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

  • 结果: NK-LGLL为一少见疾病, 临床以全身症状明显, 肝 、 脾 、 淋巴结肿大多见.

  • 互联网摘选 2025-01-18 16:05:15

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