中华医学杂志
中華醫學雜誌
중화의학잡지
National Medical Journal of China
2014年
21期
1639-1642
,共4页
钱若兵%吴旻%魏祥品%凌士营%计颖%傅先明%汪业汉%牛朝诗
錢若兵%吳旻%魏祥品%凌士營%計穎%傅先明%汪業漢%牛朝詩
전약병%오민%위상품%릉사영%계영%부선명%왕업한%우조시
肿瘤,神经上皮%脑胶质瘤病%诊断%磁共振成像%外科手术
腫瘤,神經上皮%腦膠質瘤病%診斷%磁共振成像%外科手術
종류,신경상피%뇌효질류병%진단%자공진성상%외과수술
Neoplasms,neuroepithelial%Gliomatosis cerebri%Diagnosis%Magnetic resonance
目的:探讨脑胶质瘤病的影像学诊断特点及不同手术方式的疗效。方法回顾性分析2008年9月-2013年9月安徽医科大学附属省立医院神经外科收治的26例脑胶质瘤病患者,术前行头颅CT、MR等多模态影像学检查,11例行立体定向多靶点活体组织检查术,15例行大骨瓣开颅脑叶切除术,术后选择放射治疗和(或)替莫唑胺化疗,随访分析立体定向活体组织检查和开颅脑叶切除术两组患者的生存期差异。结果根据多模态神经影像学表现,脑胶质瘤病分为两型:(1)Ⅰ型(19例)表现为以胼胝体为中心的侵犯多个脑叶或脑区的弥漫性、浸润性病变,增强扫描无明显强化;(2)Ⅱ型(7例)表现为在Ⅰ型的基础上,增强扫描时出现散在或结节状强化。病理学类型:毛细胞型星形细胞瘤2例、弥漫性星形细胞瘤13例、少突胶质细胞瘤3例,少突-星形细胞瘤1例、间变性星形细胞瘤5例、胶质母细胞瘤2例;肿瘤的恶性程度越高,术后生存期越短,其中开颅脑叶切除术组的术后平均生存期(23±7)个月,明显长于立体定向手术活体组织检查组(13±3)个月(P<0.05)。结论脑胶质瘤病是一种弥漫性、浸润性生长又保留神经系统大体结构的脑内原发性胶质性肿瘤,多模态神经影像学结合病理检查可以明确诊断;手术结合放、化疗的综合治疗可以提高患者的生存时间。
目的:探討腦膠質瘤病的影像學診斷特點及不同手術方式的療效。方法迴顧性分析2008年9月-2013年9月安徽醫科大學附屬省立醫院神經外科收治的26例腦膠質瘤病患者,術前行頭顱CT、MR等多模態影像學檢查,11例行立體定嚮多靶點活體組織檢查術,15例行大骨瓣開顱腦葉切除術,術後選擇放射治療和(或)替莫唑胺化療,隨訪分析立體定嚮活體組織檢查和開顱腦葉切除術兩組患者的生存期差異。結果根據多模態神經影像學錶現,腦膠質瘤病分為兩型:(1)Ⅰ型(19例)錶現為以胼胝體為中心的侵犯多箇腦葉或腦區的瀰漫性、浸潤性病變,增彊掃描無明顯彊化;(2)Ⅱ型(7例)錶現為在Ⅰ型的基礎上,增彊掃描時齣現散在或結節狀彊化。病理學類型:毛細胞型星形細胞瘤2例、瀰漫性星形細胞瘤13例、少突膠質細胞瘤3例,少突-星形細胞瘤1例、間變性星形細胞瘤5例、膠質母細胞瘤2例;腫瘤的噁性程度越高,術後生存期越短,其中開顱腦葉切除術組的術後平均生存期(23±7)箇月,明顯長于立體定嚮手術活體組織檢查組(13±3)箇月(P<0.05)。結論腦膠質瘤病是一種瀰漫性、浸潤性生長又保留神經繫統大體結構的腦內原髮性膠質性腫瘤,多模態神經影像學結閤病理檢查可以明確診斷;手術結閤放、化療的綜閤治療可以提高患者的生存時間。
목적:탐토뇌효질류병적영상학진단특점급불동수술방식적료효。방법회고성분석2008년9월-2013년9월안휘의과대학부속성립의원신경외과수치적26례뇌효질류병환자,술전행두로CT、MR등다모태영상학검사,11례행입체정향다파점활체조직검사술,15례행대골판개로뇌협절제술,술후선택방사치료화(혹)체막서알화료,수방분석입체정향활체조직검사화개로뇌협절제술량조환자적생존기차이。결과근거다모태신경영상학표현,뇌효질류병분위량형:(1)Ⅰ형(19례)표현위이변지체위중심적침범다개뇌협혹뇌구적미만성、침윤성병변,증강소묘무명현강화;(2)Ⅱ형(7례)표현위재Ⅰ형적기출상,증강소묘시출현산재혹결절상강화。병이학류형:모세포형성형세포류2례、미만성성형세포류13례、소돌효질세포류3례,소돌-성형세포류1례、간변성성형세포류5례、효질모세포류2례;종류적악성정도월고,술후생존기월단,기중개로뇌협절제술조적술후평균생존기(23±7)개월,명현장우입체정향수술활체조직검사조(13±3)개월(P<0.05)。결론뇌효질류병시일충미만성、침윤성생장우보류신경계통대체결구적뇌내원발성효질성종류,다모태신경영상학결합병리검사가이명학진단;수술결합방、화료적종합치료가이제고환자적생존시간。
Objective To explore the neuroimaging diagnosis and therapeutic efficacy of different surgical methods of gliomatosis cerebri.Methods 26 cases of gliomatosis cerebri at our department between September 2008 and September 2013 were retrospectively analyzed.Preoperative cranial computed tomography ( CT) , magnetic resonance imaging ( MRI) and other multimodal imaging scans were performed.The procedures included stereotactic brain biopsy (n=11) and large craniotomy lobotomy (n=15).Whole brain radiotherapy and/or temozolomide therapy was performed postoperatively according to the malignancy of tumors.Follow-ups were conducted to analyze the survival differences between stereotactic brain biopsy and large craniotomy lobotomy groups.Results According to the different features of multimodal imaging , gliomatosis cerebri could be divided into two types:(1) typeⅠ(n=19) showed a diffuse infiltrating lesion infringing multiple brain lobes or regions with central corpus callosum but without obvious enhancement ;(2) type Ⅱ( n =7 ) appeared as sporadic or tuberous enhancement in addition to the features of type Ⅰ.Pathological diagnosis:pilocytic astrocytoma (n=2), diffuse astrocytoma (n=13), oligodendroglial tumors (n=3), oligoastrocytoma (n=1), anaplastic astrocytoma (n=5) and glioblastoma (n=2).The degree of malignancy was a prognostic factor for postoperative survival in patients with gliomatosis cerebri .The mean survival time ( MST ) of large craniotomy lobotomy group ( 23 ±7 ) was significantly longer than that of stereotactic brain biopsy group(13 ±3)(P<0.05).Conclusion Gliomatosis cerebri is a primary brain glial tumor with diffuse infiltrative growth but retaining the general structure of central nervous system .Multimodal imaging studies plus pathological examination yield a definitive diagnosis.Comprehensive treatment of operation plus chemo-or radio-therapy can prolong postoperative MST.