重症合并免疫缺陷婴儿合并SARS-COV-2的造血干细胞移植中的细胞因子风暴:PICU挑战-一例报告

B. Kirthiga, I. Jayakumar, R. Uppuluri, Revathi Raj
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引用次数: 0

摘要

造血干细胞移植(HSCT)是严重联合免疫缺陷(SCID)的唯一潜在治疗选择,因为它们极易感染。免疫受损的儿童感染严重急性呼吸系统综合征冠状病毒2型的风险更高,病毒脱落时间更长,但与成年人不同,其疾病较轻。然而,随着中性粒细胞减少和移植早期,死亡风险增加。由于这些原因,当患者感染严重急性呼吸系统综合征冠状病毒2型时,HSCT通常会推迟。这个决定必须是个性化的,考虑到移植延迟导致疾病进展的风险。我们描述了一例SCID婴儿,其患有多发性危及生命的感染(耐甲氧西林金黄色葡萄球菌肝脓肿、大肠杆菌败血症和播散性卡美氏杆菌Guerinosis),转诊进行HSCT。不幸的是,在单倍体干细胞移植的条件处理开始后,他感染了严重急性呼吸系统综合征冠状病毒2型。预见到新冠肺炎的许多挑战,移植手术在儿科重症监护室(PICU)进行。PICU对移植后细胞因子释放过度综合征和胰腺炎的预期、识别和及时干预使其取得了成功。据我们所知,这是迄今为止最年轻的患有严重急性呼吸系统综合征冠状病毒2型的儿科HSCT,也是印度首例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cytokine storm in HSCT for severe combined immunodeficiency infant with SARS-COV-2: PICU challenges - A case report
Hematopoietic stem cell transplant (HSCT) is the only potentially curative option for severe combined immunodeficiency (SCID) as they are extremely vulnerable to infections. Immunocompromised children are at a higher risk of SARS-CoV-2 infection with prolonged virus shedding, but have a milder disease unlike adults. However, mortality risk increases with neutropenia and in the early transplant period. For these reasons, HSCT is generally deferred when a patient is infected with SARS-COV-2. This decision has to be individualized taking into account the risk of disease progression with delay in transplant. We describe a case of a SCID infant, who had multiple, life-threatening infections (methicillin-resistant Staphylococcus aureus liver abscess, Escherichia coli sepsis, and disseminated Bacillus Calmette-Guerinosis) referred for HSCT. He unfortunately developed SARS-COV-2 infection after the conditioning was commenced for haploidentical stem cell transplant. Foreseeing many challenges with COVID, the transplant was undertaken in the pediatric intensive care unit (PICU) setting. Anticipation, recognition, and timely intervention in the PICU of exaggerated posttransplant cytokine release syndrome and pancreatitis enabled a successful outcome. To the best of our knowledge, this is the youngest pediatric HSCT performed to date with active SARS-COV-2 and first in India.
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