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dc.rights.licenseopenen_US
hal.structure.identifierHôpital Pellegrin
dc.contributor.authorHUGUENIN, Yoann
hal.structure.identifierHôpital Pellegrin
hal.structure.identifierEtablissement Français du Sang Nouvelle Aquitaine [Bordeaux] [EFS Bordeaux Nouvelle Aquitaine]
dc.contributor.authorLEVOIR, Laure
hal.structure.identifierHôpital Pellegrin
hal.structure.identifierEtablissement Français du Sang Nouvelle Aquitaine [Bordeaux] [EFS Bordeaux Nouvelle Aquitaine]
dc.contributor.authorBOUTON, Muriel
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
dc.contributor.authorFIORE, Mathieu
dc.date.accessioned2023-03-10T08:25:07Z
dc.date.available2023-03-10T08:25:07Z
dc.date.issued2023-01-01
dc.identifier.issn1421-9662en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/172244
dc.description.abstractEnImmunization against the platelet αIIbβ3 glycoprotein due to blood transfusion represents one of the most severe complications in Glanzmann thrombasthenia (GT) disease. Anti-αIIbβ3 isoantibodies development may lead to ineffective platelet transfusion and can, in case of pregnancy, cross the placenta leading to fetal thrombocytopenia. We describe here the case of a girl with type I GT who developed high rates of anti-αIIbβ3 isoantibodies after first and unique blood transfusion. Surprisingly, this patient had only received red blood cell concentrates and immunization was presumably stimulated by the residual presence of platelets in concentrates. This study emphasizes the need for regular anti-αIIbβ3 antibodies screening in GT, even though patients have never been previously transfused with platelet concentrates.
dc.language.isoENen_US
dc.subjectArticle recherche
dc.subject.enPregnancy
dc.subject.enFemale
dc.subject.enHumans
dc.subject.enThrombasthenia
dc.subject.enIsoantibodies
dc.subject.enPlatelet Glycoprotein GPIIb-IIIa Complex
dc.subject.enBlood Platelets
dc.subject.enPlatelet Membrane Glycoproteins
dc.subject.enErythrocytes
dc.title.enHigh Rates of Anti-αIIbβ3 Antibodies Produced by a Glanzmann Thrombasthenia Patient after First and Unique Red Blood Cells Administration.
dc.title.alternativeActa Haematolen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1159/000526224en_US
dc.subject.halSciences du Vivant [q-bio]/Médecine humaine et pathologieen_US
dc.identifier.pubmed36103848en_US
bordeaux.journalActa Haematologicaen_US
bordeaux.page44-46en_US
bordeaux.volume146en_US
bordeaux.hal.laboratoriesBiologie des maladies cardiovasculaires (BMC) - UMR 1034en_US
bordeaux.issue1en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04022771
hal.version1
hal.date.transferred2023-03-10T08:25:10Z
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
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