Korean J Intern Med.
1997 Jan;12(1):80-83.
A case of coagulation factor V deficiency complicated with intracranial
hemorrhage
- Affiliations
-
- 1Institute for Clinical molecular Biology Research, College of Medicine,
Soonchunhyang University, Seoul, Korea.
Abstract
- Factor V deficiency is a relatively uncommon disorder, inherited as an autosomal
recessive trait that manifests clinically only in individuals who inherit the
defective gene from both parents. The hemorrhage of nasal and oral cavity and
ecchymosis are common but intracranial hemorrhage is very rare. We experienced a
53 year old male patient with intracranial hemorrhage due to factor V
deficiency. The laboratory tests showed prolongation of APTT and PT, normal
bleeding time and normal thrombin time. The levels of the coagulation profiles
on the patient revealed a significant decrease factor V, below 1% of normal
range (60-140%). Other coagulation factors were normal. He was treated with
fresh frozen plasma and completely recovered 3 weeks after treatment.