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IgG4相关性鼻窦炎的临床及影像学特征分析

[Analyses of clinical and radiological characteristics of IgG4-related rhinosinusitis].

作者信息

Wang M J, Gao Y, Zhou B, Li Y C, Cui S J, Huang Q, Sun Y

机构信息

Department of Otorhinolaryngology Head and Neck Surgery, Beijing TongRen Hospital, Capital Medical University, Key Laboratory of Otolaryngology Head and Neck Surgery, Ministry of Education(Capital Medical University), Beijing 100730, China.

Department of Rheumatology, Beijing TongRen Hospital, Capital Medical University, Beijing 100730, China.

出版信息

Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2019 Mar 7;54(3):187-191. doi: 10.3760/cma.j.issn.1673-0860.2019.03.005.

Abstract

To discuss the clinical and radiological features of IgG4-related rhinosinusitis. In this retrospective research, the clinical data of 16 patients diagnosed with IgG4 related rhinosinusitis, who were enrolled in Beijing Tongren Hospital from November 2013 to September 2017, were collected. The clinical features, laboratory findings, radiological findings, histological features, treatment and prognosis were all summarized. There were 12 males and 4 females among 16 patients, and male-to-female ratio was 3︰1. The age was between 30 to 70 years old, with median age of 52 years old. The chief nasal complaints were nasal obstruction and hyposmia, complicated with proptosis and eyelid swelling in 11 patients (11/16). Serum IgG4 levels were elevated in all patients and the value was over 1.44 g/L, and one patient serum IgG4 level was up to 49.70 g/L. Computed tomography (CT) showed the mainly affected sinuses were bilateral ethmoid sinus and olfactory cleft. The classic feature of CT scans was thickening of the involved bilateral ethmoid sinus mucous membrane with ethmoid bone absorption, which was mainly at midline. Histological features were severe inflammation of the mucosal tissue with mass of neutrophils and plasma cell infiltration. All patients were treated by methylprednisolone combined with cyclophosphamide or methotrexate. Remission of symptoms was detected in all patients. The clinical features of IgG4-related rhinosinusitis are often accompanied by orbital tissue involvement, elevated IgG4 serum concentration, associated sinus imaging changes, and sensitive glucocorticoid and immunosuppressive therapy.

摘要

探讨IgG4相关性鼻-鼻窦炎的临床及影像学特征。在这项回顾性研究中,收集了2013年11月至2017年9月在北京同仁医院就诊的16例诊断为IgG4相关性鼻-鼻窦炎患者的临床资料。总结了其临床特征、实验室检查结果、影像学表现、组织学特征、治疗及预后情况。16例患者中男性12例,女性4例,男女比例为3∶1。年龄在30至70岁之间,中位年龄为52岁。主要鼻部症状为鼻塞和嗅觉减退,11例患者(11/16)伴有眼球突出和眼睑肿胀。所有患者血清IgG4水平均升高,数值均超过1.44 g/L,1例患者血清IgG4水平高达49.70 g/L。计算机断层扫描(CT)显示主要受累鼻窦为双侧筛窦及嗅裂。CT扫描的典型表现为双侧受累筛窦黏膜增厚伴筛骨吸收,主要位于中线部位。组织学特征为黏膜组织重度炎症,有大量中性粒细胞和浆细胞浸润。所有患者均接受甲泼尼龙联合环磷酰胺或甲氨蝶呤治疗。所有患者症状均缓解。IgG4相关性鼻-鼻窦炎的临床特征常伴有眶周组织受累、血清IgG4浓度升高、鼻窦相关影像学改变,以及对糖皮质激素和免疫抑制治疗敏感。

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