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ID:18275930
大小:1.96 MB
页数:49页
时间:2018-09-16
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1、急性炎症性脱髓鞘性多发性神经病AcuteInflammatoryDemyelinatingPolyneuropathy,AIDP1IntroductionLandry-Landry'sparalysis1859Landryreportedanacute,ascending,predominantlymotorparalysiswithrespiratoryfailure,leadingtodeathGuillair-Barre19162例Guillain,Barreandstrohl(1916)reportedabenignpolyneuritiswitha
2、lbuminocytologicdissociationintheCSF(raisedconcentrationofCSFproteinbutanormalcellcount)蛋白细胞分离是本病的特征2GuillainBarreLandryStrohl3IntroductionIn1956,CMillerFisherdescribedatriadofacuteophthalmoplegia,ataxia,andareflexia,nowknownasFisher’ssyndromeDuringthepast15years,GBShasbecomecleart
3、hatthisclinicalpicture,nowcalledGuillain-Barrésyndrome,andhavedifferentpathologicalsubtypes4EpidemiologyWorldwideincidence0.6-4/100000peryearthroughouttheworldChinaincidence0.66per100000forallages可发生于任何年龄,男女发病率相似,夏秋多见56临床表现:中国儿童和青少年,夏初。EMG:轴索损害,AMAN。EMG符合AMAN的为65%,符合AIDP的为24%。66%有C
4、J抗体,42%有GM1抗体,其他神经节苷脂抗体为17-26%。与西方国家不同,GM1抗体与AMAN或AIDP无关。近来发现AMAN与GD1a抗体相关密切。7临床表现:中国病理:AMAN:IgG和补体在轴索周围沉积,巨噬细胞侵入轴索周围间隙,严重者有轴索变性。AIDP:IgG和补体在髓鞘外沉积,巨噬细胞也在髓鞘外,“撕开”髓鞘。AMSAN:感觉轴索比运动轴索损害重。EMG不能预测病理。8PathogenesisandPathophysiologyThecauseofthissyndromeisunknown,butitisgenerallyviewedtobe
5、anautoimmuneresponsetoabacterialorviralinfection.病因尚未完全阐明9EtiologyCampylobacterJejuniEpstein-BarrVirus(EBV)Cytomegalovirus(CMV)HIVVaccinations···········空肠肠弯曲菌10PathogenesisandPathophysiologyAnacuteimmune-mediatedpolyneuropathy,componentofpathogenwassimilarwithmyelinsheathofperiphe
6、ralnerve与感染有关的自身免疫性疾病,病原体某些成分与周围神经的髓鞘成分相似11Pathophysiology主要病理特点(principalcharacteristicofpathology)节段性脱髓鞘(segmentaldemyelization)小血管周围炎性细胞浸润12131415Clinicalmanifestations多数患者有前驱症状(起病前1~3周)呼吸道感染症状喉痛、鼻塞、发热消化道症状腹泻、呕吐16ClinicalmanifestationsProgressiveascendingsymmetricalweaknessofthe
7、limbsInvolvementofproximalanddistalmusclesNumbnessandtinglinginthehandsandfeetBackpain17ClinicalmanifestationsDepressedorabsentreflexesInvolvementofcranialnerves(facialnervesmostcommonlyinvolved)Respiratoryfailure(involvedrespiratorymuscles)Progressiontopeakdisabilityin4wkautonomic
8、nervesymptom18AssessmentCe
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