Kumwenda Tapiwa, Hodson Daniel Z, Rambiki Kelvin, Rambiki Ethel, Fedoriw Yuri, Tymchuk Christopher, Wallrauch Claudia, Heller Tom, Painschab Matthew S
Lighthouse Clinic Trust, Kamuzu Central Hospital Area, 33 Mzimba Street, P.O. Box 106, Lilongwe, Malawi.
Division of Internal Medicine-Pediatrics, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, USA.
Trop Med Infect Dis. 2024 Dec 16;9(12):307. doi: 10.3390/tropicalmed9120307.
Kaposi sarcoma-associated herpes virus (KSHV), also known as human herpes virus 8 (HHV-8), is the primary etiologic cause of Kaposi sarcoma (KS) and KSHV Inflammatory Cytokine Syndrome (KICS). Patients with KICS demonstrate symptoms of systemic inflammation, high KSHV viral load, elevation of inflammatory markers, and increased mortality. Management requires rapid diagnosis, treatment of underlying HIV, direct treatment of KS, and addressing the hyperimmune response. While a case definition based on clinical presentation, imaging findings, laboratory values, KSHV viral load, and lymph-node biopsy has been proposed, some of the required investigations are frequently unavailable in resource-constrained settings. Due to these challenges, KICS likely remains underdiagnosed and undertreated in these settings. We report a case of a 19-year-old woman living with HIV, and intermittent adherence to her ART, who presented with hypotension and acute hypoxemic respiratory failure. She was found to have high KSHV and HIV viral loads, low CD4 count, anemia, thrombocytopenia, hypoalbuminemia, and elevated inflammatory markers. On bedside ultrasound, she was found to have bilateral pleural effusions, ascites, an enlarged spleen, and hyperechoic splenic lesions. The diagnosis of KICS was made based on this constellation of findings. Weighing the risk and benefits of steroid administration in KS patients, the patient was successfully treated by the continuation of ART and the initiation of paclitaxel chemotherapy and steroids. We propose an adapted case definition relevant to the resource-constrained context. Due to the dual burden of KSHV and HIV in sub-Saharan Africa, additional cases of KICS are likely, and this syndrome will contribute to the burden of early mortality in newly diagnosed HIV patients. Addressing the diagnostic and therapeutic challenges of KICS must be a part of the overall management of the HIV pandemic.
卡波西肉瘤相关疱疹病毒(KSHV),也称为人类疱疹病毒8型(HHV-8),是卡波西肉瘤(KS)和KSHV炎性细胞因子综合征(KICS)的主要病因。KICS患者表现出全身炎症症状、高KSHV病毒载量、炎症标志物升高以及死亡率增加。治疗需要快速诊断、治疗潜在的HIV、直接治疗KS以及应对高免疫反应。虽然已经提出了基于临床表现、影像学检查结果、实验室值、KSHV病毒载量和淋巴结活检的病例定义,但在资源有限的环境中,一些所需的检查往往无法进行。由于这些挑战,KICS在这些环境中可能仍然诊断不足和治疗不足。我们报告了一例19岁感染HIV的女性病例,她间歇性坚持抗逆转录病毒治疗(ART),出现低血压和急性低氧性呼吸衰竭。她被发现KSHV和HIV病毒载量高、CD4计数低、贫血、血小板减少、低白蛋白血症以及炎症标志物升高。床边超声检查发现她有双侧胸腔积液、腹水、脾脏肿大和脾脏高回声病变。基于这一系列检查结果做出了KICS的诊断。权衡了KS患者使用类固醇的风险和益处后,通过继续ART以及开始使用紫杉醇化疗和类固醇,该患者得到了成功治疗。我们提出了一个适用于资源有限环境的病例定义。由于撒哈拉以南非洲地区KSHV和HIV的双重负担,可能会出现更多KICS病例,并且这种综合征将加重新诊断HIV患者的早期死亡负担。应对KICS的诊断和治疗挑战必须成为HIV大流行总体管理的一部分。