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蒙多氏病作为遗传性蛋白C缺乏症和抗心磷脂抗体中的首发血栓形成事件。

Mondor's disease as first thrombotic event in hereditary protein C deficiency and anticardiolipin antibodies.

作者信息

Wester J P, Kuenen B C, Meuwissen O J, de Maat C E

机构信息

Department of Internal Medicine, St. Antonius Hospital, Nieuwegein, Netherlands.

出版信息

Neth J Med. 1997 Feb;50(2):85-7. doi: 10.1016/s0300-2977(96)00072-1.

Abstract

A 45-year-old Caucasian woman presented with superficial thrombophlebitis of the right arm and right anterior thoracic wall after bilateral breast surgery followed by spontaneous left anterior thoracic vein thrombophlebitis 3 months later. Besides breast surgery and use of oral contraceptives, hereditary protein C deficiency and anticardiolipin antibodies were found as causes for this bilateral Mondor's disease.

摘要

一名45岁的白种女性在双侧乳房手术后出现右臂和右前胸壁浅静脉血栓性静脉炎,3个月后又自发出现左前胸壁静脉血栓性静脉炎。除了乳房手术和口服避孕药外,还发现遗传性蛋白C缺乏和抗心磷脂抗体是导致双侧蒙多氏病的原因。

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