Chest CT Findings of Pneumocystis jirovecii Pneumonia in a Large Cohort of Patients Who Are Immunocompromised.

IF 4.5 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Aaron M Pulsipher, Kealy Ham, Holenarasipur R Vikram, Kyle J Henry, Emily R Thompson, Michael B Gotway
{"title":"Chest CT Findings of <i>Pneumocystis jirovecii</i> Pneumonia in a Large Cohort of Patients Who Are Immunocompromised.","authors":"Aaron M Pulsipher, Kealy Ham, Holenarasipur R Vikram, Kyle J Henry, Emily R Thompson, Michael B Gotway","doi":"10.1148/ryct.250361","DOIUrl":null,"url":null,"abstract":"<p><p>Purpose To assess chest CT imaging manifestations of <i>Pneumocystis jirovecii</i> pneumonia (PJP) in a large, well-characterized cohort of patients who were immunocompromised and determine whether CT findings differ by immunocompromise etiology. Materials and Methods This retrospective study identified patients with proven or probable PJP across a multicenter hospital system over a 7-year period. Available chest CT scans were reviewed for the presence and distribution of ground-glass opacity (GGO), consolidation, interlobular septal thickening, fibrosis, nodules (characterized by size and distribution), and other findings. Imaging features and their evolution at follow-up CT were compared across immunocompromise etiologies and with the overall cohort using the Fisher exact test and Kruskal-Wallis test, as applicable. Results Among 701 evaluated patients, 675 (median age, 65 years [IQR, 54-73 years]; 423 male) had chest CT examinations available for review. Immunocompromise etiologies included hematologic malignancy (32.7%), solid neoplasia receiving chemotherapy (22.5%), autoimmune disease (17.3%), solid organ transplant (13.0%), bone marrow transplant (8.3%), corticosteroid therapy (8.1%), HIV infection (7.6%), and miscellaneous causes (4.6%). Across all etiologies, diffusely distributed GGO without distinguishing features was the most common CT finding (96.7%), with a random axial distribution in 80.1% of patients and peripheral dominance in 14.2%. Consolidation was present in 51.1% of patients. PJP CT findings substantially overlapped across immunocompromise etiologies, with no imaging pattern specific to a particular etiology. Follow-up CT was available in 71.6% of patients (median interval, 31 days; range, 2-1344 days), demonstrating PJP improvement in 66.0%, worsening in 25.5%, no change in 9.1%, and new CT patterns in 11.8%. Respiratory coinfection was present in 31.9% of patients. Conclusion PJP most commonly manifested as diffusely distributed GGO on chest CT scans, regardless of the underlying cause of immunocompromise. CT findings did not distinguish between HIV- and non-HIV-related immunosuppression, and respiratory coinfection was common. <b>Keywords:</b> <i>Pneumocystis jirovecii</i> Pneumonia, Immunosuppression, Immunocompromise, CT, Ground-Glass Opacity <i>Supplemental material is available for this article.</i> © RSNA, 2026.</p>","PeriodicalId":21168,"journal":{"name":"Radiology. Cardiothoracic imaging","volume":"8 2","pages":"e250361"},"PeriodicalIF":4.5000,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Radiology. Cardiothoracic imaging","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1148/ryct.250361","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING","Score":null,"Total":0}
引用次数: 0

Abstract

Purpose To assess chest CT imaging manifestations of Pneumocystis jirovecii pneumonia (PJP) in a large, well-characterized cohort of patients who were immunocompromised and determine whether CT findings differ by immunocompromise etiology. Materials and Methods This retrospective study identified patients with proven or probable PJP across a multicenter hospital system over a 7-year period. Available chest CT scans were reviewed for the presence and distribution of ground-glass opacity (GGO), consolidation, interlobular septal thickening, fibrosis, nodules (characterized by size and distribution), and other findings. Imaging features and their evolution at follow-up CT were compared across immunocompromise etiologies and with the overall cohort using the Fisher exact test and Kruskal-Wallis test, as applicable. Results Among 701 evaluated patients, 675 (median age, 65 years [IQR, 54-73 years]; 423 male) had chest CT examinations available for review. Immunocompromise etiologies included hematologic malignancy (32.7%), solid neoplasia receiving chemotherapy (22.5%), autoimmune disease (17.3%), solid organ transplant (13.0%), bone marrow transplant (8.3%), corticosteroid therapy (8.1%), HIV infection (7.6%), and miscellaneous causes (4.6%). Across all etiologies, diffusely distributed GGO without distinguishing features was the most common CT finding (96.7%), with a random axial distribution in 80.1% of patients and peripheral dominance in 14.2%. Consolidation was present in 51.1% of patients. PJP CT findings substantially overlapped across immunocompromise etiologies, with no imaging pattern specific to a particular etiology. Follow-up CT was available in 71.6% of patients (median interval, 31 days; range, 2-1344 days), demonstrating PJP improvement in 66.0%, worsening in 25.5%, no change in 9.1%, and new CT patterns in 11.8%. Respiratory coinfection was present in 31.9% of patients. Conclusion PJP most commonly manifested as diffusely distributed GGO on chest CT scans, regardless of the underlying cause of immunocompromise. CT findings did not distinguish between HIV- and non-HIV-related immunosuppression, and respiratory coinfection was common. Keywords: Pneumocystis jirovecii Pneumonia, Immunosuppression, Immunocompromise, CT, Ground-Glass Opacity Supplemental material is available for this article. © RSNA, 2026.

大量免疫功能低下患者的肺囊虫肺炎的胸部CT表现。
目的评估免疫功能低下患者的大型、特征明确的队列中的肺囊虫肺炎(PJP)的胸部CT影像学表现,并确定CT表现是否因免疫功能低下的病因而不同。材料和方法本回顾性研究确定了7年多中心医院系统中已证实或可能患有PJP的患者。回顾现有的胸部CT扫描,检查磨玻璃影(GGO)、实变、小叶间隔增厚、纤维化、结节(以大小和分布为特征)和其他表现的存在和分布。采用Fisher精确试验和Kruskal-Wallis试验(如适用)比较不同免疫功能低下病因的影像学特征及其随访CT的演变。结果701例患者中,675例(中位年龄65岁[IQR, 54-73岁];423例男性)有胸部CT检查可复查。免疫功能低下的病因包括血液恶性肿瘤(32.7%)、接受化疗的实体瘤(22.5%)、自身免疫性疾病(17.3%)、实体器官移植(13.0%)、骨髓移植(8.3%)、皮质类固醇治疗(8.1%)、HIV感染(7.6%)和其他原因(4.6%)。在所有病因中,无明显特征的弥漫性GGO是最常见的CT表现(96.7%),80.1%的患者呈随机轴向分布,14.2%的患者以外周为主。51.1%的患者出现实变。PJP CT的发现在免疫功能低下的病因上有很大的重叠,没有特定病因的特异性成像模式。71.6%的患者有随访CT(中位间隔31天,范围2-1344天),66.0%的患者PJP改善,25.5%的患者恶化,9.1%的患者无变化,11.8%的患者有新的CT表现。31.9%的患者存在呼吸道合并感染。结论PJP在胸部CT扫描上最常见的表现是弥漫性分布的GGO,与免疫功能低下的潜在原因无关。CT表现不能区分HIV相关和非HIV相关的免疫抑制,呼吸道合并感染很常见。关键词:乙基肺囊虫肺炎,免疫抑制,免疫功能低下,CT,毛玻璃混浊。©rsna, 2026。
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
CiteScore
20.40
自引率
1.40%
发文量
0
期刊介绍:
×
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:604180095
Book学术官方微信
小红书