中华放射学杂志
中華放射學雜誌
중화방사학잡지
Chinese Journal of Radiology
2014年
5期
422-424
,共3页
李美蓉%张忠阳%李玉华%李惠民%吴主强
李美蓉%張忠暘%李玉華%李惠民%吳主彊
리미용%장충양%리옥화%리혜민%오주강
星形细胞瘤%磁共振成像%儿童
星形細胞瘤%磁共振成像%兒童
성형세포류%자공진성상%인동
Astrocytoma%Magnetic resonance imaging%Child
目的:探讨儿童毛细胞黏液样星形细胞瘤( PMA )的MRI表现。方法回顾性分析2011年至2013年间经手术病理证实的7例PMA的MRI表现。男3例、女4例;年龄10~32个月,中位年龄21个月。结果肿瘤病灶边界清楚,6例位于下丘脑-视交叉-第三脑室区域,2例累及双侧颞叶,1例合并神经纤维瘤病-Ⅰ型( NF-Ⅰ);1例位于基底节区。实性肿块4例,实性伴囊变3例。T1 WI中,液体衰减反转恢复序列( FLAIR)检查6例,5例呈低信号,1例呈等信号;FSE序列1例,呈低信号。 T2 WI中,FLAIR序列检查3例,1例呈高信号,2例呈等信号;FSE序列5例,4例呈高信号,1例呈等信号。 DWI 6例,4例呈低信号,1例呈等信号,1例呈等低信号。增强后明显强化,4例均匀强化,3例不均匀强化,1例边缘强化,2例瘤内见不规则低信号区。2例脑脊液播散,1例瘤周轻度水肿,4例脑积水。 MRS检查2例,胆碱(Cho)/肌酸(Cr)升高,N-乙酰天冬氨酶(NAA)/Cr降低。结论PMA的MRI表现具有特征性,好发于3岁以下婴幼儿;下丘脑-视交叉-第三脑室区常见,强化方式多样,肿瘤内出血和周围水肿少见,脑脊液播散较常见。
目的:探討兒童毛細胞黏液樣星形細胞瘤( PMA )的MRI錶現。方法迴顧性分析2011年至2013年間經手術病理證實的7例PMA的MRI錶現。男3例、女4例;年齡10~32箇月,中位年齡21箇月。結果腫瘤病竈邊界清楚,6例位于下丘腦-視交扠-第三腦室區域,2例纍及雙側顳葉,1例閤併神經纖維瘤病-Ⅰ型( NF-Ⅰ);1例位于基底節區。實性腫塊4例,實性伴囊變3例。T1 WI中,液體衰減反轉恢複序列( FLAIR)檢查6例,5例呈低信號,1例呈等信號;FSE序列1例,呈低信號。 T2 WI中,FLAIR序列檢查3例,1例呈高信號,2例呈等信號;FSE序列5例,4例呈高信號,1例呈等信號。 DWI 6例,4例呈低信號,1例呈等信號,1例呈等低信號。增彊後明顯彊化,4例均勻彊化,3例不均勻彊化,1例邊緣彊化,2例瘤內見不規則低信號區。2例腦脊液播散,1例瘤週輕度水腫,4例腦積水。 MRS檢查2例,膽堿(Cho)/肌痠(Cr)升高,N-乙酰天鼕氨酶(NAA)/Cr降低。結論PMA的MRI錶現具有特徵性,好髮于3歲以下嬰幼兒;下丘腦-視交扠-第三腦室區常見,彊化方式多樣,腫瘤內齣血和週圍水腫少見,腦脊液播散較常見。
목적:탐토인동모세포점액양성형세포류( PMA )적MRI표현。방법회고성분석2011년지2013년간경수술병리증실적7례PMA적MRI표현。남3례、녀4례;년령10~32개월,중위년령21개월。결과종류병조변계청초,6례위우하구뇌-시교차-제삼뇌실구역,2례루급쌍측섭협,1례합병신경섬유류병-Ⅰ형( NF-Ⅰ);1례위우기저절구。실성종괴4례,실성반낭변3례。T1 WI중,액체쇠감반전회복서렬( FLAIR)검사6례,5례정저신호,1례정등신호;FSE서렬1례,정저신호。 T2 WI중,FLAIR서렬검사3례,1례정고신호,2례정등신호;FSE서렬5례,4례정고신호,1례정등신호。 DWI 6례,4례정저신호,1례정등신호,1례정등저신호。증강후명현강화,4례균균강화,3례불균균강화,1례변연강화,2례류내견불규칙저신호구。2례뇌척액파산,1례류주경도수종,4례뇌적수。 MRS검사2례,담감(Cho)/기산(Cr)승고,N-을선천동안매(NAA)/Cr강저。결론PMA적MRI표현구유특정성,호발우3세이하영유인;하구뇌-시교차-제삼뇌실구상견,강화방식다양,종류내출혈화주위수종소견,뇌척액파산교상견。
Objective To investigate the MRI features of pilomyxoid astrocytoma ( PMA ) in children.Methods MRI features of seven children with pathologically proven PMA in 2011-2013 were retrospectively analyzed.The ages of the patients ranged from 10 months to 32 months at initial diagnosis.Results All tumors were well-circumscribed masses.Six tumors were located in the hypothalamic-chiasmatic-third ventricular region , two tumor involved the bilateral temporal lobe , and one tumor was associated with NF-I.One occurred in the basal ganglia region.Four tumors were solid masses , whereas the other three showed cystic components.Six tumors were hypointense and one was isointense on T 1-weighted image.Five tumors were hyperintense and three were isointense on T 2-weighted image.Four tumors were hypointense , one was iso-hypointense and one was isointense on DWI.After contrast administration , four tumors enhanced homogenously and three tumors enhanced heterogeneously , with intratumoral irregular hypointense region in two tumors and rim enhancement in one tumor.Cerebrospinal fluid ( CSF ) dissemination, hydrocephalus and peritumor edema were observed in 2, 4 and 1 of cases, respectively.Proton magnetic resonance spectrum of two PMA showed elevated Cho /Cr ratios and decreased NAA/Cr ratios.Conclusions The imaging features of pilomyxoid astrocytoma include common origination from the midline of the neuroaxis in younger children about 2-3 years old.The CSF dissemination is common.The presence of hemorrhage and peritumor edema is not common.