中华病理学杂志
中華病理學雜誌
중화병이학잡지
Chinese Journal of Pathology
2015年
2期
111-117
,共7页
牛会林%徐涛%王凤华%陈峥嵘%高秋%伊鹏%夏健清
牛會林%徐濤%王鳳華%陳崢嶸%高鞦%伊鵬%夏健清
우회림%서도%왕봉화%진쟁영%고추%이붕%하건청
神经母细胞瘤%基因,myc%儿童%预后
神經母細胞瘤%基因,myc%兒童%預後
신경모세포류%기인,myc%인동%예후
Neuroblastoma%Genes,myc%Child%Prognosis
目的 分析小儿神经母细胞肿瘤(NT)的临床病理学特征,探讨MYCN扩增病例形态学改变及其在NT预后的意义.方法 回顾性分析267例小儿NT的临床病理资料.其中119例经荧光原位杂交(FISH)检测MYCN基因扩增情况,探讨MYCN扩增及其与病理形态学指标的关系,并进行预后分析.结果 267例小儿NT中,年龄1 d至13岁,中位数为27个月;男女比例为1.43∶ 1.00;组织学预后良好型157例(59.9%),组织学预后不良型110例(40.1%);临床分期,Ⅰ期38例(14.2%),Ⅱ期43例(16.1%),Ⅲ期71例(26.6%),Ⅳ期115例(43.1%,其中Ⅳs期8例).119例NT中18例MYCN扩增(15.1%),MYCN与第2号染色体信号比值为4.08~43.29;MYCN无扩增101例,其中包括获得79例(66.3%),阴性22例(18.5%).MYCN的表达在不同年龄、性别、NT分型以及核分裂-核碎裂指数(MKI)高低组间差异有统计学意义(P =0.000),而与组织学预后分组及临床分期无关(P>0.05).18例MYCN扩增病例中未分化型3例,其余15例为分化差型;17例具有高MKI,1例为中MKI;均属组织学预后不良组.3例存活,15例死亡,平均生存期为(17.9±2.4)个月.MYCN未扩增病例101例,69例存活(68.3%),32例死亡(31.7%),平均生存期(29.8±1.3)个月.生存分析结果显示,MYCN扩增患儿预后较差(P<0.05).结论 NT发病年龄小,易转移,组织学分型多为预后良好型;MYCN基因扩增病例组织学均表现为预后不良型,多伴高MKI;MYCN基因扩增患儿预后差.
目的 分析小兒神經母細胞腫瘤(NT)的臨床病理學特徵,探討MYCN擴增病例形態學改變及其在NT預後的意義.方法 迴顧性分析267例小兒NT的臨床病理資料.其中119例經熒光原位雜交(FISH)檢測MYCN基因擴增情況,探討MYCN擴增及其與病理形態學指標的關繫,併進行預後分析.結果 267例小兒NT中,年齡1 d至13歲,中位數為27箇月;男女比例為1.43∶ 1.00;組織學預後良好型157例(59.9%),組織學預後不良型110例(40.1%);臨床分期,Ⅰ期38例(14.2%),Ⅱ期43例(16.1%),Ⅲ期71例(26.6%),Ⅳ期115例(43.1%,其中Ⅳs期8例).119例NT中18例MYCN擴增(15.1%),MYCN與第2號染色體信號比值為4.08~43.29;MYCN無擴增101例,其中包括穫得79例(66.3%),陰性22例(18.5%).MYCN的錶達在不同年齡、性彆、NT分型以及覈分裂-覈碎裂指數(MKI)高低組間差異有統計學意義(P =0.000),而與組織學預後分組及臨床分期無關(P>0.05).18例MYCN擴增病例中未分化型3例,其餘15例為分化差型;17例具有高MKI,1例為中MKI;均屬組織學預後不良組.3例存活,15例死亡,平均生存期為(17.9±2.4)箇月.MYCN未擴增病例101例,69例存活(68.3%),32例死亡(31.7%),平均生存期(29.8±1.3)箇月.生存分析結果顯示,MYCN擴增患兒預後較差(P<0.05).結論 NT髮病年齡小,易轉移,組織學分型多為預後良好型;MYCN基因擴增病例組織學均錶現為預後不良型,多伴高MKI;MYCN基因擴增患兒預後差.
목적 분석소인신경모세포종류(NT)적림상병이학특정,탐토MYCN확증병례형태학개변급기재NT예후적의의.방법 회고성분석267례소인NT적림상병리자료.기중119례경형광원위잡교(FISH)검측MYCN기인확증정황,탐토MYCN확증급기여병리형태학지표적관계,병진행예후분석.결과 267례소인NT중,년령1 d지13세,중위수위27개월;남녀비례위1.43∶ 1.00;조직학예후량호형157례(59.9%),조직학예후불량형110례(40.1%);림상분기,Ⅰ기38례(14.2%),Ⅱ기43례(16.1%),Ⅲ기71례(26.6%),Ⅳ기115례(43.1%,기중Ⅳs기8례).119례NT중18례MYCN확증(15.1%),MYCN여제2호염색체신호비치위4.08~43.29;MYCN무확증101례,기중포괄획득79례(66.3%),음성22례(18.5%).MYCN적표체재불동년령、성별、NT분형이급핵분렬-핵쇄렬지수(MKI)고저조간차이유통계학의의(P =0.000),이여조직학예후분조급림상분기무관(P>0.05).18례MYCN확증병례중미분화형3례,기여15례위분화차형;17례구유고MKI,1례위중MKI;균속조직학예후불량조.3례존활,15례사망,평균생존기위(17.9±2.4)개월.MYCN미확증병례101례,69례존활(68.3%),32례사망(31.7%),평균생존기(29.8±1.3)개월.생존분석결과현시,MYCN확증환인예후교차(P<0.05).결론 NT발병년령소,역전이,조직학분형다위예후량호형;MYCN기인확증병례조직학균표현위예후불량형,다반고MKI;MYCN기인확증환인예후차.
Objective To summarize the clinicopathologic features of neuroblastic tumors (NT),and to explore the prognostic significance of MYCN amplification in NT.Methods The clinicopathologic data of 267 NT were reviewed.MYCN gene amplification was detected by fluorescence in situ hybridization (FISH) in 119 cases and the relationship with pathological characteristics and prognostic significance were analyzed.Results The study included 267 cases of children NT from patients aged from 1 day to 13 years (median 27 months).The male to female ratio was 1.43.There were 38 cases (14.2%),43 cases (16.1%),71 cases (26.6%),and 115 cases (43.1%)of INSS stages Ⅰ,Ⅱ,Ⅲ and Ⅳ respectively.Favorable histology group had 157 cases (59.9%) ; unfavorable histology group had 110 cases (40.1%).Of the 119 NT cases with MYCN FISH performed,18 cases (15.1%) showed amplification and the signal ratio of MYCN to CEP2 was 4.08-43.29.One hundred and one cases of non-amplified MYCN included MYCN gain in 79 cases (66.3%) and MYCN negative in 22 cases (18.5%).MYCN expression showed significant difference (P =0.000) between ages,gender,NT type and MKI,but not INPC and clinical stage (P > O.05).Of the 18 cases with MYCN amplification,3 were undifferentiated,and 15 poorly differentiated; 17 had high MKI and one moderate MKI.All 18 cases were in unfavorable histology group; the overall survival rate was 3/18,with an average survival time of (17.9 ± 2.4) months.Of the 101 MYCN non-amplification cases,the overall survival rate was 68.3% (69/101),with an average survival time of (29.8 ± 1.3) months.Survival analysis showed the cases with MYCN amplification had worseprognosis (P.< 0.05).Conclusions NT were commonly diagnosed in early ages and easily to metastasize.Most of cases with favorable histology.The cases of MYCN amplification showed unfavorable histology,andthe majority cases with high MKI; The patients with MYCN gene amplification had poor prognosis.