王恩彤 單希征,2
上半規(guī)管裂綜合征的認(rèn)識(shí)與處理
王恩彤1單希征1,2
上半規(guī)管裂綜合征是指因上半規(guī)管的先天性或后天性骨質(zhì)缺損—上半規(guī)管裂所導(dǎo)致的一種綜合征,可表現(xiàn)有眩暈、耳聾等前庭與耳蝸癥狀。上半規(guī)管裂綜合征臨床較少見,臨床醫(yī)師對(duì)其認(rèn)識(shí)不足,容易發(fā)生誤診誤治。本文就上半規(guī)管裂綜合征的病因、發(fā)病機(jī)理、臨床表現(xiàn)特點(diǎn)和診療策略等進(jìn)行綜述,以幫助臨床醫(yī)師對(duì)上半規(guī)管裂綜合征的認(rèn)識(shí),提高對(duì)該病的診療能力。
上半規(guī)管裂;上半規(guī)管裂綜合征;眩暈
上半規(guī)管裂綜合征(superior canal dehiscence syndrome,SCDS)是指因上半規(guī)管的先天性或后天性骨質(zhì)缺損即上半規(guī)管裂(SCD)所導(dǎo)致的一種綜合征,可表現(xiàn)有眩暈、耳聾等前庭與耳蝸癥狀。對(duì)SCDS的認(rèn)識(shí)僅有20來年的歷史。1998年Minor等[1]首先報(bào)告了8例SCDS病例,此后SCDS陸續(xù)見諸文獻(xiàn)報(bào)告,迄今已報(bào)告有 600 余例[2],國內(nèi)也偶有報(bào)告[3,4]。因該病臨床少見,臨床醫(yī)師對(duì)其尚缺少足夠的認(rèn)識(shí),容易發(fā)生誤診誤治,本文就其病因、發(fā)病機(jī)理、臨床表現(xiàn)特點(diǎn)和診療策略等綜述如下,以幫助臨床醫(yī)師對(duì)SCDS的認(rèn)識(shí),提高對(duì)該病的診療能力。
Carey等[5]對(duì)576例尸頭1000個(gè)顳骨標(biāo)本的研究發(fā)現(xiàn),SCD發(fā)生率為0.7%,另有1.3%顯示上半規(guī)管頂部覆蓋骨質(zhì)偏薄(≤0.1mm)。由于SCD通常需借助于CT證實(shí),隨著高分辨率CT(HRCT)的應(yīng)用,其發(fā)現(xiàn)率明顯增加。HRCT研究顯示SCD在兒童與成人中的發(fā)生率在3%-10%[6-12]。但CT所示SCD發(fā)生率可能被高估,因一些研究其HRCT層厚偏大甚至超過中顱窩底厚度,可能帶來SCD假陽性結(jié)果[8,13]。顳骨解剖及病理研究或手術(shù)探查報(bào)告的SCD發(fā)生率明顯低于影像學(xué)研究之發(fā)生率或發(fā)現(xiàn)率。如Crovetto等[14]比較了604耳的CT和尸頭顳骨研究結(jié)果,發(fā)現(xiàn)CT之SCD發(fā)現(xiàn)率為3.6%,而解剖學(xué)觀察SCD發(fā)生率僅為0.6%。SCD常雙側(cè)發(fā)生。尸頭或影像學(xué)研究顯示,一側(cè)表現(xiàn)有SCD者其對(duì)側(cè)亦出現(xiàn)SCD或半規(guī)管頂骨質(zhì)變薄者可占到1/3-1/2[5,15]。SCD發(fā)生率無明顯的側(cè)別差異[9]。需注意的是,許多SCD可不表現(xiàn)有臨床癥狀,因此,SCD發(fā)生率并不等同于SCDS發(fā)生率。SCDS在一般人群中的發(fā)生率尚無確切的數(shù)據(jù)。近期一多學(xué)科眩暈診療中心大樣本研究報(bào)告顯示,在其17000余例眩暈與頭暈病例中,SCDS所占比例不到1%[16]。SCDS可見于任何年齡段人群,但以中年人居多[4,17-19]。CT顯示SCD的發(fā)生率并無性別差異[9]。近期Xie等[20]報(bào)告顯示,在1996-2015年接受手術(shù)治療的SCDS患者中,男110例,女132例,平均年齡47.8±10.6歲。
SCDS由SCD所致,但SCD發(fā)生原因尚不十分清楚且尚有爭(zhēng)論,可能為先天性發(fā)育異常,也可能為后天性形成[21],抑或是多種因素作用的結(jié)果[22]。
SCD系為中顱窩底覆蓋上半規(guī)管頂面的骨質(zhì)缺損所致[1]。一般認(rèn)為,SCD可能系上半規(guī)管頂部骨質(zhì)先天性發(fā)育不全的結(jié)果[2]。兒童SCD發(fā)生率明顯高于成人[23]。許多學(xué)者觀察到,SCD的CT發(fā)現(xiàn)率在嬰幼兒較高,但在 3 歲以上兒童開始降低[11,12,24]。且SCD常常雙側(cè)發(fā)生,一側(cè)有SCD者其對(duì)側(cè)亦出現(xiàn)SCD或半規(guī)管頂骨質(zhì)變薄者占到1/3-1/2[5,15]。這些均支持SCD先天性發(fā)育異常學(xué)說[12]。SCDS累及雙側(cè)者約占25%,這也符合先天性異常的特征[25]。盡管曾有家族性SCDS的病例報(bào)告[5,26],但SCDS明顯的遺傳關(guān)系并未確定。
SCD也可能在后天形成。CT觀察顯示,一些高齡患者其上半規(guī)管頂部表面骨質(zhì)變薄[27],甚至有報(bào)告顯示SCD可隨齡加重[28],這些則支持SCD系后天性形成的理論。一些學(xué)者認(rèn)為,SCD的發(fā)生可能與頭部外傷或氣壓傷有關(guān),上半規(guī)管表面薄層骨質(zhì)可因外傷而裂開[10]。
一般認(rèn)為,SCDS發(fā)病的病理生理機(jī)理可以“第3 窗”(third window)理論來解釋[2]。正常情況下,鐙骨底板所附著之卵圓窗負(fù)責(zé)內(nèi)耳傳入聲音的調(diào)節(jié),而圓窗則負(fù)責(zé)聲及聲能由內(nèi)耳鼓階的釋放。當(dāng)存在有SCD時(shí),在卵圓窗和圓窗之外則出現(xiàn)了所謂的“第3個(gè)活動(dòng)窗”,而擾亂了內(nèi)淋巴液的正常流動(dòng)力學(xué)模式,當(dāng)受到強(qiáng)聲刺激或中耳與顱內(nèi)壓增加時(shí),正常的聲及聲能傳導(dǎo)路徑發(fā)生改變,非經(jīng)正常的耳蝸路徑而經(jīng)迷路這條低阻抗傳導(dǎo)路徑進(jìn)行傳導(dǎo),從而導(dǎo)致聽力減退及骨導(dǎo)聽覺過敏,并可誘發(fā)眩暈及眼震的出現(xiàn)。
SCDS 臨床表現(xiàn)不盡相同[2,17,29,30]。典型 SCDS 患者可表現(xiàn)有耳蝸與前庭癥狀。但有些患者可僅表現(xiàn)有耳蝸癥狀或前庭癥狀。還有一些患者雖其CT顯示有SCD的存在,但患者并不表現(xiàn)有相關(guān)的癥狀。SCD的表現(xiàn)癥狀及程度與SCD的大小有關(guān)[31]。有些患者存在輕度或隱性SCD,平時(shí)可不表現(xiàn)有明顯的癥狀,當(dāng)遇有誘因時(shí)(如外傷),可能使已有的輕度或隱性SCD加重而出現(xiàn)典型癥狀。
聽覺過敏與自聲增強(qiáng):約1/4的SCDS患者訴有骨導(dǎo)聽覺過敏相關(guān)癥狀,多表現(xiàn)為自聲增強(qiáng)(autophony),如患者不能耐受自己說話的聲音而不敢大聲講話和唱歌,還有患者因?qū)β曇舸碳っ舾卸桓矣没级勇犑謾C(jī),有些患者能聽到自己血管搏動(dòng)的聲音,表現(xiàn)為與脈搏同步的搏動(dòng)性耳鳴,感覺自己咀嚼聲過響,能聽到自己的腳步聲、心跳聲、眼球運(yùn)動(dòng)聲(眨眼聲)、腸蠕動(dòng)聲,甚至可聽到關(guān)節(jié)運(yùn)動(dòng)的聲音等。
聽力減退:通常表現(xiàn)為漸進(jìn)性聽力減退[21,28],但聽力減退在一段時(shí)間內(nèi)亦可沒有明顯的變化[19],有時(shí)也可表現(xiàn)為外傷后聽力突然減退。其聽力減退以低頻聽力下降多見[3],常表現(xiàn)為低頻傳導(dǎo)性聽力減退。一些患者尚可表現(xiàn)有耳悶脹感。
眩暈與眼震:多數(shù)患者可表現(xiàn)有前庭癥狀,如患者出現(xiàn)慢性平衡障礙和眩暈癥狀。部分患者會(huì)出現(xiàn)站立不穩(wěn)、易傾倒等平衡功能紊亂癥狀。眩暈可呈發(fā)作性,其眩暈發(fā)作可由強(qiáng)聲刺激所誘發(fā),有些患者明顯不能耐受外界環(huán)境噪聲。強(qiáng)聲刺激不僅可誘發(fā)眩暈癥狀,還可誘發(fā)眼震,即出現(xiàn)所謂Tullio現(xiàn)象[29,32],患者還常表現(xiàn)有強(qiáng)聲刺激所誘發(fā)的失衡或視物晃動(dòng)、視野偏斜等癥狀,其誘發(fā)癥狀可反復(fù)發(fā)生,持續(xù)時(shí)間較短暫[32]。眩暈與眼震也可由中耳或顱內(nèi)壓力的增加(如摒氣用力、咳嗽、打噴嚏、擤鼻涕、捏鼻鼓氣)所誘發(fā),即出現(xiàn)所謂的Hennebert征[33]。
純音測(cè)聽:典型SCDS其純音聽力多表現(xiàn)為低頻(250Hz-1000Hz)傳導(dǎo)性聾, 由于患者氣導(dǎo)聽力下降而骨導(dǎo)聽力增強(qiáng),甚至骨導(dǎo)聽閾呈負(fù)值的情況,從而存在有較大的骨氣導(dǎo)差[2]。但有些SCDS患者也可表現(xiàn)為感音神經(jīng)性聾或混合性聾。
聲導(dǎo)抗檢查:?jiǎn)渭僑CD患者其聲導(dǎo)抗測(cè)試通??杀憩F(xiàn)出正常鼓室導(dǎo)抗圖及鐙骨肌聲反射。
耳蝸電圖:SCDS患者的耳蝸電圖可出現(xiàn)SP/AP比值增加。
前庭誘發(fā)肌源性電位(VEMP):VEMP對(duì)SCDS有較好的診斷價(jià)值,尤其是oVEMP對(duì)診斷SCDS有較好的特異性和敏感性[22,34-36]。因此,VEMP可作為一項(xiàng)必要的SCDS診斷試驗(yàn)[2]。SCDS患者常表現(xiàn)有VEMP異常,一般來說,患側(cè)cVEMP閾值較正常側(cè)降低,而 oVEMP 波幅增大[2,19,29,36]。
CT顯示有SCD是診斷SCDS的主要依據(jù)之一。薄層、多平面顳骨CT掃描對(duì)發(fā)現(xiàn)SCD是一種十分有價(jià)值的方法[9]。CT層厚對(duì)SCD的發(fā)現(xiàn)和診斷非常關(guān)鍵,其層厚應(yīng)小于1mm,最好在0.625mm以下[2],且應(yīng)在上半規(guī)管平面重組,否則SCD難以被發(fā)現(xiàn)或出現(xiàn)假陽性結(jié)果[9]。MR也可用于SCD的診斷與評(píng)價(jià)[22,37]。
由于 CT 診斷 SCD 具有一定的假陽性率[8,13,14],且許多患者顳骨CT顯示有SCD,但并未表現(xiàn)有SCDS癥狀,因此,單憑CT檢查結(jié)果尚不足以做出SCDS診斷[2],SCDS診斷應(yīng)基于CT發(fā)現(xiàn)和臨床表現(xiàn)[8]。Minor[29]認(rèn)為SCDS診斷需符合以下標(biāo)準(zhǔn):①表現(xiàn)有SCDS相關(guān)癥狀;②顳骨HRCT及上半規(guī)管重組提示上半規(guī)管表面存在有骨質(zhì)缺損。近來,Ward等[2]提出了新的SCDS診斷標(biāo)準(zhǔn):
①高分辨率CT(層厚≤0.625mm):上半規(guī)管平面CT重組顯示有骨裂存在。
②至少表現(xiàn)有下述SCDS癥狀之一:
A.骨導(dǎo)聽覺過敏(表現(xiàn)為自聲增強(qiáng),可聽到眨眼聲、腳步聲等);
B.聲誘發(fā)性眩暈;
C.壓力誘發(fā)性眩暈 (捏鼻鼓氣、摒氣或外耳道受到壓力刺激);
D.博動(dòng)性耳鳴。
③下述提示存在第3窗的診斷性試驗(yàn)中至少有一項(xiàng)呈陽性:
A.純音測(cè)聽顯示骨導(dǎo)聽閾呈負(fù)值;
B.VEMP反應(yīng)增強(qiáng)(cVEMP閾值降低、oVEMP振幅增大);
C.無感音神經(jīng)性聾情況下,耳蝸電圖顯示SP/AP比值增加。
SCDS的治療選擇取決于患者的癥狀程度[22],如僅有偶發(fā)癥狀或癥狀較輕微者可采取保守治療[19],對(duì)于癥狀較重者,伴有明顯功能障礙者,保守治療難以奏效者,而影響到患者的正常學(xué)習(xí)、工作和生活時(shí),可考慮手術(shù)治療。SCDS兒童選擇手術(shù)治療應(yīng)慎重,因3歲以下兒童其上半規(guī)管可能仍處于發(fā)育過程之中,應(yīng)予以觀察及保守治療包括試配助聽器[30]。雙側(cè)SCD在選擇手術(shù)治療時(shí),應(yīng)先選擇有癥狀一側(cè)或癥狀較重一側(cè)手術(shù)。
保守治療措施包括隨訪觀察,并可進(jìn)行前庭康復(fù)治療,避開外界強(qiáng)聲或噪聲刺激以減少誘發(fā)癥狀,避免自己大聲叫喊,如患者主要癥狀為強(qiáng)聲誘導(dǎo)的眩暈,避免強(qiáng)聲刺激可使其相關(guān)癥狀得到改善,應(yīng)防止頭部及耳部外傷以防SCD加重,目前SCDS尚無有效的治療藥物,但可采用前庭抑制劑對(duì)癥治療[2]。
通??刹捎肧CD修補(bǔ)手術(shù),以消除“第3活動(dòng)窗”而達(dá)到治療目的。術(shù)式及手術(shù)徑路的選擇可依據(jù)患者的顳骨解剖特點(diǎn)和手術(shù)醫(yī)師的手術(shù)經(jīng)驗(yàn)與技巧而定[2,30]。術(shù)式主要包括 SCD 堵塞術(shù)(plugging)、覆蓋術(shù)(resurfacing)及戴帽術(shù)(capping)等,戴帽術(shù)通常是指在上半規(guī)管頂部蓋以羥基磷灰石水泥來修復(fù)其骨質(zhì)缺損[38]。手術(shù)路徑主要有中顱窩入路和乳突入路,應(yīng)采用哪種手術(shù)入路尚有爭(zhēng)論。顱中窩入路SCD堵塞修補(bǔ)術(shù)目前仍被視為治療SCDS的標(biāo)準(zhǔn)術(shù)式[2]。但因該入路屬入顱手術(shù),發(fā)生手術(shù)并發(fā)癥的潛在風(fēng)險(xiǎn)較大。目前更趨于采用乳突入路手術(shù)[2]。一些學(xué)者采用乳突入路SCD修補(bǔ)術(shù)取得了較好的治療效果[39-41]。認(rèn)為,乳突入路較中顱窩入路更為安全、有效、創(chuàng)傷小[42-45]。近來系統(tǒng)評(píng)價(jià)表明,與顱中窩入路SCD堵塞術(shù)相比,乳突入路手術(shù)的并發(fā)癥發(fā)生率低,再手術(shù)率亦較低,且住院時(shí)間短,建議采用經(jīng)乳突入路SCD堵塞術(shù)[46]。SCD封堵修補(bǔ)材料則可采用筋膜、肌肉、軟骨膜、骨粉、骨渣、骨水泥、骨蠟及纖維蛋白膠等。
SCD修補(bǔ)術(shù)為治療SCDS的有效手段,術(shù)后可有效地緩解患者聲或壓力誘發(fā)性眩暈等前庭癥狀。不管采用何種手術(shù)方法和技術(shù),多數(shù)患者在SCD修補(bǔ)術(shù)后其癥狀可得到改善[29,38,43,44,47-49]。近來系統(tǒng)評(píng)價(jià)顯示,患者術(shù)后主要以前庭癥狀的改善為主,而聽力減退則缺少明確的改善[46]。總的來說,覆蓋術(shù)的效果不及堵塞術(shù),且覆蓋術(shù)通常需經(jīng)中顱窩入路,發(fā)生手術(shù)并發(fā)癥的潛在風(fēng)險(xiǎn)較大。堵塞術(shù)對(duì)SCDS的癥狀緩解成功率較高,但其發(fā)生內(nèi)耳創(chuàng)傷引起感音神經(jīng)性聾的機(jī)會(huì)增加[22]。Ward等[2]研究顯示,SCDS經(jīng)中顱窩入路SCD堵塞術(shù)治療后其低頻骨氣導(dǎo)差有所縮小,但有25%的患者發(fā)生有輕度高頻感音神經(jīng)性聾。而以羥基磷灰石施以“戴帽術(shù)”可獲得較高的前庭癥狀緩解成功率并可減少術(shù)后并發(fā)癥[30]。
早期一項(xiàng)薈萃分析顯示,在64例接受SCD修補(bǔ)術(shù)的病例,多采用顱中窩入路,包括堵塞術(shù)33例、覆蓋術(shù)16例和戴帽術(shù)15例,其成功率分別為97%、50%和93%,感音神經(jīng)性聾和平衡功能障礙為其主要的手術(shù)并發(fā)癥[50]。近來,Xie等[20]回顧了他們?cè)?996-2015年間242例SCDS手術(shù)病例的手術(shù)并發(fā)癥發(fā)生情況,其中95.5%的病例采取中顱窩入路,4.5%的病例采取乳突入路,多數(shù)病例(89.3%)采用覆蓋術(shù)加堵塞術(shù)治療,其中27例(11.2%)出現(xiàn)手術(shù)并發(fā)癥,但多數(shù)程度較輕,其中發(fā)生BPPV者11例,感音神經(jīng)性聾6例,而嚴(yán)重并發(fā)癥發(fā)生率較低。近期Gioacchini等[51]通過對(duì)20項(xiàng)研究150例手術(shù)病例的系統(tǒng)評(píng)價(jià)顯示,SCD修補(bǔ)術(shù)包括戴帽術(shù)、堵塞術(shù)、覆蓋術(shù)及堵塞加覆蓋術(shù)的總成功率達(dá)94%,各種術(shù)式的成功率及并發(fā)癥發(fā)生率無明顯的差別。Sharon等[52]近來研究顯示,222例接受SCD修補(bǔ)術(shù)的成人患者中,因初次手術(shù)失敗而接受再手術(shù)者21例(23例次),再手術(shù)率約為10%;初次手術(shù)采用顱中窩入路者14例次(61%),采用乳突入路者9例次(39%);再手術(shù)顯示,初次手術(shù)所使用的修補(bǔ)材料尚在SCD處但未能將之完全遮蓋者17例,修補(bǔ)位置臨近骨質(zhì)變薄者4例;再手術(shù)后癥狀完全緩解者、部分緩解者和未緩解者約各占1/3,說明一些初次手術(shù)失敗者通過再手術(shù)仍可得到治愈,但再手術(shù)失敗率可能較高。
近年來,有些學(xué)者嘗試采用新的手術(shù)入路及術(shù)式來治療SCDS,如外耳道入路圓窗龕封堵術(shù)(round window niche occlusion) 或圓窗封固術(shù)(round window reinforcement),也收到較好的效果,這類手術(shù)尤適于伴有明顯聲音過敏的患者[53,54],但此類手術(shù)的長期效果尚有待于觀察[2]。
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10.16542/j.cnki.issn.1007-4856.2017.05.026
1中國武警總醫(yī)院眩暈病研究所(北京,100039)
2中國武警總醫(yī)院耳鼻咽喉頭頸外科(北京)
單希征,主任醫(yī)師.Email:sxzent@163.com
(收稿:2017-08-16)