中华超声影像学杂志
中華超聲影像學雜誌
중화초성영상학잡지
CHINESE JOURNAL OF ULTRASONOGRAPHY
2011年
7期
605-608
,共4页
吕国荣%赵艳春%刘金蓉%陈晓康%李丽雅%何韶铮%徐振宏
呂國榮%趙豔春%劉金蓉%陳曉康%李麗雅%何韶錚%徐振宏
려국영%조염춘%류금용%진효강%리려아%하소쟁%서진굉
超声检查,产前%小脑延髓池%颅窝,后
超聲檢查,產前%小腦延髓池%顱窩,後
초성검사,산전%소뇌연수지%로와,후
Ultrasonography,prenatal%Cisterna magna%Cranial fossa,posterior
目的 探讨不同孕龄胎儿小脑延髓池间隔(CMS)的正常声像图表现及正常值,并评估CMS的临床意义.方法 前瞻性选择416例不同孕周正常胎儿,采用二维超声对CMS的长径和宽径进行检测,并对其测值与孕周进行回归分析.回顾性总结我院6年间25例CMS消失的病例和12例CMS增大胎儿的临床资料.结果 ①胎儿CMS的长径和宽径在14~22孕周随着孕周的增加而增大,在23~36孕周变化不大,在37孕周后有变小趋势,与菱脑胚胎发育过程一致.②CMS消失常见于Dandy-Walker畸形、全前脑、严重脑积水、神经管缺陷、菱脑融合症、Arnold-Chiari畸形;CMS增大可见于小脑延髓池生理性增大.结论 CMS是菱脑发育正常的标志之一.CMS增大和消失与多种胎儿中枢神经系统畸形有关,尤其是后颅窝畸形.
目的 探討不同孕齡胎兒小腦延髓池間隔(CMS)的正常聲像圖錶現及正常值,併評估CMS的臨床意義.方法 前瞻性選擇416例不同孕週正常胎兒,採用二維超聲對CMS的長徑和寬徑進行檢測,併對其測值與孕週進行迴歸分析.迴顧性總結我院6年間25例CMS消失的病例和12例CMS增大胎兒的臨床資料.結果 ①胎兒CMS的長徑和寬徑在14~22孕週隨著孕週的增加而增大,在23~36孕週變化不大,在37孕週後有變小趨勢,與蔆腦胚胎髮育過程一緻.②CMS消失常見于Dandy-Walker畸形、全前腦、嚴重腦積水、神經管缺陷、蔆腦融閤癥、Arnold-Chiari畸形;CMS增大可見于小腦延髓池生理性增大.結論 CMS是蔆腦髮育正常的標誌之一.CMS增大和消失與多種胎兒中樞神經繫統畸形有關,尤其是後顱窩畸形.
목적 탐토불동잉령태인소뇌연수지간격(CMS)적정상성상도표현급정상치,병평고CMS적림상의의.방법 전첨성선택416례불동잉주정상태인,채용이유초성대CMS적장경화관경진행검측,병대기측치여잉주진행회귀분석.회고성총결아원6년간25례CMS소실적병례화12례CMS증대태인적림상자료.결과 ①태인CMS적장경화관경재14~22잉주수착잉주적증가이증대,재23~36잉주변화불대,재37잉주후유변소추세,여릉뇌배태발육과정일치.②CMS소실상견우Dandy-Walker기형、전전뇌、엄중뇌적수、신경관결함、릉뇌융합증、Arnold-Chiari기형;CMS증대가견우소뇌연수지생이성증대.결론 CMS시릉뇌발육정상적표지지일.CMS증대화소실여다충태인중추신경계통기형유관,우기시후로와기형.
Objective To establish normative data for the fetal cisterna magna septa (CMS) at various gestational age,and to evaluate its clinical significance.Methods A total of consecutive fetal between 14 and 40 gestational week(GW) were included in this prospective study.The length and width of CMS were measured by two-dimensional ultrasonography.Regression analysis was used to study the relationship between the width and length of the fetal cisterna magna septa and gestational age.Twenty-five case of fetuses with the absence of CMS and 12 case of fetuses with the enlargement of CMS were retrospectively analyzed in the past six years in our hospital.Results ①The fetal CMS length and width increased gradually between 14 and 22 GW,then plateaued between 23 GW and 36 GW,and decreased after 37 GW.This ultrasonographic pattern was in agreement with normal development of rhombencephalon.②The absence of CMS in the fetuses were common in Dandy-Walker syndrome,holoprosencephaly,severe hydrocephalus,neural tube defects,rhombencephalon synapsis and Arnold-Chiari malformation.The enlargement of CMS in the fetuses may be shown in physiologic enlargement of posterior fossa.ConclusionsCMS is a potential new marker for normal development of rhombencephalon.The enlargement and absence of CMS are related to various malformations of central neural system,especially in the abnormalities of posterior fossa.