一家三甲医院的造影剂多载体计算机断层扫描在评估儿科先天性肺畸形中的作用:观察性研究

K. Sravya, Sarukolla Meena Madhuri, M. Veena, B. Vanaja, Sunitha Bajaj, Vijaya Kumari
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引用次数: 0

摘要

摘要 由于多载体 CT(MDCT)的引入,计算机断层扫描(CT)在先天性肺部畸形的无创检查中发挥了更大的作用。如果怀疑有手术病灶,通常需要使用 CT 等横断面成像技术来确诊、进一步确定病灶和进行术前评估。 本研究旨在加深对儿童先天性肺部畸形的发生和种类的理解,并评估和比较 MDCT 与手术干预的诊断精确度。 该研究使用东芝 8 片 CT 对有呼吸系统主诉、产前有胎儿畸形定向成像(TIFFA)或先天性肺畸形(CLMs)可疑病史的儿童进行了造影剂 CT MDCT 检查;研究人群包括 40 名有 TIFFA 怀孕期间胸部异常病史或 18 个月内胸部 X 光片异常怀疑肺部异常的儿童患者。 在一项对 40 名接受造影剂 MDCT 检查以评估 CLM 的儿科患者进行的研究中,有 6 名患者因在普通 CT 上未发现肺部异常而被排除在造影剂的进一步评估之外,剩下的 34 例患者可能被诊断为 s CLM。其中,囊性肺气道畸形(CPAM)(41.1%)最为常见,其次是先天性大叶肺气肿(17.6%)、支气管源性囊肿(14.7%)、肺发育不全(11.6%)和系统性肺。 为了了解CLMs的特征和相关异常,并帮助对CLMs进行术前评估,该研究得出结论,造影剂MDCT是成像的首选。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of Multidetector Computed Tomography with Contrast in Evaluation of Congenital Lung Malformations in Pediatric Age Group at a Tertiary Care Hospital: An Observational Study
ABSTRACT Computed tomography (CT) has a larger role in the noninvasive examination of congenital lung abnormalities, thanks to the introduction of multidetector CT (MDCT). If a surgical lesion is suspected, it is often necessary to use cross-sectional imaging, such as CT, for diagnosis confirmation, further lesion definition, and preoperative evaluation. The aim of this study was to enhance comprehension of the occurrence and varieties of congenital lung abnormalities in children, as well as to assess and compare the diagnostic precision of MDCT with that of surgical intervention. MDCT with contrast CT was performed in children with respiratory complaints and prenatal history of suspicion in targeted imaging for fetal anomalies (TIFFA) or congenital lung malformations (CLMs) using TOSHIBA 8 slice CT; the study population consisted of 40 pediatric patients with a history of chest anomalies during pregnancy in TIFFA or children with abnormal chest X-ray suspicion of lung anomalies for 18 months. In a study of 40 pediatric patients who underwent MDCT with contrast to evaluate CLMs, 6 were excluded from further evaluation with contrast due to the absence of pulmonary anomalies on plain CT, leaving a possible diagnosis of s CLM in the remaining 34 cases. Of these, cystic pulmonary airway malformations (CPAM) (41.1%) were the most common, followed by congenital lobar emphysema (17.6%), bronchogenic cyst (14.7%), lung agenesis (11.6%), and phylogenetic lung. To notice the characteristics and related anomalies of CLMs and aid in the presurgical evaluation of CLMs, the study concludes that MDCT with contrast is the imaging of choice.
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