非人类免疫缺陷病毒部分免疫抑制患者的典型巨细胞病毒视网膜炎:病例系列

Alok Pratap Singh, Archit Pandharipande, Anubha Ojha, Sanjeev Yadav, M. R. Behera, Kumudini Sharma
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引用次数: 0

摘要

本研究旨在分析人类免疫缺陷病毒(HIV)阴性、部分免疫抑制的患者发生严重、典型巨细胞病毒(CMV)视网膜炎(CMVR)的情况,强调 CMVR 临床表现的不一致性,并评估联合抗 CMV 治疗在此类患者治疗中的作用。 本研究是一项回顾性、观察性、非比较性病例系列研究。我们对连续的 HIV 阴性成人 CMVR 患者进行了检查和治疗。在治疗前和治疗后进行了基于血液的 CMV 基因组聚合酶链反应分析。我们还收集了基础系统疾病的详细信息。患者同时接受了玻璃体内和静脉注射(IV)抗 CMV 治疗。随访期为 1 年。所有结果均为回顾性结果。 在艾滋病毒阴性患者中,共有 4 名连续患者的 6 只眼睛被确诊为 CMVR。患者仅有部分免疫抑制,但表现出典型的严重暴发性 CMVR。患者共接受了两次玻璃体内注射更昔洛韦,并静脉注射更昔洛韦/口服缬更昔洛韦。所有患者都在治疗期内实现了完全愈合。 与一般看法不同的是,典型的、暴发性、严重的 CMVR 可能会发生在免疫功能受限的患者身上。我们的报告强调了部分免疫抑制患者 CMVR 临床表现的不一致性。患者的免疫状态似乎是决定 CMVR 临床表型的一个重要因素。玻璃体内和静脉注射更昔洛韦/口服缬更昔洛韦联合疗法成功治疗了这组 CMVR 患者。
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Typical cytomegalovirus retinitis in non-human immunodeficiency virus partially immunosuppressed patients: A case series
The purpose of the study was to analyze the occurrence of severe, typical cytomegalovirus (CMV) retinitis (CMVR) in human immunodeficiency virus (HIV) negative, partially immunosuppressed patients, emphasizing inconsistency in the clinical presentation of CMVR and to evaluate the role of combined anti-CMV therapy in the management of such patients. This study was a retrospective, observational, noncomparative case series. We examined and treated consecutive HIV-negative adult patients of CMVR. Blood-based polymerase chain reaction analysis of the CMV genome was done pre- and posttreatment. Details of underlying systemic conditions were collected. Patients were treated with simultaneous administration of intravitreal and intravenous (IV) anti-CMV therapy. Follow-up was for 1 year. All outcomes were determined retrospectively. A total of 6 eyes of 4 consecutive patients were diagnosed with CMVR in HIV-negative patients. Patients were only partially immunosuppressed but revealed typical severe fulminant CMVR. Patients received a total of 2 intravitreal ganciclovir injections, and IV ganciclovir/oral valganciclovir was given. All patients achieved complete healing within the treatment period. As opposed to the general perception, typical, fulminant, severe CMVR may occur in patients with limited immune dysfunction. Our report underlines this inconsistency in the clinical presentation of CMVR in partially immunosuppressed patients. The immune status of the patients seems a significant factor in determining the clinical phenotypes of CMVR. Combined intravitreal and IV ganciclovir/oral valganciclovir therapy was successful in treating this group of CMVR patients.
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审稿时长
27 weeks
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