巨细胞动脉炎所致肺动脉瘤的多模式成像:病例系列。

Bardia Nadim, Emma Blassel, Anthony R Sheets, Richard N Mitchell, Ayaz Aghayev
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引用次数: 0

摘要

肺动脉瘤(PAA)是一种罕见但重要的血管现象,具有非特异性症状和体征。有些患者没有症状,有些则表现为胸痛、呼吸困难或咯血等严重症状。PAAs 通常是偶然诊断出来的,其潜在病因多种多样,包括先天性、后天性和特发性。巨细胞动脉炎(GCA)是导致 PAA 的一个非常罕见的病因,文献中的病例报道非常有限。本系列病例将回顾四例由 GCA 引起的孤立性 PAA 患者的临床表现、多模态成像和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multimodality imaging of pulmonary artery aneurysms due to giant cell arteritis: a case series.

Pulmonary artery aneurysms (PAAs) are rare, but important vascular phenomena with nonspecific signs and symptoms. While some patients remain asymptomatic, others manifest with serious symptoms such as chest pain, dyspnea, or hemoptysis. Often diagnosed incidentally, PAAs have various underlying etiologies, including congenital, acquired, and idiopathic. Giant cell arteritis (GCA) is a very rare cause of PAAs, with limited reported cases in the literature. This case series will review the clinical presentation, multimodality imaging, and management of four patients with isolated PAA due to GCA.

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