Departments of Translational Medical Sciences, Pediatric Pulmonology, Federico II University, Naples, Italy.
Departments of Advanced Biomedical Sciences, Radiology Unit, Federico II University, Naples, Italy.
Ital J Pediatr. 2023 Jul 22;49(1):92. doi: 10.1186/s13052-023-01473-0.
Tracheal compression (TC) due to vascular anomalies is an uncommon, but potentially serious cause of chronic respiratory disease in childhood. Vascular slings are congenital malformations resulting from abnormal development of the great vessels; in this group of disorders the most prevalent entity is the aberrant innominate artery (AIA). Here we provide a report on diagnosis and treatment of AIA in nine children with unexplained chronic respiratory symptoms. We describe the cases, perform a literature review, and provide a discussion on the diagnostic workup and treatment that can help manage AIA.
Clinical history, diagnostic procedures and treatment before and after the AIA diagnosis were retrospectively reviewed in nine children (5 boys and 4 girls), who were referred for recurrent-to-chronic respiratory manifestations over 10 years (2012-2022). We performed a comprehensive report on the ongoing clinical course and treatment as well as an electronic literature search on the topic.
Diagnoses at referral, before AIA was identified, were chronic dry barking cough associated with recurrent pneumonia (n = 8, 89%), lobar/segmental atelectasis (n = 3, 33%), atopic/non atopic asthma (n = 3, 33%); pneumomediastinum with subcutaneous emphysema complicated the clinical course in one case. When referred to our Unit, all patients had been previously treated with repeated antibiotic courses (n = 9, 100%), alone (n = 6, 67%) or combined with prolonged antiasthma medications (n = 3, 33%) and/or daily chest physiotherapy (n = 2, 22%), but reported only partial clinical benefit. Median ages at symptom onset and at AIA diagnosis were 1.5 [0.08-13] and 6 [4-14] years, respectively, with a relevant delay in the definitive diagnosis (4.5 years). Tracheal stenosis at computed tomography (CT) was ≥ 51% in 4/9 cases and ≤ 50% in the remaining 5 subjects. Airway endoscopy was performed in 4 cases with CT evidence of tracheal stenosis ≥ 51% and confirmed CT findings. In these 4 cases, the decision of surgery was made based on endoscopy and CT findings combined with persistence of clinical symptoms despite medical treatment. The remaining 5 children were managed conservatively.
TC caused by AIA may be responsible for unexplained chronic respiratory disease in childhood. Early diagnosis of AIA can decrease the use of expensive investigations or unsuccessful treatments, reduce disease morbidity, and accelerate the path toward a proper treatment.
由于血管异常引起的气管压迫(TC)是儿童慢性呼吸道疾病的一种不常见但潜在严重的原因。血管吊带是由大血管异常发育引起的先天性畸形;在这组疾病中,最常见的实体是异常无名动脉(AIA)。在这里,我们报告了 9 例因不明原因慢性呼吸道症状而患有 AIA 的儿童的诊断和治疗情况。我们描述了这些病例,进行了文献复习,并讨论了有助于管理 AIA 的诊断和治疗。
对 9 名(5 名男孩和 4 名女孩)因反复至慢性呼吸道表现而在 10 年内(2012-2022 年)转诊的儿童的临床病史、诊断程序和 AIA 诊断前后的治疗进行回顾性分析。我们对正在进行的临床病程和治疗进行了全面报告,并对该主题进行了电子文献检索。
转诊时的诊断,在识别出 AIA 之前,为慢性干性吠叫咳嗽伴反复肺炎(n=8,89%)、肺叶/节段性肺不张(n=3,33%)、特应性/非特应性哮喘(n=3,33%);一例病例并发纵隔气肿伴皮下气肿,使临床病程复杂化。当转至我们科室时,所有患者均曾接受过反复抗生素治疗(n=9,100%),单独治疗(n=6,67%)或联合长期抗哮喘药物治疗(n=3,33%)和/或每日胸部物理治疗(n=2,22%),但仅报告部分临床获益。症状发作和 AIA 诊断的中位年龄分别为 1.5[0.08-13]岁和 6[4-14]岁,明确诊断存在明显延迟(4.5 年)。9 例中,4 例 CT 显示气管狭窄程度≥51%,5 例剩余病例狭窄程度≤50%。4 例 CT 显示气管狭窄程度≥51%的病例进行了气道内镜检查,并证实了 CT 结果。在这 4 例中,手术决策是基于内镜和 CT 检查结果做出的,同时考虑到尽管进行了药物治疗但仍存在临床症状。其余 5 例患儿采用保守治疗。
AIA 引起的 TC 可能是儿童不明原因慢性呼吸道疾病的原因。早期诊断 AIA 可以减少昂贵的检查或无效治疗的使用,降低疾病发病率,并加速治疗进程。