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血管紧张素II 1型受体阻滞剂诱发的免疫性血小板减少症:一例报告

Angiotensin II type 1 receptor blocker-induced immune thrombocytopenia: a case report.

作者信息

Patel Dhiren K, Bilkha Nikhil, Schnee David

机构信息

VA Boston Healthcare System, 940 Belmont Street, Brockton, MA 02301, USA.

出版信息

J Med Case Rep. 2013 Jul 15;7:183. doi: 10.1186/1752-1947-7-183.

Abstract

INTRODUCTION

The development of thrombocytopenia after a dose increase in losartan and subsequently after switching the patient to valsartan is reported.

CASE PRESENTATION

A 61-year-old Caucasian man presented with epistaxis and gingival bleeding of three weeks duration. Laboratory evaluation revealed a hemoglobin level of 144g/L, a leukocyte count of 16.2×109 cells/L (72.51% neutrophils, 20.1% lymphocytes, 6.8% monocytes, 0.4% eosinophils, 0.2% bands), and a platelet count of 15.0×109 cells/L. Flow cytometry of his peripheral blood showed normal CD4:CD8 ratio and no evidence of any lymphoproliferative disorder. A peripheral smear showed decreased platelets with a few areas of clumping. Four weeks before presentation to the emergency room, his losartan dose was increased to 100mg once daily due to continuously elevated blood pressure readings. He had been maintained on losartan 50mg once daily for five years and previous routine laboratory measurements revealed a baseline platelet count of 248.0×109 cells/L.The patient began receiving an oral prednisone taper and his platelet count returned to a stable value of >200×109 cells/L. Because there was no other probable cause, he was thought to have developed immune thrombocytopenia from the increased losartan dose. Losartan was discontinued and one week later he was switched to valsartan 160mg once daily.Forty-seven days after starting valsartan, the patient presented once again to the emergency room with intermittent epistaxis and gingival bleeding while brushing his teeth of two weeks duration. Laboratory measurement revealed a platelet count of 37×109 cells/L. Valsartan was held and another prednisone taper was initiated. The patient's platelet count recovered upon valsartan discontinuation and in four weeks, his platelet count improved to 214×109 cells/L.

CONCLUSIONS

A 61-year-old Caucasian man developed immune thrombocytopenia after an increase in losartan dose and developed immune thrombocytopenia again after he was switched to valsartan.

摘要

引言

据报道,一名患者在氯沙坦剂量增加后出现血小板减少,随后在换用缬沙坦后再次出现血小板减少。

病例介绍

一名61岁的白种男性出现鼻出血和牙龈出血,持续三周。实验室检查显示血红蛋白水平为144g/L,白细胞计数为16.2×10⁹个/升(中性粒细胞72.51%,淋巴细胞20.1%,单核细胞6.8%,嗜酸性粒细胞0.4%,杆状核细胞0.2%),血小板计数为15.0×10⁹个/升。其外周血流式细胞术显示CD4:CD8比值正常,无任何淋巴增殖性疾病的迹象。外周血涂片显示血小板减少,有少量聚集区域。在到急诊室就诊前四周,由于血压持续升高,他的氯沙坦剂量增加至每日100mg。他曾每日服用50mg氯沙坦五年,之前的常规实验室检查显示基线血小板计数为248.0×10⁹个/升。患者开始接受口服泼尼松逐渐减量治疗,其血小板计数恢复至>200×10⁹个/升的稳定值。由于没有其他可能的原因,认为他因氯沙坦剂量增加而发生了免疫性血小板减少。停用氯沙坦,一周后换用每日一次160mg的缬沙坦。开始使用缬沙坦47天后,患者再次因持续两周的间歇性鼻出血和刷牙时牙龈出血到急诊室就诊。实验室检查显示血小板计数为37×10⁹个/升。停用缬沙坦并再次开始泼尼松逐渐减量治疗。停用缬沙坦后患者的血小板计数恢复,四周内,其血小板计数升至214×10⁹个/升。

结论

一名61岁的白种男性在氯沙坦剂量增加后发生免疫性血小板减少,换用缬沙坦后再次发生免疫性血小板减少。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/574b/3751637/5ddcb58d7fc9/1752-1947-7-183-1.jpg

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