2018, Number 1
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Rev Latin Infect Pediatr 2018; 31 (1)
Antiphospholipid syndrome in a one-month-old patient. Case report on a Latin American infant and literature review
Moya-Barquín LA, Coronel-Martínez DL, Arredondo-García JL
Language: Spanish
References: 18
Page: 36-39
PDF size: 399.45 Kb.
ABSTRACT
Background: The real antiphospholipid syndrome (APS) prevalence is unknown. The SAF clinical spectrum includes: positivity to antiphospholipid antibodies (aPL) without clinical data, positive aPL with non-trombotic manifestations, vascular thrombosis based SAF and y catastrophic SAF.
Case report: One month and seven days old boy that presented clinical data of thrombosis, with purple colored lesions, Raynaud’s phenomenonpor and profound cianosis in the left upper extremity and inferior extremities; with thrombocytopenia and positive lupic anticoagulant; SAF was clinical diagnosed, requiring mechanic ventilation support, anticoagulant therapy and vasodilators, with good evolution of the lesions, achieving the preservation of the lower limbs (infracondilealleve). The patient had good evolution and was discharged.
Conclusion: The classification criteria are useful for clinical research, not for diagnosis. The «non-classic» patients can fall in other clinical SAF spectrum and get lost. SAF in children differs from the adult´s presentation. In a thrombotic event, SAF should be suspected and treated, independently of the laboratory confirmation.
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