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显微镜下多血管炎的头颈部表现:19例患者的回顾性分析及文献复习

Head and Neck Manifestations of Granulomatosis with Polyangiitis: A Retrospective analysis of 19 Patients and Review of the Literature.

作者信息

Carnevale Claudio, Arancibia-Tagle Diego, Sarría-Echegaray Pedro, Til-Pérez Guillermo, Tomás-Barberán Manuel

机构信息

Department of Otorhinolaryngology, Hospital Universitari Son Espases, Palma de Mallorca, Illes Balears, Spain.

Department of Otorhinolaryngology and Head and Neck Surgery, Hospital Universitari Son Espases, Palma de Mallorca, Illes Balears, Spain.

出版信息

Int Arch Otorhinolaryngol. 2019 Apr;23(2):165-171. doi: 10.1055/s-0038-1675759. Epub 2019 Mar 1.

Abstract

Granulomatosis with Polyangiitis (GPA) is a small vessel vasculitis characterized by a necrositing granulomatous inflammation of the upper and lower respiratory tracts and focal/proliferative glomerulonephritis. In more than 70% of the cases, the presenting symptoms are head and neck manifestations that are often misdiagnosed as infectious or allergic in etiology.  The present study provides an analysis of head and neck manifestations in a series of patients diagnosed with GPA. It also evaluates their medical and surgical treatment and provides a review of the relevant literature.  A retrospective analysis of 19 patients diagnosed with GPA at a public tertiary care hospital between 2006 and 2017 was performed.  A total of 19 patients were included in the present study, and 16 of them presented head and neck manifestations. Sinonasal symptoms were the most common, affecting 56% of the patients, followed by laryngotracheal (31.25%) and ear (25%) symptoms. In 7 patients, sinonasal symptoms were the first manifestation of the disease (43.75%). Four patients underwent surgery at some stage of the disease.  Head and neck involvement is common in GPA and may stand for the first or the only manifestation of the disease. The otolaryngologists play a central role in the diagnosis and long-term treatment of these patients, and they have to keep this pathology in mind when treating patients with ENT symptoms that do not respond as expected to the treatment.

摘要

肉芽肿性多血管炎(GPA)是一种小血管血管炎,其特征为上、下呼吸道的坏死性肉芽肿性炎症以及局灶性/增殖性肾小球肾炎。在超过70%的病例中,首发症状为头颈部表现,病因常被误诊为感染性或过敏性。 本研究对一系列诊断为GPA的患者的头颈部表现进行了分析。它还评估了他们的内科和外科治疗,并对相关文献进行了综述。 对2006年至2017年间在一家公立三级护理医院诊断为GPA的19例患者进行了回顾性分析。 本研究共纳入19例患者,其中16例有头颈部表现。鼻窦症状最为常见,影响了56%的患者,其次是喉气管症状(31.25%)和耳部症状(25%)。7例患者中,鼻窦症状是疾病的首发表现(43.75%)。4例患者在疾病的某个阶段接受了手术。 头颈部受累在GPA中很常见,可能是该疾病的首发或唯一表现。耳鼻喉科医生在这些患者的诊断和长期治疗中起着核心作用,在治疗有耳鼻喉症状但对治疗无预期反应的患者时,他们必须牢记这种病理情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26b7/6449134/8b8f63cbf331/10-1055-s-0038-1675759-i0790or-1.jpg

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