Clin Lab. 2024 Jun 1;70(6). doi: 10.7754/Clin.Lab.2023.231227.
IgG4-related disease (IgG4-RD) is an immune-mediated systemic inflammatory fibrotic disease, which is a relatively rare and novel disease that can involve multiple organs or tissues, with variable clinical manifestations, and for which pulmonary involvement has been reported relatively infrequently.
Here we report a case of pulmonary infection that was initially suspected and received anti-inflammatory treatment, but the symptoms did not improve. CT examination indicated progression of the pulmonary lesion, and the nature of the lesion could not be determined by tracheoscopy and bronchoalveolar lavage. The diagnosis of IgG4 related lung disease (IgG4-RLD) was confirmed by percutaneous lung biopsy. A joint literature analysis was conducted to improve clinicians' understanding of this disease.
The patient's history, symptoms, signs and relevant examination results were analyzed. The final diagnosis was IgG4-RLD.
When the clinical symptoms and imaging manifestations of the patients are consistent with IgG4-RLD, pathological examination can be appropriately performed to clarify the nature of the lesions. More consideration should be given to the possibility of disease diagnosis to avoid misdiagnosis and underdiagnosis, and proper treatment should be given at an early stage.
IgG4 相关疾病(IgG4-RD)是一种免疫介导的系统性炎症性纤维性疾病,是一种相对罕见和新颖的疾病,可以累及多个器官或组织,具有多变的临床表现,其中肺部受累相对较少报道。
我们在此报告一例肺部感染,最初被怀疑并接受了抗炎治疗,但症状没有改善。CT 检查提示肺部病变进展,经气管镜和肺泡灌洗无法确定病变性质。经经皮肺活检确诊为 IgG4 相关肺疾病(IgG4-RLD)。进行了联合文献分析,以提高临床医生对这种疾病的认识。
分析了患者的病史、症状、体征和相关检查结果。最终诊断为 IgG4-RLD。
当患者的临床症状和影像学表现符合 IgG4-RLD 时,可以进行适当的病理检查以明确病变性质。应更多地考虑疾病诊断的可能性,避免误诊和漏诊,并在早期给予适当的治疗。