Combined Pulmonary Fibrosis and Emphysema: A Case Report and Literature Review

Shaghayegh Badriahmadi, Mahnaz Mozdourian
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Abstract

The syndrome of combined emphysema of the upper lobes and fibrosis of the lower lobes on chest computed tomography results in a characteristic functional profile, with preserved lung volumes, hypoxemia at exercise. Despite subnormal spirometry, combined pulmonary fibrosis and emphysema is a severe entity. The presence of pulmonary arterial hypertension at diagnosis is a critical determinant of prognosis.
合并肺纤维化和肺气肿1例报告并文献复习
胸部计算机断层扫描显示上肺叶合并肺气肿和下肺叶纤维化综合征,表现为特征性的功能特征,肺容量保留,运动时低氧血症。尽管肺活量低于正常,合并肺纤维化和肺气肿是一个严重的实体。肺动脉高压在诊断时的存在是预后的关键决定因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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