[Acquired coagulation disorders].


Journal

[Rinsho ketsueki] The Japanese journal of clinical hematology
ISSN: 0485-1439
Titre abrégé: Rinsho Ketsueki
Pays: Japan
ID NLM: 2984782R

Informations de publication

Date de publication:
2020
Historique:
entrez: 8 8 2020
pubmed: 8 8 2020
medline: 25 9 2020
Statut: ppublish

Résumé

Acquired coagulation inhibitors have become a popular area of research because they cause severe bleeding tendency in many patients. The use of acquired coagulation inhibitors requires rapid and precise diagnosis. Some acquired coagulation inhibitors show prolongation in the activated partial thromboplastin time (APTT) and/or prothrombin time (PT). To diagnose these disorders, mixing test is very useful. However, lupus anticoagulant related disorders, such as lupus anticoagulant hypoprothrombinemia syndrome (LAHPS), are difficult to diagnose because they are sometimes associated with a reduction in factor VIII and are thus difficult to distinguish from acquired hemophilia. Acquired factor XIII deficiency and acquired von Willebrand syndrome (AvWS) are easily overlooked because they show normal value in several patients with APTT and PT. Here I describe the diagnostic method for these disorders. In particular, five acquired coagulation inhibitors that appear to be clinically significant are studied.

Identifiants

pubmed: 32759565
doi: 10.11406/rinketsu.61.779
doi:

Substances chimiques

Lupus Coagulation Inhibitor 0

Types de publication

Journal Article

Langues

jpn

Sous-ensembles de citation

IM

Pagination

779-784

Auteurs

Nobuaki Suzuki (N)

Department of Transfusion Medicine, Nagoya University Hospital.

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Classifications MeSH