Good's syndrome remains a mystery after 55 years: A systematic review of the scientific evidence

被引:169
|
作者
Kelesidis, Theodoros [1 ]
Yang, Otto [1 ,2 ,3 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Div Infect Dis, Dept Med, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, UCLA AIDS Inst, Los Angeles, CA 90095 USA
关键词
Good's syndrome; Immunodeficiency; Infections; Hypogammaglobulinemia; Thymoma; RED-CELL APLASIA; PRIMARY ACQUIRED HYPOGAMMAGLOBULINEMIA; CHRONIC MUCOCUTANEOUS CANDIDIASIS; THYMOMA GOOD-SYNDROME; T-SUPPRESSOR CELLS; OF-THE-LITERATURE; MALIGNANT THYMOMA; LICHEN-PLANUS; MYASTHENIA-GRAVIS; CYTOMEGALOVIRUS-INFECTION;
D O I
10.1016/j.clim.2010.01.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Good syndrome (GS) is a rare association of thymoma and immunodeficiency first described more than 50 years ago. However, this syndrome still remains a mystery to clinicians. We systematically reviewed all the clinical, laboratory and immunologic findings from 152 patients with Good syndrome. The syndrome has a worldwide distribution and approximately half of the cases (47%) have been described in Europe. The diagnosis of thymoma preceded the diagnosis of hypogammaglobulinemia, infection, or diarrhea in 42% of patients whereas in 38% of patients the diagnoses were made almost simultaneously within 2 months of each other. We found significant mortality in patients with this syndrome (44.5%). Astute clinical acumen and increased awareness about the clinical and immunological profile of this syndrome may increase early recognition of this syndrome and prevent mortality. Further studies are needed to elucidate this clinical entity. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:347 / 363
页数:17
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