中华病理学杂志
中華病理學雜誌
중화병이학잡지
Chinese Journal of Pathology
2012年
6期
371-375
,共5页
黄文涛%李小秋%姚晓红%陆永明%盛伟琪%陆洪芬%周晓燕
黃文濤%李小鞦%姚曉紅%陸永明%盛偉琪%陸洪芬%週曉燕
황문도%리소추%요효홍%륙영명%성위기%륙홍분%주효연
淋巴瘤,大细胞%原位杂交,荧光%易位,遗传
淋巴瘤,大細胞%原位雜交,熒光%易位,遺傳
림파류,대세포%원위잡교,형광%역위,유전
Lymphoma,large cell%In situ hybridization,fluorescence%Translocation,genetic
目的 利用荧光原位杂交(FISH)技术观察间变性大细胞淋巴瘤(ALCL)中间变性淋巴瘤激酶(ALK)基因相关染色体易位,探讨其在临床病理学中的应用价值.方法 收集复旦大学附属肿瘤医院和上海交通大学附属新华医院病理科1999至2006年间病例55例(其中45例ALCL,10例淋巴结反应性增生),以LSI ALK双色分离重排探针,利用FISH法检测ALCL中ALK相关染色体易位,并与前期免疫组织化学(IHC)、逆转录聚合酶链反应(RT-PCR)检测结果进行对比分析.结果 FISH检测结果显示,45例ALCL中,38例成功检测到清晰的红绿信号,其中24例(24/38,63.2%)见明显的荧光分离信号,表明存在ALK相关染色体易位,其中1例表现为ALK基因多拷贝;14例(36.8%,14/38)仅见红绿融合荧光信号,表明不存在ALK相关染色体易位;7例无荧光信号或信号太弱无法判断结果,检测失败.FISH法检测AI.K相关染色体易位与前期IHC检测AIK蛋白、RT-PCR法检测ALK相关融合基因的结果基本一致(均P<0.01),10例淋巴结反应性增生病例中,均未见ALK相关染色体易位.结论 ALCL是一类具有特殊临床表现、病理形态及ALK表达异常的淋巴瘤.FISH法能有效地检测出ALCL中ALK相关染色体易位,但其可能受蜡块存放时间影响较大,与IHC、RT-PCR法互相补充,有助于ALK+ ALCL与ALK ALCL的鉴别诊断.
目的 利用熒光原位雜交(FISH)技術觀察間變性大細胞淋巴瘤(ALCL)中間變性淋巴瘤激酶(ALK)基因相關染色體易位,探討其在臨床病理學中的應用價值.方法 收集複旦大學附屬腫瘤醫院和上海交通大學附屬新華醫院病理科1999至2006年間病例55例(其中45例ALCL,10例淋巴結反應性增生),以LSI ALK雙色分離重排探針,利用FISH法檢測ALCL中ALK相關染色體易位,併與前期免疫組織化學(IHC)、逆轉錄聚閤酶鏈反應(RT-PCR)檢測結果進行對比分析.結果 FISH檢測結果顯示,45例ALCL中,38例成功檢測到清晰的紅綠信號,其中24例(24/38,63.2%)見明顯的熒光分離信號,錶明存在ALK相關染色體易位,其中1例錶現為ALK基因多拷貝;14例(36.8%,14/38)僅見紅綠融閤熒光信號,錶明不存在ALK相關染色體易位;7例無熒光信號或信號太弱無法判斷結果,檢測失敗.FISH法檢測AI.K相關染色體易位與前期IHC檢測AIK蛋白、RT-PCR法檢測ALK相關融閤基因的結果基本一緻(均P<0.01),10例淋巴結反應性增生病例中,均未見ALK相關染色體易位.結論 ALCL是一類具有特殊臨床錶現、病理形態及ALK錶達異常的淋巴瘤.FISH法能有效地檢測齣ALCL中ALK相關染色體易位,但其可能受蠟塊存放時間影響較大,與IHC、RT-PCR法互相補充,有助于ALK+ ALCL與ALK ALCL的鑒彆診斷.
목적 이용형광원위잡교(FISH)기술관찰간변성대세포림파류(ALCL)중간변성림파류격매(ALK)기인상관염색체역위,탐토기재림상병이학중적응용개치.방법 수집복단대학부속종류의원화상해교통대학부속신화의원병이과1999지2006년간병례55례(기중45례ALCL,10례림파결반응성증생),이LSI ALK쌍색분리중배탐침,이용FISH법검측ALCL중ALK상관염색체역위,병여전기면역조직화학(IHC)、역전록취합매련반응(RT-PCR)검측결과진행대비분석.결과 FISH검측결과현시,45례ALCL중,38례성공검측도청석적홍록신호,기중24례(24/38,63.2%)견명현적형광분리신호,표명존재ALK상관염색체역위,기중1례표현위ALK기인다고패;14례(36.8%,14/38)부견홍록융합형광신호,표명불존재ALK상관염색체역위;7례무형광신호혹신호태약무법판단결과,검측실패.FISH법검측AI.K상관염색체역위여전기IHC검측AIK단백、RT-PCR법검측ALK상관융합기인적결과기본일치(균P<0.01),10례림파결반응성증생병례중,균미견ALK상관염색체역위.결론 ALCL시일류구유특수림상표현、병리형태급ALK표체이상적림파류.FISH법능유효지검측출ALCL중ALK상관염색체역위,단기가능수사괴존방시간영향교대,여IHC、RT-PCR법호상보충,유조우ALK+ ALCL여ALK ALCL적감별진단.
Objective To investigate clinicopathologic features and clinical value of the chromosonal translocation involving anaplastic lymphoma kinase (ALK) in anaplastic large cell lymphoma (ALCL) by fluorescence in situ hybridization (FISH).Methods A total of 55 cases,including45 cases of ALCL and 10 reactive lymphoid hyperplasia,were collected during 1999 to 2006 in the Department of Pathology,Fudan University Shanghai Cancer Center,and Xinhua Hospital Affiliated to Shanghai Jiaotong University.All cases were studied by FISH using dual color break apart probes of ALK for detection of chromosomal translocation,compared with the previous results of immunohistochemistry (IHC) and reversetranscriptase polymerase chain reaction ( RT-PCR ) for the detection of ALK aberrations.Results The resuh of FISH showed that the clear red and green fluorescence signals were detected in 38 cases of ALCL,in which conspicuous split signals were observed in tumor cells in 24 cases ( 63.2% ),suggesting the rearrangement of the ALK locus,with multiple copies of ALK gene in one case.In addition,the rearrangement of the ALK locus was not identified in 14 of 38 cases ( 36.8% ) ; and the FISH results were unable to be evaluated in 7 cases,because no fluorescent signals involving ALK gene were found or signals were too weak to be analyzed.The concordance for the detection ALK aberrations in ALCL between FISH and RT-PCR,FISH and IHC were both statistically significant ( P < 0.01 ).Chromosomal translocation involving ALK gene was not found in all 10 cases of reactive lymphoid hyperplasia.Conclusions ALCL is an entity of lymphoma characterized by special clinical presentation,morphology,and ALK aberrations.FISH is helpful for detection of the chromosomal translocations involving ALK in ALCL,however,the detection efficiency by FISH may be affected by storage time of the parafin-embedded tissue; and therefore combined detection with IHC and RT-PCR could complement each other and help for differential diagnosis of ALK + ALCL from ALK- ALCL.