简介：通常当孩子的父母或监护人发现孩子有什么不好时，会带孩子来给我们看。这篇文章更多关注给婴幼儿的建设性意见，他们往往很难评价。这不是详细的介绍列表或诊断技术，而是一个新的视点。一般原则

简介：放射治疗是许多头颈部肿瘤的有效治疗,随着放疗技术的改进,肿瘤得到较好的控制,头颈部肿瘤尤其是鼻咽癌放疗后的5年生存率明显提高.生存期的延长,生存质量越来越受到重视,本文就听觉系统的放射损伤与防治的有关文献进行综述.

简介：目的探讨真菌性角膜炎药物诊疗经验。方法对36例真菌性角膜炎进行溃疡灶刮除，碘酊烧灼，抗真菌药物联合治疗。结果36眼中重型者10眼，9眼治愈或炎症明显改善，1眼溃疡面大，溃疡穿孔行眼球摘除；轻型14眼全部治愈。结论真菌性角膜炎进行溃疡灶刮除，碘酊烧灼，抗真菌药物联合治疗，费用低，疗效好，适合在我国基层医院推广应用。

简介：目的：探讨儿童瞬目症BUT情况，为临床治疗提供依据。方法：215例患者均排除全身疾患，检查角膜、结膜、屈光不正等，着重检查BUT，详细了解患者病史，不良生活习惯等，治疗上停用含有防腐剂及激素类滴眼液，避免及纠正不良卫生及生活习惯，心理治疗，合理用眼，矫正屈光不正，给予不含防腐剂的滴眼液点眼，如3g／L艾丽滴眼液3次／d点眼，需用抗生素的给予可乐必妥滴眼液3～4次／d点眼，酌情给予抗病毒及维生素类药物。结果：215例患者BUT小于10s者197例（91．6％）326眼，其中5S以下123例224眼。本组215例病例中经过7～28d治疗，173例（80．5％）治愈，37例（17．2％）好转，5例（2．3％）无效，均未患眼部疾病，且不配合治疗，仍每天看电视或玩电脑游戏2h以上。经治疗BUT正常者192例（89．3％），好转19例（8．8％）无效者4例（1．9％）。随访1～6mo，复发31例，均为长期看电视、玩电脑、习惯揉眼者，BUT检查再次异常者，重复治疗后治愈或好转。结论：泪膜的保持并发挥其生理功能与瞬目动作休息相关，我们认为泪膜稳定性差是瞬目症的另一重要因素，BUT检查在诊治儿童瞬目症中起着关键的作用，它可以正确指导医生合理用药，使患者早日康复，而且简单易行，无痛苦，儿童易接受。我们建议BUT可作为儿童瞬目症的常规检查。

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简介：目的：探讨机械性眼外伤的临床特征及诊疗结果分析。方法：收集我院收治的机械性眼外伤122例122眼的临床资料,进行记录及回顾性分析。结果：机械性眼外伤122例中,开放性眼外伤116眼（95.1%）,闭合性眼外伤6眼（4.9%）,男女之比6.18∶1,机械性眼外伤以眼球开放性损伤为最多,致伤多以异物为主,经过及时手术治疗,全部保住了眼球,与入院视力相比,出院视力得到明显提高。结论：工作和生产意外是机械性眼外伤的主要原因,病情复杂,合并症多,后果严重,应加强防范。及时的医院就诊和眼科显微手术技术的提高及玻璃体视网膜手术的开展是挽救伤眼视力、降低机械性眼外伤并发症的有效措施。

简介：资料病例1男性,65岁。因右侧鼻腔流臭脓涕8个月,门诊以＂右全组鼻窦炎＂收入院。2年前因鼻咽癌（T3N1M0）行60Co放射治疗（以下简称放疗）,剂量为70Gy。CT扫描显示：右侧鼻腔、上颌窦、筛窦密度增高,上颌窦内侧壁骨质吸收（图1）。根据病史、症状、体征,结合影像学检查,诊断为右侧全组鼻窦炎,拟行鼻内镜手术。手术在全身麻醉下进行。

简介：<正>赵××,男,32岁。左眼钝挫伤,1997年5月10日夜11时于伤后1小时来我院急诊。主诉于当日夜间宴会上饮酒过多,有醉意后头撞在门上损伤左眼。伤时左眼剧痛,流出"热泪"和血水,视力丧失。既往于4年前曾在找市某医院请俄罗斯医生施行双

简介：0引言放射状角膜切开术（radialkeratotomy，RK）最早见于19世纪末期的眼科文献，1974／1979年前苏联Fyodorov对这一手术的发展做出了巨大的贡献，获得了满意的矫正效果，在世界各地发展较快，1978年传入我国。目前该手术由于预测性差、易出现术中术后并发症等，已基本被淘汰。

简介：AIM:ToinvestigatetheregulationofEaf2proteininmouselenscellsapoptosisinducedbyultraviolet(UV)radiation.METHODS:AneyeofEaf2geneknockoutmiceornormalcontrolmicewasexposedtoUVradiation,andtheotheronewasnon-exposed.AlloflenseswereanalyzedbyTUNELandcaspase3activityassaystodeterminethedifferenceoftheapoptosisinducedbyUVradiation.Inaddition,exposedandnon-exposedlenseswereanalyzedbyquantifiedp53expressionandreal-timereversetranscription-polymerasechainreaction(RT-PCR)ofBax,Bid,Apaf-1,PumaandNoxa,tocompareEaf2geneknockoutmiceandnormalcontrolmice.RESULTS:UVradiationcausedapoptosisoflenscellsinnormalcontrolmiceandEaf2knockoutmice.Activityofcaspase3wassignificantlyhigherinnormalcontrolmicethanEaf2knockoutmice.Expressionofp53proteinwassignificantlyhigherinlensesexposedtoUVradiationthannonexposedlenses,butwassimilarbetweenEaf2geneknockoutmiceandnormalcontrolmiceinthesameUVcondition.AfterexposingtoUVradiation,theanalysisofreal-timeRT-PCRdemonstratedthatmRNAlevelsofPumaandNoxaweresignificantlyhigherinlensesofnormalcontrolmicethanEaf2geneknockoutmice,andthatmRNAlevelsofBax,BidandApaf-1werenotsignificantlydifferentbetweengeneknockoutmiceandnormalcontrolmice.CONCLUSION:Eaf2increaseslenscellsapoptosisinducedbyultravioletradiation.AndEaf2up-regulatesexpressionofthePumaandtheNoxatoactonlenscellsapoptosisafterUVradiation.

简介：目的评价带线羟基磷灰石义眼座(HA)无包裹植入的临床疗效.方法对29例眼球摘除术后患者,采用带线羟基磷灰石义眼座作为眼窝植入物,无包裹直接植入.Ⅰ期植入21例.Ⅱ期植入8例.结果分别随访5-18月,4眼术后出现球结膜裂开,2眼术后轻度上睑下垂,1眼术后五月义眼座中度暴露,均经相应治疗后恢复.其他病例手术效果良好,无植入物脱出及移位,义眼座活动度良好.结论带线羟基磷灰石义眼座直接植入术,具有操作简单、材料易得、并发症少等优点,具有良好的应用前景.

简介：AIM:Toinvestigatethediffusioncharacteristicsofwaterofopticnerveandopticradiationinhealthyadultsanditsrelatedfactorsbydiffusiontensorimaging（DTI）at3T.METHODS:Atotalof107healthyvolunteersperformedheadconventionalMRIandbilateralopticnerveandopticradiationDTI.TheprimarydataofDTIwasprocessedbypost-processingsoftwareofDTIstudio2.3,obtainingfractionalanisotropyvalue,meandiffusivityvalue,principalenginevalue,orthogonalenginevaluebymeasuring,andanalyzedbytheSPSS13.0statisticalsoftware.RESULTS:Thebilateralopticnerveandopticradiationfiberspresentedgreencolorindirectionalencodedcolor（DEC）mapsandpresentedhighsignalinfractionalanisotropy（FA）maps.TheFAvalueoftheleftopticnervewas0.598±0.069andtherightwas0.593±0.065;themeandiffusivity（MD）valueoftheleftopticnervewas（1.324±0.349）×10-3mm2/sandtherightwas（1.312±0.350）x10-3mm2/s;theprincipalenginevalue(λ?)oftheleftopticnervewas（2.297±0.522）×10-4mm2/sandtherightwas（2.277±0.526）×10-3mm2/s;theorthogonalenginevalue（λ⊥）oftheleftopticnervewas（0.838±0.285）×10-3mm2/sandtherightwas（0.830±0.280）×10-3mm2/s;theFAvalueoftheleftopticradiationwas0.636±0.057andtherightwas0.628±0.056;themeandiffusivity（MD）valueoftheleftopticradiationwas（0.907±0.103）×10-3mm2/sandtherightwas（0.889±0.125）×10-3mm2/s;theprincipaleigenvalue(λⅡ)oftheleftopticradiationwas（1.655±0.210）×10-3mm2/sandtherightwas（1.614±0.171）×10-3mn2/s;theorthogonalenginvalue（λ⊥）oftheleftopticradiationwas（0.531±0.103）×10-3mm2/sandtherightwas（0.524±0.152）×10-3m

简介：AIM:Tocomparetheregularityandaccuracyoflaserinsitukeratomileusis(LASIK)flapscreatedbytheZiemerFEMTOLDV'Classic'(Ziemer'Classic')andZiemerFEMTOLDVCrystalLinefemtosecondlaser(ZiemerCrystalLine).METHODS:Fourier-domainopticalcoherencetomography(RTVueOCT)wasusedtomeasurethemorphologyof200LASIKflapsof100consecutivepatientscreatedwiththeZiemerClassic(100flaps)ortheZiemerCrystalLine(100flaps)atoneweekpostoperatively.Flapthicknesswasevaluatedat36specifiedmeasurementpointsoneachflap.Forallprocedureswithbothlasers,thenominalflapthicknesswas110μm.RESULTS:ThemeanflapthicknessoftheZiemerCrystalLinegroup(102.49±2.68μm)wasthinnerthanthatoftheZiemerClassicgroup(107.65±5.09μm)(P<0.01).Averagethicknessofallflapswasuniformwithin4μmatallmeasurementpoints.TheflapsintheZiemerCrystalLinegroupweremoreregularthanthoseintheZiemerClassicgroupwhenmeasuredfromthecentertotheperiphery.Themaximumdeviationfromthenominal110μmof36measurementswas8μmintheZiemerClassicgroup,whileintheZiemerCrystalLinegroupitwas9μm.Withinthe3600measurementsonthe100eyes,differencesgreaterthan20μmwereobserved0.14%intheZiemerClassicgroup,and0.04%intheZiemerCrystalLinegroup.CONCLUSION:TheflapscreatedwiththeZiemerFEMTOLDVCrystalLinefemtosecondlaseraremoreuniformandthinnerthanthosecreatedbytheZiemerFEMTOLDVClassicfemtosecondlaser.

简介：AIM:Toestablishanuntransfectedhumancornealstromal(HCS)celllineandcharacterizeitsbiocompatibilitytoacellularporcinecornealstroma(aPCS).·METHODS:PrimaryculturewasinitiatedwithapurepopulationofHCScellsinDMEM/F12media(pH7.2)containing20%fetalbovineserumandvariousnecessarygrowthfactors.Theestablishedcelllinewascharacterizedbygrowthproperty,chromosomeanalysis,tumorigenicityassay,expressionofmarkerproteinsandfunctionalproteins.Furthermore,thebiocompatibilityofHCScellswithaPCSwasexaminedthroughhistologicalandimmunocytochemistryanalysesandwithlight,electronmicroscopies.·RESULTS:HCScellsproliferatedtoconfluence2weekslaterinprimarycultureandhavebeensubculturedtopassage140sofar.AcontinuousuntransfectedHCScelllinewithapopulationdoublingtimeof41.44hoursatpassage80hasbeendetermined.Resultsofchromosomeanalysis,morphology,combinedwiththeresultsofexpressionofmarkerproteinandfunctionalproteinssuggestedthatthecellsretainedHCScellproperties.Furthermore,HCScellshavenotumorigenicity,andwithexcellentbiocompatibilitytoaPCS.·CONCLUSION:Anuntransfectedandnon-tumorigenicHCScelllinehasbeenestablished,andthecellsmaintainedpositiveexpressionofmarkerproteinsandfunctionalproteins.Thecellline,withexcellentbiocompatibilitytoaPCS,mightbeusedforinvitroreconstructionoftissue-engineeredHCS.

简介：AIM:Todemonstratethemorphologyandstructureofinvitroreconstructedtissue-engineeredhumancornealepithelium(TE-HCEP)withseedercellsfromanuntransfectedHCEPcellline.·METHODS:TheTE-HCEPswerereconstructedinvitrowithseedercellsfromanuntransfectedHCEPcellline,andscaffoldcarriersofdenudedamnioticmembrane(dAM)inair-liquidinterfaceculturefor3,5,7and9days,respectively.Thespecimenswereexaminedwithhematoxylin-eosin(HE)stainingofparaffin-section,immunocytochemicalstaining,scanningandtransmissionelectronmicroscopy.·RESULTS:DuringinvitroreconstructionofTE-HCEP,HCEPcellsformeda3-4,6-7and8-10layersofanHCEP-likestructureondAMsinair-liquidinterfaceculturefor3,5and7days,respectively.Butthecellsdeceasedto5-6layersandthestructureofstraifiedepitheliumbecamelooseatday9.Andthecellsmaintainedpositiveexpressionofmarkerproteins(keratin3andkeratin12),cell-junctionproteins(zonulaoccludens-1,E-cadherin,connexin43andintegrinβ1)andmembranetransportproteinofNa+-K+ATPase.TheHCEPcellsinTE-HCEPwererichinmicrovillionapicalsurfaceandestablishednumerouscell-cellandcell-dAMjunctionsatday5.·CONCLUSION:ThemorphologyandstructureofthereconstructedTE-HCEPweresimilartothoseofHCEPinvivo.TheHCEPcellsinthereconstructedTE-HCEPmaintainedthepropertiesofHCEPcells,includingabilitiesofformingintercellularandcell-extracellularmatrixjunctionsandabilitiesofperformingmembranetransportation.TheuntransfectedHCEPcellsanddAMscouldpromisinglybeusedinreconstructionHCEPequivalentforclinicalcornealepitheliumtransplantation.