Manalac Ahmira Jade E, Lytle Erika, Khan Liaqat, George Koshy
Pediatrics and Neonatology, Edward Via College of Osteopathic Medicine, Monroe, USA.
Pediatrics, Edward Via College of Osteopathic Medicine, Monroe, USA.
Cureus. 2024 Jun 3;16(6):e61576. doi: 10.7759/cureus.61576. eCollection 2024 Jun.
This case report investigates the management of a 24-week-old neonate with congenital cytomegalovirus (CMV) infection and its sequelae, including severe intrauterine growth restriction, thrombocytopenia, and brain anomalies, ultimately progressing to lissencephaly. The diagnostic challenges included delayed clinical suspicion of congenital CMV, which was not identified until after delivery through CMV DNA polymerase chain reaction, and differentiating its symptoms from other potential causes of the neonate's condition. Aggressive interventions included antibiotics, antiviral therapy with ganciclovir, and supportive measures such as intubation, CPR, respiratory support, blood transfusions, and management of coagulopathy. Despite these efforts, the patient deteriorated due to progressive hypoperfusion, hypoxemic cardiorespiratory failure, and disseminated intravascular coagulopathy. Due to the poor prognosis and extent of multiorgan damage, support was withdrawn per parental consent. This case highlights the complications encountered when managing an advanced-stage neonatal CMV infection and emphasizes the importance of a multidisciplinary and holistic approach to guide diagnosis and treatment.
本病例报告探讨了一名24周大先天性巨细胞病毒(CMV)感染新生儿及其后遗症的治疗情况,这些后遗症包括严重的宫内生长受限、血小板减少症和脑异常,最终发展为无脑回畸形。诊断面临的挑战包括先天性CMV的临床怀疑延迟,直到分娩后通过CMV DNA聚合酶链反应才得以确诊,以及将其症状与新生儿病情的其他潜在病因相区分。积极的干预措施包括使用抗生素、更昔洛韦抗病毒治疗,以及诸如插管、心肺复苏、呼吸支持、输血和凝血病管理等支持措施。尽管采取了这些措施,患者仍因进行性低灌注、低氧性心肺衰竭和弥散性血管内凝血而病情恶化。由于预后不良和多器官损伤程度严重,经家长同意停止了支持治疗。本病例突出了晚期新生儿CMV感染治疗中遇到的并发症,并强调了多学科整体方法在指导诊断和治疗方面的重要性。