Kaliman J, Sinzinger H, Staudacher M, Mannheimer E
Wien Klin Wochenschr. 1985 Mar 29;97(7):323-6.
A case is reported of a 10 year-old girl admitted to hospital because of severe intermittent claudication. Occlusion of the left popliteal artery was diagnosed. Since successful surgical intervention the patient has been symptom-free. No causative factor was detected for this premature occlusion. During intensive laboratory check-up an extreme diminution in sensitivity of the platelets to prostacyclin and a receptor defect were discovered. This defect seems to be genetically determined. The extent to which this as yet unreported platelet defect might have contributed to the development of atherosclerosis at such an early age is discussed.
报告了一例10岁女孩因严重间歇性跛行入院的病例。诊断为左腘动脉闭塞。自成功进行手术干预以来,患者一直无症状。未检测到导致这种过早闭塞的病因。在深入的实验室检查中,发现血小板对前列环素的敏感性极度降低以及存在受体缺陷。这种缺陷似乎是由基因决定的。本文讨论了这种尚未报道的血小板缺陷在多大程度上可能促成了如此早年的动脉粥样硬化发展。