[Clinical features and CT findings of fibrosing mediastinitis associated pulmonary hypertension].

F Li, J Wan, Z G Zhai, W M Xie, Y Gao, D T Liu, R Y Dou, W Guo, Y Xiao, G F Zhu
{"title":"[Clinical features and CT findings of fibrosing mediastinitis associated pulmonary hypertension].","authors":"F Li,&nbsp;J Wan,&nbsp;Z G Zhai,&nbsp;W M Xie,&nbsp;Y Gao,&nbsp;D T Liu,&nbsp;R Y Dou,&nbsp;W Guo,&nbsp;Y Xiao,&nbsp;G F Zhu","doi":"10.3760/cma.j.cn112147-20220912-00754","DOIUrl":null,"url":null,"abstract":"<p><p><b>Objective:</b> To investigate the clinical features and CT findings of pulmonary hypertension (PH) in patients with fibrosing mediastinitis (FM). <b>Methods:</b> Thirteen patients with FM diagnosed between September 2015 and June 2022 were studied retrospectively, including patients with PH (FM-PH group) and patients without PH (FM group) confirmed on right heart catheterization. The <i>t</i> test of two independent samples, Mann-Whitney <i>U</i> rank sum and <i>Fisher's</i> test were used to compare the general information, symptoms, laboratory examination, right ventricular and pulmonary artery measurement data and pulmonary artery CT findings between the two groups, respectively. <b>Results:</b> Compared with the 7 FM patients aged 28-79 (60.00±17.69) years, the 6 patients in the FM-PH group, aged from 60 to 82 (68.83±8.35) years, had more peripheral edema, lower percentage of PaO<sub>2</sub>, wider inner diameters of pulmonary artery and right ventricle, a higher ratio of right ventricle and left ventricular transverse diameter, faster tricuspid regurgitation velocity and higher estimated systolic pulmonary artery pressure (<i>P</i><0.05). There were no differences in BNP levels and tricuspid annular plane systolic excursion between groups (<i>P</i>>0.05). Of the 6 patients with PH, 5 had precapillary PH and 1 had mixed PH. Except that the pulmonary vascular resistance in patients of the FM-PH group was significantly higher than that in the FM group (<i>P</i><0.05), there were no significant differences in cardiac output, mixed venous oxygen saturation and pulmonary capillary wedge pressure between the two groups. CT pulmonary angiography (CTPA) showed pulmonary artery and vein stenosis. Patients in the FM-PH group had more severe stenosis and occlusion of pulmonary artery and pulmonary vein (<i>P</i><0.05), and more involvement of multiple pulmonary veins (<i>P</i><0.05). <b>Conclusions:</b> The clinical manifestation of FM complicated with PH is related to the degree of involvement of pulmonary artery, vein and airway. It is recommended that the disease be evaluated in combination with multiple parameters such as clinical manifestations, cardiac ultrasound, right cardiac catheter and CTPA.</p>","PeriodicalId":23961,"journal":{"name":"Zhonghua jie he he hu xi za zhi = Zhonghua jiehe he huxi zazhi = Chinese journal of tuberculosis and respiratory diseases","volume":"46 5","pages":"460-465"},"PeriodicalIF":0.0000,"publicationDate":"2023-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zhonghua jie he he hu xi za zhi = Zhonghua jiehe he huxi zazhi = Chinese journal of tuberculosis and respiratory diseases","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3760/cma.j.cn112147-20220912-00754","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: To investigate the clinical features and CT findings of pulmonary hypertension (PH) in patients with fibrosing mediastinitis (FM). Methods: Thirteen patients with FM diagnosed between September 2015 and June 2022 were studied retrospectively, including patients with PH (FM-PH group) and patients without PH (FM group) confirmed on right heart catheterization. The t test of two independent samples, Mann-Whitney U rank sum and Fisher's test were used to compare the general information, symptoms, laboratory examination, right ventricular and pulmonary artery measurement data and pulmonary artery CT findings between the two groups, respectively. Results: Compared with the 7 FM patients aged 28-79 (60.00±17.69) years, the 6 patients in the FM-PH group, aged from 60 to 82 (68.83±8.35) years, had more peripheral edema, lower percentage of PaO2, wider inner diameters of pulmonary artery and right ventricle, a higher ratio of right ventricle and left ventricular transverse diameter, faster tricuspid regurgitation velocity and higher estimated systolic pulmonary artery pressure (P<0.05). There were no differences in BNP levels and tricuspid annular plane systolic excursion between groups (P>0.05). Of the 6 patients with PH, 5 had precapillary PH and 1 had mixed PH. Except that the pulmonary vascular resistance in patients of the FM-PH group was significantly higher than that in the FM group (P<0.05), there were no significant differences in cardiac output, mixed venous oxygen saturation and pulmonary capillary wedge pressure between the two groups. CT pulmonary angiography (CTPA) showed pulmonary artery and vein stenosis. Patients in the FM-PH group had more severe stenosis and occlusion of pulmonary artery and pulmonary vein (P<0.05), and more involvement of multiple pulmonary veins (P<0.05). Conclusions: The clinical manifestation of FM complicated with PH is related to the degree of involvement of pulmonary artery, vein and airway. It is recommended that the disease be evaluated in combination with multiple parameters such as clinical manifestations, cardiac ultrasound, right cardiac catheter and CTPA.

【纤维化性纵隔炎合并肺动脉高压的临床特征及CT表现】。
目的:探讨纤维化性纵隔炎(FM)患者肺动脉高压(PH)的临床特点及CT表现。方法:回顾性分析2015年9月至2022年6月诊断为FM的13例患者,包括经右心导管确诊的PH患者(FM-PH组)和无PH患者(FM组)。采用两个独立样本的t检验、Mann-Whitney U秩和和Fisher检验分别比较两组患者的一般资料、症状、实验室检查、右心室和肺动脉测量资料及肺动脉CT表现。结果:与7例28 ~ 79岁(60.00±17.69)岁的FM患者相比,6例60 ~ 82岁(68.83±8.35)岁的FM组患者外周水肿较多,PaO2比例较低,肺动脉和右心室内径较宽,右心室与左心室横径比值较高,三尖瓣反流速度较快,肺动脉收缩压估计较高(PP>0.05)。6例PH患者中,5例为毛细前PH, 1例为混合性PH。但FM-PH组肺血管阻力明显高于FM组(ppp)结论:FM合并PH的临床表现与肺动脉、静脉、气道的受累程度有关。建议结合临床表现、心脏超声、右心导管、CTPA等多指标评价。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信