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静脉注射免疫球蛋白替代疗法预防Good综合征患者肺部感染

Intravenous immunoglobulin replacement therapy to prevent pulmonary infection in a patient with Good's syndrome.

作者信息

Wang Ching-Hsun, Chan Edward D, Perng Cherng-Lih, Chian Chih-Feng, Chen Chien-Wen, Perng Wann-Cherng, Su Wen-Lin

机构信息

Department of Internal Medicine, Tri-Service General Hospital, Taipei, Taiwan.

Division of Pulmonary Sciences and Critical Care Medicine, University of Colorado Denver at Anschutz Medical Center, Denver, CO 80045, USA; Denver Veterans Affairs Medical Center, Denver, CO 80220, USA; Division of Mycobacterial and Respiratory Infections, Department of Medicine, National Jewish Health, Denver, CO 80206, USA.

出版信息

J Microbiol Immunol Infect. 2015 Apr;48(2):229-32. doi: 10.1016/j.jmii.2012.09.003. Epub 2012 Nov 29.

Abstract

Good's syndrome is an acquired immunodeficiency state associated with thymoma and characterized by recurrent pulmonary infections. We describe a 67-year-old woman who presented with respiratory symptoms caused by concomitant disseminated cytomegalovirus infection and Pneumocystis jiroveci pneumonia 38 months after thymectomy for a thymoma. Immunologic analysis revealed hypogammaglobulinemia with absent B-cell population as demonstrated by flow cytometry, consistent with Good's syndrome. Following treatment with sulfamethoxazole/trimethoprim and ganciclovir, the patient improved with resolution of her respiratory symptoms. However, the patient subsequently experienced additional infections, necessitating additional subsequent hospital admissions. During the last admission, intravenous immunoglobulin (IVIG) replacement therapy was initiated and continued after discharge. Infection has been prevented for one year after beginning IVIG replacement therapy. This case reveals that in patients with combined humoral and cell-mediated immune deficiency, concomitant infection with different pathogens is not unusual, and immediate specific therapy is important. Periodic IVIG infusion, to maintain adequate Ig levels, is recommended.

摘要

古德综合征是一种与胸腺瘤相关的获得性免疫缺陷状态,其特征为反复发生肺部感染。我们描述了一名67岁女性,她在因胸腺瘤行胸腺切除术后38个月,出现了由播散性巨细胞病毒感染和耶氏肺孢子菌肺炎共同引起的呼吸道症状。免疫分析显示低丙种球蛋白血症,流式细胞术证实B细胞群缺失,符合古德综合征。经磺胺甲恶唑/甲氧苄啶和更昔洛韦治疗后,患者呼吸道症状缓解,病情改善。然而,患者随后又经历了其他感染,需要再次住院。在最后一次住院期间,开始静脉注射免疫球蛋白(IVIG)替代治疗,并在出院后继续。开始IVIG替代治疗后,已预防感染一年。该病例表明,在体液免疫和细胞介导免疫联合缺陷的患者中,合并不同病原体感染并不罕见,立即进行特异性治疗很重要。建议定期输注IVIG,以维持足够的免疫球蛋白水平。

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