Volume 40, Issue 11 pp. 1661-1663

Lupus Anticoagulant Induced by the Combination of Valproate and Lamotrigine

Andoni Echaniz-Laguna

Corresponding Author

Andoni Echaniz-Laguna

Unité d'Explorations Fonctionnelles des Epilepsies, Clinique Neurologique, Hôpital Civil, Strasbourg, France

Address correspondence and reprint requests to Dr. A. Echaniz-Laguna at Unite d' Explorations Fonctionnelles des Epilepsies, Clinique Neurologique, Hôpital Civil, 1 Place de 1'Hôpital, BP 426, 67091 Strasbourg Cedex, France.Search for more papers by this author
Anne Thiriaux

Anne Thiriaux

Unité d'Explorations Fonctionnelles des Epilepsies, Clinique Neurologique, Hôpital Civil, Strasbourg, France

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Isabelle Ruolt-Olivesi

Isabelle Ruolt-Olivesi

Unité d'Explorations Fonctionnelles des Epilepsies, Clinique Neurologique, Hôpital Civil, Strasbourg, France

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Christian Marescaux

Christian Marescaux

Unité d'Explorations Fonctionnelles des Epilepsies, Clinique Neurologique, Hôpital Civil, Strasbourg, France

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Edouard Hirsch

Edouard Hirsch

Unité d'Explorations Fonctionnelles des Epilepsies, Clinique Neurologique, Hôpital Civil, Strasbourg, France

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First published: 02 August 2005
Citations: 22

Abstract

Summary: A 5-year-old boy with generalized absence seizures was treated with valproate (VPA), 30 mg/kg/day. One month after VPA introduction, routine examination showed moderate reduction in fibrinogen and prolonged partial throm-boplastin time (PTT). The search for lupus anticoagulant (LAC) was negative. After 10 months of VPA treatment, seizures persisted, and lamotrigine (LTG), 2 mg/kg/day, was progressively given with VPA. Seizures disappeared, but PTT was more prolonged than before LTG introduction. The search for LAC was positive, and enzyme-linked immunosorbent assays (ELISAs) for immunoglobulin G (IgG) anticardiolipid antibodies were positive. Serum autoantibody screen and rheumatoid factor were negative; serum complement was normal. LAC eventually disappeared with VPA discontinuation. We believe that LTG may have exacerbated an initially mild immune response induced by VPA without clinical evidence of systemic disease. We therefore suggest that careful surveillance for LAC and systemic disease should be instituted when VPA is used with LTG.

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