一例类似于成人斯蒂尔病的非典型家族性地中海热（与吡啉相关的自身炎症性疾病）成人病例。
An adult case of atypical familial Mediterranean fever (pyrin-associated autoinflammatory disease) similar to adult-onset Still's disease.
作者信息
Tsuruma Hayato, Sato Hiroe, Hasegawa Eriko, Nozawa Yukiko, Nakatsue Takeshi, Wada Yoko, Kuroda Takeshi, Suzuki Yoshiki, Nakano Masaaki, Narita Ichiei
机构信息
General Clinical Training Center Niigata University Medical and Dental Hospital Niigata Japan.
Division of Clinical Nephrology and Rheumatology Niigata University Graduate School of Medical and Dental Sciences Niigata Japan.
出版信息
Clin Case Rep. 2019 Mar 12;7(4):801-805. doi: 10.1002/ccr3.2102. eCollection 2019 Apr.
We present a 55-year-old woman with periodic fever and symptoms similar to adult-onset Still's disease (AOSD). She had a heterogeneous mutation of the gene and colchicine was effective. Atypical familial Mediterranean fever (pyrin-associated autoinflammatory disease) should be considered in patients with periodic fever accompanied by symptoms similar to AOSD.
我们报告一名55岁女性，有周期性发热及类似成人斯蒂尔病（AOSD）的症状。她存在该基因的异质性突变，秋水仙碱治疗有效。对于伴有类似AOSD症状的周期性发热患者，应考虑非典型家族性地中海热（与吡啉相关的自身炎症性疾病）。
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