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本文引用的文献

1
Mortality predictors in ANCA-associated vasculitis: Experience of a Brazilian monocentric cohort of a rheumatology center.抗中性粒细胞胞浆抗体相关性血管炎的死亡预测因子:一个巴西单中心风湿病中心的经验。
Medicine (Baltimore). 2021 Dec 23;100(51):e28305. doi: 10.1097/MD.0000000000028305.
2
Granulomatosis with polyangiitis: A case report and brief review of literature.肉芽肿性多血管炎:一例病例报告及文献简要综述。
Radiol Case Rep. 2021 Sep 5;16(11):3445-3450. doi: 10.1016/j.radcr.2021.08.028. eCollection 2021 Nov.
3
The cancer risk according to three subtypes of ANCA-associated vasculitis: A propensity score-matched analysis of a nationwide study.基于三种 ANCA 相关性血管炎亚型的癌症风险:一项全国性研究的倾向评分匹配分析。
Semin Arthritis Rheum. 2021 Aug;51(4):692-699. doi: 10.1016/j.semarthrit.2021.03.014. Epub 2021 Apr 1.
4
The biology, pathogenetic role, clinical implications, and open issues of serum anti-neutrophil cytoplasmic antibodies.血清抗中性粒细胞胞浆抗体的生物学、发病机制作用、临床意义及存在的问题。
Autoimmun Rev. 2021 Mar;20(3):102759. doi: 10.1016/j.autrev.2021.102759. Epub 2021 Jan 18.
5
ANCA-associated vasculitis.抗中性粒细胞胞浆抗体相关性血管炎。
Nat Rev Dis Primers. 2020 Aug 27;6(1):71. doi: 10.1038/s41572-020-0204-y.
6
Updates in antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis for the ENT surgeon.耳鼻喉科医师应了解的抗中性粒细胞胞浆抗体(ANCA)相关性血管炎的最新进展。
Clin Otolaryngol. 2020 May;45(3):316-326. doi: 10.1111/coa.13524. Epub 2020 Mar 20.
7
European Position Paper on Rhinosinusitis and Nasal Polyps 2020.欧洲鼻窦炎和鼻息肉 2020 年立场文件。
Rhinology. 2020 Feb 20;58(Suppl S29):1-464. doi: 10.4193/Rhin20.600.
8
Should nasal biopsy inevitably be performed for classifying granulomatosis with polyangiitis in patients with rhinosinusitis? A retrospective chart review study.对于伴有鼻-鼻窦炎的肉芽肿性多血管炎患者,是否必须进行鼻活检以进行分类?一项回顾性图表审查研究。
Rheumatol Int. 2019 May;39(5):885-892. doi: 10.1007/s00296-019-04282-z. Epub 2019 Mar 18.
9
Granulomatosis with polyangiitis causing subglottic stenosis-two cases and their management.肉芽肿性多血管炎导致声门下狭窄——两例病例及其处理
AME Case Rep. 2018 Apr 30;2:17. doi: 10.21037/acr.2018.03.01. eCollection 2018.
10
Ear, nose and throat involvement in granulomatosis with polyangiitis: how it presents and how it determines disease severity and long-term outcomes.显微镜下多血管炎累及耳鼻咽喉:其临床表现与疾病严重程度及长期预后的关系。
Clin Rheumatol. 2018 Apr;37(4):1075-1083. doi: 10.1007/s10067-018-4019-0. Epub 2018 Feb 20.

以头颈部症状为首发临床表现的肉芽肿性多血管炎:28例临床分析

[Granulomatosis with polyangiitis with head and neck symptoms as the first clinical manifestation: clinical analysis of 28 cases].

作者信息

Lu Yemin, An Yunfang, Li Qiang, Ren Ying, Chen Yibo, Ma Yongli, Zhang Zhishou, Han Lan, Zhao Changqing

机构信息

Department of Otolaryngology Head and Neck Surgery,the Second Hospital of Shanxi Medical University,Key Research Laboratory of Airway Neuroimmunology,Taiyuan,030001,China.

出版信息

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.

DOI:10.13201/j.issn.2096-7993.2022.05.008
PMID:35483687
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10128263/
Abstract

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.

摘要

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。