.肿瘤界清,均位于肾实质的皮质区,镜下观察见水肿的间质中嗜碱性瘤细胞排列成小腺泡状,灶性区可见乳头状结构,偶可见钙化或沙砾体形成;免疫组织化学染色中,肿瘤细胞PAX2、波形蛋白均阳性表达,WT-1表达局灶或弱阳性5例、阳性2例、阴性1例,广谱CK表达阳性3例,CK7表达阴性7例、局灶阳性1例,CD10、肾细胞癌标志物(RCC)、上皮细胞膜抗原、突触素、嗜铬粒素A均阴性.7例Ki-67阳性表达<2%、1例局灶区约5%.8例获得随访,时间7 ~ 57个月,均未出现复发或转移.结论 后肾腺瘤的诊断需依据独特的组织学特征,免疫表型表现为波形蛋白、PAX2恒定表达,部分病例WT-1有局灶或弱阳性表达,Ki-67阳性表达率低,其诊断需有临床及影像学资料的支持.
目的 分析和總結後腎腺瘤的臨床、影像學及病理學特徵.方法 利用光鏡觀察及免疫組織化學EnVision法分析8例後腎腺瘤,併結閤文獻討論其臨床影像學特點、病理診斷、鑒彆診斷、治療和預後.結果 患者女性6例,男性2例,年齡12 ~ 70歲,平均年齡43.6歲.腫瘤界清,均位于腎實質的皮質區,鏡下觀察見水腫的間質中嗜堿性瘤細胞排列成小腺泡狀,竈性區可見乳頭狀結構,偶可見鈣化或沙礫體形成;免疫組織化學染色中,腫瘤細胞PAX2、波形蛋白均暘性錶達,WT-1錶達跼竈或弱暘性5例、暘性2例、陰性1例,廣譜CK錶達暘性3例,CK7錶達陰性7例、跼竈暘性1例,CD10、腎細胞癌標誌物(RCC)、上皮細胞膜抗原、突觸素、嗜鉻粒素A均陰性.7例Ki-67暘性錶達<2%、1例跼竈區約5%.8例穫得隨訪,時間7 ~ 57箇月,均未齣現複髮或轉移.結論 後腎腺瘤的診斷需依據獨特的組織學特徵,免疫錶型錶現為波形蛋白、PAX2恆定錶達,部分病例WT-1有跼竈或弱暘性錶達,Ki-67暘性錶達率低,其診斷需有臨床及影像學資料的支持.
목적 분석화총결후신선류적림상、영상학급병이학특정.방법 이용광경관찰급면역조직화학EnVision법분석8례후신선류,병결합문헌토론기림상영상학특점、병리진단、감별진단、치료화예후.결과 환자녀성6례,남성2례,년령12 ~ 70세,평균년령43.6세.종류계청,균위우신실질적피질구,경하관찰견수종적간질중기감성류세포배렬성소선포상,조성구가견유두상결구,우가견개화혹사력체형성;면역조직화학염색중,종류세포PAX2、파형단백균양성표체,WT-1표체국조혹약양성5례、양성2례、음성1례,엄보CK표체양성3례,CK7표체음성7례、국조양성1례,CD10、신세포암표지물(RCC)、상피세포막항원、돌촉소、기락립소A균음성.7례Ki-67양성표체<2%、1례국조구약5%.8례획득수방,시간7 ~ 57개월,균미출현복발혹전이.결론 후신선류적진단수의거독특적조직학특정,면역표형표현위파형단백、PAX2항정표체,부분병례WT-1유국조혹약양성표체,Ki-67양성표체솔저,기진단수유림상급영상학자료적지지.
Objective To study the clinical and histopathologic features of metanephric adenoma (MA).Methods Eight cases of recently diagnosed MA were retrieved from archival file.Immunohistochemical study was carried out.The clinical characteristics,pathologic parameters,differential diagnosis,treatment options and prognosis of MA were analyzed,with literature review.Results The patients included 6 females and 2 males.The age of patients ranged from 12 to 70 years (mean =43.6 years).Eight cases were located in renal cortex and showed well-defined borders.Histologically,the tumor was composed of tubules lined by small basophilic cells and embedded in an edematous stroma.Papillary structures and psammoma bodies were focally seen.Immunohistochemical study showed that the tumor cells were positive for PAX2 and vimentin in all the 8 cases.WT-1 was positive in 2 cases,focal and weak in 5 cases,and negative in 1 case.CK-Pan was positive in 3 cases.CK7 staining was mostly negative,with focal and weak positivity only in 1 case.The proliferative index,as highlighted by Ki-67 staining,was less than 2% in 7 cases and focally around 5% in 1 case.The expressions of CK20,CD10,RCC,epithelial membrane antigen,CD56,synaptophysin and chromogranin A were negative.Follow-up information from 7 to 57 months was available in all patients; and none of them developed local recurrence or distant metastasis.Conclusions The diagnosis of MA relies primarily on thorough histologic examination and immunohistochemical study (vimentin and PAX2 positive,WT-1 focally and weakly positive in some cases,and low proliferative index).Correlation with clinical and radiologic findings would also be helpful.