韩国间质性肺疾病诊断和管理指南:隐源性组织性肺炎。

IF 2.5 Q2 RESPIRATORY SYSTEM
Yong Suk Jo, Jong Sun Park, Sun Hyo Park, Joon Sung Joh, Hye Jin Jang, Hyun-Kyung Lee
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引用次数: 0

摘要

隐源性组织性肺炎(COP)是特发性间质性肺炎(IIP)的一种,表现为急性或亚急性病程。排除继发性原因或疾病后可确诊。COP约占iip的5-10%,平均诊断年龄为50至60岁。患者主要表现为干咳和呼吸困难。他们经常出现发烧、疲劳和体重减轻的症状。高分辨率计算机断层扫描(HRCT)常见的放射学表现包括局限性实变,通常在胸膜下或位于较低区域,尽管它们可以发生在肺的所有区域。虽然治疗可以在没有组织病理学诊断的情况下开始,但当诊断不明确时,可能需要进行组织活检。对类固醇治疗的反应通常很好,临床改善迅速,预后良好,尽管复发很常见。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Korean Guidelines for Diagnosis and Management of Interstitial Lung Disease: Cryptogenic organizing pneumonia.

Cryptogenic organizing pneumonia (COP), one of the idiopathic interstitial pneumonias (IIP), exhibits an acute or subacute course. It can be diagnosed after excluding secondary causes or diseases. COP accounts for approximately 5-10% of IIPs, with the average age of diagnosis ranging from 50 to 60 years. Patients primarily present with dry cough and dyspnea. They often experience fever, fatigue, and weight loss. Common radiologic findings on high-resolution computed tomography (HRCT) include localized consolidations, which are typically subpleural or located in the lower zones, though they can occur in all regions of the lungs. While treatment can be initiated without histopathological diagnosis, tissue biopsy may be necessary when the diagnosis is unclear. Response to steroid therapy is generally good, with rapid clinical improvement and a favorable prognosis, although relapses are common.

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来源期刊
CiteScore
5.30
自引率
0.00%
发文量
42
审稿时长
12 weeks
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