Nora R E, Bell W R, Noe D A, Sholar P W
Am J Med. 1985 Jul;79(1):122-6. doi: 10.1016/0002-9343(85)90556-x.
This report presents a heretofore undescribed laboratory variant of congenital factor X deficiency, seen in conjunction with a relatively rare tumor. The patient had a history of bleeding, a prolonged prothrombin time, and a factor X value of 4.2 percent of normal activity, but the partial thromboplastin time and Russell's viper venom clotting time were normal. Management of this case required unusual measures to treat the patient's coagulopathy.