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Successful Outcome of Severe Intra-cerebral Bleeding Associated with Acquired Factor V Inhibition: Utilization of Multiple Therapeutic Agents.

ΤίτλοςSuccessful Outcome of Severe Intra-cerebral Bleeding Associated with Acquired Factor V Inhibition: Utilization of Multiple Therapeutic Agents.
Publication TypeJournal Article
Year of Publication2018
AuthorsAndreadis, P., Kafantari K., Agapidou A., Vakalopoulou S., & Vlachaki E.
JournalBalkan Med J
Volume35
Issue1
Pagination112-115
Date Published2018 01 20
ISSN2146-3131
Λέξεις κλειδιάAged, Cerebral Hemorrhage, Cyclophosphamide, Factor V, Hemophilia A, Heparin, Low-Molecular-Weight, Humans, Male, Rituximab, Treatment Outcome
Abstract

BACKGROUND: Acquired coagulation factor inhibitors are antibodies that either inhibit activity or increase the clearance of a clotting factor and lead to an increased risk of bleeding. Most of the time, the disorder is attributed to factor VIII inhibition (acquired haemophilia A); however, other coagulation factors could also be implicated.CASE REPORT: Herein, we report an interesting case of a patient who underwent coronary artery bypass grafting and received antibiotic treatment after surgery with third generation cephalosporin. A month later, he presented with extreme bleeding diathesis and cerebral haemorrhage. Following a thorough clinical and laboratory investigation, an acquired factor V inhibitor was diagnosed. The patient received treatment with corticosteroids, intravenous immunoglobulins, anti-CD20 monoclonal antibodies (rituximab), cyclophosphamide and recombinant factor VIIa. Finally, despite the poor initial prognosis, the patient managed to achieve a full recovery.CONCLUSION: As there are no clear guidelines on acquired coagulation inhibitor treatment, reports of such cases could offer insight for future therapy choices. The case was unique because the treatment regimen included a combination of multiple therapeutic agents including rituximab.

DOI10.4274/balkanmedj.2017.0158
Alternate JournalBalkan Med J
PubMed ID28903884
PubMed Central IDPMC5820439

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