巨细胞病毒感染相关免疫性血小板减少症1例报告

Rafael Siqueira Athayde Lima, Rodrigo Fonseca Halley, Tássia Ívila Freitas de Almeida, Aglaêrton Silva Pinheiro, Maiza Colares De Carvalho
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摘要

免疫性血小板减少症(ITP)是一种获得性的血小板减少症,其特征是存在针对血小板的自身抗体。它可能是主要或次要的几种情况。我们提出的情况下,一个63岁的妇女诊断为免疫性血小板减少难治性常规治疗。在检查ITP的继发原因后,诊断为急性巨细胞病毒(CMV)感染。患者接受更昔洛韦治疗,血小板计数恢复正常。在某些难治性ITP病例中,cmv相关的免疫性血小板减少症应该被考虑。如果诊断为急性巨细胞病毒感染继发的ITP,则应考虑使用更昔洛韦进行特异性抗病毒治疗。在这些情况下,免疫抑制剂,如类固醇,可能使ITP恶化,应尽可能迅速减少或停用。
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Cytomegalovirus Infection-related Immune Thrombocytopenia: A Case Report
Immune thrombocytopenia (ITP) is an acquired cause of thrombocytopenia characterized by the presence of autoantibodies against platelets. It may be primary or secondary to several conditions. We present the case of a 63-year-old woman with a diagnosis of immune thrombocytopenia refractory to conventional therapy. After she was tested for secondary causes of ITP, a diagnosis of acute cytomegalovirus (CMV) infection was made. She was treated with ganciclovir and presented normalization of platelet count. CMV-related Immune Thrombocytopenia should always be considered in certain cases of refractory ITP. If the diagnosis of ITP secondary to acute CMV infection is made, specific antiviral therapy with ganciclovir should be considered. In these cases, immunosuppressive agents, such as steroids, may worsen the ITP and should be tapered or withdrawn as rapidly as feasible.
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