| Literature DB >> 26781021 |
Yusuke Yamaga1, Kiyonobu Tokuyama, Takehiro Kato, Rie Yamada, Masanori Murayama, Tsuneko Ikeda, Noriyoshi Yamakita, Takeshige Kunieda.
Abstract
Thrombocytopenia, anasarca, fever, reticulin fibrosis, and organomegaly (TAFRO) syndrome is a unique clinicopathologic variant of multicentric Castleman's disease that has recently been identified in Japan. Previous reports have shown that affected patients typically respond to immunosuppressive therapy, such as prednisolone and tocilizumab. However, the optimal treatment for refractory TAFRO syndrome, which can be fatal, remains unclear. We herein report a case of tocilizumab-resistant TAFRO syndrome successfully treated with cyclosporin A, indicating that cyclosporine A may be an alternative therapy for refractory TAFRO syndrome.Entities:
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Year: 2016 PMID: 26781021 DOI: 10.2169/internalmedicine.55.4710
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271