@article{oai:nagasaki-u.repo.nii.ac.jp:00001592,
 author = {Shimizu, Toshimasa and Iwamoto, Naoki and Okamoto, Momoko and Endo, Yushiro and Tsuji, Sosuke and Takatani, Ayuko and Igawa, Takashi and Umeda, Masataka and Fukui, Shoichi and Sumiyoshi, Remi and Kitamura, Mineaki and Koga, Tomohiro and Kawashiri, Shin-ya and Ichinose, Kunihiro and Tamai, Mami and Nakamura, Hideki and Origuchi, Tomoki and Nishino, Tomoya and Kawakami, Atsushi},
 issue = {3},
 journal = {Internal Medicine},
 month = {Feb},
 note = {A 44-year-old Japanese man with a 14-year history of limited cutaneous systemic sclerosis (SSc) was admitted with a fever, 
hypertension, anemia, thrombocytopenia, and renal dysfunction. On admission, hypertension, hyperreninemia, acute renal dysfunction,hemolytic anemia, and thrombocytopenia led to the diagnosis of scleroderma renal crisis (SRC) complicated with thrombotic microangiopathy (TMA).
 The patient had also been infected with influenza B virus almost six days before admission. Following treatment with plasma exchange,an angiotensin-converting enzyme inhibitor, and an anti-virus agent, his general condition improved. He had no risk factors for SRC.In SSc patients, an influenza virus infection might trigger SRC complicated with TMA., Internal medicine, 58(3), pp.441-445; 2019},
 pages = {441--445},
 title = {Scleroderma Renal Crisis Complicated with Thrombotic Microangiopathy Triggered by Influenza B Virus Infection},
 volume = {58},
 year = {2019}
}