Mikhaĭlova E A, Iadrikhinskaia V N, Savchenko V G
Ter Arkh. 1999;71(7):64-9.
To validate up-to-date policy of immunosuppressive therapy of patients with aplastic anemia (AA) which has developed either at acute or chronic phase of viral hepatitis.
16 patients with AA detected within 6 months (9 patients) or 12-36 months (7 patients) after acute viral hepatitis received immunosuppressive therapy (antilymphocytic globulin, cyclosporin A, splenectomy).
Posthepatitis aplastic anemias ran a severe and treatment-resistant course in most cases. The immunosuppressive therapy produced a response in 44% of the patients. AA following acute viral hepatitis demands intensive and long-term immunosuppressive therapy with antilymphocytic globulin, cyclosporin A, splenectomy (in some cases) to achieve a persistent clinicohematological remission.
验证针对在病毒性肝炎急性期或慢性期发生的再生障碍性贫血(AA)患者的最新免疫抑制治疗策略。
16例再生障碍性贫血患者在急性病毒性肝炎后6个月内(9例)或12 - 36个月(7例)接受免疫抑制治疗(抗淋巴细胞球蛋白、环孢素A、脾切除术)。
多数情况下,肝炎后再生障碍性贫血病情严重且治疗抵抗。免疫抑制治疗使44%的患者产生反应。急性病毒性肝炎后的再生障碍性贫血需要使用抗淋巴细胞球蛋白、环孢素A、脾切除术(某些情况下)进行强化和长期免疫抑制治疗,以实现持续的临床血液学缓解。