Common pathway coagulopathy and hemorrhagic edema of infancy.
bleeding
dyscrasias
edema
microangiopathy
pediatrics
Journal
Clinical case reports
ISSN: 2050-0904
Titre abrégé: Clin Case Rep
Pays: England
ID NLM: 101620385
Informations de publication
Date de publication:
Oct 2023
Oct 2023
Historique:
received:
04
05
2023
revised:
16
08
2023
accepted:
14
09
2023
medline:
23
10
2023
pubmed:
23
10
2023
entrez:
23
10
2023
Statut:
epublish
Résumé
When screening tests of haemostasis are abnormal, it is important to identify at which point in the coagulation cascade dysfunction may be occurring. This may assist to identify a specific deficiency/dysfunction, the type of bleeding to be anticipated, and replacement therapy if required. Unmasking of an inherited coagulopathy or the development of an acquired coagulopathy may occur in the setting of a second (febrile) illness. Differentiating between inherited and acquired coagulopathies will rely on clinicians taking a thorough personal and family bleeding history, and correlating these findings with the haemostasis screening results.
Identifiants
pubmed: 37867536
doi: 10.1002/ccr3.8060
pii: CCR38060
pmc: PMC10585055
doi:
Types de publication
Case Reports
Langues
eng
Pagination
e8060Informations de copyright
© 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.
Déclaration de conflit d'intérêts
None.
Références
Haemophilia. 2008 Nov;14(6):1164-9
pubmed: 19141156
Clin Exp Dermatol. 2013 Jan;38(1):116-7
pubmed: 22731924
Semin Thromb Hemost. 2019 Jul;45(5):523-543
pubmed: 31121608
Haemophilia. 2018 Jul;24(4):648-656
pubmed: 29578313
Int J Environ Res Public Health. 2019 Mar 06;16(5):
pubmed: 30845781
Br J Haematol. 2009 Jun;146(1):17-26
pubmed: 19438479