全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...
华西医学  2011 

合并免疫指标异常的视神经脊髓炎临床特点

, PP. 1639-1641

Keywords: 视神经脊髓炎,自身免疫性疾病,多发性硬化

Full-Text   Cite this paper   Add to My Lib

Abstract:

【】 目的 分析合并免疫指标异常的视神经脊髓炎临床特点。 方法 回顾性分析2009年5月-2010年11月收治的62例视神经脊髓炎患者中24例合并免疫指标异常患者的临床资料。24例均为女性,发病年龄14~53岁。对其临床表现、视觉诱发电位、影像学检查结果、免疫检查结果进行分析。 结果 所有患者均有脊髓和视神经同时或先后受累的表现。24例视觉诱发电位检查23例异常。脊髓MRI显示病变集中于颈段、上胸段脊髓。颈段和胸段脊髓同时受累17例,单纯颈段脊髓受损6例,单纯胸段脊髓受损1例。所有患者抗核抗体滴度均≥1∶100,合并抗SSA抗体阳性14例(55.5%),同时合并抗SSB抗体阳性11例(45.8%),合并抗Rib抗体阳性1例,合并抗SCL-70抗体阳性1例,合并抗dsDNA抗体1例。 结论 视神经脊髓炎合并免疫指标异常的患者以女性较为多见,易复发,青壮年患者发病率最高。脊髓MRI示病变集中于颈段、上胸段脊髓,表现为长节段脊髓损害。视神经脊髓炎患者合并结缔组织病的病例较多。【Abstract】 Objective Toanalyzetheclinicalfeaturesofneuromyelitisoptica(NMO)combinedwithabnormalimmuneparameters. Methods Weretrospectivelyreviewedtheclinicaldataof24patientswithNMOandabnormalimmuneparametersamongthe62NMOpatientswhowereadmittedintoourdepartmentbetweenMay2009andNovember2010.Allpatientswerefemale,agedfrom14to53years.Weanalyzedtheirclinicalmanifestations,visualevokedpotentials,imagingresults,andimmunologicalexaminations. Results Allpatientshadsimultaneousorsuccessivespinalcordandopticnerveinvolvement.Twenty-threepatientshadabnormalvisualevokedpotential.MRIshowedthatthelesionsfocusedonthecervicalandupperthoracicspinalcord.Bothcervicalandthoracicspinalcordwereinvolvedin17cases;therewere6casesofsimplecervicalspinalcordinjuryand1caseofsimplethoracicspinalcorddamage.Antinuclearantibodytiterofallthepatientswas≥1∶100.Combinedpositiveanti-SSAantibodyoccurredin14patients(55.5%);Concomitantpositiveanti-SSBantibodiesoccurredin11patients(45.8%);Combinedpositiveanti-Ribantibodiesoccurredin1patient;Combinedpositiveanti-SCL-70antibodyoccurredin1patient;andcombinedpositiveanti-dsDNAantibodiesoccurredin1patient. Conclusions NMOcombinedwithabnormalimmuneparametersmainlyoccursinfemalepatients,especiallyinyoungpeople.Recurrencerateishigh.MRIshowsthatthelesionsfocusmainlyonthecervicalandupperthoracicspinalcord,manifestingthecharacteristicoflongsegmentdamage.AndNMOisfrequentlycombinedwithconnectivetissuedisease.

References

[1]   Nasir S, Kerr DA, Birnbaum J. Nineteen episodes of recurrent myelitis in a woman with neuromyelitis optica and systemic lupus erythematosus[J]. Arch Neurol, 2009, 66(9): 1160-1163.
[2]   Pellkofer HL, Hohlfeld R, Kuempfel T. Thirty-one episodes of myelitis and optic neuritis in a woman with neuromyelitis optica and systemic lupus erythematosus[J]. Arch Neurol, 2010, 67(6): 779-780.
[3]   江天丽, 郑金瓯. 35例视神经脊髓炎的临床分析[J]. 广西医学, 2007, 11(29): 1787-1788.
[4]   郁冰冰, 刘建勇, 邓勇, 等. MRI在视神经脊髓炎诊断及随访观察中的应用价值[J]. 医学影像学杂志, 2006, 16(1): 28-29.
[5]   Lennon VA, Wingerchuk DM, Kryzer TJ, et al. A serum autoantibody marker of neuromyelitis optica: distinction from multiple sclerosis[J]. Lancet, 2004, 364(9451): 2106-2112.
[6]   Poser CM, Brinar VV. Disseminated encephalomyelitis and multiple sclerosis: two different diseases-a critical review[J]. Acta Neurol Scand, 2007, 116(4): 201-206.
[7]   何晓非, 郭端, 周红雨, 等. 视神经脊髓炎临床特征分析[J]. 四川大学学报(医学版), 2010, 41(5): 919-921.
[8]   Javed A, Balabanov R, Arnason BG, et al. Minor salivary gland inflammation in Devic′s disease and longitudinally extensive myelitis[J]. Mult Scler, 2008, 14(6): 809-814.
[9]   Wingerchuk DM, Lennon VA, Lucchinetti CF, et al. The spectrum of neuromyelitis optica[J]. Lancet Neurol, 2007, 6(9): 805-815.
[10]   Wingerchuk DM, Hogancamp WF, O’Brien PC, et al. The clinical course of neuromyelitis optica (Devic’s syndrome)[J]. Neurology, 1999, 53(5): 1107-1114.
[11]   Wingerchuk DM, Lennon VA, Pittock SJ, et al. Revised diagnostic criteria for neuromyelitis optica[J]. Neurology, 2006, 66(10): 1485-1489.
[12]   Wingerchuk DM. Neuromyelitis optica: effect of gender[J]. J Neurol Sci, 2009, 286(1-2): 18-23.
[13]   Ghezzi A, Bergamaschi R, Martinelli V, et al. Clinical characteristics, course and prognosis of relapsing Devic′s neuromyelitis optica[J]. J Neurol, 2004, 251(1): 47-52.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133