Internal Medicine
Online ISSN : 1349-7235
Print ISSN : 0918-2918
ISSN-L : 0918-2918
CASE REPORTS
Eculizumab for Severe Thrombotic Microangiopathy Secondary to Surgical Invasive Stress and Bleeding
Yoko FujitaMaho TerashitaMasahiko YazawaYukitaka YamasakiTomonori ImamuraJunichiro KibayashiToshihiro SawaiYoshihiko HidakaKatsuki OhtaniNorimitsu InoueYugo Shibagaki
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ジャーナル オープンアクセス

2020 年 59 巻 1 号 p. 93-99

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Atypical hemolytic uremic syndrome (aHUS) is an extremely rare condition caused by an excessive activation of the complement pathway based on genetic or acquired dysfunctions in complement regulation, leading to thrombotic microangiopathy (TMA). A complement-amplifying condition (CAC) can trigger aHUS occurrence along with complement abnormality. We herein report a case of severe TMA after laparoscopic myomectomy in a healthy woman. This case was eventually diagnosed as complement-mediated TMA secondary to surgical invasive stress as a CAC, with no definitive diagnosis of aHUS despite a genetic test. The patient fully recovered after several eculizumab administrations.

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© 2020 by The Japanese Society of Internal Medicine
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