The Uncommon Combination of Common Variable Immunodeficiency, Macrophage Activation Syndrome, and Cytomegalovirus Retinitis

被引:16
作者
Aghamohammadi, Asghar [1 ]
Abolhassani, Hassan [1 ]
Hirbod-Mobarakeh, Armin [1 ]
Ghassemi, Fariba [2 ]
Shahinpour, Shervin [1 ]
Behniafard, Nasrin [1 ]
Naghibzadeh, Ghazal [1 ]
Imanzadeh, Amir [1 ]
Rezaei, Nima [1 ,3 ,4 ]
机构
[1] Childrens Med Ctr, Res Ctr Immunodeficiencies, Pediat Ctr Excellence, Tehran, Iran
[2] Farabi Hosp, Eye Res Ctr, Tehran, Iran
[3] Univ Tehran Med Sci, Sch Med, Mol Immunol Res Ctr, Tehran, Iran
[4] Univ Tehran Med Sci, Sch Med, Dept Immunol, Tehran, Iran
关键词
AUTOIMMUNE MANIFESTATIONS; IMMUNOCOMPETENT PATIENTS; CLINICAL PHENOTYPES; INFECTION; CHILDREN; DEFICIENCY; MANAGEMENT; DISORDERS; UPDATE; ADULTS;
D O I
10.1089/vim.2011.0060
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Common variable immunodeficiency (CVID) is a heterogeneous group of disorders with varied immunologic phenotypes and clinical manifestations. Patients with CVID are mainly characterized by decreased serum immunoglobulin levels, and increased susceptibility to recurrent bacterial infections, autoimmune disorders, and malignancies. Here we present a CVID patient who has developed a clinical polyclonal lymphocytic infiltration phenotype associated with severe and irreversible pancytopenia with unknown etiology. Progressive unilateral loss of vision and cytomegalovirus retinitis indicated the cause of patient's pancytopenia.
引用
收藏
页码:161 / 165
页数:5
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