38.3 Primary Immunodeficiencies: When is it not just "JIA"

被引:0
作者
Gowda, Nikhil C. [1 ]
Aggarwal, Amita [1 ]
机构
[1] Sanjay Gandhi Postgrad Inst Med Sci, Dept Clin Immunol & Rheumatol, Lucknow, India
来源
BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY | 2024年 / 38卷 / 03期
关键词
Inborn errors of immunity; Primary immunodeficiency; Autoinflammatory diseases; Juvenile idiopathic arthritis; JUVENILE IDIOPATHIC ARTHRITIS; PAPA SYNDROME; DEFICIENCY; DISEASES; HYPOGAMMAGLOBULINEMIA; MUTATIONS; RHEUMATOLOGY; ADULTS;
D O I
10.1016/j.berh.2024.101960
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Juvenile Idiopathic Arthritis (JIA) is sometimes considered a diagnosis of exclusion as the name signifies that no cause is evident for this form of arthritis. Despite this JIA has some classical clinical features and many categories are defined based on the phenotype. . Since there is no diagnostic test for JIA, diseases that can mimic JIA, including Primary Immunodeficiencies (PID) can sometimes be misdiagnosed as JIA. The clues to suspecting PIDs are early age of onset, presence of family history, increased susceptibility to infections, unusual features like urticaria, interstitial lung disease, sensorineural hearing loss and poor response to conventional therapy, amongst others. This review will highlight the basics of PIDs and will discuss PIDs that can present with arthritis and hence can be confused with JIA.
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