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[IgG4相关性肺病:8例分析及文献复习]

[IgG4-related lung disease: analysis of 8 cases and literature review].

作者信息

Han G J, Hu H, Mao D, Bai X, She D Y, Zhao S F, Wen Z L, Gao J

机构信息

Respiratory Department of People's Liberation Army General Hospital, Beijing 100853, China.

出版信息

Zhonghua Jie He He Hu Xi Za Zhi. 2017 Mar 12;40(3):193-198. doi: 10.3760/cma.j.issn.1001-0939.2017.03.010.

Abstract

To improve the understanding and treatment of IgG4-related lung disease (IgG4-RLD). The clinical characteristics, serum IgG4 levels, pathological features, chest CT, therapy and prognosis of 8 patients with IgG4-RLD were retrospectively analyzed. These patients were admitted to the People's Liberation Army General Hospital and the pathological diagnosis was made between December 2005 and March 2016. Relevant literatures were reviewed. The 8 patients with IgG4-RLD included 4 men and 4 women, with an average age of (59±4) years (range, 37-74). The respiratory symptoms included shortness of breath, cough, and expectoration. Extra-pulmonary symptoms included abdominal pain, facial edema, and fever. Extrapulmonary organs were involved in 7 cases. Serum IgG4 levels were elevated in 8 cases, with an average concentration of(17±6)g/L. Chest CT showed solid lung nodules in 6, alveolar-interstitial infiltration in 5, bronchovascular lesions in 3 and ground glass shadows in 2 cases. PET/CT was performed in 2 cases and it showed multiple organ involvement with higher radioactivity uptake(SUVmax2.9-4.2). The pathological examination found lymphocyte and plasma cell infiltration in 7, fibrous tissue hyperplasia in 5, and occlusive vasculitis in 2 cases. On immunohistochemical staining, the ratio of IgG4-positive plasma cells to IgG-positive plasma cells was higher than 40%in 3 cases. The number of IgG4-positive plasma cells was 10-50/HP in 8 cases. The misdiagnosis rate was 100% before the final diagnosis was made. Three cases received glucocorticoids with immunosuppressant therapy, 2 received surgery combined with glucocorticoid therapy, 2 received glucocorticoid therapy alone, and 1 only received surgery. The follow-up time was 4-132 months, with remission in 7 cases, and disease progression in 1 case, but no death. A total of 195 cases of IgG4-RLD were reviewed from the literature, among whom 111 cases were admitted with respiratory symptoms, 144 with extra-pulmonary involvement. Serum IgG4 levels were detected in 179 cases, with an average concentration of 5.408 g/L. The nodular type was predominant, accounting for 36.9%. Of these cases, 178 received glucocorticoid treatment with disease remission. The major clinical manifestations of IgG4-RLD were shortness of breath, cough and expectoration. Multiple organ lesions were common. The misdiagnosis rate was extremely high. The diagnosis could be made based on pathological features and IgG4 serum levels . Glucocorticoid treatment was effective.

摘要

为提高对IgG4相关性肺病(IgG4-RLD)的认识及治疗水平。回顾性分析8例IgG4-RLD患者的临床特征、血清IgG4水平、病理特征、胸部CT、治疗及预后情况。这些患者均入住解放军总医院,病理诊断时间为2005年12月至2016年3月。并复习相关文献。8例IgG4-RLD患者中,男性4例,女性4例,平均年龄(59±4)岁(范围37-74岁)。呼吸系统症状包括气短、咳嗽、咳痰。肺外症状包括腹痛、面部水肿、发热。7例累及肺外器官。8例血清IgG4水平升高,平均浓度为(17±6)g/L。胸部CT表现为实性肺结节6例,肺泡-间质浸润5例,支气管血管病变3例,磨玻璃影2例。2例行PET/CT检查,显示多器官受累,放射性摄取增高(SUVmax 2.9-4.2)。病理检查发现7例有淋巴细胞和浆细胞浸润,5例有纤维组织增生,2例有闭塞性血管炎。免疫组化染色显示,3例IgG4阳性浆细胞与IgG阳性浆细胞之比高于40%。8例IgG4阳性浆细胞数为10-50/HP。最终诊断前误诊率为100%。3例接受糖皮质激素联合免疫抑制剂治疗,2例接受手术联合糖皮质激素治疗,2例仅接受糖皮质激素治疗,1例仅接受手术治疗。随访时间4-132个月,7例缓解,1例疾病进展,但无死亡病例。从文献中复习了共195例IgG4-RLD病例,其中111例以呼吸系统症状入院,144例有肺外受累。179例检测血清IgG4水平,平均浓度为5.408 g/L。结节型为主,占36.9%。其中178例接受糖皮质激素治疗后病情缓解。IgG4-RLD的主要临床表现为气短、咳嗽、咳痰。多器官病变常见。误诊率极高。可根据病理特征及IgG4血清水平作出诊断。糖皮质激素治疗有效。

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