Nilsen A, Matre R
Acta Med Scand. 1980;207(1-2):123-5.
This paper reports the findings of an "acquired" hereditary angioedema-like syndrome in a patient with myelofibrosis. No previous personal or family history of angioedema was present. The serum complement pattern showed a marked reduction of Cl esterase inhibitor, Clq and C4. All family members had a normal complement profile. Because of frequent attacks of laryngeal angioedema, prophylactic treatment with danazol was started. A striking clinical response was observed as well as a normalizing effect on the underlying biochemical abnormality.
本文报告了一名骨髓纤维化患者出现“获得性”遗传性血管性水肿样综合征的研究结果。患者既往无个人或家族性血管性水肿病史。血清补体模式显示Cl酯酶抑制剂、Clq和C4显著降低。所有家庭成员的补体谱均正常。由于喉部血管性水肿频繁发作,开始使用达那唑进行预防性治疗。观察到显著的临床反应以及对潜在生化异常的正常化作用。