Bessias Nikolaos, Moulakakis Konstantinos G, Lioupis Christos, Bakogiannis Konstantinos, Sfyroeras Giorgos, Kakaletri Konstantina, Andrikopoulos Vassilios
Department of Vascular Surgery, Red Cross Hospital, Athens, Greece.
J Vasc Surg. 2005 Oct;42(4):800-4. doi: 10.1016/j.jvs.2005.05.038.
We report a rare case of a pregnant woman with Wegener's granulomatosis whose disease involved the lungs, the spleen, and a limb. Wegener's granulomatosis was clinically manifested in the 34th week of pregnancy with pulmonary infiltrates, splenic infarcts, and acute limb ischemia. Successive thrombectomies failed to maintain arterial flow in the distal limb due to the development of active vasculitis. Thrombosis of the tibial arteries and recurrence of thrombosis was a persistent clinical observation. In the meantime, a cesarean section was performed, with a successful delivery of a healthy male newborn. Because of the recent cesarean section, the patient did not undergo thrombolysis. The woman finally underwent amputation of the limb. According to the reviewed literature, this is the sixth reported case of Wegener's granulomatosis presenting with digital ischemia and the first manifested during pregnancy.
我们报告了一例罕见的患有韦格纳肉芽肿病的孕妇,其疾病累及肺部、脾脏和一个肢体。韦格纳肉芽肿病在妊娠第34周临床表现为肺部浸润、脾梗死和急性肢体缺血。由于活动性血管炎的发展,连续的血栓切除术未能维持远端肢体的动脉血流。胫动脉血栓形成和血栓复发是持续的临床观察结果。与此同时,进行了剖宫产,成功分娩出一名健康的男婴。由于近期剖宫产,患者未接受溶栓治疗。该女性最终接受了肢体截肢术。根据文献回顾,这是第六例报告的出现手指缺血的韦格纳肉芽肿病病例,也是第一例在妊娠期出现的病例。