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肝移植患者的免疫性血小板减少性紫癜

Immune thrombocytopenic purpura in a liver transplant patient.

作者信息

Ünlüsoy Aksu Aysel, Eğritaş Gürkan Ödül, Sarı Sinan, Yenicesu İdil, Dalgıç Buket

机构信息

Department of Pediatric Gastroenterology, Hepatology and Nutrition, Gazi University, Ankara, Turkey.

出版信息

Exp Clin Transplant. 2014 Mar;12 Suppl 1:175-7.

Abstract

Thrombocytopenia is common during the early posttransplant period. Most cases are mild and recover in 1 month. Occasionally, severe thrombocytopenia may occur in the late posttransplant period. We report a 10-year-old boy with severe thrombocytopenia 3.5 years after liver transplant. We exclude secondary causes of thrombocytopenia. Bone marrow aspiration findings and treatment response were suggestive for immune thrombocytopenic purpura. The patient was treated with intravenous immunoglobulin at thrombocytopenia periods successfully. We continued tacrolimus, but preferred a reduced dose. In conclusion, immune thrombocytopenic purpura should be borne in mind as a reason of late onset, severe thrombocytopenia after liver transplant.

摘要

血小板减少症在移植后早期很常见。大多数病例症状较轻,1个月内可恢复。偶尔,严重的血小板减少症可能发生在移植后期。我们报告了一名10岁男孩,在肝移植3.5年后出现严重血小板减少症。我们排除了血小板减少症的继发原因。骨髓穿刺结果和治疗反应提示为免疫性血小板减少性紫癜。患者在血小板减少期成功接受了静脉注射免疫球蛋白治疗。我们继续使用他克莫司,但选择了较低剂量。总之,免疫性血小板减少性紫癜应被视为肝移植后迟发性、严重血小板减少症的一个原因。

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