• 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

技术报告:肺内囊状含气腔隙:23例患者呼气期高分辨率CT上的大小变化

Technical report: Cystic air spaces in the lung: change in size on expiratory high-resolution CT in 23 patients.

作者信息

Worthy S A, Brown M J, Müller N L

机构信息

Department of Radiology, University of British Columbia and Vancouver Hospital and Health Sciences Centre, Canada.

出版信息

Clin Radiol. 1998 Jul;53(7):515-9. doi: 10.1016/s0009-9260(98)80172-4.

DOI:10.1016/s0009-9260(98)80172-4
PMID:9714392
Abstract

PURPOSE

To determine the presence of change in size of air-filled cysts in the lung on expiration by comparison between inspiratory and expiratory high-resolution computed tomography (CT) scans.

MATERIALS AND METHODS

Inspiratory and expiratory high-resolution (1-mm collimation) CT scans were obtained in 23 patients with lung cysts due to a variety of lung diseases. The 23 patients had a total of 27 types of cystic lesions including bullae (n=7), honeycomb cysts due to fibrosing alveolitis (n=11), lymphangioleiomyomatosis (LAM, n=2), cystic adenomatoid malformation (n=1), and bronchiectasis (n=6). An adequate expiratory effort, with at least 5% decrease in the anteroposterior or transverse thoracic diameter, was required for inclusion in the study. Inspiratory and expiratory scans at corresponding anatomic levels were compared to determine any change in size of the cysts on expiration.

RESULTS

Cystic lesions due to bronchiectasis, LAM and fibrosing alveolitis decreased in size on expiratory CT. In six of seven cases bullae decreased in size, and in one patient with a single bulla it remained unchanged. In one case a single cyst due to cystic adenomatoid malformation increased in size on expiration.

CONCLUSION

The majority of lung cysts decrease in size on expiration suggesting that they communicate with the airways.

摘要

目的

通过吸气和呼气高分辨率计算机断层扫描(CT)的比较,确定肺部含气囊肿在呼气时大小是否改变。

材料与方法

对23例因各种肺部疾病导致肺囊肿的患者进行吸气和呼气高分辨率(1毫米准直)CT扫描。这23例患者共有27种囊性病变,包括肺大疱(n = 7)、纤维化肺泡炎所致蜂窝状囊肿(n = 11)、淋巴管平滑肌瘤病(LAM,n = 2)、囊性腺瘤样畸形(n = 1)和支气管扩张(n = 6)。纳入研究要求有足够的呼气动作,前后径或横径至少减少5%。比较相应解剖层面的吸气和呼气扫描,以确定囊肿在呼气时大小的任何变化。

结果

支气管扩张、LAM和纤维化肺泡炎所致的囊性病变在呼气CT上大小减小。7例肺大疱中有6例大小减小,1例单个肺大疱患者大小无变化。1例囊性腺瘤样畸形所致单个囊肿在呼气时大小增加。

结论

大多数肺囊肿在呼气时大小减小,提示它们与气道相通。

相似文献

1
Technical report: Cystic air spaces in the lung: change in size on expiratory high-resolution CT in 23 patients.技术报告:肺内囊状含气腔隙:23例患者呼气期高分辨率CT上的大小变化
Clin Radiol. 1998 Jul;53(7):515-9. doi: 10.1016/s0009-9260(98)80172-4.
2
Cystic lung disease: a comparison of cystic size, as seen on expiratory and inspiratory HRCT scans.囊性肺疾病:呼气和吸气 HRCT 扫描所见囊肿大小的比较。
Korean J Radiol. 2000 Apr-Jun;1(2):84-90. doi: 10.3348/kjr.2000.1.2.84.
3
Computed tomography differentiation between cystic bronchiectasis and bullae.
J Thorac Imaging. 1991 Dec;7(1):83-5. doi: 10.1097/00005382-199112000-00011.
4
Respiratory change in size of honeycombing: inspiratory and expiratory spiral volumetric CT analysis of 97 cases.蜂窝状结构大小的呼吸变化:97例吸气和呼气螺旋容积CT分析
J Comput Assist Tomogr. 1999 Mar-Apr;23(2):174-80. doi: 10.1097/00004728-199903000-00003.
5
Air trapping on expiratory high-resolution CT scans in the absence of inspiratory scan abnormalities: correlation with pulmonary function tests and differential diagnosis.呼气期高分辨率CT扫描显示空气潴留而吸气期扫描无异常:与肺功能检查的相关性及鉴别诊断
AJR Am J Roentgenol. 1998 May;170(5):1349-53. doi: 10.2214/ajr.170.5.9574614.
6
Accuracy of high-resolution CT in diagnosing lung diseases.
AJR Am J Roentgenol. 1998 Jun;170(6):1507-12. doi: 10.2214/ajr.170.6.9609163.
7
Is There a Relationship Between Paratracheal Air Cysts and Upper Lobe Fibrosis?气管旁气囊肿与上叶纤维化之间有关系吗?
J Comput Assist Tomogr. 2016 Mar-Apr;40(2):256-60. doi: 10.1097/RCT.0000000000000362.
8
Congenital masses of the lung, cystic adenomatoid malformation versus congenital lobar emphysema: prenatal diagnosis and implications for postnatal treatment.
J Ultrasound Med. 2004 Oct;23(10):1379-84. doi: 10.7863/jum.2004.23.10.1379.
9
Lymphangioleiomyomatosis: pulmonary and abdominal findings with pathologic correlation.淋巴管平滑肌瘤病:肺部和腹部表现及其病理相关性
Radiographics. 2002 Oct;22 Spec No:S185-98. doi: 10.1148/radiographics.22.suppl_1.g02oc13s185.
10
Serial changes of cystic air spaces in fibrosing alveolitis: a CT-pathological study.纤维化肺泡炎中囊状气腔的系列变化:一项CT病理研究。
Clin Radiol. 1995 Jun;50(6):357-63. doi: 10.1016/s0009-9260(05)83131-9.

引用本文的文献

1
Unlocking the clinical potential of paired inspiratory and expiratory CT scans in the differential diagnosis of cystic lung diseases: A systematic review.揭示吸气与呼气配对CT扫描在囊性肺疾病鉴别诊断中的临床潜力:一项系统评价
PLoS One. 2024 Dec 3;19(12):e0314572. doi: 10.1371/journal.pone.0314572. eCollection 2024.
2
Narrowing the Differential Diagnosis of Cystic Lesions in Smokers with Expiratory CT Acquisition Using the Cyst-Airway Communication Hypothesis.应用含气支气管征假说缩小吸烟患者肺部含气囊腔病变的鉴别诊断范围。
Lung. 2022 Dec;200(6):817-820. doi: 10.1007/s00408-022-00576-5. Epub 2022 Oct 22.
3
Automated CT scan scores of bronchiectasis and air trapping in cystic fibrosis.
支气管扩张症和囊性纤维化空气潴留的 CT 扫描自动评分。
Chest. 2014 Mar 1;145(3):593-603. doi: 10.1378/chest.13-0588.
4
Natural history of honeycombing: follow-up of patients with idiopathic pulmonary fibrosis treated with single-lung transplantation.蜂窝肺的自然史:接受单肺移植治疗特发性肺纤维化患者的随访。
Radiol Med. 2013 Feb;118(1):40-50. doi: 10.1007/s11547-012-0810-4. Epub 2012 Mar 19.
5
Cystic lung disease: a comparison of cystic size, as seen on expiratory and inspiratory HRCT scans.囊性肺疾病:呼气和吸气 HRCT 扫描所见囊肿大小的比较。
Korean J Radiol. 2000 Apr-Jun;1(2):84-90. doi: 10.3348/kjr.2000.1.2.84.