Johansen S, Johnsen B, Jansen J
Neuromedicinsk afdeling, Centralsygehuset Hillerød.
Ugeskr Laeger. 1991 Jan 7;153(2):116-7.
A 28 year old woman with a previous history of labile hypertension, migraine and transitory cerebral ischemia was admitted with cerebral infarction. One month later she developed livedo reticularis and amaurosis fugax, which led to the diagnosis of Sneddon's disease (livedo reticularis, labile hypertension and neurological symptoms) and the anticardiolipin antibody (ACA) syndrome. Treatment with prednisone and phenprocoumon resulted in lowering of ACA-titers, but the symptoms did not subside until acetylsalicylic acid was added.
一名28岁女性,既往有不稳定型高血压、偏头痛和短暂性脑缺血病史,因脑梗死入院。一个月后,她出现了网状青斑和一过性黑矇,这导致了Sneddon病(网状青斑、不稳定型高血压和神经症状)和抗心磷脂抗体(ACA)综合征的诊断。使用泼尼松和苯丙香豆素治疗使ACA滴度降低,但直到加用乙酰水杨酸后症状才消退。