北京大学学报(医学版) ›› 2018, Vol. 50 ›› Issue (6): 1039-1043. doi: 10.19723/j.issn.1671-167X.2018.06.017

• 论著 • 上一篇    下一篇

免疫球蛋白G4相关疾病患者发病形式及就诊行为特征分析

朱星昀1,刘燕鹰1,(),孙学娟2,于萍3,刘爽4,付美艳5,刘栩1,任立敏1,栗占国1   

  1. 1. 北京大学人民医院风湿免疫科, 北京 100044
    2. 廊坊市人民医院风湿免疫科, 河北廊坊 065000
    3. 唐山开滦总医院风湿免疫科, 河北唐山 063000
    4. 昆明医科大学第一附属医院风湿免疫科, 昆明 650032
    5. 乌鲁木齐市友谊医院风湿免疫科, 乌鲁木齐 830049
  • 出版日期:2018-12-18 发布日期:2018-12-18
  • 通讯作者: 刘燕鹰 E-mail:liuyanying20030801@msn.com
  • 基金资助:
    国家重点研发计划(2017YFA0105802、北京大学人民医院研究与发展基金RDH 2017-02)

A cross-sectional study of the clinical features and physician visit patterns at onset of immunoglobulin G4 related disease

Xing-yun ZHU1,Yan-ying LIU1,(),Xue-juan SUN2,Ping YU3,Shuang LIU4,Mei-yan FU5,Xu LIU1,Li-min REN1,Zhan-guo LI1   

  1. 1. Department of Rheumatology and Immunology, Peking University People’s Hospital, Beijing 100044, China
    2. Department of Rheumatology and Immunology, The People’s Hospital of Langfang City, Langfang 065000, Hebei, China
    3. Department of Rheumatology and Immunology, Kailuan General Hospital, Tangshan 063000, Hebei, China
    4. Department of Rheumatology and Immunology, First Affiliated Hospital of Kuiming Medical University, Kunming 650032, China
    5. Department of Rheumatology and Immunology, Urumuqi Youyi Hospital, Urumuqi 830049, China
  • Online:2018-12-18 Published:2018-12-18
  • Contact: Yan-ying LIU E-mail:liuyanying20030801@msn.com

摘要:

目的: 了解免疫球蛋白G4相关疾病(immunoglobulin G4-related disease,IgG4RD)患者的起病形式和就诊行为现况。方法: 采用流行病学研究方法,对在北京大学人民医院就诊的112例IgG4RD患者进行调查,其中资料完整者100例,内容包括患者的性别、年龄、身高、体重、病史、就诊过程及患病对工作的影响等。结果: 本组IgG4RD患者平均发病年龄为(51.51±12.9)岁,男女患病比为1 :0.75,女性发病年龄显著早于男性(P<0.001)。IgG4RD患者常见受累器官比例依次是颌下腺69%、泪腺59%、胰腺28%、腮腺28%,女性患者泪腺受累较多(P<0.05)。62%的患者合并有过敏性疾病。IgG4RD患者首诊科室主要为普通外科(9/100)、口腔及颌面外科(17/100)、风湿免疫科(16/100),确诊科室集中在风湿免疫科(67/100)、口腔颌面外科(16/100)和消化内科(7/100)。2010年后发病的患者平均发病到确诊月数较2010年前显著降低(P<0.01)。未明确诊断前接受过手术的患者有43例,首诊于外科的患者更易接受手术(P<0.01)。18%的患者因患病影响了工作。结论: IgG4RD女性患者并不少见,且发病年龄多早于男性,唾液腺、泪腺为最常见受累器官,且多为首发。过敏性疾病为IgG4RD常见的临床表现。临床漏诊、误诊普遍,近半数患者在诊断前接受了不必要的手术治疗,近年来延误诊断的情况略有改善,但仍应引起临床医师更多重视。

关键词: 自身免疫病, 免疫球蛋白G, 体征和症状, 就诊行为特征

Abstract:

Objective: To comprehend clinical features and patient’s physician visit patterns at onset of immunoglobulin G4 related disease (IgG4RD). Methods: In the study, 100 patients with IgG4RD who received treatments in the Department of Rheumatology and Immunology of Peking University People’s Hospital from Apr. 1st, 2017 to Apr. 1st, 2018 were investigated, including gender, age, height, body weight, age of onset, physician visit history, primary history and how did the disease affected their life, etc. Results: In this 100 IgG4RD cohort (57 males and 43 females), the male/female ratio was 1 :0.75, the mean age of onset was (51.51±12.9) years, and the median duration was 49 months (ranging from 4 to 231 months). The onset age of males was significantly older than that of females (P<0.01). The manifestations showed that up to 69% patients had submaxillay glands lesion, 59% patients had lacrimal glands lesion, 28% patients had pancreas involvement and 28% patients had parotid glands involvement. The females had more lacrimal glands involvement (P<0.05). 62% patients were complicated with anaphylactic disease. The primary physician visit departments concentrated upon general surgery department (19/100), oral and maxillofacial surgery department (17/100), rheumatology and immunology department (16/100), ophthalmology department (15/100) and gastroenterology department (10/100). The departments where the confirmed diagnose was made concentrated upon rheumatology department (67/100),oral and maxillofacial surgery department (16/100) and gastroenterology department (7/100). The mean diagnosis duration after 2010 was (16.96±2.163) months, significantly shorter than that before 2010, which was (113.3±11.01) months. Before the definite diagnose was made, 43% patients underwent surgeries and 12% patients had more than one time surgeries. The patients whose first-visit department was a surgery department were more likely to undergo surgeries (P<0.01). 18% patients (18/100) stated that the disease had affected their work. Conclusion: In this cohort of the IgG4RD patients, female is common and has earlier onset age than male. The major manifestations of IgG4RD are salivary glands, lacrimal glands and pancreas involvement. The common chief complains are salivary glands and lacrimal glands enlargement. Accompanied by anaphylactic disease is a marked manifestation of this disease. Delayed diagnoses are not rare, though this situation has been improved since 2010, and more attention still should be paid to the disease.

Key words: Autoimmune diseases, Immunoglobulin G, Signs and symptoms, Physicians visit pattern

中图分类号: 

  • R593.2

图1

IgG4相关疾病患者的首发症状(n=100)"

表1

100例IgG4相关疾病患者的受累器官"

Organs n %
Submaxillary gland 69 69.0
Lacrimal gland 59 59.0
Pancreas 28 28.0
Parotid gland 28 28.0
Skin 24 24.0
Lymph node 22 22.0
Biliary tract 15 15.0
Retroperitoneal 11 11.0
Paranasal sinuses 11 11.0
Lung 10 10.0
Aorta 3 3.0
Prostate gland 2 2.0

表2

100例IgG4相关疾病患者的首诊科室分布"

Departments n %
General surgery 19 19.0
Oral and maxillofacial surgery 17 17.0
Rheumatology and immunology 16 16.0
Ophthalmology 15 15.0
Gastroenterology 10 10.0
Otolaryngology and head neck surgery 8 8.0
Urology 3 3.0
Nephrology 3 3.0
General medicine 3 3.0
Oncology 2 2.0
Respiratory 1 1.0
Emergency 1 1.0
Dermatology 1 1.0
Liver disease 1 1.0

表3

100例IgG4相关疾病患者的确诊科室分布"

Departments n %
Rheumatology and immunology 67 67.0
Oral and maxillofacial surgery 16 16.0
Gastroenterology 7 7.0
General surgery 4 4.0
Ophthalmology 2 2.0
Nephrology 1 1.0
Otolaryngology and head neck surgery 1 1.0
Respiratory 1 1.0
Infectious disease 1 1.0

图2

100例IgG4相关疾病患者发病到确诊的时长"

[1] Kamisawa T, Funata N, Hayashi Y , et al. A new clinicopatholo-gical entity of IgG4-related autoimmune disease[J]. J Gastroenterol, 2003,38(10):982-984.
doi: 10.1007/s00535-003-1175-y pmid: 14614606
[2] Umehara H, Nakajima A, Nakamura T , et al. IgG4-related di-sease and its pathogenesis-cross-talk between innate and acquired immunity[J]. Int Immunol, 2014,26(11):585-595.
doi: 10.1093/intimm/dxu074 pmid: 4201844
[3] Su Y, Sun W, Wang C , et al. Detection of serum IgG4 levels in patients with IgG4-related disease and other disorders[J]. PLoS One, 2015,10(4):e0124233.
doi: 10.1371/journal.pone.0124233 pmid: 4401680
[4] Inoue D, Yoshida K, Yoneda N , et al. IgG4-related disease: dataset of 235 consecutive patients[J]. Medicine (Baltimore), 2015,94(15):e680.
doi: 10.1097/MD.0000000000000680
[5] Lin W, Lu S, Chen H , et al. Clinical characteristics of immunoglobulin G4-related disease: a prospective study of 118 Chinese patients[J]. Rheumatology (Oxford), 2015,54(11):1982-1990.
doi: 10.1093/rheumatology/kev203 pmid: 26106212
[6] Zhang J, Chen H, Ma Y , et al. Characterizing IgG4-related di-sease with 18F-FDG PET/CT: a prospective cohort study [J]. Eur J Nucl Med Mol Imaging, 2014,41(8):1624-1634.
doi: 10.1007/s00259-014-2729-3 pmid: 4089015
[7] Uchida K, Masamune A, Shimosegawa T , et al. Prevalence of IgG4-related disease in Japan based on nationwide survey in 2009[J]. Int J Rheumatol, 2012,2012:358371.
doi: 10.1155/2012/358371 pmid: 22899936
[8] Takahashi H, Yamamoto M, Suzuki C , et al. The birthday of a new syndrome: IgG4-related diseases constitute a clinical entity[J]. Autoimmun Rev, 2010,9(9):591-594.
doi: 10.1016/j.autrev.2010.05.003 pmid: 20457280
[9] Umehara H, Okazaki K, Masaki Y , et al. Comprehensive diagnostic criteria for IgG4-related disease (IgG4-RD), 2011[J]. Mod Rheumatol, 2012,22(1):21-30.
doi: 10.3109/s10165-011-0571-z
[10] Kamisawa T, Zen Y, Pillai S , et al. IgG4-related disease[J]. Lancet, 2015,385(9976):1460-1471.
doi: 10.1016/S0140-6736(14)60720-0
[11] Masaki Y, Dong L, Kurose N , et al. Proposal for a new clinical entity, IgG4-positive multiorgan lymphoproliferative syndrome: analysis of 64 cases of IgG4-related disorders[J]. Ann Rheum Dis, 2009,68(8):1310-1315.
doi: 10.1136/ard.2008.089169 pmid: 18701557
[12] Zen Y, Nakanuma Y . IgG4-related disease: a cross-sectional study of 114 cases[J]. Am J Surg Pathol, 2010,34(12):1812-1819.
doi: 10.1097/PAS.0b013e3181f7266b
[13] Fong W, Liew I, Tan D , et al. IgG4-related disease: features and treatment response in a multi-ethnic cohort in Singapore[J]. Clin Exp Rheumatol, 2018,36(Suppl. 112):89-93.
pmid: 29846168
[14] Finkelman FD, Boyce JA, Vercelli D , et al. Key advances in mechanisms of asthma, allergy, and immunology in 2009[J]. J Allergy Clin Immunol, 2010,125(2):312-318.
doi: 10.1016/j.jaci.2011.12.968 pmid: 2671063
[15] Gao Y, Zheng M, Cui L , et al. IgG4-related disease: association between chronic rhino-sinusitis and systemic symptoms[J]. Eur Arch Otorhinolaryngol, 2018,275(8):2013-2019.
doi: 10.1007/s00405-018-5013-5
[16] Hirano K, Tada M, Isayama H , et al. Long-term prognosis of autoimmune pancreatitis with and without corticosteroid treatment[J]. Gut, 2007,56(12):1719-1724.
doi: 10.1136/gut.2006.115246 pmid: 2095691
[17] Hong X, Zhang YY, Li W , et al. Treatment of immunoglobulin G4-related sialadenitis: outcomes of glucocorticoid therapy combined with steroid-sparing agents[J]. Arthritis Res Ther, 2018,20(1):12.
doi: 10.1186/s13075-017-1507-6 pmid: 5791187
[1] 宁晓然,王子乔,张珊珊,张霞,唐素玫,刘燕鹰. 超声评分系统在IgG4相关涎腺炎评估中的应用[J]. 北京大学学报(医学版), 2019, 51(6): 1032-1035.
[2] 杨红霞,田小兰,江薇,李文丽,刘青艳,彭清林,王国春,卢昕. 免疫介导坏死性肌病的临床和病理特征分析[J]. 北京大学学报(医学版), 2019, 51(6): 989-995.
[3] 刘恩阳, 刘静芳, 邵文威, 肖琳, 李国辉, 昌晓红, 邱晓彦. 肿瘤来源的IgG抑制脐带血中T细胞的增殖[J]. 北京大学学报(医学版), 2017, 49(5): 824-828.
[4] 冯向辉, 张立, 徐莉, 孟焕新, 陈智滨, 释栋, 路瑞芳. 侵袭性牙周炎患者抗伴放线聚集杆菌血清c型IgG滴度分析[J]. 北京大学学报(医学版), 2015, 47(5): 820-824.
[5] 刘丹, 李茹, 刘佳钰, 姚海红, 陈庆平, 贾园, 苏茵 . 显微镜下多血管炎合并自身免疫性溶血性贫血的临床特点及治疗转归[J]. 北京大学学报(医学版), 2015, 47(4): 657-660.
[6] 顿耀军, 于路平, 杜依青, 盛正祚, 王功伟, 李雪, 杨冰, 徐涛, 黄晓波, 王晓峰. IgG4相关性腹膜后纤维化5例临床特征及文献回顾[J]. 北京大学学报(医学版), 2015, 47(4): 622-627.
[7] 朱一丹, 魏建荣, 黄露, 王绍华, 田寒梅, 郭新彪. 不同大气污染程度地区学龄儿童呼吸系统疾病及症状发生的比较[J]. 北京大学学报(医学版), 2015, 47(3): 395-399.
[8] 王琳琳, 杨娜, 袁悦, 任爱国. 人叶酸受体自身抗体IgG酶联免疫吸附试验检测方法的建立及评价[J]. 北京大学学报(医学版), 2014, 46(3): 483-487.
[9] 张颖健, 赵金霞, 刘蕊, 刘湘源. 肺受累的IgG4相关硬化性疾病1例[J]. 北京大学学报(医学版), 2012, 44(2): 311-315.
[10] 石宇红, 李茹 , 陈适 , 苏茵 , 贾园. 91例混合性结缔组织病患者的临床特点及转归[J]. 北京大学学报(医学版), 2012, 44(2): 270-274.
[11] 王欣, 邓芙蓉, 吕海波, 吴少伟, 郭新彪. 北京市大气污染对成人呼吸系统症状发生的长期影响 [J]. 北京大学学报(医学版), 2011, 43(3): 356-359.
[12] 李珺, 曲贞, 张宜苗, 于峰, 黄婧, 杨瑞, 赵明辉, 刘刚. 检测血、尿IgG4在特发性膜性肾病中的临床意义[J]. 北京大学学报(医学版), 2010, 42(6): 671-674.
[13] 冯向辉, 徐莉, 孟焕新, 张立, 陈智滨, 释栋. 慢性牙周炎患者抗伴放线放线杆菌IgG滴度改变的临床意义[J]. 北京大学学报(医学版), 2010, 42(2): 207-210.
[14] 安媛, 张学武, 栗占国. 青年发病的原发性干燥综合征发病形式和临床特点研究[J]. 北京大学学报(医学版), 2009, 41(3): 324-327.
[15] 卢恬, 朱晓辉, 柳世庆, 郑杰, 邱晓彦. 白细胞介素2促进宫颈癌细胞系HeLaS3免疫球蛋白G的表达[J]. 北京大学学报(医学版), 2009, 41(2): 158-161.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
[1] 张三. 中文标题测试[J]. 北京大学学报(医学版), 2010, 42(1): 1 -10 .
[2] 赵磊, 王天龙 . 右心室舒张末期容量监测用于肝移植术中容量管理的临床研究[J]. 北京大学学报(医学版), 2009, 41(2): 188 -191 .
[3] 万有, , 韩济生, John E. Pintar. 孤啡肽基因敲除小鼠电针镇痛作用增强[J]. 北京大学学报(医学版), 2009, 41(3): 376 -379 .
[4] 张燕, 韩志慧, 钟延丰, 王盛兰, 李玲玲, 郑丹枫. 骨骼肌活组织检查病理诊断技术的改进及应用[J]. 北京大学学报(医学版), 2009, 41(4): 459 -462 .
[5] 赵奇, 薛世华, 刘志勇, 吴凌云. 同向施压测定自酸蚀与全酸蚀粘接系统粘接强度[J]. 北京大学学报(医学版), 2010, 42(1): 82 -84 .
[6] 林红, 王玉凤, 吴野平. 学校生活技能教育对小学三年级学生行为问题影响的对照研究[J]. 北京大学学报(医学版), 2007, 39(3): 319 -322 .
[7] 丰雷, 程嘉, 王玉凤. 注意缺陷多动障碍儿童的运动协调功能[J]. 北京大学学报(医学版), 2007, 39(3): 333 -336 .
[8] 李岳玲, 钱秋瑾, 王玉凤. 儿童注意缺陷多动障碍成人期预后及其预测因素[J]. 北京大学学报(医学版), 2007, 39(3): 337 -340 .
[9] . 书讯[J]. 北京大学学报(医学版), 2007, 39(3): 225 -328 .
[10] 牟向东, 王广发, 刁小莉, 阙呈立. 肺黏膜相关淋巴组织型边缘区B细胞淋巴瘤一例[J]. 北京大学学报(医学版), 2007, 39(4): 346 -350 .