文章编号:1003-2754(2013)05-0396-03线粒体神经胃肠型脑肌病的临床和病理分析许二赫,张弥兰,董会卿,贾建平收稿日期:2012-12-26;修订日期:2013-03-15作者单位:(首都医科大学宣武医院神经内科,北京100053)通讯作者:许二赫,E-mail:xuerhe@163.com摘要:目的探讨线粒体神经胃肠型脑肌病(MitochondrialNeurogastrointestinalEncephalopathyDisease,MNGIE)的临床和病理特点。方法通过1例临床确诊为线粒体神经胃肠型脑肌病病例的临床表现、影像学检查及病理检查,系统回顾线粒体神经胃肠型脑肌病的发病机制、临床表现、病理特点。结果该患有长期的腹痛、腹泻史,神经系统首发症状为听力障碍,此后出现头晕、走路不稳、记忆力逐渐下降。神经系统检查有眼外肌麻痹、听力障碍、周围神经损害。肌电图:广泛神经源性损害。头部MRI表现为广泛的白质脑病。肌肉活检为HE染色中出现嗜碱的肌纤维,在GT染色中为典型和不典型的RRF,在NADH染色和SDH染色中深染。结论线粒体神经胃肠型脑肌病是一种特殊类型的线粒体肌病,具有上述临床及影像学特点,加上血及(或)脑脊液乳酸水平升高,肌肉活检示组织学线粒体肌病的表现。如果发现血清白细胞中胸苷磷酸化酶活性降低或基因检测发现胸苷磷酸化酶(thymidinephosphorylase,TYMP)基因位点突变更能进一步确诊。关键词:线粒体神经胃肠型脑肌病;线粒体;胸苷磷酸化酶中图分类号:R746文献标识码:AClinicalandpathologicalanalysisofmitochondrialneurogastrointestinalencephalopathydiseaseXUEr-he,ZHANGMi-lan,DONGHui-qing,etal.(DepartmentofNeurology,XuanwuHospital,CapitalMedicalUniversety,Beijing100053,China)Abstract:ObjectiveToexploretheclinicalandpathologicalfeaturesofmitochondrialneurogastrointestinalen-cephalopathydisease(MNGIE).MethodsClinicalmanifestations,imaging,andpathologicexaminationresultsofoneconfirmedcaseofMNGIEwerestudied.Thepathogenesis,clinicalmanifestations,andpathologicalcharacteristicsofMNG-IEweresystematicallyreviewed.ResultsThepatienthadalonghistoryofchronicabdominalpainanddiarrhea.Theini-tialnervoussystemsymptomswerehearingdisorder,followedbydizziness,ataxia,andgradualmemoryimpairment.Nervoussystemexaminationshowedexternalophthalmoplegia,hearingimpairment,andperipheralnervedamage.Electromyogramshowedextensiveneurogenicdamage.HeadMRIshowedextensiveleukoencephalopathy.H&Estainingofmusclebiopsyspecimensshowedbasophilicmusclefibers,andGTstainingrevealedtypicalandatypicalraggedredfibers,whichweredarklystainedinSDHstainingandNADHstaining.ConclusionMNGIEisaspecialtypeofmitochondrialmyopathywiththeaforementionedclinicalandimagingfeatures.Inaddition,lactatelevelsinthebloodand/orcerebrospinalfluidareele-vated,andmusclebiopsyshowshistologicalmanifestationsofmitochondrialmyopathy.Thediseasemaybefurtherconfirmediftheactivityofthymidinephosphorylase(TYMP)inwhitebloodcellsisdecreasedorgenelocusmutationofTPisdetec-tedbygeneticanalysis.Keywords:Mitochondrialneurogastrointestinalencephalopathydisease;Mitochondria;Thymidinephosphoryl-ase线粒体神经胃肠型脑肌病(MitochondrialNeu-rogastrointestinalEncephalopathyDisease,MNGIE)是一种特殊类型的线粒体肌病,又被称为“多发性神经病伴眼肌麻痹、白质脑病、假性肠梗阻(POLIP)”,“眼部及胃肠肌营养不良(OGIMD)”,“线粒体脑肌病伴多发周围神经病、眼肌麻痹和假性肠梗阻(ME-POP)”。MNGIE是最常见的缩写名称。主要临床表现为胃肠道动力障碍、眼肌麻痹、周围神经病,头部MRI表现为广泛的白质脑病,肌肉活检示线粒体肌病的表现。至今中国尚无该病例报道。现将我们临床诊断MNGIE的病例做如下报道。1病例报告患者,女,28岁。因进行性双耳听力下降8年,头晕、行走不稳、记忆力下降7月于2010年10月收入院。患者于8年前(20岁)无明...