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抗中性粒细胞胞浆抗体(ANCA)相关性血管炎伴中耳炎(OMAAV)的临床特征及治疗结果:对日本全国性调查中235例患者的回顾性分析

Clinical features and treatment outcomes of otitis media with antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (OMAAV): A retrospective analysis of 235 patients from a nationwide survey in Japan.

作者信息

Harabuchi Yasuaki, Kishibe Kan, Tateyama Kaori, Morita Yuka, Yoshida Naohiro, Kunimoto Yasuomi, Matsui Takamichi, Sakaguchi Hiroshi, Okada Masahiro, Watanabe Takeshi, Inagaki Akira, Kobayashi Shigeto, Iino Yukiko, Murakami Shingo, Takahashi Haruo, Tono Tetsuya

机构信息

a Department of Otolaryngology-Head and Neck Surgery , Asahikawa Medical University , Asahikawa , Hokkaido , Japan.

b Department of Otolaryngology , Oita University Faculty of Medicine , Oita , Japan.

出版信息

Mod Rheumatol. 2017 Jan;27(1):87-94. doi: 10.1080/14397595.2016.1177926. Epub 2016 May 11.

Abstract

OBJECTIVE

We aimed to analyze clinical features and treatment outcomes of otitis media caused by antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV), i.e. otitis media with AAV (OMAAV).

METHODS

This survey was performed between December 2013 and February 2014. The study began with a preliminary survey to 123 otolaryngology institutions in Japan to inquire about their experiences with OMAAV patients during the past 10 years, and was followed by a questionnaire survey to investigate clinical and laboratory findings. OMAAV was defined using the criteria described in the text.

RESULTS

Two hundred and thirty-five patients classified as OMAAV were enrolled in this study. They were characterized as follows: (1) disease onset with initial signs/symptoms due to intractable otitis media with effusion or granulation, which did not respond to ordinary treatments such as antibiotics and insertion of tympanic ventilation tubes, followed by progressive hearing loss; (2) predominantly female (73%) and older (median age: 68 years); (3) predominantly myeloperoxidase (MPO)-ANCA-positive (60%), followed by proteinase 3 (PR3)-ANCA-positive (19%) and both ANCAs-negative (16%); (4) frequently observed accompanying facial palsy (36%) and hypertrophic pachymeningitis (28%); and (5) disease often involving lung (35%) and kidney (26%) lesions. Four factors associated with OMAAV were found to be related to an unfavorable clinical course threatening the patient's hearing and/or lives, namely facial palsy, hypertrophic pachymeningitis, both ANCAs-negative phenotype, and disease relapse. The occurrence of hypertrophic pachymeningitis was associated with facial palsy (p < 0.05), both ANCAs-negative phenotype (p < 0.001), and headache (p < 0.001). The administration of corticosteroid together with an immunosuppressant was an independent predicting factor for lack of disease relapse (odds ratio [OR] = 1.90, p = 0.03) and an improvement in hearing loss (OR =2.58, p = 0.0002).

CONCLUSION

Since OMAAV has novel clinical features, the disease may be categorized as a subentity for the classification of AAV.

摘要

目的

我们旨在分析抗中性粒细胞胞浆抗体(ANCA)相关血管炎(AAV)所致中耳炎,即伴AAV的中耳炎(OMAAV)的临床特征及治疗结果。

方法

本调查于2013年12月至2014年2月进行。研究首先对日本123家耳鼻喉科机构进行初步调查,询问其在过去10年中对OMAAV患者的诊治经验,随后进行问卷调查以调查临床和实验室检查结果。OMAAV采用文中所述标准进行定义。

结果

本研究纳入了235例归类为OMAAV的患者。其特征如下:(1)疾病起病时最初的体征/症状为顽固性渗出性中耳炎或肉芽,对抗生素和鼓膜置管等常规治疗无反应,随后出现进行性听力丧失;(2)女性居多(73%)且年龄较大(中位年龄:68岁);(3)主要为髓过氧化物酶(MPO)-ANCA阳性(60%),其次是蛋白酶3(PR3)-ANCA阳性(19%)和两种ANCA均阴性(16%);(4)常伴有面神经麻痹(36%)和肥厚性硬脑膜炎(28%);(5)疾病常累及肺部(35%)和肾脏(26%)病变。发现与OMAAV相关的四个因素与威胁患者听力和/或生命的不良临床病程有关,即面神经麻痹、肥厚性硬脑膜炎、两种ANCA均阴性表型和疾病复发。肥厚性硬脑膜炎的发生与面神经麻痹(p<0.05)、两种ANCA均阴性表型(p<0.001)和头痛(p<0.001)相关。糖皮质激素与免疫抑制剂联合使用是疾病无复发(比值比[OR]=1.90,p=0.03)和听力损失改善(OR=2.58,p=0.0002)的独立预测因素。

结论

由于OMAAV具有新的临床特征,该疾病可能可归类为AAV分类中的一个亚实体。

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