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肉芽肿性多血管炎:耳鼻喉科医生需要了解的一种罕见但具有重要临床意义的疾病。

Granulomatosis with Polyangiitis: A Rare but Clinically Important Disease for the Otolaryngologist.

机构信息

Otolaryngology and Head and Neck Surgery, Austin Hospital, Heidelberg Victoria, Australia.

Department of Rheumatology, The Alfred Hospital, Melbourne, Victoria, Australia.

出版信息

Niger J Clin Pract. 2024 Jul 1;27(7):819-826. doi: 10.4103/njcp.njcp_790_23. Epub 2024 Jul 27.

Abstract

INTRODUCTION

Granulomatosis with polyangiitis (GPA) is rare but debilitating autoimmune disease and commonly presents with sinonasal as well as other head and neck symptoms.

AIMS

To summarize the ear, nose, and throat-specific symptomatology and management of GPA.

METHODS AND RESULTS

We performed a literature review by using the PubMed search engine to provide a summary of recent and important literature that is pertinent to an otolaryngologist's clinical practice. We provide a guide on the pathophysiology, epidemiology, clinical features, investigation, and management (operative and nonoperative) of this important disease.

CONCLUSIONS

This review illustrates the important role that an otolaryngologist can play in the work up and symptom management of patients with GPA. Knowledge of the common presenting symptoms as well as more rare presentations of GPA is extremely important for otolaryngologists as prompt diagnosis and management is extremely important to avoid significant morbidity and mortality.

摘要

简介

肉芽肿性多血管炎(GPA)是一种罕见但使人虚弱的自身免疫性疾病,常伴有鼻-鼻窦以及其他头颈部症状。

目的

总结 GPA 的耳部、鼻部和喉部的具体症状及治疗方法。

方法与结果

我们使用 PubMed 搜索引擎进行文献回顾,总结了与耳鼻喉科医生临床实践相关的近期重要文献。我们提供了关于该疾病病理生理学、流行病学、临床特征、检查和治疗(手术和非手术)的指南。

结论

本综述说明了耳鼻喉科医生在 GPA 患者的检查和症状管理中可以发挥重要作用。了解 GPA 的常见表现以及更罕见的表现对于耳鼻喉科医生非常重要,因为及时诊断和治疗对于避免严重的发病率和死亡率至关重要。

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