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获得性异常纤维蛋白原血症诱导红细胞聚集所致的手指缺血和坏疽。

Digital ischemia and gangrene due to red blood cell aggregation induced by acquired dysfibrinogenemia.

作者信息

Kwaan H C, Levin M, Sakurai S, Kucuk O, Rooney M W, Lis L J, Kauffman J W

机构信息

Department of Medicine, Northwestern University Medical School, Chicago, IL, USA.

出版信息

J Vasc Surg. 1997 Dec;26(6):1061-8. doi: 10.1016/s0741-5214(97)70021-1.

Abstract

Digital gangrene was observed in a patient who had angiographic findings of digital arterial occlusion. The patient's blood showed a marked red blood cell aggregation with rouleaux formation in long chains, which could not be dispersed at shear rates up to 200 sec-1. Studies of the patient's blood revealed the presence of an abnormal fibrinogen capable of aggregating normal red blood cells. This fibrinogen was found by Raman spectroscopy to have an increased alpha-helical content, whereas the beta-sheet content was decreased. Defibrinogenation therapy with ancrod resulted in a dramatic symptomatic relief. The disappearance of the abnormal fibrinogen 6 months later and an absence of a family history indicate that this dysfibrinogenemia was acquired.

摘要

在一名具有指动脉闭塞血管造影表现的患者中观察到了指端坏疽。该患者的血液显示出明显的红细胞聚集,形成长链状的缗钱状,在高达200秒-1的剪切速率下也无法分散。对该患者血液的研究发现存在一种能够聚集正常红细胞的异常纤维蛋白原。通过拉曼光谱法发现这种纤维蛋白原的α-螺旋含量增加,而β-折叠含量减少。用安克洛酶进行去纤维蛋白原治疗后症状显著缓解。6个月后异常纤维蛋白原消失且无家族史表明这种异常纤维蛋白原血症是后天获得的。

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