Hemophagocytic syndrome (HPS) often occurred at the onset of AOSD and half of them did not have leukopenia in the literature reviewed.

 
  • 我們回顧文獻中成人史提爾氏病合并嗜血癥候群的病例,嗜血癥候群多發(fā)生在成人史提爾氏病發(fā)病的時(shí)候,且其中大約有一半的病患的白血球增加或正常。
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