Tomşa Nicoleta-Ana, Meliţ Lorena Elena, Bucur Gabriela, Văsieșiu Anca-Meda, Mărginean Cristina Oana
Pediatrics Clinic, Emergency Clinical County Hospital, 540140 Targu Mures, Romania.
Department of Pediatrics 1, George Emil Palade University of Medicine, Pharmacy, Science and Technology of Targu Mures, 540136 Targu Mures, Romania.
Children (Basel). 2024 Aug 19;11(8):1010. doi: 10.3390/children11081010.
Cytomegalovirus (CMV) infection is present in a latent state in 70-90% of the immunocompetent population, and its reactivation might be triggered by inflammatory conditions such as post-COVID multisystem inflammatory syndrome (MIS-C) or by immunosuppression induced by steroids. The aim of this paper was to highlight the unexpected complications associated with SARS-CoV-2 infection that require a complex clinical approach for accurate diagnosis.
We present the case of a 4-year-old male patient who, during an initially favorable course of PIMS, experienced symptoms of respiratory failure.
The patient initially presented with clinical and paraclinical signs of PIMS with cardiac involvement, for which high-dose corticosteroid therapy was initiated, followed by gradual tapering, along with immunoglobulins, anticoagulants, antiplatelet agents, and symptomatic treatment. After 10 days of favorable progress, the patient's general condition deteriorated, showing tachypnea, desaturation, and a ground-glass appearance on thoracic CT. Negative inflammatory markers and favorable cardiac lesion evolution ruled out MIS-C relapse. The presence of anti-CMV IgM antibodies and viral DNA in the blood confirmed acute CMV infection, likely triggered by prior severe-acute-respiratory-syndrome-related coronavirus 2 (SARS-CoV-2) infection and secondary immunosuppression due to steroids. Non-specific immunomodulatory treatment was initiated but led to worsening of pulmonary lesions, prompting the initiation of specific antiviral treatment with ganciclovir, resulting in rapid clinical and imaging improvement.
CMV infection can be reactivated by immunosuppression induced by corticosteroid therapy for MIS-C and may require specific etiological treatment.
巨细胞病毒(CMV)感染以潜伏状态存在于70-90%的免疫功能正常人群中,其重新激活可能由炎症状态触发,如新冠后多系统炎症综合征(MIS-C),或由类固醇诱导的免疫抑制引发。本文旨在强调与严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染相关的意外并发症,这些并发症需要复杂的临床方法来进行准确诊断。
我们报告一例4岁男性患者的病例,该患者在最初PIMS病情良好的过程中出现了呼吸衰竭症状。
患者最初表现出PIMS伴心脏受累的临床和辅助检查体征,为此开始了高剂量皮质类固醇治疗,随后逐渐减量,同时使用免疫球蛋白、抗凝剂、抗血小板药物及对症治疗。经过10天的良好进展后,患者的一般状况恶化,出现呼吸急促、血氧饱和度下降,胸部CT显示磨玻璃样改变。炎症指标阴性及心脏病变进展良好排除了MIS-C复发。血液中抗CMV IgM抗体和病毒DNA的存在证实了急性CMV感染,可能是由先前的SARS-CoV-2感染及类固醇导致的继发性免疫抑制引发。开始了非特异性免疫调节治疗,但导致肺部病变恶化,促使开始使用更昔洛韦进行特异性抗病毒治疗,从而使临床和影像学迅速改善。
CMV感染可因MIS-C的皮质类固醇治疗诱导的免疫抑制而重新激活,可能需要特异性病因治疗。