Literature DB >> 33025591

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

Francesco Saettini1, Alessandro Cattoni2, Martina Redaelli1, Daniela Silvestri3, Giulia Maria Ferrari1, Andrea Biondi1,2, Momcilo Jankovic1, Marco Spinelli1.   

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. ©2020 Foundation Acta Paediatrica. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  ITP; autoimmune disease; children; primary immunodeficiencies

Mesh:

Year:  2020        PMID: 33025591     DOI: 10.1111/apa.15593

Source DB:  PubMed          Journal:  Acta Paediatr        ISSN: 0803-5253            Impact factor:   2.299


  2 in total

Review 1.  Splenomegaly in Children and Adolescents.

Authors:  Meinolf Suttorp; Carl Friedrich Classen
Journal:  Front Pediatr       Date:  2021-07-09       Impact factor: 3.418

2.  Case Report: Hypomorphic Function and Somatic Reversion in DOCK8 Deficiency in One Patient With Two Novel Variants and Sclerosing Cholangitis.

Authors:  Francesco Saettini; Grazia Fazio; Daniele Moratto; Marta Galbiati; Nicola Zucchini; Davide Ippolito; Marco Emilio Dinelli; Luisa Imberti; Mario Mauri; Maria Luisa Melzi; Sonia Bonanomi; Alessio Gerussi; Marinella Pinelli; Chiara Barisani; Cristina Bugarin; Marco Chiarini; Mauro Giacomelli; Rocco Piazza; Giovanni Cazzaniga; Pietro Invernizzi; Silvia Clara Giliani; Raffaele Badolato; Andrea Biondi
Journal:  Front Immunol       Date:  2021-04-16       Impact factor: 7.561

  2 in total

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