Japanese Journal of Neurosurgery
Online ISSN : 2187-3100
Print ISSN : 0917-950X
ISSN-L : 0917-950X
CASE REPORTS
A Case of Congenital Hemophilia A with Severe Intracranial Hemorrhage after Instrumental Delivery
Kokyo SakuradaChihiro WatanabeMasae KurohaMami YamashitaMaya KonoSatoshi Ihara
Author information
JOURNAL OPEN ACCESS

2023 Volume 32 Issue 7 Pages 443-447

Details
Abstract

  Hemophilia A, a deficiency of coagulation factor Ⅷ, is the most common congenital bleeding disorder. If the family history suggests hemophilia A, instrumental delivery should be avoided to prevent bleeding complications from birth injuries. However, instrumental delivery may be considered in cases with no family history of hemophilia A. Here, we present the case of a neonatal patient with hemophilia A who underwent instrumental delivery due to the lack of a family history. The patient developed severe intracranial hemorrhage that required a craniotomy for hematoma removal. Although activated partial thromboplastin time (APTT) prolongation is the key to diagnosing hemophilia, it should be noted that APTT can be physiologically prolonged in neonates. In addition, since administration of fresh frozen plasma (FFP) alone does not have sufficient hemostatic effects in hemophilia A, care must be taken during surgery.

Content from these authors
© 2023 The Japanese Congress of Neurological Surgeons

この記事はクリエイティブ・コモンズ [表示 - 非営利 - 改変禁止 4.0 国際]ライセンスの下に提供されています。
https://creativecommons.org/licenses/by-nc-nd/4.0/deed.ja
Previous article Next article
feedback
Top