Ruiz-Argüelles G J, Ruiz-Argüelles A, Pérez-Romano B, Alarcón-Segovia D
Centro de Hematología y Medicina Interna, Instituto Nacional de la Nutrición Salvador Zubirán, México City, México.
Acta Haematol. 1993;89(4):206-8. doi: 10.1159/000204525.
We describe here a female patient with mixed connective tissue disease, secondary antiphospholipid syndrome, pulmonary hypertension and severe acquired, probably autoimmune, antibody-mediated type I coagulation protein S deficiency (total, free and C4bp-bound). No previous instance of anti-PS antibody-associated PS deficiency had been reported. The patient was treated initially with prednisone, but the protein S levels did not rise until danazol was added, and dropped again after its withdrawal.
我们在此描述一名患有混合性结缔组织病、继发性抗磷脂综合征、肺动脉高压以及严重获得性(可能为自身免疫性)抗体介导的I型凝血蛋白S缺乏(总蛋白S、游离蛋白S及与C4结合蛋白结合的蛋白S)的女性患者。此前尚无抗PS抗体相关的蛋白S缺乏的病例报道。该患者最初接受泼尼松治疗,但直到加用达那唑后蛋白S水平才升高,停药后又再次下降。