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经病理证实的特发性胸膜肺弹力纤维增生症 1 例报告。

Idiopathic pleuroparenchymal fibroelastosis confirmed by pathology: a case report.

机构信息

Department of Respiratory and Critical Care Medicine, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China.

出版信息

J Int Med Res. 2021 Feb;49(2):300060521992217. doi: 10.1177/0300060521992217.

Abstract

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.

摘要

现报道 1 例活动后出现咳嗽和哮喘,且持续时间均为 1 个月的患者。患者的胸部高分辨率计算机断层扫描(HRCT)显示双肺上叶(尤其是右肺)脏层胸膜增厚,伴有纤维带和胸膜附近斑块,且伴有支气管扩张。经胸腔镜肺活检证实为特发性胸膜肺弹力纤维组织增生症。患者接受乙酰半胱氨酸治疗,但活动后哮喘加重,10 个月后肺功能显著下降。特发性胸膜肺弹力纤维组织增生症是一种罕见的新型特发性间质性肺炎,除肺移植外,尚无有效治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c803/7917883/dd281a095df5/10.1177_0300060521992217-fig1.jpg

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