Hemostatic abnormalities and increased vascular endothelial cell markers in patients with red cell fragmentation syndrome induced by mitomycin C
✍ Scribed by Shozaburo Nagaya; Hideo Wada; Kouzi Oka; Motoaki Tanigawa; Shigehisa Tamaki; Kouta Tsuzi; Eiki Miyanishi; Yoshihiro Wakita; Nobuyuki Minami; Katsumi Deguchi; Kozi Suzuki; Takeshi Nakano; Hiroshi Shiku
- Book ID
- 102699615
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 574 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0361-8609
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✦ Synopsis
Abstract
We examined red cell fragmentation syndrome (RCFS) induced by mitomycin C (MMC) (13 patients), by thrombotic thrombocytopenic purpura (TTP) (17 patients), and by disseminated intravascular coagulation (DIC) (15 patients). Plasma cytokine levels were increased in the TTP and DIC patients, but not in those whose RCFS was induced by MMC, suggesting that the activation of the immune system plays an important role in the pathogenesis of RCFS due to TTP and DIC but did not in RCFS due to MMC. Plasma thrombomodulin, tissue type plasminogen activator, and plasminogen activator inhibitor‐I levels were increased in all RCFS patients, suggesting that RCFS, whether MMC induced, or due to TTP or DIC, might be associated with vascular endothelial cell injury. In TTP, von Willebrand factor (vWF) antigen and high molecular weight vWF multimer levels were reduced, possibly as a result of microthrombus consumption. The hemostatic data in this study showed that the TTP patients were in a hypercoagulable state without hyperfibrinolysis, and that DIC patients were in both a hypercoagulable and a hyperfibrinolytic state, whereas hemostatic abnormalities were slight in patients with MMC induced RCFS. These findings suggest that vascular endothelial cell injuries might be associated with RCFS, and that those injuries in MMC‐induced RCFS might not be related to microthrombi or an activated immune system.