Acquired haemophilia due to factor VIII inhibitors in ovarian hyperstimulation syndrome: case report.

TitleAcquired haemophilia due to factor VIII inhibitors in ovarian hyperstimulation syndrome: case report.
Publication TypeJournal Article
Year of Publication2003
AuthorsNakauchi-Tanaka T, Sohda S, Someya K, Kono K, Hamada H, Yoshikawa H
Volume18
Issue3
Pagination6
Date PublishedMar
ISSN0268-1161
Accession Number12615815
KeywordsAdult, Blood Coagulation Factors / tu [Therapeutic Use], Delivery, Obstetric, Factor VIII / ai [Antagonists & Inhibitors], Female, Hemophilia A / dt [Drug Therapy], Hemophilia A / et [Etiology], Humans, IM, Infant, Newborn, Male, Ovarian Hyperstimulation Syndrome / co [Complications], Ovarian Hyperstimulation Syndrome / me [Metabolism], Pregnancy
Abstract

A 31-year-old nulligravida woman developed an acquired factor VIII inhibitor associated with severe ovarian hyperstimulation syndrome (OHSS). She developed haematouria, ecchymosis, and intramuscular bleeding following the severe OHSS. Laboratory examinations showed a markedly prolonged activated partial thromboplastin time and a low level of factor VIII activity. Treatment with prothrombin complex concentrate and factor VIII inhibitor bypassing agent was successful in reducing the inhibitor so that she delivered a healthy baby via spontaneous vaginal delivery. Acquired haemophilia is a life-threatening disorder. This is the first case report of acquired haemophilia in OHSS.

URLhttp://ovidsp.ovid.com/ovidweb.cgi?T=JS&CSC=Y&NEWS=N&PAGE=fulltext&D=med4&AN=12615815
Alternate JournalHum.Reprod.
Notify Library Reference ID1760

Related Incidents