Lupus anticoagulant-hypoprothrombinemia syndrome and catastrophic antiphospholipid syndrome in a patient with antidomain I antibodies
Affiliation auteurs | !!!! Error affiliation !!!! |
Titre | Lupus anticoagulant-hypoprothrombinemia syndrome and catastrophic antiphospholipid syndrome in a patient with antidomain I antibodies |
Type de publication | Journal Article |
Year of Publication | 2016 |
Auteurs | Galland J, Mohamed S, Revuz S, De Maistre E, de Laat B, Marie P-Y, Zuily S, Levy B, Regnault V, Wahl D |
Journal | BLOOD COAGULATION & FIBRINOLYSIS |
Volume | 27 |
Pagination | 580-582 |
Date Published | JUL |
Type of Article | Article |
ISSN | 0957-5235 |
Mots-clés | antidomain I antibodies, catastrophic antiphospholipid antibody syndrome, lupus anticoagulant-hypoprothrombinemia syndrome, Systemic lupus erythematosus |
Résumé | Lupus anticoagulant-hypoprothrombinemia syndrome is a rare condition characterized by the association of acquired factor II deficiency and lupus anticoagulant. Contrary to classical antiphospholipid syndrome, it may cause severe life-threatening bleeding (89% of published cases). We report a patient, positive for antidomain I antibodies, with initially primary lupus anticoagulant-hypoprothrombinemia syndrome without previous clinical manifestation or underlying systemic disease. Five years later, he experienced the first systemic lupus erythematous flare. Within a few days, catastrophic antiphospholipid syndrome was diagnosed with heart, liver and kidney involvement. The patient recovered under pulse steroids, intravenous heparin and intravenous immunoglobulins. Copyright (C) 2016 Wolters Kluwer Health, Inc. All rights reserved. |
DOI | 10.1097/MBC.0000000000000545 |