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患者男,16岁。因不明原因面色苍白、皮肤出血、发热8个月于1985年1月入院。血象:Hb35g/L,网织红细胞0.005,WBC2.5×10~9/L,PBC36×10~9/L。N0.35、L0.64、E0.01。骨髓象:增生低下,三系均减少,淋巴细胞增高(0.64),浆、网状细胞易见,巨核细胞全片未见,散在血小板少。诊断为再障,经丙睾、左旋咪唑、输血等治疗,血象进步,症状好转出院。1990年7月症状复发再次入院。查体:T38℃,重度贫血貌,全身皮肤可见出血点,肝、脾未扪及。血象:Hb39g/L,WBC3.5×10~9/L,plt14×10~9/L,网织红细胞0.01,分类N0.36、L0.45、
Male patient, 16 years old. For unknown reasons pale, skin bleeding, fever 8 months in January 1985 admitted. Blood: Hb35g / L, reticulocytes 0.005, WBC2.5 × 10 ~ 9 / L, PBC36 × 10 ~ 9 / L. N0.35, L0.64, E0.01. Bone marrow like: hyperplasia, all three lines are reduced, lymphocytes increased (0.64), plasma, reticulocytes, megakaryocytes showed no whole piece, scattered in less platelets. Diagnosis of aplastic anemia, by the testis, levamisole, blood transfusions and other treatment, blood, progress, symptoms improved discharge. July 1990 recurrence of symptoms and re-admission. Physical examination: T38 ℃, severe anemia appearance, systemic skin bleeding, liver, spleen not palpable. Blood: Hb39g / L, WBC3.5 × 10 ~ 9 / L, plt14 × 10 ~ 9 / L, reticulocyte 0.01, classification N0.36, L0.45,