中华病理学杂志
中華病理學雜誌
중화병이학잡지
Chinese Journal of Pathology
2012年
8期
534-537
,共4页
张建国%胡文忠%李玉%赵瑞皎%孔令非
張建國%鬍文忠%李玉%趙瑞皎%孔令非
장건국%호문충%리옥%조서교%공령비
肿瘤,神经上皮%癫痫%诊断,鉴别%免疫组织化学
腫瘤,神經上皮%癲癇%診斷,鑒彆%免疫組織化學
종류,신경상피%전간%진단,감별%면역조직화학
Neoplasms,neuroepithelial%Epilepsy%Diagnosis,differential%Immunohistochemistry
目的 探讨胚胎发育不良性神经上皮肿瘤(DNT)的临床病理学、影像学特征、治疗及其预后情况.方法 回顾性分析10例经病理确诊的DNT患者资料,归纳其临床病理和影像学特征.结果 临床均以顽固性癫痫为主要症状,肿瘤位于颞叶5例、额叶3例、顶叶2例.CT扫描病灶呈低密度影,MRI呈T1WI低信号,增强后无强化,T2WI高信号,液体衰减反转恢复序列(FLAIR)检查瘤内可见等信号分隔,边缘环状高信号;无占位效应和瘤周水肿.肿瘤由特异性胶质神经元成分构成,包括少突胶质样细胞,“漂浮”神经元和星形胶质细胞.免疫组织化学:OLC阳性表达Olig2和S-100蛋白,神经元和部分OLC表达NeuN、突触素;Ki-67阳性指数均<1%.治疗:9例行肿瘤全切术,1例为次全切,术后未行放疗和化疗.预后:均获随访,9例无复发,1例复发.结论 DNT确诊需结合临床病理、免疫组织化学及影像学检查.手术效果良好,术中脑电图描记可有效切除癫痫灶,术后无须放疗和化疗.
目的 探討胚胎髮育不良性神經上皮腫瘤(DNT)的臨床病理學、影像學特徵、治療及其預後情況.方法 迴顧性分析10例經病理確診的DNT患者資料,歸納其臨床病理和影像學特徵.結果 臨床均以頑固性癲癇為主要癥狀,腫瘤位于顳葉5例、額葉3例、頂葉2例.CT掃描病竈呈低密度影,MRI呈T1WI低信號,增彊後無彊化,T2WI高信號,液體衰減反轉恢複序列(FLAIR)檢查瘤內可見等信號分隔,邊緣環狀高信號;無佔位效應和瘤週水腫.腫瘤由特異性膠質神經元成分構成,包括少突膠質樣細胞,“漂浮”神經元和星形膠質細胞.免疫組織化學:OLC暘性錶達Olig2和S-100蛋白,神經元和部分OLC錶達NeuN、突觸素;Ki-67暘性指數均<1%.治療:9例行腫瘤全切術,1例為次全切,術後未行放療和化療.預後:均穫隨訪,9例無複髮,1例複髮.結論 DNT確診需結閤臨床病理、免疫組織化學及影像學檢查.手術效果良好,術中腦電圖描記可有效切除癲癇竈,術後無鬚放療和化療.
목적 탐토배태발육불량성신경상피종류(DNT)적림상병이학、영상학특정、치료급기예후정황.방법 회고성분석10례경병리학진적DNT환자자료,귀납기림상병리화영상학특정.결과 림상균이완고성전간위주요증상,종류위우섭협5례、액협3례、정협2례.CT소묘병조정저밀도영,MRI정T1WI저신호,증강후무강화,T2WI고신호,액체쇠감반전회복서렬(FLAIR)검사류내가견등신호분격,변연배상고신호;무점위효응화류주수종.종류유특이성효질신경원성분구성,포괄소돌효질양세포,“표부”신경원화성형효질세포.면역조직화학:OLC양성표체Olig2화S-100단백,신경원화부분OLC표체NeuN、돌촉소;Ki-67양성지수균<1%.치료:9례행종류전절술,1례위차전절,술후미행방료화화료.예후:균획수방,9례무복발,1례복발.결론 DNT학진수결합림상병리、면역조직화학급영상학검사.수술효과량호,술중뇌전도묘기가유효절제전간조,술후무수방료화화료.
Objective To study the clinicopathologic features,radiologic findings,treatment options and prognosis of dysembryoplastic neuroepithelial tumor (DNT).Methods The clinicopathologic and radiologic features were retrospectively analyzed in 10 cases of DNT.Results Intractable partial seizure was the main presenting symptom in all patients. The tumor was located in temporal lobe ( number =5 ),frontal lobe (number =3 ) or parietal lobe (number =2 ).CT scan displayed a hypodense lesion.MRI scan revealed the tumor was non-enhancing T1 WI hypointense and T2WI hyperintense,with internal septation and hyperintense ring around the tumor seen on FLAIR image.There was neither peritumoral edema nor mass effect.Histologically,the tumor showed the presence of glioneuronal element,with oligodendrocyte-like cells, floating neurons, astrocytes and associated microcystic changes, Immunohistochemical study demonstrated positivity for NeuN and synaptophysin in the neurons and some oligodendrocyte-like cells.Olig2 and S-100 protein were also expressed in the oligodendrocyte-like cells.Ki-67 index were lower than 1% in all cases.Nine cases were treated by complete surgical excision and the remaining case was subtotally excised. No post-operative chemotherapy or radiotherapy was given.One of the 10 cases recurred on follow up. Conclusions Correct diagnosis of DNT requires correlation with clinicopathologic,radiologic and immunohistochemical findings.Complete resection of the tumor and epileptogenic foci is the mainstay of treatment for DNT,with intraoperative EEG monitoring.Post-operative chemotherapy or radiotherapy is not required.