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原发性免疫缺陷、自身免疫性甲状腺功能亢进、乳糜泻和系统性红斑狼疮与儿童免疫性血小板减少症。

Primary immunodeficiencies, autoimmune hyperthyroidism, coeliac disease and systemic lupus erythematosus in childhood immune thrombocytopenia.

作者信息

Saettini Francesco, Cattoni Alessandro, Redaelli Martina, Silvestri Daniela, Ferrari Giulia Maria, Biondi Andrea, Jankovic Momcilo, Spinelli Marco

机构信息

Department of Pediatric Onco-Hematology, San Gerardo Hospital, Fondazione MBBM, Università degli Studi di Milano-Bicocca, Monza, Italy.

Department of Pediatrics, San Gerardo Hospital, Fondazione MBBM, Università degli Studi di Milano-Bicocca, Monza, Italy.

出版信息

Acta Paediatr. 2021 Feb;110(2):643-651. doi: 10.1111/apa.15593. Epub 2020 Oct 13.

Abstract

AIM

To evaluate the cumulative prevalence of coeliac disease, systemic lupus erythematosus, autoimmune hyperthyroidism and primary immunodeficiencies in children with either newly diagnosed/persistent or chronic immune thrombocytopenia (ITP).

METHODS

Monocentric retrospective analysis of the clinical and biochemical features of 330 consecutive patients with ITP referred to our Pediatric Hematology Unit between January 2009 and December 2018.

RESULTS

The prevalence of systemic lupus erythematosus (0.3%), coeliac disease (0.3%) and autoimmune hyperthyroidism (0.6%) was not increased compared to general paediatric population. Of note, the prevalence of underlying primary immunodeficiencies was 2.4%, remarkably higher than the general paediatric population (P = .005). All the patients diagnosed with immunodeficiency developed either bi-/trilinear cytopenia or splenomegaly.

CONCLUSION

Whilst autoimmune and immunological screening is already recommended at the onset of immune thrombocytopenia, we recommend that primary immunodeficiencies be regularly screened during follow-up, especially in case of additional cytopenia or lymphoproliferation.

摘要

目的

评估新诊断/持续性或慢性免疫性血小板减少症(ITP)患儿中乳糜泻、系统性红斑狼疮、自身免疫性甲状腺功能亢进症和原发性免疫缺陷的累积患病率。

方法

对2009年1月至2018年12月期间转诊至我们儿科血液科的330例连续性ITP患者的临床和生化特征进行单中心回顾性分析。

结果

与普通儿科人群相比,系统性红斑狼疮(0.3%)、乳糜泻(0.3%)和自身免疫性甲状腺功能亢进症(0.6%)的患病率并未增加。值得注意的是,潜在原发性免疫缺陷的患病率为2.4%,显著高于普通儿科人群(P = 0.005)。所有被诊断为免疫缺陷的患者均出现双系/三系血细胞减少或脾肿大。

结论

虽然在免疫性血小板减少症发病时已建议进行自身免疫和免疫学筛查,但我们建议在随访期间定期筛查原发性免疫缺陷,尤其是在出现额外血细胞减少或淋巴细胞增殖的情况下。

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