Clinicopathological features of TAFRO syndrome complicated by acquired hemophilia A and development of cardiopulmonary arrest that were successfully treated with VA-ECMO and tocilizumab
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
http://link.springer.com/article/10.1007/s12185-019-02604-2/fulltext.html
Reference15 articles.
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2. Hasegawa E, Sato H, Wada Y, Takai K, Wakamatsu A, Nozawa Y, et al. Characterization of patients with systemic lupus erythematosus who meet the diagnostic criteria for TAFRO syndrome. Lupus. 2018;27:417–27.
3. Fujimoto S, Kawabata H, Nurose N, Kawanami-iwao H, Sakai T, Kawanami T, et al. Sjögren’s syndrome manifesting as clinicopathological features of TAFRO syndrome: a case report. Medicine (Baltimore). 2017;96:e9220.
4. Masaki Y, Kawabata H, Takai K, Kojima M, Tsukamoto N, Ishigaki Y, et al. Proposed diagnostic criteria, disease severity classification and treatment strategy for TAFRO syndrome, 2015 version. Int J Hematol. 2016;103:686–92.
5. Shetty S, Bhave M, Ghosh K. Acquired hemophilia a: diagnosis, an etiology, clinical spectrum and treatment options. Autoimmun Rev. 2011;10:311–6.
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3. 血友病インヒビター治療薬factor VIIa/factor X製剤の現状と展望;Japanese Journal of Thrombosis and Hemostasis;2023
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