Lu Yemin, An Yunfang, Li Qiang, Ren Ying, Chen Yibo, Ma Yongli, Zhang Zhishou, Han Lan, Zhao Changqing
Department of Otolaryngology Head and Neck Surgery,the Second Hospital of Shanxi Medical University,Key Research Laboratory of Airway Neuroimmunology,Taiyuan,030001,China.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2022 May;36(5):362-368. doi: 10.13201/j.issn.2096-7993.2022.05.008.
To investigate the early clinical features and diagnosis of granulomatous polyangiitis(GPA) with head and neck symptoms as the first presentation. The data of 28 patients with GPA diagnosed in the Second Hospital of Shanxi Medical University from 2014 to 2021, whose first symptoms appeared on the head and neck, were collected. All patients underwent relevant imaging examinations, laboratory tests, endoscopy, and pathological tissue biopsies. Systemic glucocorticoid or combined immunosuppressive therapy was administered and followed up for 1-5 years. Two patients refused treatment and were lost to follow-up; 26 patients were discharged with improved symptoms, complaining of nasal ventilation, resolution of supraorbital swelling, reduced dyspnoea, and renal symptoms. Five patients were repeatedly admitted to the hospital due to recurrent renal involvement. Although GPA often begins with head and neck symptoms, it is non-specific and can easily be confused with chronic inflammatory disease, leading to misdiagnosis. If suspicious cases are identified, they should be combined with endoscopy, pathological tissue biopsy, and special laboratory tests as early as possible to shorten the time to diagnosis, and obtain early diagnosis and treatment.
探讨以头颈部症状为首发表现的肉芽肿性多血管炎(GPA)的早期临床特征及诊断方法。收集了2014年至2021年在山西医科大学第二医院确诊的28例GPA患者的数据,这些患者的首发症状出现在头颈部。所有患者均接受了相关影像学检查、实验室检查、内镜检查及病理组织活检。给予全身糖皮质激素或联合免疫抑制治疗,并随访1至5年。2例患者拒绝治疗并失访;26例患者症状改善出院,诉鼻通气改善、眶上肿胀消退、呼吸困难减轻及肾脏症状缓解。5例患者因肾脏受累复发而再次入院。虽然GPA常以头颈部症状起病,但症状不具特异性,易与慢性炎症性疾病混淆,导致误诊。若发现可疑病例,应尽早结合内镜检查、病理组织活检及特殊实验室检查,以缩短诊断时间,实现早诊断、早治疗。