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Pediatric antiphospholipid syndrome: is it the same as an adult?
Viсtoria Bitsadze1, Jamilya Khizroeva1, Arina Lazarchuk1
1Department of Obstetrics, Gynecology and Perinatal Medicine, N. F. Filatov Clinical Institute of Children's Health, I. M. Sechenov First Moscow State Medical University (Sechenov University), Moscow, Russia.
Insights
Antiphospholipid syndrome (APS) in children is rare but serious, causing blood clots and other issues. This review discusses pediatric APS features, differences from adult APS, and the need for updated diagnostic and treatment criteria.
Area of Science:
- Pediatric Rheumatology
- Hematology
- Immunology
Background:
- Antiphospholipid syndrome (APS) is a rare, potentially life-threatening autoimmune condition.
- It manifests in neonates and children with arterial and/or venous thrombosis and various non-thrombotic complications.
- Pediatric APS presents unique challenges in diagnosis and management compared to adult cases.
Purpose of the Study:
- To review the current understanding of pediatric Antiphospholipid Syndrome (APS).
- To highlight differences between pediatric and adult APS.
- To emphasize the need for revised diagnostic and treatment guidelines for pediatric APS.
Main Methods:
- Literature review of existing studies on pediatric Antiphospholipid Syndrome.
- Analysis of clinical features, including thrombotic and non-thrombotic manifestations.
- Examination of the role of genetic thrombophilia in pediatric APS.
Main Results:
- Pediatric APS exhibits distinct clinical features and potential differences from adult APS.
- The catastrophic form of APS is a rare but severe presentation in children.
- Genetic thrombophilia may influence the manifestation of APS in pediatric patients.
Conclusions:
- Pediatric APS requires specific diagnostic and therapeutic approaches.
- Early recognition and management are crucial due to potential severe outcomes.
- Further research is needed to refine diagnostic criteria and treatment strategies for children with APS.
Importance:
Antiphospholipid syndrome in neonates and children is a rare, but in some cases life-threatening condition with arterial and/or venous thrombosis and/or non-thrombotic neurological, skin, ophthalmological and other manifestations.
Observations:
This review highlights the available information about the features of pediatric APS, including the rare catastrophic form, the differences between pediatric and adult APS, and the role of genetic thrombophilia in APS manifestation.
Conclusions And Relevance:
The clinical manifestations and treatment options for APS in children may differ from those in adults, and prescribing therapy can be challenging due to the unique clinical and morphological characteristics of the pediatric patient. Pediatric APS may be a predictor of the development of certain autoimmune diseases and classic manifestations of APS in adulthood, therefore, a revision of the existing criteria for the diagnosis and treatment of APS in children is necessary.
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