Immune thrombocytopenic purpura in children: An update

Bennani Kenza 1, 2, *, Tlamçani Imane 1, 2 and Amrani Hassani Moncef 1, 2

1 Department of Hematology, Central Laboratory of Medical Biological Analyses, Hassan II University Hospital, Fez, Morocco.
2 Faculty of Medicine, Pharmacy, and Dental Medicine of Fez, Sidi Mohamed Ben Abdellah University, Fez, Morocco.
 
Research Article
World Journal of Advanced Research and Reviews, 2024, 23(02), 1456–1461
Article DOI10.30574/wjarr.2024.23.2.2485
 
Publication history: 
Received on 09 July 2024; revised on 15 August 2024; accepted on 17 August 2024
 
Abstract: 
Immune thrombocytopenic purpura, also known as Werlhof's disease, is the most common cause of thrombocytopenia in children. While the majority of childhood Immune thrombocytopenic purpura cases are benign and resolve spontaneously, a rigorous evaluation of bleeding potential using the Buchanan score remains essential. Indeed, in rare situations, the disease can progress to severe forms threatening life prognosis. The diagnosis of immune thrombocytopenic purpura relies on a combination of clinical, biological criteria, and exclusion of other causes of thrombocytopenia. Management of Immune thrombocytopenic purpura  varies based on its form, severity of bleeding, and impact on the child's quality of life. For mild cases, watchful waiting may be sufficient. However, for severe forms or those with high bleeding risk, specific treatments are considered. These include intravenous immunoglobulins, corticosteroid therapy, splenectomy, immunosuppressants, and thrombopoietin analogs. In recent years, significant progress has been made in the genetics of constitutional thrombocytopenia, allowing a revision of chronic Immune thrombocytopenic purpura diagnoses by identifying inherited genetic abnormalities. The growing understanding of Immune thrombocytopenic purpura mechanisms, combined with genetic and therapeutic advances, offers promising prospects for optimizing disease management and improving the quality of life of affected children.
 
Keywords: 
Purpura; Immune thrombocytopenia; Child; Update
 
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