Broekmans A W, van Rooyen W, Westerveld B D, Briët E, Bertina R M
Gastroenterology. 1987 Jan;92(1):240-2. doi: 10.1016/0016-5085(87)90867-5.
Protein S deficiency is inherited as an autosomal dominant trait. Heterozygotes with a reduction of 50% in the plasma protein S concentration are at risk for the development of venous thromboembolism, often occurring at an early age without an apparent cause. In the majority of the patients thrombosis is restricted to the superficial or deep venous system of the legs. In this case report we describe the presence of mesenteric vein thrombosis in a 30-yr-old man with hereditary protein S deficiency. In his family protein S deficiency was also recognized in his mother, brother, and niece. Both his mother and brother had a history of thrombotic disease.
蛋白S缺乏症作为常染色体显性性状遗传。血浆蛋白S浓度降低50%的杂合子有发生静脉血栓栓塞的风险,常于早年无明显诱因发病。大多数患者的血栓形成局限于腿部浅静脉或深静脉系统。在本病例报告中,我们描述了一名30岁患有遗传性蛋白S缺乏症男性患者出现肠系膜静脉血栓形成的情况。在他的家族中,其母亲、兄弟和侄女也被诊断为蛋白S缺乏症。他的母亲和兄弟都有血栓形成病史。