Wu M, Wang L, Ji Y, Shang G G, Hong Q Y
Department of Pulmonary Medicine, Zhongshan Hospital, Fudan University, Shanghai 200032, China (is now working at the Department of Pulmonary Medicine, Fujian Province Geriatrics Hospital).
Zhonghua Yi Xue Za Zhi. 2018 Nov 13;98(42):3442-3446. doi: 10.3760/cma.j.issn.0376-2491.2018.42.013.
To improve the understanding and treatment of IgG4-related lung disease (IgG4-RLD) by analyzing the clinical characteristics of patients. A total of 13 patients with IgG4-related lung disease (IgG4-RLD) diagnosed by pathology at Zhongshan Hospital affiliated to Fudan University during December 2007 to December 2017 were included. The clinical characteristics, chest CT, pathological features, serum IgG4 levels, therapy and prognosis of these 13 patients were analyzed. The 13 patients with IgG4-RLD included 8 men and 5 women, with an average age of (51.1±14.8) years. The clinical manifestations were varied, 10 patients showed respiratory symptoms, mainly including cough (=9), expectoration (=6), hemoptysis (=6), chest tightness (=2) and breathless (=2). Multiple organs were involved in 12 cases. Chest CT showed solid lung nodules (=9), ground glass shadows (=1), alveolar-interstitial infiltration (=3), bronchovascular lesions (=3), and the solid lung nodules was predominant. Enlargement of lymph nodes in the mediastinal and bilateral hilum of the lung were present in 10 cases. Serum IgG4 levels were elevated in all the 13 cases, with an average concentration of (7.92 ±13.98)g/L. Quite amount of lymphocytes, plasma cell infiltration and fibrosis were common pathologic findings. Immunohistochemical staining showed a large number of IgG4 positive plasma cells infiltration with IgG4 positive plasma cells count 10-320/HP in 13 cases. The ratio of IgG4 positive plasma cells to IgG positive plasma cells was higher than 40%. Eight patients received glucocorticoid therapy alone, five received glucocorticoids with immunosuppressant therapy. After treatment, 10 patients were with remission, and disease progressed in 3 patients, but no death. The clinical manifestations and imaging features of IgG4-RLD are diverse, and lesions can often involve multiple organs. The diagnosis could be made based on pathological features and IgG4 serum levels. Glucocorticoid can be used as the first choice for the treatment of IgG4-RLD.
通过分析患者的临床特征,以提高对IgG4相关性肺病(IgG4-RLD)的认识和治疗水平。纳入2007年12月至2017年12月期间在复旦大学附属中山医院经病理诊断的13例IgG4相关性肺病(IgG4-RLD)患者。分析这13例患者的临床特征、胸部CT、病理特征、血清IgG4水平、治疗及预后情况。13例IgG4-RLD患者中,男性8例,女性5例,平均年龄(51.1±14.8)岁。临床表现多样,10例患者出现呼吸道症状,主要包括咳嗽(9例)、咳痰(6例)、咯血(6例)、胸闷(2例)和气促(2例)。12例患者累及多个器官。胸部CT表现为实性肺结节(9例)、磨玻璃影(1例)、肺泡-间质浸润(3例)、支气管血管病变(3例),以实性肺结节为主。10例患者出现纵隔及双侧肺门淋巴结肿大。13例患者血清IgG4水平均升高,平均浓度为(7.92±13.98)g/L。病理常见大量淋巴细胞、浆细胞浸润及纤维化。免疫组化染色显示13例均有大量IgG4阳性浆细胞浸润,IgG4阳性浆细胞计数为10~320/HP。IgG4阳性浆细胞与IgG阳性浆细胞的比值高于40%。8例患者仅接受糖皮质激素治疗,5例患者接受糖皮质激素联合免疫抑制剂治疗。治疗后,10例患者缓解,3例患者病情进展,但无死亡病例。IgG4-RLD的临床表现和影像特征多样,病变常累及多个器官。可根据病理特征和血清IgG4水平进行诊断。糖皮质激素可作为IgG4-RLD治疗的首选药物。