{"title":"Laryngotracheoesophageal Cleft Type IV in a Preterm Neonate. A Case Report and Literature Review.","authors":"Rozeta Sokou, Anastasia Batsiou, Aikaterini Konstantinidi, Paschalia Kopanou-Taliaka, Marina Tsaousi, Maria Lampridou, Evangelia-Filothei Tavoulari, Konstantinos Mitropoulos, Paraskevi Liakou, Stamatina Willadara-Gamage, Petros V Vlastarakos, Zoi Iliodromiti, Theodora Boutsikou, Nicoletta Iacovidou","doi":"10.14712/23362936.2024.4","DOIUrl":null,"url":null,"abstract":"<p><p>We present a case of a preterm neonate with a type IV laryngo-tracheo-oesophageal cleft, an uncommon congenital malformation, resulting from the failure of separation of the trachea and the oesophagus during fetal development, often associated with other deformities as well. Data in the literature shows that the long-term morbidity from the entity has declined over the last decades, even though prognosis remains unfavourable for types III and IV. This report emphasizes the complex issues neonatologists are faced with, when treating neonates with this rare disorder in the first days of life, what will raise suspicion of this rare medical entity, and that direct laryngoscopy/bronchoscopy finally depicts the exact extension of the medical condition. At the same time extensive evaluation for coexisting congenital anomalies should be performed. For all the above reasons, these neonates should be treated in specialized tertiary pediatric centers for multidisciplinary prompt management, which may improve, the outcome.</p>","PeriodicalId":35490,"journal":{"name":"Prague medical report","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Prague medical report","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14712/23362936.2024.4","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0
Abstract
We present a case of a preterm neonate with a type IV laryngo-tracheo-oesophageal cleft, an uncommon congenital malformation, resulting from the failure of separation of the trachea and the oesophagus during fetal development, often associated with other deformities as well. Data in the literature shows that the long-term morbidity from the entity has declined over the last decades, even though prognosis remains unfavourable for types III and IV. This report emphasizes the complex issues neonatologists are faced with, when treating neonates with this rare disorder in the first days of life, what will raise suspicion of this rare medical entity, and that direct laryngoscopy/bronchoscopy finally depicts the exact extension of the medical condition. At the same time extensive evaluation for coexisting congenital anomalies should be performed. For all the above reasons, these neonates should be treated in specialized tertiary pediatric centers for multidisciplinary prompt management, which may improve, the outcome.
我们接诊了一例患有 IV 型喉-气管-食道裂的早产新生儿,这是一种不常见的先天性畸形,是由于气管和食道在胎儿发育过程中未能分离造成的,通常还伴有其他畸形。文献数据显示,尽管 III 型和 IV 型患者的预后仍然不佳,但在过去几十年中,该病的长期发病率已有所下降。本报告强调了新生儿科医生在治疗生命最初几天患有这种罕见疾病的新生儿时所面临的复杂问题,即怎样才能引起对这种罕见病症的怀疑,以及直接喉镜/支气管镜检查最终能准确描述病情的延伸。同时,还应对并存的先天性畸形进行广泛评估。鉴于上述原因,这些新生儿应在专业的三级儿科中心接受治疗,接受多学科的及时处理,以改善预后。