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TAFRO syndrome with refractory thrombocytopenia responding to tocilizumab and romiplostim: a case report

Thrombocytopenia, anasarca, fever, reticulin fibrosis, organomegaly (TAFRO) syndrome is a unique clinicopathologic subtype of multicentric Castleman’s disease that has recently been identified in Japan. However, little is known about its renal histological changes and the optimal treatment for TAFRO...

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שמור ב:
מידע ביבליוגרפי
הוצא לאור ב:CEN Case Rep
Main Authors: Noda-Narita, Shoko, Sumida, Keiichi, Sekine, Akinari, Hoshino, Junichi, Mise, Koki, Suwabe, Tatsuya, Hayami, Noriko, Yamanouchi, Masayuki, Ueno, Toshiharu, Mizuno, Hiroki, Kawada, Masahiro, Hiramatsu, Rikako, Hasegawa, Eiko, Sawa, Naoki, Takaichi, Kenmei, Ohashi, Kenichi, Fujii, Takeshi, Ubara, Yoshifumi
פורמט: Artigo
שפה:Inglês
יצא לאור: Springer Japan 2018
נושאים:
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC5886949/
https://ncbi.nlm.nih.gov/pubmed/29468524
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13730-018-0319-0
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