Acquired factor VIII inhibitor in a patient with multiple sclerosis treated with interferon β-1a.


Journal

Journal of neuroimmunology
ISSN: 1872-8421
Titre abrégé: J Neuroimmunol
Pays: Netherlands
ID NLM: 8109498

Informations de publication

Date de publication:
15 03 2020
Historique:
received: 19 08 2019
revised: 07 01 2020
accepted: 08 01 2020
pubmed: 17 1 2020
medline: 29 8 2020
entrez: 17 1 2020
Statut: ppublish

Résumé

Acquired Factor VIII inhibitor is a rare acquired clotting disorder which has been seen in the setting of particular medications, autoimmune disease, and malignancy. Reports of this disorder in patients receiving immunomodulatory therapies for multiple sclerosis are rare. We present a case of a 48 year-old woman with likely development of acquired Factor VIII inhibitor in the setting of interferon beta monotherapy for multiple sclerosis, and discuss the pathogenesis of this disorder which involves shifts in helper T cell populations and increased production of immunoglobulins.

Identifiants

pubmed: 31945592
pii: S0165-5728(19)30404-7
doi: 10.1016/j.jneuroim.2020.577146
pii:
doi:

Substances chimiques

Autoantibodies 0
Autoantigens 0
Factor VIII 9001-27-8
Interferon beta-1a XRO4566Q4R

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

577146

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Auteurs

D Pandya (D)

Temple University Hospital, Department of Neurology, 3401 North Broad Street, Philadelphia, PA 19140, USA. Electronic address: darshan.pandya@tuhs.temple.edu.

V Hellerslia (V)

Temple University Hospital, Department of Pharmacy Practice, Philadelphia, PA 19140, USA.

E Gettings (E)

Temple University Hospital, Department of Neurology, Philadelphia, PA 19140, USA.

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Classifications MeSH