Morita Yuka, Takahashi Kuniyuki, Izumi Shuji, Kubota Yamato, Ohshima Shinsuke, Horii Arata
Department of Otolaryngology Head and Neck Surgery, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Otol Neurotol. 2017 Jan;38(1):97-101. doi: 10.1097/MAO.0000000000001223.
Otitis media (OM) with antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (OMAAV) is a novel concept of ear disease that is characterized by progressive mixed or sensorineural hearing loss with occasional systemic involvement. Considering the accumulating knowledge about the characteristics of and treatment for auditory dysfunction in OMAAV, the objective of this study was to investigate the vestibular function and symptoms of patients with OMAAV.
Retrospective chart review.
University hospital.
Thirty-one OMAAV patients met criteria proposed by the OMAAV study group in Japan.
Clinical characteristics and vestibular tests.
Eleven of 31 OMAAV patients had vestibular symptoms; 3 patients had acute vertigo attack with sudden hearing loss and 8 patients had chronic dizziness. Episodic vertigo was not seen in any of the patients. Three patients who received a less intensive therapy without immunosuppressive agents developed intractable persistent dizziness. All symptomatic patients and six of the nine OMAAV patients without vestibular symptoms showed unilateral or bilateral caloric weakness; therefore, vestibular involvement was present in 84% of OMAAV patients. Gain of vestibulo-ocular reflex was reduced in symptomatic patients. The eye-tracking test and optokinetic nystagmus revealed no evidence of central dysfunction.
Vestibular dysfunction was seen in 84% of OMAAV patients. One-third of OMAAV patients showed vestibular symptoms such as acute vertigo attack or chronic dizziness, which are of peripheral origin. One-third of the symptomatic patients developed intractable dizziness. Initial intensive treatment by combination therapy with steroid and immunosuppressive agents may be essential for preventing the development of intractable dizziness.
抗中性粒细胞胞浆抗体(ANCA)相关血管炎伴中耳炎(OMAAV)是一种耳部疾病的新概念,其特征为进行性混合性或感音神经性听力损失,偶尔伴有全身受累。鉴于关于OMAAV中听觉功能障碍的特征和治疗的知识不断积累,本研究的目的是调查OMAAV患者的前庭功能和症状。
回顾性病历审查。
大学医院。
31例OMAAV患者符合日本OMAAV研究组提出的标准。
临床特征和前庭测试。
31例OMAAV患者中有11例有前庭症状;3例患者出现急性眩晕发作并伴有突然听力损失,8例患者有慢性头晕。所有患者均未出现发作性眩晕。3例接受强度较低的非免疫抑制剂治疗的患者出现难治性持续性头晕。所有有症状的患者以及9例无前庭症状的OMAAV患者中的6例均表现为单侧或双侧冷热试验减弱;因此,84%的OMAAV患者存在前庭受累。有症状患者的前庭眼反射增益降低。眼跟踪测试和视动性眼球震颤未显示中枢功能障碍的证据。
84%的OMAAV患者存在前庭功能障碍。三分之一的OMAAV患者表现出前庭症状,如急性眩晕发作或慢性头晕,这些症状源于外周。三分之一的有症状患者出现难治性头晕。初始采用类固醇和免疫抑制剂联合治疗的强化治疗可能对预防难治性头晕的发生至关重要。