Isolated Factor VII Deficiency Diagnosed after a Life-Threatening Brain Haemorrhage

Author:

Tsuda T1,Okamoto Y1,Sakaguchi R1,Katayama N1,Ota K1

Affiliation:

1. Department of Blood Transfusion Medicine and Clinical Haematology, Wakayama Medical College, Wakayama City, Japan

Abstract

A 65-year-old man was admitted to another hospital with a life-threatening brain haemorrhage, and laboratory examinations on admission revealed prolonged prothrombin time with normal activated partial thromboplastin time. To establish the cause of his abnormal coagulation, he was referred to our clinic. Neither the patient nor his family had any previous history of bleeding symptoms. His liver function was within normal limits but coagulation tests showed increased plasma activities of factors II, VIII, IX, X, with reduced activities of factors V and VII. The activity of factor VII was less than 2% but no inhibitor of factor VII was detected in the plasma. We concluded that the patient had a rare congenital isolated factor VII deficiency although he had not shown earlier bleeding problems, presumably because of compensation for the factor VII deficiency by enhanced activities of components of the extrinsic coagulation pathway, factors II, VIII, IX and X.

Publisher

SAGE Publications

Subject

Biochemistry (medical),Cell Biology,Biochemistry,General Medicine

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Congenital Factor XIII Deficiency;Congenital Bleeding Disorders;2018

2. rFVII for Pediatric Acute Intracranial Hemorrhage;Stroke;2007-07

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