新医学
新醫學
신의학
NEW CHINESE MEDICINE
2014年
5期
316-319
,共4页
邓玲%邵建永%张旭%汤涛%邵琼%李银珍
鄧玲%邵建永%張旭%湯濤%邵瓊%李銀珍
산령%소건영%장욱%탕도%소경%리은진
NK/T细胞淋巴瘤%实时定量PCR%原位杂交
NK/T細胞淋巴瘤%實時定量PCR%原位雜交
NK/T세포림파류%실시정량PCR%원위잡교
NK/T-cell lymphoma%Real-time quantitative PCR%In situ hybridization
目的:探讨EB病毒(EBV)-DNA拷贝数和EBV编码的小RNA (EBERs)原位表达在鼻NK/T细胞淋巴瘤(NKTCL)是否具有一致性。方法回顾性分析50例鼻NKTCL的临床病理特征,免疫组织化学检测CD3、CD45RO、CD20、CD56、CD79a、TIA1、Granzyme B表达情况;分别运用实时定量PCR检测石蜡组织中EBV-DNA的拷贝数以及原位杂交检测EBERs,分析与EBV感染与鼻NKTCL的关系。结果鼻NKTCL大部分发生部位位于鼻腔占88%(44/50),伴有出血、坏死以及溃疡者高达100%(50/50)。CD3、CD56、TIA1、Granzyme B及EBV-DNA 和EBERs阳性表达率达100%。所有患者的EBV-DNA拷贝数均处于一个较高的水平,最小拷贝数为127.105,最大拷贝数为1450000,其中位拷贝数是23750。结论实时定量PCR检测EBV-DNA拷贝数与原位杂交技术检测EBERs表达具有高度一致性。因此鉴于鼻NKTCL具有组织形态复杂多样性的特点,在诊断鼻NKTCL时需综合考虑临床表现、形态学改变、免疫表型及EBV-DNA或EBERs高水平表达,方能明确诊断。
目的:探討EB病毒(EBV)-DNA拷貝數和EBV編碼的小RNA (EBERs)原位錶達在鼻NK/T細胞淋巴瘤(NKTCL)是否具有一緻性。方法迴顧性分析50例鼻NKTCL的臨床病理特徵,免疫組織化學檢測CD3、CD45RO、CD20、CD56、CD79a、TIA1、Granzyme B錶達情況;分彆運用實時定量PCR檢測石蠟組織中EBV-DNA的拷貝數以及原位雜交檢測EBERs,分析與EBV感染與鼻NKTCL的關繫。結果鼻NKTCL大部分髮生部位位于鼻腔佔88%(44/50),伴有齣血、壞死以及潰瘍者高達100%(50/50)。CD3、CD56、TIA1、Granzyme B及EBV-DNA 和EBERs暘性錶達率達100%。所有患者的EBV-DNA拷貝數均處于一箇較高的水平,最小拷貝數為127.105,最大拷貝數為1450000,其中位拷貝數是23750。結論實時定量PCR檢測EBV-DNA拷貝數與原位雜交技術檢測EBERs錶達具有高度一緻性。因此鑒于鼻NKTCL具有組織形態複雜多樣性的特點,在診斷鼻NKTCL時需綜閤攷慮臨床錶現、形態學改變、免疫錶型及EBV-DNA或EBERs高水平錶達,方能明確診斷。
목적:탐토EB병독(EBV)-DNA고패수화EBV편마적소RNA (EBERs)원위표체재비NK/T세포림파류(NKTCL)시부구유일치성。방법회고성분석50례비NKTCL적림상병리특정,면역조직화학검측CD3、CD45RO、CD20、CD56、CD79a、TIA1、Granzyme B표체정황;분별운용실시정량PCR검측석사조직중EBV-DNA적고패수이급원위잡교검측EBERs,분석여EBV감염여비NKTCL적관계。결과비NKTCL대부분발생부위위우비강점88%(44/50),반유출혈、배사이급궤양자고체100%(50/50)。CD3、CD56、TIA1、Granzyme B급EBV-DNA 화EBERs양성표체솔체100%。소유환자적EBV-DNA고패수균처우일개교고적수평,최소고패수위127.105,최대고패수위1450000,기중위고패수시23750。결론실시정량PCR검측EBV-DNA고패수여원위잡교기술검측EBERs표체구유고도일치성。인차감우비NKTCL구유조직형태복잡다양성적특점,재진단비NKTCL시수종합고필림상표현、형태학개변、면역표형급EBV-DNA혹EBERs고수평표체,방능명학진단。
Objective To explore whether the EBV-DNA copy number and EBERs expression are concordant with nasal NK/T cell lymphoma (NKTCL)diagnosis. Methods 50 patients diagnosed as nasal NKTCL were investigated in this study retrospectively. Expressions of CD3,CD45RO,CD20,CD56,CD79a, TIA1 ,Granzyme B were applied with immunohistochemistry staining. EBV-encoded small RNAs (EBERs) was measured by in situ hybridization,and EBV-DNA copy numbers with real-time quantitative PCR,respec-tively. Results 88% (44/50)of the nasal NKTCL occurred in nasal cavity. All cases exhibits necrosis,ul-ceration and bleeding. Expressions of CD3,CD56,TIA1 and Granzyme B as well as high level of EBV-DNA and EBERs were observed in all cases. The median EBV-DNA copy number was shown as 23,750 (the range of 1 27.1 05 to 1 450 000). Conclusions The high consistency between EBV-DNA copy numbers and EBERs expression was confirmed. Due to its complex morphological diversity,clinical manifestation,pathological changes,and phenotyping with EBV-DNA copy numbers/EBERs expression should be appiled when nasal NK-TCL was considered.