Result:NK-LGLL is a rare disease, its clinical characters are obviously general symptom, hepatomegaly, splenomegaly, lymphadenectasis.

 
  • 結果:NK-LGLL為一少見(jiàn)疾病,臨床以全身癥狀明顯,肝、脾、淋巴結腫大多見(jiàn)。
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