中华神经外科杂志
中華神經外科雜誌
중화신경외과잡지
Chinese Journal of Neurosurgery
2009年
3期
222-225
,共4页
郭志旺%漆松涛%王浩%方陆雄%潘军%张喜安
郭誌旺%漆鬆濤%王浩%方陸雄%潘軍%張喜安
곽지왕%칠송도%왕호%방륙웅%반군%장희안
神经元胶质混合性肿瘤%癫痫%磁共振成像
神經元膠質混閤性腫瘤%癲癇%磁共振成像
신경원효질혼합성종류%전간%자공진성상
Mixed neuranal-glial tumors%Epilepsy%Magnetic resonance imaging
目的 分析低级别脑神经元-胶质混合性肿瘤MRI及临床特点.方法 回顾病理证实的18例该类患者临床及影像资料.结果 患者术前均有癫痫史,14例为药物难治性癫痫.MRI上病变边界清晰,均位于或累及皮层;多呈实性,少数为囊实性或囊性,实性成分更靠近皮层;病变呈长T1长T2信号,部分实性成分为等信号;信号均匀少有强化,囊实性者可小壁结节样强化,壁可部分强化;肿瘤无明显占位效应,瘤周水肿少见或轻微.术后平均随访25.6个月无复发.结论 低级别脑神经元-胶质混合性肿瘤位于或累及皮层,多以癫痫起病,手术全切可较好控制症状.
目的 分析低級彆腦神經元-膠質混閤性腫瘤MRI及臨床特點.方法 迴顧病理證實的18例該類患者臨床及影像資料.結果 患者術前均有癲癇史,14例為藥物難治性癲癇.MRI上病變邊界清晰,均位于或纍及皮層;多呈實性,少數為囊實性或囊性,實性成分更靠近皮層;病變呈長T1長T2信號,部分實性成分為等信號;信號均勻少有彊化,囊實性者可小壁結節樣彊化,壁可部分彊化;腫瘤無明顯佔位效應,瘤週水腫少見或輕微.術後平均隨訪25.6箇月無複髮.結論 低級彆腦神經元-膠質混閤性腫瘤位于或纍及皮層,多以癲癇起病,手術全切可較好控製癥狀.
목적 분석저급별뇌신경원-효질혼합성종류MRI급림상특점.방법 회고병리증실적18례해류환자림상급영상자료.결과 환자술전균유전간사,14례위약물난치성전간.MRI상병변변계청석,균위우혹루급피층;다정실성,소수위낭실성혹낭성,실성성분경고근피층;병변정장T1장T2신호,부분실성성분위등신호;신호균균소유강화,낭실성자가소벽결절양강화,벽가부분강화;종류무명현점위효응,류주수종소견혹경미.술후평균수방25.6개월무복발.결론 저급별뇌신경원-효질혼합성종류위우혹루급피층,다이전간기병,수술전절가교호공제증상.
Objective To Analyze the MRI and clinical features of low grade cerebral mixed neuronal-glial tumors. Method We retrospectively studied the clinical features and imaging data of 18 cases of low grade cerebral mixed neuronal-glial tumors which were pathologically confirmed. Results All the patients had a history of epilepsy,of which 14 cases onset with drug intractable epilepsy. The lesions showed clear sharp border on MRI and located or involved in the cortex. They were solid for the vast majority of them, involving a small portion of solid-cystic combination or cystic mass merely. The solid component situated closer to the cortex. Most of them manifested as slightly hypointcnse on T1WI and hyperintense relative gray matter on T2WI, involving a small part of isointense solid lesions on MRI scan. The signals were even and enhancement were rare. The solid-cystic lesions could be small nodular enhancement. They showed no mass effect, with rare or minor edema. No recurrence occurred during a mean follow-up period of 25.6 months. Conclusions Most of the low grade cerebral mixed neuronal-glial tumors occurred or involved in the cortex, onset with drug intractable epilepsy. Total surgical removal lesions can control the clinical symptoms perfectly.