Thromb Haemost 1969; 22(02): 316-325
DOI: 10.1055/s-0038-1651357
Originalarbeiten-Original Articles-Travaux Originaux
Schattauer GmbH

Congenital Combined Deficiency of Factor V and Factor VIII

A Case Report and the Effect of Transfusion of Normal Plasma and Hemophilic Blood[*]
H Saito
1   1st Department of Internal Medicine, Nagoya University, School of Medicine, Nagoya, Japan
,
M Shioya
1   1st Department of Internal Medicine, Nagoya University, School of Medicine, Nagoya, Japan
,
K Koie
1   1st Department of Internal Medicine, Nagoya University, School of Medicine, Nagoya, Japan
,
T Kamiya
1   1st Department of Internal Medicine, Nagoya University, School of Medicine, Nagoya, Japan
,
O Katsumi
1   1st Department of Internal Medicine, Nagoya University, School of Medicine, Nagoya, Japan
› Author Affiliations
Further Information

Publication History

Publication Date:
10 June 2018 (online)

Summary

A case of congenital combined deficiency of factor V and factor VIII was reported. The patient, a 9 year old boy, gave a history of epistaxis, hematomas, and of hemorrhages following dental extraction since the age of 2 ; plasma levels of factor V and factor VIII were found to be 16% and 8% of normal, respectively. No one in his family had a deficiency of either factor. The effects of transfusion of normal fresh plasma and whole blood from a patient with hemophilia A were studied. While the former were similar to the pattern as seen in classical hemophilia, the latter consisted of an immediate increase of factor V activity and a delayed increase of factor VIII activity, despite the fact that factor VIII activity was almost absent from the donor’s blood.

* Present address: The Children’s Cancer Research Foundation, 35 Binney Street, Boston, Massachusetts 02115, U.S.A.


 
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