Incidence of idiopathic syrinx in pediatric patients diagnosed with VACTERL association.

IF 2.1 3区 医学 Q3 CLINICAL NEUROLOGY
Joanna E Papadakis, Daniel Weber, John S Albanese, Ashley K Birch, Benjamin Warf
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Abstract

Objective: While the association of a syrinx with a tethered spinal cord in the context of VACTERL (vertebral defects [V], imperforate anus or anal atresia [A], cardiac malformations [C], tracheoesophageal defects [T] with or without esophageal atresia [E], renal anomalies [R], and limb defects [L]) association is known, the incidence of idiopathic syrinxes among these patients has not previously been reported. The authors aimed to characterize the incidence of syrinxes and the pattern of congenital anomalies in pediatric patients with VACTERL association, with a specific focus on the presence of idiopathic syrinxes in this population.

Methods: An institutional database was retrospectively queried for all pediatric patients with VACTERL association. Patients were assessed for the presence of a syrinx. Those with no accompanying lesion to which the syrinx could be ascribed were designated idiopathic. Descriptive statistics and qualitative analyses characterized the clinical presentation and outcomes of this population.

Results: The authors retrospectively identified 186 patients between 1993 and 2023 with VACTERL association. Of these 186 patients, 141 (75.8%) had a tethered spinal cord and 44 (23.7%) had a syrinx. Most syrinxes could be ascribed to the presence of a tethered spinal cord and/or Chiari malformation; however, 4 (9.1%) of the 44 appeared idiopathic, suggesting the incidence of idiopathic syrinxes in this patient population may be as high as 2.2% (4/186). Most patients remained asymptomatic aside from a single patient who presented with mild gait dysfunction that resolved over time. All syrinxes were managed conservatively, and all but one decreased or remained stable in size on follow-up imaging.

Conclusions: Although limited, current estimates suggest the general incidence of an idiopathic syrinx is between 5.6 and 8.4 per 100,000 people; these findings in a pediatric cohort with VACTERL association suggest an incidence of 2200 per 100,000 (i.e., 2.2%). Thus, an idiopathic syrinx may be 200-400 times as prevalent in the pediatric VACTERL population.

诊断为VACTERL关联的儿童患者中特发性鼻鸣的发生率。
目的:虽然已知在VACTERL(椎体缺损[V]、肛门闭锁或肛门闭锁[a]、心脏畸形[C]、气管食管缺损[T]伴或不伴食管闭锁[E]、肾脏异常[R]和肢体缺损[L])的情况下,鼻塞与脊髓栓系的关联,但这些患者中特发性鼻塞的发生率此前未见报道。作者旨在描述与VACTERL相关的儿童患者中鼻窦的发生率和先天性异常的模式,特别关注这一人群中特发性鼻窦的存在。方法:回顾性查询机构数据库中所有与VACTERL相关的儿科患者。评估患者是否存在鸣管。那些没有伴随病变的鼻鸣可归因于被指定为特发性。描述性统计和定性分析描述了该人群的临床表现和结果。结果:作者回顾性地确定了186例1993年至2023年间存在VACTERL关联的患者。在这186例患者中,141例(75.8%)有脊髓栓系,44例(23.7%)有注射器。大多数鼻鸣可归因于脊髓栓系和/或Chiari畸形的存在;但44例中有4例(9.1%)为特发性,提示特发性注射器在该患者群体中的发病率可能高达2.2%(4/186)。除了一名患者表现出轻微的步态功能障碍,随着时间的推移,大多数患者仍无症状。所有的注射器都进行了保守的管理,在随访成像中,除一个外,所有的注射器都缩小或保持稳定。结论:虽然有限,但目前的估计表明,特发性鼻炎的一般发病率在每10万人5.6至8.4人之间;在与VACTERL相关的儿科队列中,这些发现表明发病率为2200 / 10万(即2.2%)。因此,在儿童VACTERL人群中,特发性鼻鸣的发生率可能是其200-400倍。
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来源期刊
Journal of neurosurgery. Pediatrics
Journal of neurosurgery. Pediatrics 医学-临床神经学
CiteScore
3.40
自引率
10.50%
发文量
307
审稿时长
2 months
期刊介绍: Information not localiced
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