Bibbo Christopher, Davis W Hodges
Foot and & Ankle Service, Department of Orthopaedic Surgery, Marshfield Clinic, Wisconsin, USA.
J Foot Ankle Surg. 2005 Jul-Aug;44(4):301-6. doi: 10.1053/j.jfas.2005.04.009.
The thrombotic thrombocytopenic-hemolytic uremic (TTP-HUS) syndrome is a thrombotic microangiopathy involving end-organ vascular beds. Microcirculatory thrombosis results in ischemic changes in any number of organ systems, especially the central nervous and renal systems. Musculoskeletal system involvement is less well described, but when it occurs, acral ischemia may be severe. TTP-HUS is well recognized as a complication of organ transplantation, drug therapy, in pregnancy, and as a chronic, relapsing congenital disorder. Bacterial sepsis may also result in a thrombotic microangiopathy of the central nervous and renal systems (TTP-HUS). This article presents a case report and discusses the pathogenesis and lower-extremity manifestations of TTP-HUS, and outlines management strategies.
血栓性血小板减少性-溶血性尿毒症(TTP-HUS)综合征是一种累及终末器官血管床的血栓性微血管病。微循环血栓形成会导致多个器官系统出现缺血性改变,尤其是中枢神经系统和肾脏系统。肌肉骨骼系统受累的情况描述较少,但一旦发生,肢端缺血可能会很严重。TTP-HUS被公认为器官移植、药物治疗、妊娠的并发症,以及一种慢性复发性先天性疾病。细菌败血症也可能导致中枢神经系统和肾脏系统的血栓性微血管病(TTP-HUS)。本文报告了一例病例,并讨论了TTP-HUS的发病机制和下肢表现,概述了治疗策略。