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新生儿 MIS-C:应对细胞因子风暴。

Neonatal MIS-C: Managing the Cytokine Storm.

机构信息

Fortis Hospital, Anandapur, Kolkata, India

Fortis Hospital, Anandapur, Kolkata, India.

出版信息

Pediatrics. 2021 Nov;148(5). doi: 10.1542/peds.2020-042093. Epub 2021 Aug 25.

Abstract

A term infant girl with uneventful antenatal history had an erythematous rash followed by fever from day 8. She was diagnosed with late-onset sepsis and was treated accordingly. She received immunoglobulin for persistent thrombocytopenia, after which there was transient improvement. The patient was transferred to our hospital on day 25 after recurrence of fever, watery diarrhea, and a generalized maculopapular rash. On admission, she had tachycardia, tachypnoea, anemia, thrombocytopenia, hypoalbuminemia, and generalized edema. Reverse transcriptase-polymerase chain reaction results for coronavirus disease 2019 (COVID-19) was positive. Within 12 hours of admission, she developed cardiogenic shock with pulmonary edema and needed invasive ventilation. Echocardiography revealed ejection fraction of 40% with mild pericardial effusion. N-terminal pro-brain natriuretic peptide was 33000 g/L, D-dimer 16500 µg/L, and ferritin 16000 ng/mL. Methylprednisolone, immunoglobulin, and enoxaparin was started, with a diagnosis of multisystem inflammatory syndrome in children, associated with COVID-19. She developed seizures, pulmonary hemorrhage, and cardiac arrest the following day, along with acute kidney injury. She was extubated after 5 days. Steroid was stopped after 5 days because she developed hypertension and echocardiography had normalized. Five days after extubation, she again developed respiratory distress and was ventilated again for 2 days. Echocardiography revealed moderate left ventricular dysfunction, along with secondary elevation of ferritin. Methylprednisolone was restarted and continued for 5 days followed by tapering dose of oral prednisolone, on which she was finally discharged. Although mild myocarditis with COVID-19 has been reported, multisystem inflammatory syndrome in children in a newborn with refractory myocarditis, along with gastrointestinal and renal manifestations, is a rare entity. Dermatologic manifestation of neonatal COVID-19 is also unique.

摘要

一名无特殊病史的足月女婴,在生后第 8 天出现红斑性皮疹,继而发热。她被诊断为晚发型败血症,并接受了相应的治疗。由于持续性血小板减少症,她接受了免疫球蛋白治疗,之后血小板短暂性升高。入院第 25 天,患儿因发热、水样腹泻和全身性斑丘疹复发,转入我院。入院时,患儿心动过速、呼吸急促、贫血、血小板减少、低白蛋白血症和全身性水肿。新冠病毒 2019 型(COVID-19)逆转录-聚合酶链反应结果为阳性。入院后 12 小时内,患儿出现心源性休克伴肺水肿,需要进行有创通气。超声心动图显示射血分数为 40%,伴有轻度心包积液。N 端脑利钠肽前体为 33000 g/L,D-二聚体为 16500 µg/L,铁蛋白为 16000 ng/mL。患儿开始接受甲泼尼龙、免疫球蛋白和依诺肝素治疗,诊断为 COVID-19 相关儿童多系统炎症综合征。第 2 天,患儿出现惊厥、肺出血和心脏骤停,并伴有急性肾损伤。入院后第 5 天患儿拔管。入院后第 5 天,患儿因出现高血压而停用激素,此时超声心动图已恢复正常。拔管后 5 天,患儿再次出现呼吸窘迫,再次插管通气 2 天。超声心动图显示中度左心室功能障碍,铁蛋白再次升高。患儿重新开始使用甲泼尼龙,连续使用 5 天后,逐渐减少口服泼尼松剂量,最终患儿出院。虽然 COVID-19 相关轻度心肌炎已有报道,但新生儿伴难治性心肌炎、胃肠道和肾脏表现的儿童多系统炎症综合征是一种罕见疾病。新生儿 COVID-19 的皮肤表现也很独特。

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