Siegert G, Plat M
Institut für Klinische Chemie und Laboratoriumsdiagnostik, Medizinischen Akademie Carl Gustav Carus, Dresden.
Z Gesamte Inn Med. 1988 May 1;43(9):228-31.
Deficiency conditions in the contact phase system of the blood coagulation belong to the rare hereditary defects. Clinically, there is as a rule no inclination to haemorrhage but an increased risk of thrombosis. Therefore, the diagnosis is frequently made on the basis of incidental findings within the framework of routine examinations. Indicating sign is a greatly prolonged partial thromboplastin time (PTT) without clinical signs of haemorrhage. 3 patients with factor XII deficiency are presented and the diagnostic method in prolonged PTT is explained.
血液凝固接触相系统的缺陷状况属于罕见的遗传性缺陷。临床上,通常没有出血倾向,而是血栓形成风险增加。因此,诊断往往是在常规检查过程中基于偶然发现做出的。指示性体征是部分凝血活酶时间(PTT)显著延长且无出血的临床体征。本文介绍了3例因子Ⅻ缺乏症患者,并解释了PTT延长时的诊断方法。