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Idiopathic pleuroparenchymal fibroelastosis confirmed by pathology: a case report

机译:经发染性胸膜安全肌肉囊泡通过病理证实:案例报告

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摘要

The case of a patient with cough and asthma after activity that each had a 1-month duration is reported. Chest high-resolution computed tomography (HRCT) showed visceral pleural thickening in both upper lungs (especially the right lung), which was accompanied by fibrous strips and patches near the pleura, and these were accompanied by distraction bronchiectasis. Idiopathic pleuropulmonary elastosis was confirmed by thoracoscopic lung biopsy. The patient was treated with acetylcysteine, but their asthma worsened after activity and their lung function decreased significantly after 10 months. Idiopathic pleuroparenehymal fibroelastosis is a rare new type of idiopathic interstitial pneumonia, which has no effective treatment except for lung transplantation.
机译:据报道,患有咳嗽和哮喘的患者的患者报告了每一个持续时间。胸部高分辨率计算断层扫描(HRCT)在上肺(特别是右肺)中显示了内脏胸膜增稠,伴随着胸膜附近的纤维条和贴片,并且这些伴随着分散的支气管扩张。通过胸镜肺活检证实了特发性胸膜尿素弹性。患者用乙酰半胱氨酸处理,但活性后哮喘恶化,其肺功能在10个月后显着降低。特发性胸膜肝肌肌肌纤维素是一种罕见的新型特发性肺炎,除了肺移植外没有有效的待遇。

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