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[1]李芳芳,李崇巍,郑荣秀.儿童IgA血管炎相关神经系统损害的临床分析[J].天津医科大学学报,2023,29(06):662-665.
 LI Fang-fang,LI Chong-wei,ZHENG Rong-xiu.Clinical analysis of neurological damage associated with IgA vasculitis in children[J].Journal of Tianjin Medical University,2023,29(06):662-665.
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儿童IgA血管炎相关神经系统损害的临床分析(PDF)
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《天津医科大学学报》[ISSN:1006-8147/CN:12-1259/R]

卷:
29卷
期数:
2023年06期
页码:
662-665
栏目:
临床医学
出版日期:
2023-11-20

文章信息/Info

Title:
Clinical analysis of neurological damage associated with IgA vasculitis in children
文章编号:
1006-8147(2023) 06-0662-04
作者:
李芳芳12李崇巍2郑荣秀1
(1.天津医科大学总医院儿科,天津 300052;2.天津市儿童医院风湿免疫科,天津 300134)
Author(s):
LI Fang-fang12LI Chong-wei2ZHENG Rong-xiu1
(1.Department of Pediatrics,General Hospital,Tianjin Medical University,Tianjin 300052,China;2.Department of Rheumatology & Immunology,Tianjin Children′s Hospital,Tianjin 300134,China)
关键词:
IgA血管炎神经系统损害大脑后部可逆性脑病综合征静脉窦血栓
Keywords:
IgA vasculitisneurological damageposterior reversible encephalopathy syndromevenous sinus thrombosis
分类号:
R725.9
DOI:
-
文献标志码:
A
摘要:
目的:总结IgA血管炎引起的神经系统损害,探讨其危险因素、治疗及转归。方法:选择天津市儿童医院2016年1月至2022年1月收治的IgA血管炎患儿1 879例,其中出现神经系统损害的患儿34例(A组),随机抽取同期非神经系统损害病例72例(B组),对两组临床表现、实验室检查、治疗及转归进行回顾性分析。结果:IgA血管炎相关神经系统损害发生率为1.8%,A组和B组均有典型紫癜样皮疹,A组出现消化道症状、消化道出血、皮疹在非典型部位的发生率分别为97.1%、32.4%、67.6%,B组分别为72.2%、8.3%、40.3%,差异存在统计学意义(χ2=9.571、9.895、6.922,均P<0.05),但尿常规、尿微量白蛋白、尿转铁蛋白、血Ig、便钙卫蛋白等无统计学差异(均P>0.05)。A组中16例脑电图显示背景活动慢波;15例神经电生理显示周围神经损害;2例头颅MRI提示大脑后部可逆性脑病综合征;1例头颅MRI提示静脉窦血栓。A组均接受糖皮质激素治疗,其中强化治疗19例,大剂量甲强龙冲击治疗8例,使用环磷酰胺15例,静脉应用丙种球蛋白10例,7例采用了甲强龙冲击联合环磷酰胺治疗,5例应用甲强龙冲击联合环磷酰胺及丙种球蛋白治疗。B组仅3例应用甲强龙冲击治疗,2例应用环磷酰胺,其中1例应用甲强龙冲击联合环磷酰胺治疗,其余68例仅予常规剂量糖皮质激素或对症治疗后好转。两组患儿出院时病情均好转,出院后随访6个月均未遗留后遗症。结论:IgA血管炎罕见出现神经系统损害,出现消化道症状、消化道出血和皮疹发生在非典型部位的患儿更容易发生神经系统损害。
Abstract:
Objective: To summarize the neurological damage caused by IgA vasculitis and explore the associated risk factors,treatment,and outcomes. Methods:A retrospective analysis was conducted on 1 879 cases of IgA vasculitis admitted to Tianjin Children′s Hospital between January 2016 and January 2022. Among these cases,34 children with neurological damage were categorized into group A,while 72 cases without neurological damage were randomly selected for group B. Clinical manifestations,laboratory examinations,treatments,and outcomes were retrospectively analyzed for both groups. Results:The incidence of IgA vasculitis-related neurological damage was found to be 1.8%. A typical purpura rash was observed in both group A and group B. The incidence of gastrointestinal symptoms,gastrointestinal bleeding,and rash was significantly higher in group A(97.1%,37.4% and 67.6% respectively) compared to group B(72.2%,8.3%,and 40.3% respectively,χ2= 9.571,9.895,6.922,all P< 0.05). However,there were no significant differences between the two groups in terms of urine routine,microalbumin,transferrin,blood Ig levels,and fecal calprotectin(all P> 0.05). In group A children,16 EEGs showed background activity slow waves,15 neuroelectrophysiology tests indicated peripheral nerve damage,2 cases had head MRI findings suggestive of posterior brain reversible encephalopathy syndrome,and 1 child had head MRI findings suggestive of venous sinus thrombosis. All children in group A received glucocorticoid treatment,with 19 cases undergoing intensive treatment,8 cases received high-dose methylprednisolone pulse therapy,15 cases received cyclophosphamide,and 10 cases were treated with intravenous gamma globulin(IVIG),7 cases were treated with methylprednisolone pulse therapy combined with cyclophosphamide,and 5 cases were treated with methylprednisolone pulse therapy combined with cyclophosphamide and IVIG. In group B,only 3 children received methylprednisolone pulse therapy and 2 children were treated with cyclophosphamide,while 1 case received both treatments. The remaining 68 patients in group B were only treated with conventional dose glucocorticoids or symptomatic treatment. Both groups showed improvement at discharge,and no sequelae were observed during the follow-up in June. Conclusion:IgA vasculitis in children rarely causes neurological damage,and those presenting with gastrointestinal symptoms,gastrointestinal bleeding,and rash occurring in atypical areasare more likely to experience neurological damage.

参考文献/References:

[1] ONI L,SAMPATH S. Childhood IgA vasculitis(Henoch Schonlein purpura)-advances and knowledge gaps[J]. Front Pediatr,2019,7:257.
[2] 中华医学会儿科学分会免疫学组,《中华儿科杂志》编辑委员会. 儿童过敏性紫癜循证诊治建议[J]. 中华儿科杂志,2013,51(7):502-507.
[3] OZEN S,PISTORIO A,IUSAN S M,et al. EULAR/PRINTO/PRES criteria for Henoch-Sch?觟nlein purpura,childhood polyarteritis nodosa,childhood Wegener granulomatosis and childhood Takayasu arteritis:Ankara 2008. Part Ⅱ:final classification criteria[J]. Ann Rheum Dis,2010,69(5):798-806.
[4] PACHEVA I H,IVANOV I S,STEFANOVA K,et al. Central nervous system involvement in Henoch-Schonlein purpura in children and adolescents[J]. Case Rep Pediatr,2017,2017:5483543.
[5] GARZONI L,VANONI F,RIZZI M,et al. Nervous system dysfunction in Henoch-Schonlein syndrome: systematic review of the literature[J]. Rheumatology(Oxford),2009,48(12):1524-1529.
[6] 何松蔚,陈芳,胡艳,等. 过敏性紫癜合并中枢神经系统损害18例[J]. 中华实用儿科临床杂志,2013,28(23):1821-1824.
[7] 何庭艳,黄瑛,杨军. 儿童过敏性紫癜合并可逆性后部脑白质病临床分析[J]. 罕少疾病杂志,2017,24(5):21-23,34.
[8] FUNKEN D,G?魻TZ F,BüLTMANN E,et al. Focal seizures and posterior reversible encephalopathy syndrome as presenting signs of IgA vasculitis/Henoch-Schoenlein purpura-an educative case and systematic review of the literature[J]. Front Neurol,2021,12:759386.
[9] NINOMIYA H,KUBOTA K,KIMURA T,et al. Immunoglobulin A vasculitis complicated with posterior reversible encephalopathy syndrome and reversible cerebral vasoconstriction syndrome[J]. Pediatr Int,2019,61(8):836-838.
[10] NIE Y L,SONG Z X,TAO J,et al. Correlations of serological markers with development of systemic involvement in adult immunoglobulin A vasculitis: a retrospective study of 259 patients in central China[J]. Curr Med Sci,2021,41(5):888-893.
[11] ZHENG Q,HE Q,HUANG H,et al. Venous sinus thrombosis in a case of immunoglobulin A vasculitis and a systemic review of literature[J]. Int J Rheum Dis,2023,26(3):539-543.
[12] B?魪RUB?魪 M D,BLAIS N,LANTHIER S. Neurologic manifestations of Henoch-Sch?觟nlein purpura[J]. Handb Clin Neurol,2014,120:1101-1111.
[13] ABEND N S,LICHT D J,SPENCER C H. Lupus anticoagulant and thrombosis following Henoch-S?觟honlein purpura[J]. Pediatr Neurol,2007,36(5):345-347.
[14] 卢祖能. 周围神经病治疗应关注的问题[J]. 卒中与神经疾病,2016,23(4):219-224.
[15] AK?覶ABOY M, FIDAN K, KANDUR Y, et al. Cerebral vasculitis in Henoch-Sch?觟nlein purpura: a case report[J]. Arch Rheumatol, 2017,32(3):264-267.
[16] NISHIO M,YOSHIOKA K,YAMAGAMI K,et al. Reversible posterior leukoencephalopathy syndrome:a possible manifestation of Wegener′s granulomatosis-mediated endothelial injury[J]. Mod Rheumatol,2008,18(3):309-314.

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备注/Memo

备注/Memo:
作者简介 李芳芳(1982-),女,副主任医师,硕士在读,研究方向:儿科学;通信作者:郑荣秀,E-mail:rzheng@tmu.edu.cn。
更新日期/Last Update: 2023-12-01