脾切除术治疗成人免疫性血小板减少症的疗效评价

A. Żyluk
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摘要

摘要简介:免疫性血小板减少症(IT)是一种获得性免疫介导的疾病,其特征是抗血小板自身抗体介导的血小板破坏增加导致血小板计数减少。被自身抗体“标记”的血小板首先在脾脏中被识别和破坏,因此,脾切除术是一种治疗选择,特别是在保守治疗难治性病例中。本研究的目的是确定脾切除术治疗成年IT患者的长期预后。材料与方法:11例患者行脾切除术,男7例,女4例,平均年龄43岁,平均生存时间30个月。手术指征均为保守性类固醇治疗失败。9例患者术后平均5年评估手术结果。结果:所有患者均获得良好的治疗反应(缓解)。所有患者均未继续治疗,随访时血小板计数均高于100 G/L。无严重并发症。结论:在保守治疗失败的情况下,脾切除术是一种有效且相对安全的二线治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An assessment of the effectiveness of splenectomy in the treatment of immune thrombocytopenia in adults
Abstract Introduction: Immune thrombocytopenia (IT) is an acquired immune-mediated disease characterized by a decrease in platelet count due to antiplatelet autoantibody-mediated increased platelet destruction. Platelets which are “labelled” by autoantibodies are recognized and destroyed first of all in the spleen, and, therefore, splenectomy is one of the treatment options, particularly in cases refractory to conservative treatment. The objective of this study was to determine long-term outcomes of splenectomy in the treatment of IT in adult patients. Materials and methods: Eleven patients, 7 men and 4 women with a mean age of 43 years and IT lasting 30 months on average underwent splenectomy. Indication to surgery was failed conservative steroid therapy in all patients. Outcomes of surgery were assessed in 9 patients on average 5 years following the surgery. Results: In all patients, good response to the treatment was obtained (remission). None of the patients continued therapy against the disease and all had platelet count at the follow-up higher than 100 G/L. No serious complications were observed. Conclusion: Splenectomy is an effective and relatively safe, second-line treatment of IT, in cases in which conservative therapy fails.
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