A case report of severe bleeding due to lupus anticoagulant hypoprothrombinemia syndrome.
Coagulation factor II
Corticosteroids
Hemorrhagic disorders
Hypoprothrombinemia
Lupus anticoagulant
Journal
Journal of thrombosis and thrombolysis
ISSN: 1573-742X
Titre abrégé: J Thromb Thrombolysis
Pays: Netherlands
ID NLM: 9502018
Informations de publication
Date de publication:
Feb 2020
Feb 2020
Historique:
pubmed:
14
9
2019
medline:
11
11
2020
entrez:
14
9
2019
Statut:
ppublish
Résumé
Association of acquired factor II deficiency and lupus anticoagulant is a rare disease that can be related to sudden, severe or fatal haemorrhage. We present a 74-years-old woman with history of myelodysplastic syndrome, admitted to the Emergency Department due to spontaneous mucocutaneous bleeding. Coagulation assays revealed prolonged prothrombin time and activated partial thromboplastin time with evidence of an immediate acting inhibitor. Antithrombotic therapy usage, drug ingestion, disseminated intravascular coagulation, liver dysfunction and sepsis were excluded. Patient was admitted for close monitoring and etiological evaluation. A comprehensive bleeding diathesis workup was performed showing factor II levels severely decreased and transient positive lupus anticoagulant. Immunosuppression with methylprednisolone lasted for 3 days, followed by prednisolone. After 20 days she was discharged and follow-up was scheduled. Early diagnosis of lupus anticoagulant hypoprothrombinemia syndrome is critical, as it may result in fatal complications if not treated appropriately. There is no consensus regarding the best treatment, most being based on immunosuppression.
Identifiants
pubmed: 31515751
doi: 10.1007/s11239-019-01955-1
pii: 10.1007/s11239-019-01955-1
doi:
Substances chimiques
Lupus Coagulation Inhibitor
0
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
334-336Références
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