• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

定量CT成像分析预测先天性肺气道畸形患者的病理特征。

Quantitative CT imaging analysis to predict pathology features in patients with a congenital pulmonary airway malformation.

作者信息

Hermelijn Sergei M, Mackenbach Maarten J, van Horik Cathy, Ciet Pierluigi, Wolf Janina L, von der Thüsen Jan H, Wijnen René M H, Tiddens Harm A W M, Schnater J Marco

机构信息

Department of Pediatric Surgery, Erasmus Medical Center, Sophia Children's Hospital, Molewaterplein 40. 3015 GD Rotterdam, Mailing address: Postbus 2060, Rotterdam 3000 CB, the Netherlands.

Department of Pediatric Metabolic Diseases, Erasmus Medical Center, Sophia Children's Hospital, Rotterdam, the Netherlands.

出版信息

J Pediatr Surg. 2022 Aug;57(8):1567-1572. doi: 10.1016/j.jpedsurg.2021.10.008. Epub 2021 Oct 14.

DOI:10.1016/j.jpedsurg.2021.10.008
PMID:34809963
Abstract

BACKGROUND

Risk for infection and potential malignant degeneration are the most common arguments for resecting asymptomatic Congenital Pulmonary Airway Malformations (CPAM). We aimed to investigate if CT- imaging characteristics can be used to predict histopathological features, by using an objective quantitative CT scoring method.

METHODS

Archival CPAM tissue samples were histologically re-assessed and patients who had a pre-operative volumetric CT-scan were included. Lung disease was quantified using the newly-developed congenital lung abnormality quantification(CLAQ) scoring method and obtained percentages were used to predict histopathological signs of inflammation and presence of mucinous proliferation (MP). Because MP is presumed a precursor for mucinous adenocarcinoma in situ (AIS) this method was also used to compare CT-scans of patients with AIS to those with only CPAM.

RESULTS

Thirty-three CPAM patients were included of which 13(39%) had histological signs of inflammation and 8(24%) had a MP. Patients with inflammation had a significantly smaller lesion (14% vs 38%) while those with MP had more extensive disease (54%vs17%). Patients with AIS had a significantly smaller lesion compared to CPAM patients (5%vs29%). Significant predictors for inflammation were smaller lesion size and percentage hypodensity within lesions while a larger lesion size and percentage parenchymal hyperdensity (solid lung tissue components) were predictors for MP as well as AIS.

CONCLUSIONS

Smaller CPAM lesions may be more susceptible to inflammation while larger lesions may be associated with the presence of MP. Parenchymal hyperdensity is found as a predictor for MP as well as AIS and should therefore elicit more extensive gross sampling.

LEVEL OF EVIDENCE

Level III.

摘要

背景

感染风险和潜在恶性变是切除无症状先天性肺气道畸形(CPAM)最常见的理由。我们旨在通过使用一种客观的定量CT评分方法,研究CT成像特征是否可用于预测组织病理学特征。

方法

对存档的CPAM组织样本进行组织学重新评估,并纳入术前进行容积CT扫描的患者。使用新开发的先天性肺异常量化(CLAQ)评分方法对肺部疾病进行量化,并将获得的百分比用于预测炎症的组织病理学征象和黏液性增殖(MP)的存在。由于MP被认为是原位黏液腺癌(AIS)的前体,该方法还用于比较AIS患者与仅患有CPAM患者的CT扫描结果。

结果

纳入了33例CPAM患者,其中13例(39%)有炎症的组织学征象,8例(24%)有MP。有炎症的患者病变明显较小(14%对38%),而有MP的患者疾病范围更广(54%对17%)。与CPAM患者相比,AIS患者的病变明显较小(5%对29%)。炎症的显著预测因素是病变较小和病变内低密度百分比,而较大的病变大小和实质高密度百分比(实性肺组织成分)是MP以及AIS的预测因素。

结论

较小的CPAM病变可能更容易发生炎症,而较大的病变可能与MP的存在有关。实质高密度被发现是MP以及AIS的预测因素,因此应进行更广泛的大体标本采集。

证据水平

三级。

相似文献

1
Quantitative CT imaging analysis to predict pathology features in patients with a congenital pulmonary airway malformation.定量CT成像分析预测先天性肺气道畸形患者的病理特征。
J Pediatr Surg. 2022 Aug;57(8):1567-1572. doi: 10.1016/j.jpedsurg.2021.10.008. Epub 2021 Oct 14.
2
Congenital lung abnormality quantification by computed tomography: The CLAQ method.先天性肺异常的 CT 定量:CLAQ 方法。
Pediatr Pulmonol. 2020 Nov;55(11):3152-3161. doi: 10.1002/ppul.25032. Epub 2020 Aug 26.
3
Early KRAS oncogenic driver mutations in nonmucinous tissue of congenital pulmonary airway malformations as an indicator of potential malignant behavior.先天性肺气道畸形非黏液组织中 KRAS 原癌基因驱动突变作为潜在恶性行为的指标。
Hum Pathol. 2020 Sep;103:95-106. doi: 10.1016/j.humpath.2020.07.015. Epub 2020 Jul 16.
4
Thoracic MDCT findings of a combined congenital lung lesion: Bronchial atresia associated with congenital pulmonary airway malformation.先天性肺气道畸形合并支气管闭锁的胸部 MDCT 表现
Pediatr Pulmonol. 2021 Sep;56(9):2903-2910. doi: 10.1002/ppul.25556. Epub 2021 Jul 21.
5
Computed tomography features can distinguish type 4 congenital pulmonary airway malformation from other cystic congenital pulmonary airway malformations.计算机断层扫描特征可将 4 型先天性肺气道畸形与其他囊性先天性肺气道畸形区分开来。
Eur J Radiol. 2020 May;126:108964. doi: 10.1016/j.ejrad.2020.108964. Epub 2020 Mar 19.
6
Two's Company: Multiple Thoracic Lesions on Prenatal US and MRI.双胎妊娠:产前超声及 MRI 发现多发胸内病变。
Fetal Diagn Ther. 2020;47(8):642-652. doi: 10.1159/000507783. Epub 2020 Jun 29.
7
Congenital Pulmonary Airway Malformations With a Reconsideration and Current Perspective on the Stocker Classification.先天性肺气道畸形的再思考及对斯多克分类的最新观点。
Pediatr Dev Pathol. 2023 May-Jun;26(3):241-249. doi: 10.1177/10935266221146823. Epub 2023 Feb 21.
8
Lung Ultrasound Findings in Congenital Pulmonary Airway Malformation.先天性肺气道畸形的肺部超声表现。
Am J Perinatol. 2018 Oct;35(12):1222-1227. doi: 10.1055/s-0038-1645861. Epub 2018 May 1.
9
Congenital pulmonary airway malformation: A case report of a rare cause of neonatal respiratory distress and review of the literature.先天性肺气道畸形:一例新生儿呼吸窘迫罕见病因的病例报告及文献复习
Niger J Clin Pract. 2019 Nov;22(11):1621-1625. doi: 10.4103/njcp.njcp_20_19.
10
Mucinous adenocarcinoma of the lung in association with congenital pulmonary airway malformation.肺黏液腺癌合并先天性肺气道畸形。
J Pediatr Surg. 2010 Nov;45(11):2256-9. doi: 10.1016/j.jpedsurg.2010.07.008.

引用本文的文献

1
Analysis of anatomical characteristics of congenital pulmonary airway malformation lesions based on CT images.基于CT图像的先天性肺气道畸形病变的解剖学特征分析
Front Pediatr. 2025 May 23;13:1576380. doi: 10.3389/fped.2025.1576380. eCollection 2025.
2
Impact of pulmonary infection on thoracoscopic surgery outcomes in children with CPAM: a retrospective study.肺部感染对先天性肺气道畸形患儿胸腔镜手术结局的影响:一项回顾性研究
BMC Surg. 2025 Mar 10;25(1):94. doi: 10.1186/s12893-025-02827-7.
3
Integrative analysis of bulk and single-cell RNA sequencing reveals the gene expression profile and the critical signaling pathways of type II CPAM.
对 bulk 和单细胞 RNA 测序的综合分析揭示了 II 型先天性肺气道畸形(CPAM)的基因表达谱和关键信号通路。
Cell Biosci. 2024 Jul 18;14(1):94. doi: 10.1186/s13578-024-01276-8.
4
Congenital Cystic Adenomatoid Malformation (CCAM) Type II: A Rare Case of Sudden Infant Death.先天性囊性腺瘤样畸形(CCAM)II型:一例罕见的婴儿猝死病例。
Children (Basel). 2022 Nov 26;9(12):1830. doi: 10.3390/children9121830.