迁移性空洞形成作为肉芽肿性多血管炎某一特定病例的主要受累表现。
Migrant cavitation as primary involvement in a particular case of granulomatosis with polyangiitis.
作者信息
Manti Francesco, Battaglia Caterina, Pelaia Corrado, Petullà Maria, Bertucci Bernardo, Laganà Domenico
机构信息
Radiodiagnostic Institute, "Magna Græcia" University of Catanzaro, Catanzaro, Italy.
Respiratory Medicine Unite, "Magna Græcia" University of Catanzaro, Catanzaro, Italy.
出版信息
Radiol Case Rep. 2022 Jul 28;17(10):3535-3538. doi: 10.1016/j.radcr.2022.06.074. eCollection 2022 Oct.
Granulomatosis with polyangiitis (GPA), previously known as Wegener's granulomatosis, is a necrotizing granulomatous vasculitis of the small and medium vessels involving the upper respiratory tract, lungs, and kidneys. In this case report, we will describe the case of a 60-year-old man who presented to our observation with recurrent episodes of hemoptoe, fever, and mucopurulent sputum. The diagnosis was made by radiological and laboratory tests.
肉芽肿性多血管炎（GPA），以前称为韦格纳肉芽肿，是一种累及上呼吸道、肺和肾脏的中小血管坏死性肉芽肿性血管炎。在本病例报告中，我们将描述一名60岁男性的病例，该患者因反复咯血、发热和黏液脓性痰前来我院就诊。诊断通过影像学和实验室检查做出。
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