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成功治疗一名 HIV 阳性患者的卡波西肉瘤免疫重建炎症综合征。

Successful treatment of an HIV-positive patient with unmasking Kaposi's sarcoma immune reconstitution inflammatory syndrome.

机构信息

School of Dentistry and Oral Health, Griffith University, Queensland, Australia.

出版信息

J Clin Virol. 2013 Jul;57(3):282-5. doi: 10.1016/j.jcv.2013.03.005. Epub 2013 Apr 8.

DOI:10.1016/j.jcv.2013.03.005
PMID:23578530
Abstract

BACKGROUND

Kaposi's sarcoma (KS) continues to be the most common human immunodeficiency virus (HIV)-associated neoplasm with considerable morbidity and mortality. While lesions normally resolve upon initiation of antiretroviral therapy (ART), recrudescence or unmasking of KS lesions may occur as part of immune reconstitution inflammatory syndrome (IRIS). Treatment of unmasking KS-IRIS is not yet standardised.

OBJECTIVES

To report the successful treatment of a patient with fulminating mucocutaneous unmasking KS-IRIS by maintaining ART and using pegylated liposomal doxorubicin (PLD).

STUDY DESIGN

The patient, a 39-year-old HIV-positive male with no previous history of KS presented with a 2-week history of cutaneous and oral KS lesions that had disseminated rapidly over the preceding 4 days. The KS lesions appeared 8 weeks after recommencing ART. At the time of this presentation, his CD4+ count was 742 cells/mm(3) with a HIV viral load <400 copies/ml. ART was maintained and treatment with PLD commenced.

RESULTS

Despite the rapid dissemination of KS lesions, virus was undetectable in plasma. In a late-stage vasoformative lesion, immunohistochemistry (IHC) for human herpesvirus 8 (HHV-8) antigen was light and diffuse, with stippled deposits within endothelial cell nuclei. Virus extracted from the lesion was HHV-8 subtype A. The patient responded well to PLD, relapsed a year later, but after further PLD, has remained well for the following 5 years.

CONCLUSION

Despite the absence of HHV-8 viraemia, this is clearly a case of unmasking KS-IRIS. It demonstrates that this entity can be successfully treated by maintaining ART and administering PLD.

摘要

背景

卡波西肉瘤(KS)仍然是最常见的人类免疫缺陷病毒(HIV)相关肿瘤,具有相当高的发病率和死亡率。虽然在开始抗逆转录病毒治疗(ART)后,病变通常会消退,但 KS 病变的复发或显露可能是免疫重建炎症综合征(IRIS)的一部分。未掩盖 KS-IRIS 的治疗尚未标准化。

目的

报告一例通过维持 ART 和使用聚乙二醇化脂质体多柔比星(PLD)成功治疗爆发性黏膜未掩盖 KS-IRIS 的患者。

研究设计

患者为一名 39 岁 HIV 阳性男性,以前没有 KS 病史,出现了 2 周的皮肤和口腔 KS 病变,这些病变在过去 4 天内迅速扩散。KS 病变在重新开始 ART 8 周后出现。在本次就诊时,他的 CD4+计数为 742 个细胞/mm3,HIV 病毒载量<400 拷贝/ml。维持 ART,并开始使用 PLD 治疗。

结果

尽管 KS 病变迅速扩散,但血浆中无法检测到病毒。在晚期血管形成病变中,人类疱疹病毒 8(HHV-8)抗原的免疫组化(IHC)呈轻度弥漫性,内皮细胞核内有点状沉积物。从病变中提取的病毒是 HHV-8 亚型 A。患者对 PLD 反应良好,一年后复发,但进一步使用 PLD 后,在接下来的 5 年中一直保持良好。

结论

尽管没有 HHV-8 病毒血症,但这显然是一个未掩盖的 KS-IRIS 病例。它表明,通过维持 ART 和给予 PLD,可以成功治疗这种疾病。

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