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IgG4 相关疾病伴气管支气管粟粒状结节和哮喘:病例报告及文献复习。

IgG4-related disease with tracheobronchial miliary nodules and asthma: a case report and review of the literature.

机构信息

Center for Respiratory Diseases, China-Japan Friendship Hospital; Department of Pulmonary and Critical Care Medicine, China-Japan Friendship Hospital; National Clinical Research Center for Respiratory Diseases, Peking University Health Science Center, No 2, East Yinghua Road, Chaoyang District, Beijing, 100029, People's Republic of China.

Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, No 167, Beilishi Road, Xicheng District, Beijing, 100037, People's Republic of China.

出版信息

BMC Pulm Med. 2019 Oct 30;19(1):191. doi: 10.1186/s12890-019-0957-9.

Abstract

BACKGROUND

IgG4-related disease (IgG4-RD) is a systemic autoimmune disease that can affect multiple organs of the body. Pulmonary manifestations of IgG4-RD include pulmonary solid nodules, thickening of bronchovascular bundles, interstitial involvement, and ground glass opacities. Here we present a rare case of IgG4-RD with tracheobronchial nodules and review the relevant literature.

CASE PRESENTATION

A 52-year-old man was admitted to our hospital with a history of intermittent cough for 27 months and recurrent wheezing for 17 months. He had been diagnosed with asthma prior to admission and was responsive to oral prednisone (30 mg/day, with gradual tapering). Bronchoscopy performed 2 years prior to admission showed tracheal and bronchial mucosal hyperemia, edema, and miliary nodules. Pathological tests showed chronic inflammation with focal lymphocytic infiltration in the bronchial mucosa. The patient had recurrent cough and wheezing after prednisone was stopped or the dose reduced. At the time of admission to our hospital, his serum immunoglobulin G4 (IgG4) level had increased to 7.35 g/L. Following bronchoscopy, the IgG4 expression in the bronchial mucosa was compared with that observed during the last two bronchoscopies. Bronchoscopy performed 7 months prior to admission revealed IgG4+ plasma cell infiltration in the bronchial tissue, with > 10 IgG4+ plasma cells per high power field and an IgG4+/IgG+ cell ratio of > 40%. The current bronchoscopy revealed a decrease in IgG4 expression in the bronchial tissue, probably because of the intermittent prednisone treatment. The case fulfilled the comprehensive clinical diagnostic criteria for IgG4-RD. He received prednisone and azathioprine, and he has never developed recurrence.

CONCLUSIONS

Our case exhibited three important clinical indication: First, tracheobronchial miliary nodules could be the presentation of IgG4-related disease. Second, IgG4-related disease with pulmonary involvement has close connection with asthma. Last, IgG4-related disease can be very sensitive to prednisone, the infiltration of IgG4 positive plasma cells decreased after prednisone treatment and symptoms significantly improved in our case. In conclusion, we reported the first case of IgG4-RD presenting with miliary nodules on the tracheal and bronchial tube walls combined with asthma. The findings will further our understanding of the characteristics of IgG4-RD.

摘要

背景

IgG4 相关疾病(IgG4-RD)是一种系统性自身免疫性疾病,可影响身体的多个器官。IgG4-RD 的肺部表现包括肺部实性结节、支气管血管束增厚、间质性浸润和磨玻璃影。在这里,我们报告一例罕见的 IgG4-RD 伴气管支气管结节,并复习相关文献。

病例介绍

一名 52 岁男性,因间歇性咳嗽 27 个月和反复喘息 17 个月而入院。入院前被诊断为哮喘,对口服泼尼松(30mg/天,逐渐减量)有反应。入院前 2 年支气管镜检查显示气管和支气管黏膜充血、水肿和粟粒状结节。病理检查显示支气管黏膜慢性炎症伴局灶性淋巴细胞浸润。泼尼松停药或减量后,患者反复出现咳嗽和喘息。入院时,患者血清 IgG4 水平升高至 7.35g/L。支气管镜检查后,比较了支气管黏膜的 IgG4 表达,与前两次支气管镜检查结果进行了比较。入院前 7 个月的支气管镜检查显示,支气管组织中有 IgG4+浆细胞浸润,高倍视野下>10 个 IgG4+浆细胞,IgG4+/IgG+细胞比值>40%。目前的支气管镜检查显示,支气管组织中的 IgG4 表达减少,可能是由于间歇性使用泼尼松治疗。该病例符合 IgG4-RD 的综合临床诊断标准。他接受了泼尼松和硫唑嘌呤治疗,从未复发。

结论

我们的病例表现出三个重要的临床特征:首先,气管支气管粟粒结节可能是 IgG4 相关疾病的表现。其次,伴有肺部受累的 IgG4 相关疾病与哮喘密切相关。最后,IgG4 相关疾病对泼尼松非常敏感,我们的病例在泼尼松治疗后 IgG4 阳性浆细胞浸润减少,症状明显改善。总之,我们报告了首例 IgG4-RD 表现为气管和支气管管壁粟粒结节并伴有哮喘的病例。这些发现将进一步加深我们对 IgG4-RD 特征的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60e5/6822466/9199212a691a/12890_2019_957_Fig1_HTML.jpg

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