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嗜酸性粒细胞增多综合征1例分析

Analysis of one case of hypereosinophilic syndrome
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摘要 嗜酸性粒细胞增多综合征是一种涉及多学科的临床少见病,多因早期嗜酸性粒细胞未得到有效控制最终死于嗜酸性粒细胞增多性心肌病和心脏扩大引起的心力衰竭。本例患者为老年男性,以支气管哮喘、肺炎为首发症状,迁延不愈3年,嗜酸性粒细胞持续升高至72%(嗜酸性粒细胞百分比正常值为0.4%~8%),期间常年口服复方甲氧那明胶囊(商品名:阿斯美)、孟鲁司特钠片(商品名:顺尔宁)等仍控制不佳,几乎每天咳嗽,多次因支气管扩张合并感染入院治疗,3年后呼吸系统症状突然消失,转而出现以下肢足部红斑性水肿、紫癜为表现的皮肤症状及以四肢麻木、瘫痪为表现的神经源性损害症状。本研究报告了该病例发病、实验室检查、治疗、转归等完整的诊疗过程,并通过文献复习,以期对嗜酸性粒细胞增多综合征及相关疾病加深认识,做到早期诊断,正确治疗。 Hypereosinophilic syndrome is a rare clinical disease involving many disciplines.Most of them died of heart failure caused by hypereosinophilic cardiomyopathy and cardiac enlargement.This patient is an elderly man,with bronchial asthma and pneumonia as the first symptoms,which had been prolonged for 3 years,eosinophils continued to rise to 72%(eosinophil percentage normal value of 0.4%-8%).He took compound methoxypheniramine capsules(trade name:Asmeton),montelukast sodium tablets(trade name:Singulair),etc.orally during this period,but still had poor control,coughing almost every day,and was hospitalized several times for bronchodilatation.3 years later,his respiratory symptoms suddenly disappeared,and developed skin symptoms manifested by erythematous edema and purpura of the lower limbs and neurogenic damage manifested by numbness and paralysis of the limbs.This study reported the complete diagnosis and treatment process,such as the onset,laboratory examination,treatment and outcome,and through the literature review,in order to deepen the understanding of hypereosinophilic syndrome and related diseases,and achieve early diagnosis and correct treatment.
作者 陈天丽 李鹏涛 CHEN Tian-li;LI Peng-tao(Department of Dermatology,Huangdao District Central Hospital,Qingdao 266555,China)
出处 《中国实用医药》 2025年第10期161-164,共4页 China Practical Medicine
关键词 嗜酸性粒细胞增多综合征 病例报告 红斑水肿 Hypereosinophilic syndrome Case report Erythematous edema
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  • 1杨青.慢性阻塞性肺疾病急性加重期嗜酸性粒细胞水平和预后的关系分析[J].世界最新医学信息文摘,2020(46):70-70. 被引量:2
  • 2王树才,曹秉振.系统性红斑狼疮的神经系统损害及发病机制[J].国际神经病学神经外科学杂志,2005,32(5):451-454. 被引量:6
  • 3Tefferi A, Gotlib J, Pardanani A, et al. Hypereosinophilic syn- drome and clonal eosinophilia: point-of-care diagnostic algo- rithm and treatment update [J~. Mayo Clin Proc, 2010, 85 (2) : 158-164.
  • 4Gotlib J. World Health Organization-defined eosinophilic disor- ders: 2014 update on diagnosis, risk stratification, and manage- ment[J]. Am J Hematol,2014,89(3) :325-337.
  • 5Klion AD, Bochner BS, Gleich GJ, et al. Approaches to the trea~- merit of hypereosinophilic syndromes: a workshop summary re- port[J]. Allergy Clin Immunol,2006, 10(6) : 1292-1302.
  • 6Van Grotel M, de Hoog M, de Krijger RR, et al. Hypereosino- philic syndrome in children[J!. Leuk Res,2012,36(10) : 1249- 1254.
  • 7Weller PF, Bubley GJ. The idiopathic hypereosinophilic syn- drome[J]. Blood, 1994,83 (10) :2759-2779.
  • 8Grolla E, Dalla-Vestra M, Bonanni L, et al. A rare case of aor- tic valve thrombosis in patient with idiopathic hypereosinophilic syndrome [ J 1. Case Rep Cardiol, 2015,9 (8) : 852-860.
  • 9LefevreG, Copin MC, Staumont-Salle D, et al. The lymphoid variant of hypereosinophilic syndrome-study of 21 patients with CD3- CD4~ aberrant T- cell phenotype [J ]. Medicine, 2014, 93 (2) :255-266.
  • 10Derakhshan D, Ilkhanipoor H, Derakhshan A, et al. Eosino- philie cystitis and idiopathic Hypereosinophilie syndrome in an eight-year-old girl [J]. Saudi J Kidney Dis Transpl, 2014, 25(6) : 1301-1303.

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