{"title":"快速进展性间质性肺病患者的 HIV 筛查测试呈阳性:病例报告。","authors":"Xue Chen, Miaotian Cai, Yingmin Ma, Tong Zhang, Yulin Zhang","doi":"10.2147/IDR.S481681","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Interstitial lung diseases (ILDs) comprise a heterogeneous group of disorders characterized by inflammation and fibrosis of the pulmonary interstitium, posing significant challenges in identifying their underlying causes. Pneumocystis pneumonia (PCP) is the leading cause of ILD in people living with HIV (PLWH). In individuals with connective tissue diseases, ILD is a frequent complication with significant morbidity and mortality.</p><p><strong>Methods: </strong>A case is presented that details the intricate diagnostic process of rapidly progressive interstitial lung disease (RP-ILD).</p><p><strong>Results: </strong>The patient initially presented with clinical features consistent with ILD, including progressive respiratory symptoms and radiological findings typical of pulmonary inflammation. Coupled with a positive HIV screening result, these findings led to an initial misdiagnosis of PCP, a common opportunistic infection in PLWH. However, despite standard anti-PCP treatment, the patient's condition did not improve, prompting further diagnostic evaluations. Subsequent investigations revealed the presence of serum anti-melanoma differentiation-associated gene 5 (anti-MDA5) antibody, a biomarker strongly associated with rapidly progressive ILD in clinically amyopathic dermatomyositis (CADM).</p><p><strong>Conclusion: </strong>This case report offers a novel perspective on the diagnostic process of ILD, particularly emphasizing the importance of distinguishing false-positive antibodies caused by autoimmune diseases in the context of positive HIV screening tests, thereby improving the accuracy of RP-ILD diagnosis and mitigating the mortality burden associated with this condition.</p>","PeriodicalId":13577,"journal":{"name":"Infection and Drug Resistance","volume":"17 ","pages":"5111-5116"},"PeriodicalIF":2.9000,"publicationDate":"2024-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11586118/pdf/","citationCount":"0","resultStr":"{\"title\":\"Positive HIV Screening Test in a Patient with Rapidly Progressive Interstitial Lung Disease: A Case Report.\",\"authors\":\"Xue Chen, Miaotian Cai, Yingmin Ma, Tong Zhang, Yulin Zhang\",\"doi\":\"10.2147/IDR.S481681\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>Interstitial lung diseases (ILDs) comprise a heterogeneous group of disorders characterized by inflammation and fibrosis of the pulmonary interstitium, posing significant challenges in identifying their underlying causes. Pneumocystis pneumonia (PCP) is the leading cause of ILD in people living with HIV (PLWH). In individuals with connective tissue diseases, ILD is a frequent complication with significant morbidity and mortality.</p><p><strong>Methods: </strong>A case is presented that details the intricate diagnostic process of rapidly progressive interstitial lung disease (RP-ILD).</p><p><strong>Results: </strong>The patient initially presented with clinical features consistent with ILD, including progressive respiratory symptoms and radiological findings typical of pulmonary inflammation. Coupled with a positive HIV screening result, these findings led to an initial misdiagnosis of PCP, a common opportunistic infection in PLWH. However, despite standard anti-PCP treatment, the patient's condition did not improve, prompting further diagnostic evaluations. Subsequent investigations revealed the presence of serum anti-melanoma differentiation-associated gene 5 (anti-MDA5) antibody, a biomarker strongly associated with rapidly progressive ILD in clinically amyopathic dermatomyositis (CADM).</p><p><strong>Conclusion: </strong>This case report offers a novel perspective on the diagnostic process of ILD, particularly emphasizing the importance of distinguishing false-positive antibodies caused by autoimmune diseases in the context of positive HIV screening tests, thereby improving the accuracy of RP-ILD diagnosis and mitigating the mortality burden associated with this condition.</p>\",\"PeriodicalId\":13577,\"journal\":{\"name\":\"Infection and Drug Resistance\",\"volume\":\"17 \",\"pages\":\"5111-5116\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2024-11-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11586118/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Infection and Drug Resistance\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.2147/IDR.S481681\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"INFECTIOUS DISEASES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Infection and Drug Resistance","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2147/IDR.S481681","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0
摘要
目的:间质性肺疾病(ILDs)是以肺间质炎症和纤维化为特征的一组异质性疾病,给确定其根本原因带来了巨大挑战。肺孢子虫肺炎(PCP)是导致艾滋病病毒感染者(PLWH)患上 ILD 的主要原因。在患有结缔组织疾病的患者中,ILD 是一种常见的并发症,发病率和死亡率都很高:方法:本文介绍了一个病例,详细阐述了快速进展性间质性肺病(RP-ILD)的复杂诊断过程:患者最初表现出与间质性肺病一致的临床特征,包括进行性呼吸道症状和典型的肺部炎症放射学检查结果。再加上艾滋病毒筛查结果呈阳性,这些发现导致患者最初被误诊为五氯苯酚,这是艾滋病毒感染者常见的机会性感染。然而,尽管进行了标准的抗五氯苯酚治疗,患者的病情并没有好转,因此需要进一步进行诊断评估。随后的检查发现患者血清中存在抗黑色素瘤分化相关基因5(anti-MDA5)抗体,这种生物标记物与临床淀粉样变性皮肌炎(CADM)中快速进展的ILD密切相关:本病例报告为 ILD 的诊断过程提供了一个新的视角,特别强调了在 HIV 筛查检测呈阳性的情况下区分由自身免疫性疾病引起的假阳性抗体的重要性,从而提高了 RP-ILD 诊断的准确性,减轻了与这种疾病相关的死亡率负担。
Positive HIV Screening Test in a Patient with Rapidly Progressive Interstitial Lung Disease: A Case Report.
Objective: Interstitial lung diseases (ILDs) comprise a heterogeneous group of disorders characterized by inflammation and fibrosis of the pulmonary interstitium, posing significant challenges in identifying their underlying causes. Pneumocystis pneumonia (PCP) is the leading cause of ILD in people living with HIV (PLWH). In individuals with connective tissue diseases, ILD is a frequent complication with significant morbidity and mortality.
Methods: A case is presented that details the intricate diagnostic process of rapidly progressive interstitial lung disease (RP-ILD).
Results: The patient initially presented with clinical features consistent with ILD, including progressive respiratory symptoms and radiological findings typical of pulmonary inflammation. Coupled with a positive HIV screening result, these findings led to an initial misdiagnosis of PCP, a common opportunistic infection in PLWH. However, despite standard anti-PCP treatment, the patient's condition did not improve, prompting further diagnostic evaluations. Subsequent investigations revealed the presence of serum anti-melanoma differentiation-associated gene 5 (anti-MDA5) antibody, a biomarker strongly associated with rapidly progressive ILD in clinically amyopathic dermatomyositis (CADM).
Conclusion: This case report offers a novel perspective on the diagnostic process of ILD, particularly emphasizing the importance of distinguishing false-positive antibodies caused by autoimmune diseases in the context of positive HIV screening tests, thereby improving the accuracy of RP-ILD diagnosis and mitigating the mortality burden associated with this condition.
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ISSN: 1178-6973
Editor-in-Chief: Professor Suresh Antony
An international, peer-reviewed, open access journal that focuses on the optimal treatment of infection (bacterial, fungal and viral) and the development and institution of preventative strategies to minimize the development and spread of resistance.