Dong-Ge Han, Chun-Lin Ying, Tian-Qi Zhao, Qiao-Yun Tong, Wei Liu
{"title":"igg4相关肺部疾病的临床特征:基于单中心的经验","authors":"Dong-Ge Han, Chun-Lin Ying, Tian-Qi Zhao, Qiao-Yun Tong, Wei Liu","doi":"10.1007/s10067-025-07678-4","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>IgG4-related lung disease (IgG4-RLD) is a rare autoimmune condition. This study aims to systematically analyze the clinical characteristics of IgG4-RLD to enhance clinicians' awareness and improve patient outcomes.</p><p><strong>Methods: </strong>This retrospective analysis investigates the clinical data of 20 patients diagnosed with IgG4-RLD at the Yichang Central People's Hospital between January 2019 and April 2025.</p><p><strong>Results: </strong>The mean age at diagnosis among the 20 patients with IgG4-RLD was 60.10 ± 10.34 years, with a male-to-female ratio of 3:1. The most frequent clinical manifestations were hemoptysis and abnormalities in pulmonary imaging. Eight patients (40.00%) presented with isolated pulmonary involvement, while 12 patients (60.00%) exhibited extra-pulmonary organ involvement, with lymph node involvement being the most prevalent. The pulmonary imaging characteristics primarily included solid nodular patterns in 10 patients (50.00%) and round ground-glass opacity (GGO) patterns in 9 patients (45.00%). Patients with round GGO patterns exhibited a higher incidence of hemoptysis and predominantly had a history of respiratory conditions (P < 0.05). Patients with solid nodular patterns exhibited significantly higher percentages of eosinophils and lymphocytes, as well as elevated serum IgG levels, compared to those with round GGO patterns (P < 0.05). By contrast, patients with round GGO patterns demonstrated significantly higher percentages of neutrophils and a markedly increased neutrophil-to-lymphocyte ratio (NLR) compared to those with solid nodular patterns (P < 0.05).</p><p><strong>Conclusions: </strong>The clinical manifestations of IgG4-RLD are complex and heterogeneous. Clinicians need to acquire a thorough understanding of these features in order to develop personalized diagnostic and therapeutic approaches, thereby enhancing patient outcomes. Key Points • The pulmonary imaging characteristics of IgG4-RLD were primarily manifested as solid nodular patterns and round GGO patterns. • Patients with round GGO patterns were more likely to experience hemoptysis, and the majority of these patients presented with a history of respiratory conditions. • Patients with solid nodular patterns demonstrated significantly higher percentages of eosinophils, lymphocytes, and serum IgG levels compared to those with round GGO patterns. • Patients with round GGO patterns demonstrated significantly higher percentages of neutrophils and a markedly increased NLR compared to those with solid nodular patterns.</p>","PeriodicalId":10482,"journal":{"name":"Clinical Rheumatology","volume":" ","pages":""},"PeriodicalIF":2.8000,"publicationDate":"2025-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Clinical characteristics of IgG4-related lung disease: a single-center based experience.\",\"authors\":\"Dong-Ge Han, Chun-Lin Ying, Tian-Qi Zhao, Qiao-Yun Tong, Wei Liu\",\"doi\":\"10.1007/s10067-025-07678-4\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>IgG4-related lung disease (IgG4-RLD) is a rare autoimmune condition. This study aims to systematically analyze the clinical characteristics of IgG4-RLD to enhance clinicians' awareness and improve patient outcomes.</p><p><strong>Methods: </strong>This retrospective analysis investigates the clinical data of 20 patients diagnosed with IgG4-RLD at the Yichang Central People's Hospital between January 2019 and April 2025.</p><p><strong>Results: </strong>The mean age at diagnosis among the 20 patients with IgG4-RLD was 60.10 ± 10.34 years, with a male-to-female ratio of 3:1. The most frequent clinical manifestations were hemoptysis and abnormalities in pulmonary imaging. Eight patients (40.00%) presented with isolated pulmonary involvement, while 12 patients (60.00%) exhibited extra-pulmonary organ involvement, with lymph node involvement being the most prevalent. The pulmonary imaging characteristics primarily included solid nodular patterns in 10 patients (50.00%) and round ground-glass opacity (GGO) patterns in 9 patients (45.00%). Patients with round GGO patterns exhibited a higher incidence of hemoptysis and predominantly had a history of respiratory conditions (P < 0.05). Patients with solid nodular patterns exhibited significantly higher percentages of eosinophils and lymphocytes, as well as elevated serum IgG levels, compared to those with round GGO patterns (P < 0.05). By contrast, patients with round GGO patterns demonstrated significantly higher percentages of neutrophils and a markedly increased neutrophil-to-lymphocyte ratio (NLR) compared to those with solid nodular patterns (P < 0.05).</p><p><strong>Conclusions: </strong>The clinical manifestations of IgG4-RLD are complex and heterogeneous. Clinicians need to acquire a thorough understanding of these features in order to develop personalized diagnostic and therapeutic approaches, thereby enhancing patient outcomes. Key Points • The pulmonary imaging characteristics of IgG4-RLD were primarily manifested as solid nodular patterns and round GGO patterns. • Patients with round GGO patterns were more likely to experience hemoptysis, and the majority of these patients presented with a history of respiratory conditions. • Patients with solid nodular patterns demonstrated significantly higher percentages of eosinophils, lymphocytes, and serum IgG levels compared to those with round GGO patterns. • Patients with round GGO patterns demonstrated significantly higher percentages of neutrophils and a markedly increased NLR compared to those with solid nodular patterns.</p>\",\"PeriodicalId\":10482,\"journal\":{\"name\":\"Clinical Rheumatology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2025-09-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical Rheumatology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s10067-025-07678-4\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"RHEUMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Rheumatology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s10067-025-07678-4","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"RHEUMATOLOGY","Score":null,"Total":0}
Clinical characteristics of IgG4-related lung disease: a single-center based experience.
Background: IgG4-related lung disease (IgG4-RLD) is a rare autoimmune condition. This study aims to systematically analyze the clinical characteristics of IgG4-RLD to enhance clinicians' awareness and improve patient outcomes.
Methods: This retrospective analysis investigates the clinical data of 20 patients diagnosed with IgG4-RLD at the Yichang Central People's Hospital between January 2019 and April 2025.
Results: The mean age at diagnosis among the 20 patients with IgG4-RLD was 60.10 ± 10.34 years, with a male-to-female ratio of 3:1. The most frequent clinical manifestations were hemoptysis and abnormalities in pulmonary imaging. Eight patients (40.00%) presented with isolated pulmonary involvement, while 12 patients (60.00%) exhibited extra-pulmonary organ involvement, with lymph node involvement being the most prevalent. The pulmonary imaging characteristics primarily included solid nodular patterns in 10 patients (50.00%) and round ground-glass opacity (GGO) patterns in 9 patients (45.00%). Patients with round GGO patterns exhibited a higher incidence of hemoptysis and predominantly had a history of respiratory conditions (P < 0.05). Patients with solid nodular patterns exhibited significantly higher percentages of eosinophils and lymphocytes, as well as elevated serum IgG levels, compared to those with round GGO patterns (P < 0.05). By contrast, patients with round GGO patterns demonstrated significantly higher percentages of neutrophils and a markedly increased neutrophil-to-lymphocyte ratio (NLR) compared to those with solid nodular patterns (P < 0.05).
Conclusions: The clinical manifestations of IgG4-RLD are complex and heterogeneous. Clinicians need to acquire a thorough understanding of these features in order to develop personalized diagnostic and therapeutic approaches, thereby enhancing patient outcomes. Key Points • The pulmonary imaging characteristics of IgG4-RLD were primarily manifested as solid nodular patterns and round GGO patterns. • Patients with round GGO patterns were more likely to experience hemoptysis, and the majority of these patients presented with a history of respiratory conditions. • Patients with solid nodular patterns demonstrated significantly higher percentages of eosinophils, lymphocytes, and serum IgG levels compared to those with round GGO patterns. • Patients with round GGO patterns demonstrated significantly higher percentages of neutrophils and a markedly increased NLR compared to those with solid nodular patterns.
期刊介绍:
Clinical Rheumatology is an international English-language journal devoted to publishing original clinical investigation and research in the general field of rheumatology with accent on clinical aspects at postgraduate level.
The journal succeeds Acta Rheumatologica Belgica, originally founded in 1945 as the official journal of the Belgian Rheumatology Society. Clinical Rheumatology aims to cover all modern trends in clinical and experimental research as well as the management and evaluation of diagnostic and treatment procedures connected with the inflammatory, immunologic, metabolic, genetic and degenerative soft and hard connective tissue diseases.