Fritzler M J, Hart D A
Faculty of Medicine, Department of Medicine, University of Calgary, Alberta, Canada.
Arthritis Rheum. 1990 Feb;33(2):274-6. doi: 10.1002/art.1780330218.
We describe a patient with systemic sclerosis (SSc; scleroderma) characterized by severe Raynaud's phenomenon, cutaneous sclerosis, and digital ulceration and subsequent amputation who was treated with recombinant tissue plasminogen activator (rt-PA) after acute myocardial infarction. She showed prompt improvement of the Raynaud's phenomenon and healing of the digital ulceration. After 18 months of followup, the Raynaud's phenomenon has remained mild, and there has been improvement in the cutaneous sclerosis. Since the pathophysiology of SSc has been associated with disorders of fibrinolysis and coagulation, this patient represents an interesting index case that might prompt further evaluation of rt-PA therapy in carefully selected patients.
我们描述了一名系统性硬化症(SSc;硬皮病)患者,其特征为严重雷诺现象、皮肤硬化、指端溃疡并随后截肢,该患者在急性心肌梗死后接受了重组组织型纤溶酶原激活剂(rt-PA)治疗。她的雷诺现象迅速改善,指端溃疡愈合。经过18个月的随访,雷诺现象仍较轻微,皮肤硬化也有所改善。由于SSc的病理生理学与纤维蛋白溶解和凝血紊乱有关,该患者代表了一个有趣的索引病例,可能会促使对精心挑选的患者进一步评估rt-PA治疗。