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先天性梨状窝瘘新生儿的影像学表现:45例回顾性研究

Imaging Findings in Neonates With Congenital Pyriform Sinus Fistula: A Retrospective Study of 45 Cases.

作者信息

Li Li, Zhao Dong-Ji-Hui, Yao Tao-Yue, Xiang Yong-Hua, Liu Hong, Ma Qiu-Hong, Jin Ke, He Si-Ping

机构信息

Department of Radiology, Hunan Children's Hospital, University of South China, Changsha, China.

Otorhinolaryngology, Head and Neck Surgery, Hunan Children's Hospital, University of South China, Changsha, China.

出版信息

Front Pediatr. 2021 Nov 2;9:721128. doi: 10.3389/fped.2021.721128. eCollection 2021.

Abstract

Congenital pyriform sinus fistula (CPSF) is a rare branchial cleft deformity. The characteristics and management of CPSF in neonates are different from those in children or adults, and a comprehensive understanding of the imaging features of neonatal CPSF can facilitate its preoperative diagnosis. Thus, the aim of this study was to summarize the ultrasonography (US) and CT imaging findings of CPSF in neonates. Forty-five full-term neonates with CPSF, confirmed by pathology after surgical resection from January 2012 to October 2020, were included in this retrospective study. All patients underwent preoperative cervical US and contrast-enhanced CT examinations, and the imaging findings were analyzed. Forty-six cervical cystic masses were found in 45 neonates, including one case with bilateral lesions, three cases with lesions on the right side, and 41 cases on the left side. Both US and CT detected neck abnormality among all cases, while the diagnostic accuracy of US (15/46, 32.6%) was lower than that of CT (42/46, 91.3%). Moreover, CT showed significantly higher detection rates of intralesional air bubbles, involvement of the ipsilateral thyroid, deviation of the airway, and expansion into the mediastinal and retropharyngeal space compared with the US. As the age increased, it was more likely to present some features including the absence of air-containing, thick cyst wall, and poorly defined border (ρ <0.05). CPSF in the neonates showed distinctive imaging findings on contrast-enhanced CT scan, which provides important supplementary information for the diagnosis of CPSF after the initial US examination.

摘要

先天性梨状窝瘘(CPSF)是一种罕见的鳃裂畸形。新生儿CPSF的特征及处理方法与儿童或成人不同,全面了解新生儿CPSF的影像学特征有助于其术前诊断。因此,本研究旨在总结新生儿CPSF的超声(US)及CT影像学表现。本回顾性研究纳入了2012年1月至2020年10月期间经手术切除并经病理证实的45例足月CPSF新生儿。所有患者均接受了术前颈部超声及增强CT检查,并对影像学表现进行了分析。45例新生儿共发现46个颈部囊性肿物,其中1例为双侧病变,3例为右侧病变,41例为左侧病变。所有病例超声和CT均检测到颈部异常,然而超声的诊断准确率(15/46,32.6%)低于CT(42/46,91.3%)。此外,与超声相比,CT显示病变内气泡、同侧甲状腺受累、气道偏移以及向纵隔和咽后间隙扩展的检出率显著更高。随着年龄增长,更易出现一些特征,包括无含气现象、囊肿壁增厚及边界不清(ρ<0.05)。新生儿CPSF在增强CT扫描上表现出独特的影像学特征,为初次超声检查后CPSF的诊断提供了重要的补充信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39d5/8593330/ff445c7720f6/fped-09-721128-g0001.jpg

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