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一名新生儿多系统炎症综合征患者的主-髂动脉血栓形成和肾动脉狭窄:病例报告及文献复习

Aortoiliac arterial thrombosis and renal artery stenosis in a patient with neonatal multisystem inflammatory syndrome: a case report and review of literature.

作者信息

Lertkovit Oranooj, Isaranimitkul Daranee, Pornrattanarungsri Suwanna, Sirimongkolchaiyakul Ornatcha, Tangcheewinsirikul Sirikarn, Saengrat Pichada

机构信息

Division of Hematology and Oncology, Department of Pediatrics, Faculty of Medicine Vajira Hospital, Navamindradhiraj University, Bangkok, Thailand.

Division of Cardiology, Department of Pediatrics, Faculty of Medicine Vajira Hospital, Navamindradhiraj University, Bangkok, Thailand.

出版信息

Front Pediatr. 2025 Jan 10;12:1474192. doi: 10.3389/fped.2024.1474192. eCollection 2024.

Abstract

BACKGROUND

Multisystem inflammatory syndrome in neonates (MIS-N) is a rare condition thought to be associated with prenatal exposure to maternal severe acute respiratory syndrome coronavirus 2 infection. This immune-mediated hyperinflammation has been described in neonates with multiorgan dysfunction, including cardiopulmonary, encephalopathy, coagulopathy, and vascular complications. However, renovascular complications in MIS-N are rare. Here, we present a case with aortoiliac arterial thrombosis and renovascular stenosis in MIS-N.

CASE PRESENTATION

A 2-day-old, full-term, male neonate presented with fever, respiratory failure, hypotensive shock, and elevated inflammatory markers. He was transferred to our neonatal intensive care unit for comprehensive monitoring and treated with antibiotics for early-onset neonatal sepsis. However, his clinical condition deteriorated. His mother reported a history of severe acute respiratory syndrome coronavirus 2 infection during the late second trimester. He was diagnosed with MIS-N based on the fulfillment of the diagnostic criteria for multiorgan involvement and laboratory findings. He responded to intravenous immunoglobulin, corticosteroids, and aspirin. However, he later developed significant hypertension, which was associated with aortoiliac arterial thrombosis and right renal artery stenosis. An elevated ferritin level was observed. The ongoing inflammatory condition was considered, and corticosteroids were restarted along with treatment for documented thrombosis using enoxaparin and aspirin. After treatment, partial resolution of aortoiliac arterial thrombus was observed. However, narrowing of the proximal part of right renal artery persisted, and blood pressure remained difficult to control, requiring multiple antihypertensive agents. Finally, the patient underwent percutaneous transluminal balloon angioplasty to control hypertension.

CONCLUSION

Our case revealed the clinical course of MIS-N with renovascular complications. The condition's hyperinflammatory state may have played a pathophysiological role in the development of this life-threatening complication. Although there is an increased risk of bleeding in MIS-N, thromboprophylaxis should be considered in high-risk patients. An early multidisciplinary approach is recommended to ensure prompt diagnosis and improve outcomes.

摘要

背景

新生儿多系统炎症综合征(MIS-N)是一种罕见疾病,被认为与产前暴露于母亲严重急性呼吸综合征冠状病毒2感染有关。这种免疫介导的过度炎症已在患有多器官功能障碍的新生儿中被描述,包括心肺、脑病、凝血病和血管并发症。然而,MIS-N中的肾血管并发症很少见。在此,我们报告一例MIS-N合并主髂动脉血栓形成和肾血管狭窄的病例。

病例介绍

一名2日龄、足月男婴,出现发热、呼吸衰竭、低血压休克和炎症标志物升高。他被转入我们的新生儿重症监护病房进行全面监测,并接受抗生素治疗以治疗早发性新生儿败血症。然而,他的临床状况恶化。他的母亲报告在孕中期晚期有严重急性呼吸综合征冠状病毒2感染史。根据多器官受累的诊断标准和实验室检查结果,他被诊断为MIS-N。他对静脉注射免疫球蛋白、皮质类固醇和阿司匹林有反应。然而,他后来出现了严重高血压,这与主髂动脉血栓形成和右肾动脉狭窄有关。观察到铁蛋白水平升高。考虑到持续的炎症状态,重新开始使用皮质类固醇,并使用依诺肝素和阿司匹林治疗已记录的血栓形成。治疗后,观察到主髂动脉血栓部分溶解。然而,右肾动脉近端狭窄仍然存在,血压仍然难以控制,需要多种抗高血压药物。最后,患者接受了经皮腔内球囊血管成形术以控制高血压。

结论

我们的病例揭示了MIS-N合并肾血管并发症的临床过程。该疾病的过度炎症状态可能在这种危及生命的并发症的发生发展中起到了病理生理作用。尽管MIS-N有出血风险增加,但对于高危患者应考虑进行血栓预防。建议采用早期多学科方法以确保及时诊断并改善预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc85/11757169/7c9e96ca526b/fped-12-1474192-g001.jpg

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