Dessein P H, Lamparelli R D, Phillips S A, Rubenchik I A, Zwi S
Department of Medicine, University of the Witwatersrand Medical School, Johannesburg, South Africa.
J Rheumatol. 1989 Nov;16(11):1494-6.
A 49-year-old woman with clinical features of systemic lupus erythematosus, systemic sclerosis, Sjögren's and the antiphospholipid syndromes developed severe immune thrombocytopenia and skin infarctions. Both complications responded to immunosuppressive agents.
一名49岁女性，具有系统性红斑狼疮、系统性硬化症、干燥综合征及抗磷脂综合征的临床特征，出现了严重的免疫性血小板减少症和皮肤梗死。这两种并发症对抗免疫抑制剂均有反应。
