变应性肉芽肿性血管炎

变应性肉芽肿性血管炎的相关文献在1999年到2021年内共计73篇,主要集中在内科学、神经病学与精神病学、儿科学 等领域,其中期刊论文63篇、会议论文10篇、专利文献560555篇;相关期刊50种,包括工企医刊、现代医院、临床肺科杂志等; 相关会议9种,包括2015年第十三届全国风湿病学术会议、2015北京医学会神经病学学术年会、全国第十届中西医结合风湿病学术会议等;变应性肉芽肿性血管炎的相关文献由228位作者贡献,包括于清宏、林翊萍、刘秀云等。

变应性肉芽肿性血管炎—发文量

期刊论文>

论文:63 占比:0.01%

会议论文>

论文:10 占比:0.00%

专利文献>

论文:560555 占比:99.99%

总计:560628篇

变应性肉芽肿性血管炎—发文趋势图

变应性肉芽肿性血管炎

-研究学者

  • 于清宏
  • 林翊萍
  • 刘秀云
  • 史哲
  • 吴齐雁
  • 张智斌
  • 焦维克
  • 薛青
  • 邢岩
  • 丁强
  • 期刊论文
  • 会议论文
  • 专利文献

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    • 麻恒; 庄起东; 张巧丽; 丁群力; 邓在春; 陈众博
    • 摘要: 嗜酸性粒细胞增多综合征(HES)是一种病因尚未明确的罕见疾病,以血液和组织内嗜酸性粒细胞持续增多为特征,可造成多脏器损伤,主要靶器官包括皮肤、心脏、呼吸道、胃肠道及神经系统,临床诊断存在一定困难.我院近期诊断了1例HES,以发热、咳嗽为主要临床症状,伴有胸闷气促,皮肤出现红黑色皮下结节,实验室检查主要以血嗜酸性粒细胞增高为主,影像学表现以肺内浸润影为主要表现,经过正规激素治疗后症状明显改善,体温回归正常,皮肤结节消失,目前病情稳定未复发.嗜酸性粒细胞增多综合征(HES)是一种临床罕见疾病,以血液和组织内嗜酸性粒细胞持续增多为特征,可造成多脏器损伤,主要靶器官包括皮肤、心脏、呼吸道、胃肠道及神经系统.该疾病由Hardy和Anderson于1968年首次提出,在人群中的发病率较低.根据WHO在2015年更新的监测及统计数据显示,HES发病率为0.036/100000,死亡率约为9.3%[1].因病例数量缺乏,该疾病发生发展以及治疗方案等多个方面在临床上尚无明确标准,许多该疾病有关的论点需要更多临床案例为基础进一步研究,本文报告1例嗜酸性粒细胞增多综合征患者的临床资料,为疾病研究提供实例支持.
    • 赵海燕; 刘向一; 孙阿萍; 张朔; 樊东升
    • 摘要: 目的 分析变应性肉芽肿性血管炎(Churg-Strauss sydrome,CSS)的临床特点以及周围神经受损的表现,以提高诊治水平.方法 收集自2005年1月~2016年12月在北京大学第三医院收治的14例CSS患者的临床资料,回顾性分析其临床表现及周围神经受损的情况.结果 14例CSS患者中男性10例(71.4%),年龄20~78岁(53.6±16.2);外周血嗜酸性粒细胞平均升高20.7%(10.3% ~55%);呼吸系统是最常受累的器官(100%),哮喘9例(64.3%),肺部浸润12例(85.7%);6例(42.9%)存在周围神经受损,以四肢周围神经尤其是下肢神经轴索损害为主,同时累及运动与感觉神经;CSS起病初期误诊率高达64.3%,起病至确诊间隔平均15.9 m(1~72 m).结论 CSS是一种误诊率较高的全身多系统受累的血管炎,存在嗜酸性粒细胞升高,且临床和电生理结果提示非对称性以轴索损害为主的周围神经病患者,需注意CSS的可能.%Objective Analyze the clinical characteristics of eosinophilic granulomatosis with polyangiitis ( Churg-Strauss syndrome,CSS) and peripheral neuropathy,and to improve the diagnosis and treatment of CSS. Methods Medical records from all patients diagnosed with CSS who had been treated at Peking University Third Hospital,China,between Jan-uary 2005 and December 2016 were retrospectively reviewed to identify the clinical manifestations and the damage of pe-ripheral nerve. Results 14 patients were diagnosed with CSS. 10 (71. 4%) of them were males,and from 20 to 78 (53. 6 ± 16. 2) years old. Peripheral blood eosinophils increased,and the mean of eosinophils was 20. 7%,(10. 3% ~55%). The most frequently involved organ respiratory system (100%),9 cases of asthma (64. 3%) and 12 cases of pulmonary in-vasion (85. 7%). Peripheral nerve injuries occurred in 6 patients (42. 9%),especially in the lower extremities,and both the motor and sensory nerves were involved. The misdiagnosis rate of CSS at the early onset was very high (64. 3%),and mean time of the onset to diagnosis interval was 15. 9 months (1~72 months). Conclusion CSS was a vasculitis involved multisystem,and with a high rate of misdiagnosis. The patients with elevated eosinophils and axonal impairment of peripher-al neuropathy,should be paid attention to the possibility of CSS.
    • 苏凡; 邱茜; 蔡冬梅; 梁柳琴; 杨岫岩
    • 摘要: Objective To evaluate the clinical features,treatment and prognosis of Eosinophilic Granulomatous Vasculitis.Methods We analyzed retrospectively the clinical and laboratory features,treatment and prognosis of 43 patients with Eosinophilic Granulomatous Vasculitis who admitted to the Department of Rheumatology of the First Affiliated University Hospital of Sun Yat-sen University between 2005 and 2014.Results Of the 43 patients,31 patients (72.1%) had allergic symptoms in the disease course and 16 patients (37.2%) had asthma and lung wheezing sound when performing the physical examination.Organs involvements included skin,acra,lung,kidney,central and peripheral nervous system,digestive system and heart.Positive antineutrophilic cytoplasmic antibody (ANCA) which mainly with MPO-ANCA was found in 18 patients (41.9%).Thirty-nine patients (90.7%)had high blood eosinophil level while all patients (100%) had elevated IgE.Two patients died of multiple organ failure in their acute phase,and the others had favorable prognosis after receiving the treatment of glucocorticoid combine with cyclophosphamide or methotrexate.Conclusions Eosinophilic Granulomatous Vasculitiscould make damage to organs and tissues.Only 72.1% patients had allergic symptoms and 37.2% patients had asthma and lung wheezing sound.More than half patients have the negative ANCA.Glucocorticoidcombine with cyclophosphamide or methotrexate can achieve satisfactory therapeutic effects.%目的 探讨嗜酸性肉芽肿性血管炎患者的临床特征、治疗和预后.方法 分析2005至2014年中山大学附属第一医院风湿免疫科诊断和治疗随访的43例嗜酸性肉芽肿性血管炎患者,总结临床与实验室特征、治疗与转归.结果 在43例中31例(72.1%)在既往史、现病史和体检中存在变应性症状,其中有哮喘症状或听诊肺部哮鸣音者16例(37.2%).组织和脏器受累包括皮肤、肢端、肺脏、肾脏、中枢和周围神经系统、消化系统、心脏等.中性粒细胞胞质抗体(ANCA)阳性18例(41.9%),以MPO-ANCA阳性为主.血嗜酸性粒细胞增高者39例(90.7%),43例(100%)均有血IgE增高.2例在急性期死于多脏器衰竭,其余41例经用激素和环磷酰胺或甲氨蝶呤治疗,预后良好.结论 嗜酸性肉芽肿性血管炎可以损害各个脏器和组织;仅72.1%的患者存在变应性症状,只有37.2%的患者存在哮喘或肺部哮鸣音;超半数的患者ANCA阴性;激素联合环磷酰胺或甲氨蝶呤治疗可取得较好的疗效.
    • 吉连梅; 贺玲玲; 赵东宝
    • 摘要: Objective To analyze the clinical features of eosinophilic granulomatosis with polyangiitis (EGPA).Methods The clinical characteristics,laboratory test,therapeutic regimen,pathology and imaging diagnosis in 23 cases with EGPA from the First Affiliated Changhai Hospital of Second Military Medical University within June 2007 to January 2013 were retrospectively analyzed.Results There were 14 males and 9 females,with the age ranged from 21 to 68 years.The mean age was (42±9) years.The overall prevalence of asthma was 78%(18/23).The allergic rhinitis accounted for 61%(14/23).The maxillary sinuses were the most frequendy involved,which accounted for 57%(13/23).Skin involvement was 57%(13/23),peripheral neuritis was 70%(16/23).Central nervous system involvement presented cerebrovascular event.Cardiac involvement accounted for 48%(11/23),digestive system involvement accounted for 17%(4/23).The outcome of auxiliary laboratory test revealed that 96%(22/23) patients expressed significantly higher levels of IgE and 70%(16/23) patients carried anti-neutrophil cytoplasmic antibodies (ANCA) which were presented as the perinuclear ANCA (p-ANCA).The patchy infiltrates of lung CT scan accounted for 69% (11/23).EMG showed mononeuritis multiplex and symmetric sensory motor neuropathy.The abnormal ratios of ECG and Echocardiography were 48%(11/23),79%(11/14) respectively.The pathological manifestations were necrotizing vasculitis,eosinophilic tissue infiltration,and extravascular granulomas.Conclusion Our results confirm the heterogenicity in clinical presentation and lack of specificity.Early diagnosis and treatment will be helpful for good prognosis.%目的 探讨嗜酸性肉芽肿性多血管炎(EGPA)的临床特点,以提高对本病的认识.方法 回顾性分析2007年6月至2013年1月在第二军医大学第一附属长海医院住院诊治的23例EGPA患者的资料,对其临床症状、实验室及影像资料、病理等进行分析和总结.结果 23例EGPA患者中,男性14例,女性9例,发病年龄21~68岁,平均(42±9)岁.病变累及全身多个系统及器官,病程中出现哮喘的占78%(18/23),变应性鼻炎占61%(14/23),鼻窦炎占57%(13/23),以上颌窦炎为主;皮肤受累占57%(13/23);周围神经炎占70%(16/23).中枢神经系统受累多表现为脑血管事件;心脏受累占48%(11/23);消化系统受累占17%(4/23).实验室检查中,IgE升高占96%(22/23),ANCA阳性占70%(16/23),以核周型ANCA(p-ANCA)为主.肺部CT多表现为斑片渗出影,占69%(11/23);肌电图多表现为多发性单神经炎和对称性感觉运动神经末梢病变;心电图异常占48%(11/23);超声心动图异常占79%(11/14).病理表现主要为坏死性血管炎、嗜酸性粒细胞浸润和血管外肉芽肿形成.结论 EGPA临床表现复杂多样,但缺乏特异性.早期诊断、早期治疗可有效改善其预后.
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