Zhang Yiyun, Ke Yihan, Shi Mengwen, Wang Xiaoying, Yuan Jie, Sun Yu
Department of Otorhinolaryngology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.
Hubei Province Clinical Research Center for Deafness and Vertigo, Wuhan 430022, China.
Diagnostics (Basel). 2025 Aug 13;15(16):2026. doi: 10.3390/diagnostics15162026.
Cytomegalovirus (CMV) represents the most prevalent cause of congenital viral infection in newborns and the leading non-genetic etiology of sensorineural hearing loss (SNHL) in children. Notably, only 10-15% of congenitally infected infants possibly present with classic clinical symptoms at birth, including Small for gestational age, Microcephaly, Petechiae or purpura, Blueberry muffin rash, Jaundice, Hepatomegaly, Splenomegaly and abnormal neurologic signs. In contrast, approximately 90% of infected neonates exhibit no apparent symptoms initially. Current research predominantly focuses on symptomatic cases due to their severe acute presentations and high rates of long-term sequelae (40-60%), including SNHL and neurodevelopmental impairments. However, significant controversy persists regarding the management of asymptomatic infants. Emerging evidence reveals that 8-15% of asymptomatic carriers develop Late-onset Hearing Loss (LOHL) beyond the neonatal period. Additionally, 5-10% may manifest neurodevelopmental abnormalities including mild intellectual disability, learning difficulties, or motor coordination disorders. Crucially, given the substantial population of asymptomatic cCMV cases, these delayed complications account for 30-40% of all cCMV-related long-term morbidity, underscoring their considerable public health impact. This review synthesizes current evidence and controversies regarding cCMV-related SNHL in asymptomatic or mildly symptomatic children, with a focus on screening, diagnostic classification, and antiviral management gaps, to heighten clinical awareness of this underrecognized cause of hearing loss.
巨细胞病毒(CMV)是新生儿先天性病毒感染的最常见原因,也是儿童感音神经性听力损失(SNHL)的主要非遗传病因。值得注意的是,只有10%-15%的先天性感染婴儿在出生时可能出现典型临床症状,包括小于胎龄儿、小头畸形、瘀点或紫癜、蓝莓松饼样皮疹、黄疸、肝肿大、脾肿大和异常神经体征。相比之下,约90%的感染新生儿最初并无明显症状。目前的研究主要集中在有症状的病例上,因为这些病例急性表现严重,长期后遗症发生率高(40%-60%),包括SNHL和神经发育障碍。然而,对于无症状婴儿的管理仍存在重大争议。新出现的证据表明,8%-15%的无症状携带者在新生儿期后会出现迟发性听力损失(LOHL)。此外,5%-10%可能表现出神经发育异常,包括轻度智力残疾、学习困难或运动协调障碍。至关重要的是,鉴于无症状先天性CMV感染病例数量众多,这些延迟并发症占所有先天性CMV感染相关长期发病率的30%-40%,凸显了它们对公共卫生的重大影响。本综述综合了关于无症状或轻度症状儿童中与先天性CMV感染相关的SNHL的现有证据和争议,重点关注筛查、诊断分类和抗病毒治疗方面的差距,以提高对这种未得到充分认识的听力损失原因的临床认识。