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      椎動(dòng)脈起源異常與發(fā)育不良關(guān)系的研究

      2015-01-03 00:03:52朱玄1辛世杰1王雷李晰呂俊遠(yuǎn)
      關(guān)鍵詞:主動(dòng)脈弓起源椎動(dòng)脈

      朱玄1,,辛世杰1,,王雷,李晰,呂俊遠(yuǎn)

      (中國(guó)醫(yī)科大學(xué)附屬第一醫(yī)院1.鞍山醫(yī)院普通外科,遼寧 鞍山 114001;中國(guó)醫(yī)科大學(xué)附屬第一醫(yī)院2.普外教研室,血管甲狀腺外科,沈陽(yáng) 110001)

      椎動(dòng)脈起源異常與發(fā)育不良關(guān)系的研究

      朱玄1,2,辛世杰1,2,王雷2,李晰2,呂俊遠(yuǎn)2

      (中國(guó)醫(yī)科大學(xué)附屬第一醫(yī)院1.鞍山醫(yī)院普通外科,遼寧 鞍山 114001;中國(guó)醫(yī)科大學(xué)附屬第一醫(yī)院2.普外教研室,血管甲狀腺外科,沈陽(yáng) 110001)

      目的探討椎動(dòng)脈起源異常和椎動(dòng)脈發(fā)育不良(VAH)的發(fā)生率以及他們之間的關(guān)系,為影像診斷及臨床手術(shù)提供資料和參考。方法回顧性分析2 370例患者的胸部增強(qiáng)MSCT影像資料,對(duì)原始圖像進(jìn)行技術(shù)重組,重點(diǎn)觀察分析椎動(dòng)脈起源及椎動(dòng)脈V1段直徑變化特點(diǎn)。逐例測(cè)量椎動(dòng)脈V1段的內(nèi)徑。將椎動(dòng)脈全程均勻性纖細(xì),V1段內(nèi)徑<2.5 mm定義為VAH。結(jié)果2 370例患者中左椎動(dòng)脈起源異常131例(5.5%),均發(fā)自主動(dòng)脈弓。其中發(fā)自左頸總動(dòng)脈和左鎖骨下動(dòng)脈之間主動(dòng)脈弓126例(5.3%),發(fā)自左鎖骨下動(dòng)脈遠(yuǎn)端主動(dòng)脈弓5例(0.2%)。右椎動(dòng)脈起源于右頸總動(dòng)脈4例(0.16%),均合并迷走右鎖骨下動(dòng)脈。根據(jù)椎動(dòng)脈是否發(fā)自左頸總動(dòng)脈與左鎖骨下動(dòng)脈之間主動(dòng)脈弓,將檢查者分為起源正常組與起源變異組。正常組(n=1 985)中,左側(cè)VAH 71例,右側(cè)VAH 144例。變異組(n=126)中左側(cè)VAH共22例,右側(cè)VAH共5例。兩組差異有統(tǒng)計(jì)學(xué)意義(P= 0.000)。結(jié)論左椎動(dòng)脈直接起源于左頸總動(dòng)脈和左鎖骨下動(dòng)脈之間的主動(dòng)脈弓為最常見(jiàn)的椎動(dòng)脈起源異常,其發(fā)生率女性高于男性。左椎動(dòng)脈直接起源于主動(dòng)脈弓與左椎動(dòng)脈發(fā)育不良關(guān)系密切。

      椎動(dòng)脈變異;椎動(dòng)脈起源異常;椎動(dòng)脈發(fā)育不良

      椎動(dòng)脈為腦部血供的重要來(lái)源,主要供應(yīng)脊髓上部、腦干、小腦和雙側(cè)大腦半球后部及雙側(cè)顳葉底部的血液,占全腦血流量的1/5[1]。椎脈損傷或閉塞將會(huì)引起一系列腦缺血癥狀,如頭暈、耳鳴、視物模糊、共濟(jì)失調(diào)甚至?xí)炟省W祫?dòng)脈的變異并不少見(jiàn),已經(jīng)逐漸引起臨床醫(yī)生的重視。本研究旨在探討椎動(dòng)脈起源異常和先天性椎動(dòng)脈發(fā)育不良(vertebral artery hypoplasia,VAH)之間的關(guān)系,從而為外科手術(shù)方案的制定及影像學(xué)診斷提供參考。

      1 材料與方法

      1.1 資料來(lái)源

      收集2013年4月至2013年7月于我院門(mén)診或住院處行胸部增強(qiáng)MSCT檢查患者的影像資料。排除標(biāo)準(zhǔn):(1)年齡<18歲;(2)主動(dòng)脈旁腫物壓迫影響主動(dòng)脈弓形態(tài);(3)造影劑分布不均影響圖像質(zhì)量;(4)有主動(dòng)脈弓部手術(shù)史;(5)椎動(dòng)脈V1段顯露不充分的圖像。最后2 370例患者被納入研究對(duì)象。其中男1 348例(56.9%),女1 022例(43.1%)。年齡18~88歲,平均年齡為(58.09±12.08)歲。男女之間的年齡差異無(wú)統(tǒng)計(jì)學(xué)意義[(58.25±12.07)歲 vs(57.88±12.09)歲,P=0.478]。

      1.2 檢查方法

      使用雙源多探頭CT系統(tǒng),其中使用西門(mén)子二代雙源CT(Somatom Definition Flash,德國(guó))289例(12.2%),飛利浦256排螺旋CT(Philips Brilliance iCT256,荷蘭)1 232例(52.0%),東芝640排CT(Aquilion AquilionOne,日本)849例(35.8%)。參數(shù)設(shè)定:球管電壓為120 kV、自動(dòng)球管電流調(diào)制,層厚1.0 mm,增量1.0 mm,螺距0.870(西門(mén)子,東芝),0.798(飛利浦)。經(jīng)肘部靜脈以2.5 mL/s的流速注射非離子型碘對(duì)比劑(碘佛醇注射液,320 mg/mL,中國(guó)恒瑞制藥)80 mL。然后注射20 mL生理鹽水。椎動(dòng)脈CT掃描延遲時(shí)間設(shè)定為18~22 s。

      1.3 數(shù)據(jù)采集

      將原始橫斷面圖像傳輸?shù)綀D像后處理工作站,進(jìn)行最大密度投影(maximum intensity projection,MIP)、二維曲面重建(curved planar reconstruction,CPR)、多平面重建(multi-planar reformation,MPR)和容積再現(xiàn)(volume rendering,VR)重組。由兩名有經(jīng)驗(yàn)的臨床醫(yī)生獨(dú)立采集數(shù)據(jù),意見(jiàn)分歧由兩人協(xié)商達(dá)成一致。依據(jù)軸位圖像和曲面重建圖像觀察主動(dòng)脈弓分支的形態(tài),并對(duì)椎動(dòng)脈的起源進(jìn)行分類(lèi)。椎動(dòng)脈直徑的測(cè)量在軸位圖像上進(jìn)行。避開(kāi)迂曲及動(dòng)脈硬化斑塊導(dǎo)致的狹窄處,在椎動(dòng)脈Ⅵ段任取兩點(diǎn)測(cè)量其內(nèi)徑,平均值為該支椎動(dòng)脈的直徑,所得數(shù)據(jù)進(jìn)行分類(lèi)統(tǒng)計(jì)。對(duì)于VAH,目前尚沒(méi)有統(tǒng)一的診斷標(biāo)準(zhǔn)。將全程纖細(xì)、直徑≤2.5 mm的椎動(dòng)脈定義為VAH。這是由一組亞洲人通過(guò)測(cè)量椎動(dòng)脈的血流量而提出的定義[2]。

      1.4 統(tǒng)計(jì)學(xué)分析

      采用SPSS17.0統(tǒng)計(jì)軟件進(jìn)行分析,計(jì)量資料采用x±s描述,均數(shù)比較用u檢驗(yàn)或Kruskal-Wallis檢驗(yàn)。計(jì)數(shù)資料的比較采用χ2檢驗(yàn)。相關(guān)性分析采用Pearson檢驗(yàn)。P<0.05為差異有統(tǒng)計(jì)學(xué)意義。

      2 結(jié)果

      2.1 椎動(dòng)脈的起源

      起源正常組,即椎動(dòng)脈起源于鎖骨下動(dòng)脈且主動(dòng)脈弓無(wú)異常分支者1 985例(83.8%)。起源變異組為:(1)左椎動(dòng)脈發(fā)自左頸總動(dòng)脈和左鎖骨下動(dòng)脈之間的主動(dòng)脈弓,共126例(5.3%),其中14例(0.6%)合并頭臂干與左頸總動(dòng)脈共干,2例(0.08%)合并迷走右鎖骨下動(dòng)脈;(2)左椎動(dòng)脈發(fā)自左鎖骨下動(dòng)脈遠(yuǎn)端的主動(dòng)脈弓5例(0.2%),其中1例(0.04%)合并頭臂干與左頸總動(dòng)脈共干;(3)右椎動(dòng)脈起源于右頸總動(dòng)脈4例(0.16%),均合并迷走右鎖骨下動(dòng)脈;(4)椎動(dòng)脈正常起源于鎖骨下動(dòng)脈但主動(dòng)脈弓存在異常分支(圖1)。

      2.2 椎動(dòng)脈發(fā)育不良的發(fā)生率

      根據(jù)椎動(dòng)脈V1節(jié)段的直徑,104例(4.4%)患者被診斷為左側(cè)VAH,172例(7.3%)被診斷為右側(cè)VAH,6例(0.3%)被診斷為雙側(cè)VAH。

      2.3 年齡、性別與椎動(dòng)脈變異之間的關(guān)系

      左椎動(dòng)脈直接起源于左頸總動(dòng)脈與左鎖骨下動(dòng)脈之間的主動(dòng)脈弓的患者126例(5.3%),男女比例明顯低于正常起源椎動(dòng)脈的男女比例(57/69 vs 1 169/816,P=0.003),即女性患者多見(jiàn)。VAH患者的平均年齡明顯高于無(wú)VAH患者的平均年齡(P= 0.012)。性別差異無(wú)統(tǒng)計(jì)學(xué)意義(P=0.290,表1)。

      發(fā)自左頸總動(dòng)脈與左鎖骨下動(dòng)脈之間主動(dòng)脈弓的左椎動(dòng)脈,常并發(fā)發(fā)育不良。正常組(n=1 985)中,左側(cè)VAH 71例,右側(cè)VAH 144例。變異組中(n=126)中左側(cè)VAH 22例,右側(cè)VAH 5例,見(jiàn)表2。

      3 討論

      圖1 椎動(dòng)脈的容積再現(xiàn)或多平面重建模型Fig.1 Volume Rendering or Multiplanar Reformatting View of VA Patterns

      表1 年齡、性別與椎動(dòng)脈起源和VAH之間的關(guān)系Tab.1 Age and gender in patients with the different origin of the VA and VAH

      表2 椎動(dòng)脈發(fā)自左頸總動(dòng)脈與左鎖骨下動(dòng)脈之間的主動(dòng)脈弓與發(fā)育不良之間的關(guān)系Tab.2 Association between the vertebral artery hypoplasia and the vertebral artery that come from the aortic arch

      椎動(dòng)脈變異并不少見(jiàn),我們主要研究椎動(dòng)脈起源變異和VAH之間的關(guān)系。本項(xiàng)研究共2 370例患者,左椎動(dòng)脈起源異常131例(5.5%),右椎動(dòng)脈起源異常4例(0.16%)。左側(cè)VAH 104例(4.4%),右側(cè)VAH 172例(7.3%),雙側(cè)VAH 6例(0.3%)。近年來(lái),隨著MSCT成像技術(shù)的不斷成熟,人們對(duì)椎動(dòng)脈的形態(tài)學(xué)方面有了進(jìn)一步的認(rèn)識(shí)。椎動(dòng)脈的變異會(huì)對(duì)頸部手術(shù)及主動(dòng)脈弓部的血管腔內(nèi)治療方案的制定造成一定的影響,因此已經(jīng)逐步引起臨床醫(yī)生的關(guān)注。

      椎動(dòng)脈為鎖骨下動(dòng)脈的主要分支,從鎖骨下動(dòng)脈發(fā)出后全程分為四段,即椎前段(V1),橫突段(V2)、枕下段(V3)和顱內(nèi)段(V4),雙側(cè)椎動(dòng)脈顱內(nèi)段匯合為基底動(dòng)脈。若椎動(dòng)脈起源于鎖骨下動(dòng)脈以外的其它動(dòng)脈,即為椎動(dòng)脈起源異常。在我國(guó),最常見(jiàn)的類(lèi)型為左側(cè)椎動(dòng)脈直接發(fā)自主動(dòng)脈弓[3]。本組研究中其發(fā)生率為5.5%。曾有其它大樣本研究顯示發(fā)生率為3.7%~6.6%[4,5]。日本有學(xué)者研究發(fā)現(xiàn),椎動(dòng)脈起源異常與椎動(dòng)脈入頸椎橫突孔水平異常有關(guān)[3]。異常起源的椎動(dòng)脈進(jìn)入椎間孔的水平往往較正常起源者高,即V1段行程延長(zhǎng)迂曲且缺乏頸椎橫突的保護(hù),這樣在轉(zhuǎn)動(dòng)頸部時(shí)可能會(huì)引起椎動(dòng)脈痙攣或產(chǎn)生夾層甚至閉塞。手術(shù)操作時(shí),必須對(duì)該區(qū)域血管解剖進(jìn)行充分的評(píng)價(jià),以免損傷異常的椎動(dòng)脈,進(jìn)而影響脊髓及腦部的血供。對(duì)主動(dòng)脈弓、鎖骨下動(dòng)脈或椎動(dòng)脈進(jìn)行介入治療時(shí),若鎖骨下動(dòng)脈造影未發(fā)現(xiàn)椎動(dòng)脈,應(yīng)考慮到椎動(dòng)脈起源于主動(dòng)脈弓或頸總動(dòng)脈的情況。椎動(dòng)脈起源于頸總動(dòng)脈者罕見(jiàn),本組僅見(jiàn)4例,均為右椎動(dòng)脈起源于右頸總動(dòng)脈,且合并迷走的右鎖骨下動(dòng)脈。曾有研究顯示:迷走右鎖骨下動(dòng)脈的102例患者中,右椎動(dòng)脈與右頸總動(dòng)脈共干的發(fā)生率為20.6%,而右椎動(dòng)脈起源于右頸總動(dòng)脈的發(fā)生率為13.7%[6]??梢?jiàn),迷走右鎖骨下動(dòng)脈與右椎動(dòng)脈起源異常有一定的聯(lián)系。超過(guò)80%的迷走右鎖骨下動(dòng)脈走行于食管的右后方,其它的走行于氣管和食管之間,或走行于氣管前方[7]。我們所研究的18例均走行于食管后方。異常走行的右鎖骨下動(dòng)脈有時(shí)會(huì)壓迫食管,引起吞咽困難的癥狀,稱(chēng)為食管受壓性吞咽困難[8]。此外,右鎖骨下動(dòng)脈起源異常常合并右側(cè)喉返神經(jīng)移位,這在甲狀腺手術(shù)時(shí)應(yīng)引起注意。Schwarzacher等[9]曾報(bào)道1例起始于主動(dòng)脈弓的椎動(dòng)脈發(fā)出甲狀腺下動(dòng)脈的變異。多數(shù)研究認(rèn)為,椎動(dòng)脈直接起源于主動(dòng)脈弓是由于胚胎發(fā)育過(guò)程中,發(fā)育成椎動(dòng)脈的背外側(cè)支和參與合成主動(dòng)脈弓的背主動(dòng)脈主干之間未發(fā)生萎縮或中斷而成。椎動(dòng)脈起源異常與年齡和性別之間的聯(lián)系很少有文獻(xiàn)報(bào)導(dǎo)。Bhatia等的一項(xiàng)尸檢研究發(fā)現(xiàn)左椎動(dòng)脈直接起源于主動(dòng)脈弓凸側(cè)的左頸總動(dòng)脈和鎖骨下動(dòng)脈之間,在澳洲南部地區(qū)要比其它地區(qū)高發(fā),而且隨著時(shí)間的推移,發(fā)生率有明顯增高的趨勢(shì)[3]。并且推測(cè),社會(huì)和環(huán)境因素可能影響主動(dòng)脈弓分支的發(fā)育。我們的研究中,左椎動(dòng)脈起源于左頸總動(dòng)脈與左鎖骨下動(dòng)脈之間的主動(dòng)脈弓的發(fā)生率在女性患者中明顯增高。

      椎動(dòng)脈直徑一般為3~5 mm,雙側(cè)通常不對(duì)稱(chēng)[10]。有資料顯示,人群中約50%的個(gè)體左椎動(dòng)脈直徑明顯大于右側(cè),25%的個(gè)體右椎動(dòng)脈直徑明顯大于左側(cè),剩余25%個(gè)體左、右椎動(dòng)脈直徑相當(dāng)[10,11]。通常當(dāng)一側(cè)椎動(dòng)脈顯著變細(xì)時(shí),被認(rèn)為是VAH。曾有文獻(xiàn)報(bào)道其在正常人群中發(fā)生率為11.6%~26.5%[12,13]。VAH在椎動(dòng)脈造影中并不少見(jiàn),目前尚沒(méi)有統(tǒng)一的診斷標(biāo)準(zhǔn)。文獻(xiàn)中常用的VAH的診斷標(biāo)準(zhǔn)主要有:根據(jù)頸部血管超聲,椎動(dòng)脈內(nèi)的血流量<40 mL/min,或椎動(dòng)脈的直徑<2.5 mm,或雙側(cè)椎動(dòng)脈不對(duì)稱(chēng)比例超過(guò)1∶1.7[2,15]。根據(jù)頸部MRI判斷,如果雙側(cè)椎動(dòng)脈直徑<2 mm,則細(xì)側(cè)椎動(dòng)脈被診斷為VAH[15]。本研究中,將椎動(dòng)脈全程均勻狹窄,直徑<2.5 mm定義為VAH。統(tǒng)計(jì)數(shù)據(jù)顯示:11.9%患者被診斷為VAH。左側(cè)VAH 104例(4.4%),右側(cè)VAH 172例(7.3%),雙側(cè)VAH 6例(0.3%)。George等[16]報(bào)道,在正常人群中,左椎動(dòng)脈發(fā)育不良占5.7%,右椎動(dòng)脈發(fā)育不良占8.8%,比本組研究結(jié)果略高。由于各文獻(xiàn)報(bào)道的發(fā)生率都是以VAH的定義為基礎(chǔ),因此診斷標(biāo)準(zhǔn)不同就降低了各研究的可比性。Demarin等[17]通過(guò)遺傳學(xué)研究指出,VAH具有家族遺傳傾向,通常女性多于男性。本組研究結(jié)果顯示,VAH與性別無(wú)關(guān)而與年齡增高有關(guān)。不能排除高齡患者有血管退行性變的因素。由于我們只是根據(jù)椎動(dòng)脈直徑的大小來(lái)定義椎動(dòng)脈發(fā)育不良,所以VAH與年齡、性別的關(guān)系還有待于進(jìn)一步的探討。Chaturvedi等[18]指出,發(fā)育細(xì)小的椎動(dòng)脈會(huì)較正常側(cè)更早發(fā)生粥樣硬化及狹窄。椎動(dòng)脈直徑狹窄,會(huì)導(dǎo)致腦血流量的減少和后循環(huán)供血不足。所以,VAH也可能是腦部后循環(huán)中風(fēng)的危險(xiǎn)因素。

      本組研究結(jié)果顯示:左椎動(dòng)脈直接起源于主動(dòng)脈弓容易并發(fā)左椎動(dòng)脈發(fā)育不良。即往并沒(méi)有類(lèi)似的報(bào)導(dǎo)。椎動(dòng)脈直接起源于主動(dòng)脈弓,從流體力學(xué)上講,這種垂直發(fā)出的結(jié)構(gòu),會(huì)受到更大的壓力沖擊,理論上可以得到更充足的血液供應(yīng),從而減少椎動(dòng)脈供血不足性疾病的發(fā)生。但是若合并椎動(dòng)脈發(fā)育不良或因高血壓、動(dòng)脈粥樣硬化而產(chǎn)生病理性狹窄時(shí),細(xì)小的椎動(dòng)脈對(duì)壓力的承受能力就會(huì)減弱。這樣,主動(dòng)脈弓內(nèi)的壓力就成為導(dǎo)致狹窄的椎動(dòng)脈發(fā)生破裂或形成夾層動(dòng)脈瘤的重要原因。一般情況下,當(dāng)一側(cè)椎動(dòng)脈起源異常及發(fā)育不良時(shí),對(duì)側(cè)椎動(dòng)脈常可發(fā)生代償性增粗、迂曲,成為優(yōu)勢(shì)椎動(dòng)脈,從而保證腦部后循環(huán)的血供。但當(dāng)對(duì)側(cè)椎動(dòng)脈受到刺激而痙攣、狹窄或手術(shù)損傷時(shí),就會(huì)出現(xiàn)一系列后循環(huán)缺血癥狀,如頭痛、頭暈、耳鳴、耳聾等。我們?cè)谛蓄i部外科手術(shù)或主動(dòng)脈弓部的血管腔內(nèi)治療前,一定要充分了解雙側(cè)椎動(dòng)脈的起源及供血情況。本研究只測(cè)量了椎動(dòng)脈V1段的內(nèi)徑,要進(jìn)一步確認(rèn)二者之間的關(guān)系也許要評(píng)估椎動(dòng)脈的行程。

      以前很少有人研究椎動(dòng)脈起源異常和年齡、性別以及VAH之間的關(guān)系。本研究中,我們確定了遼寧地區(qū)活體成年人椎動(dòng)脈起源異常和椎動(dòng)脈發(fā)育不良的發(fā)生率。椎動(dòng)脈起源異常最常見(jiàn)的類(lèi)型為左椎動(dòng)脈直接發(fā)自左頸總動(dòng)脈和左鎖骨下動(dòng)脈之間的主動(dòng)脈弓,其發(fā)生率女性高于男性。左椎動(dòng)脈直接起源于主動(dòng)脈弓易并發(fā)左椎動(dòng)脈發(fā)育不良。

      [1]Caplan LR,Wityk RJ,Glass TA,et al.New england medical center posterior circulation registry[J].Ann Neurol,2004,56(3):389-398.

      [2]Chen YY,Chao AC,Hsu HY,et al.Vertebral artery hypoplasia is associated with a decrease in net vertebral flow volume[J].Ultrasound Med Biol,2010,36(1):38-43.

      [3]Bhatia K,Ghabriel MN,Henneberg M.Anatomical variations in the branches of the human aortic arch:a recent study of a South Australian population[J].Folia Morphol(Warsz),2005,64(3):217-223.

      [4]Karacan A,Türkvatan A,Karacan K.Anatomical variations of aortic arch branching:evaluation with computed tomographic angiography[J].Cardiol Young,2014,24(3):485-493.

      [5]Vucˇurevic′G,Marinkovic′S,Pu?ka? L,et al.Anatomy and radiology of the variations of aortic arch branches in 1,266 patients[J].Folia Morphol(Warsz),2013,72(2):113-122.

      [6]Tsai IC,Tzeng WS,Lee T,et al.Vertebral and carotid artery anomalies in patients with aberrant right subclavian arteries[J].Pediatr Radiol,2007,37(10):1007-1012.

      [7]Kau T,Sinziq M,Gasser J,et al.Aortic development and anomalies[J].Semin Intervent Radiol,2007,24(2):141-152.

      [8]Levitt B,Richter JE.Dysphagia lusoria:a comprehensive review[J]. Dis Esophagus,2007,20(6):455-460.

      [9]Schwarzacher SW,Krammer EB.Complex anomalies of the human aortic system:unique case with both vertebral arteries as additional branches of the aortic arch[J].Anat Rec,1989,225(3):246-250.

      [10]Cosar M,Yaman M,Eser O,et al.Basilar artery angulation and vertigo due to the hemodynamic effect of dominant vertebral artery[J].Med Hypothese,2008,70(5):941-943.

      [11]Nishikata M,Hirashima Y,Tomita T,et a1.Measurement of basilar artery bending and elongation by magnetic resonance cerebral angiography:relationship to age,sex and vertebral artery dominance[J].Arch Gerontol Geriatr,2004,38(3):251-259.

      [12]Jeng JS,Yip PK.Evaluation of vertebral artery hypoplasia and asymmetry by color-coded duplex ultrasonography[J].Ultrasound Med Biol,2004,30(5):605-609.

      [13]Park JH,Kim JM,Roh JK.Hypoplastic vertebral artery:frequency and associations with ischaemic stroke territory[J].J Neurol Neurosurg Psychiatr,2007,78(9):954-958.

      [14]Cosar M,Yaman M,Eser O,et al.Basilar artery angulation and vertigo due to the hemodynamic effect of dominant vertebral artery[J].Med Hypothese,2008,70(5):941-943.

      [15]Eskander MS,Drew JM,Aubin ME,et al.Vertebral artery anatomy:a review of two hundred fifty magnetic resonance imaging scans[J].Spine(Phila Pa 1976),2010,35(23):2035-2040.

      [16]George B,Laurian C.Pathology and surgery[M].New York:Springer Verlag,1987:20-24.

      [17]Demarin V,Skaric′-Juric′T,Lovrencic′-Huzjan A,et a1.Vertebral artery hypoplasia-sex-specific frequencies in 36 parent-off spring pairs[J].Coll Antropol,2001,25(2):501-509.

      [18]Chaturvedi S,Lukovits TG,Chen W,et al.Ischemia in the territory of a hypoplastic vertebrobasilar system[J].Neurology,1999,52(5):980-983.

      (編輯裘孝琦)

      The Relationship ofVertebralArtery Hypoplasia and Anomalous Origin of VertebralArtery

      ZHUXuan1,2,XINShi-jie1,2,WANGLei2,LIXi2,LVJun-yuan2
      (1.DepartmentofGeneralsurgery,The An Shan HospitalofThe FirstHospital,China MedicalUniversity,Anshan 114001,China;2.DepartmentofVascularand Thyroid Surgery,GeneralSurgery Department,The FirstHospital,China MedicalUniversity,Shenyang 110001,China)

      ObjectiveTo determine the prevalence ofanomalous origin ofvertebralartery(VA)and vertebralartery hypoplasia(VAH),and evaluate the association between them,in order to provide information and reference for diagnostic imaging and clinical surgery.MethodsA total of 2 370 patients who underwent thoracic enhanced computed tomography(CT)were included in this retrospective study.The original images were reorganized to observe and analyze the vertebral artery origin and diameter changes of V1 segment of the vertebral artery.The internal diameter of V1 segmentofthe vertebralartery was measured case by case.The uniformity and tenuity ofthe entire vertebralartery whose V1 segmenthad the internal diameterofless than 2.5 mm was defined as VAH.ResultsTotally 131(5.5%)in 2 370 cases ofpatients had anomalous origin ofthe leftvertebral arteries which were all originated from the bottom of the aortic arch.Among these cases,126 cases(5.3%)had vertebral artery originated directly from the aortic arch between the leftcommon carotid artery and the leftsubclavian artery,and 5 cases(0.2%)originated from the aortic arch atdistal end of left subclavian artery.There were 4 cases(0.16%)of the right vertebral artery originated from the right common carotid artery,which were merged with aberrantrightsubclavian artery.According to whetherthe vertebralartery wasfrom the bottom ofthe aortic arch between the leftcommon carotid artery and the left subclavian artery,the subjects were divided into the normal group and the variation group.There were 71 cases of left VAH and 144 casesofrightVAHin the normalgroup(n=1 985),22 cases ofleftVAH and 5 cases ofrightVAHin the variation group.Two groups were significantly different(P=0.000).ConclusionThe most common anomalous origin of vertebral artery is the left vertebral artery originated directly from the aortic arch between the left common carotid artery and the left subclavian artery.The incidence of anomalous origin is higher in women than in men.Advanced age is a risk factorfor VAH.The leftvertebralartery directly originated from arch is strongly correlated with leftvertebralartery hypoplasia.

      vertebral artery variation;anomalous origin of vertebral artery;vertebral artery hypoplasia

      R654.3

      A

      0258-4646(2015)04-0293-05

      國(guó)家自然科學(xué)基金(81170295)

      朱玄(1981-),女,主治醫(yī)師,碩士.

      辛世杰,E-mail:sjxin@mail.cmu.edu.cn

      2014-11-11

      網(wǎng)絡(luò)出版時(shí)間:

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