[组织肺炎:智利某中心10年登记资料分析]。

IF 0.3
Revista medica de Chile Pub Date : 2024-10-01 Epub Date: 2025-02-03 DOI:10.4067/s0034-98872024001001060
Miljenko Lolas, Juan Pablo Cuevas, Mauricio Salinas
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引用次数: 0

摘要

组织性肺炎(OP)是一种罕见的疾病,属于特发性间质性肺炎。它可以是隐源性(COP)或继发于各种病因。其诊断复杂且不标准化。没有出版的智利系列。我们报告了一组在国家胸科研究所(INT)接受组织治疗的肺炎患者。目的:描述智利某中心OP患者的特点。方法:回顾2013年至2022年INT的病理记录。临床和放射学资料来自医院记录。每个案例都由研究小组进行了审查。数据用均值、绝对频率和相对频率来描述。结果:在203例活检中,69例临床/放射学症状与op相符。这些受试者的平均年龄为62岁,其中男性33例(47.8%),女性36例(52.2%)。经支气管活检49例(71%),手术活检19例(27.5%)。在病因方面,37例(53.6%)被认为是隐源性的,12例(17.4%)继发于使用药物/药物,11例(15.9%)与结缔组织病有关。在治疗方面,36例(52.2%)患者接受口服类固醇治疗,10例(14.5%)患者接受皮质类固醇和免疫抑制剂混合治疗。在长期随访中,仅在6年多的时间里就有23人死亡。结论:该系列报道与文献报道具有相似的特征。本系列中描述的大多数病例被归类为COP。最常见的潜在病因是结缔组织疾病和药物。最常用的治疗方法是单独使用皮质类固醇或与免疫抑制剂混合使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Organizing Pneumonia: Analysis of 10 Years Registers in a Chilean Center].

Organized pneumonia (OP) is an uncommon disease included in the group of idiopathic interstitial pneumonias. It can be cryptogenic (COP) or secondary to various etiologies. Its diagnosis is complex and not standardized. There are no published Chilean series. We present a cohort of patients with pneumonia in organization treated at the National Thoracic Institute (INT).

Aim: To describe the characteristics of patients with OP in a Chilean center.

Methods: Pathological registries from the INT were reviewed between 2013 and 2022. Clinical and radiological information was obtained from hospital records. Each case was reviewed by the research team. Data are described by means, absolute and relative frequencies.

Results: From an initial list of 203 biopsies, 69 were obtained with clinical/radiological symptoms compatible with OP. The mean age of these subjects was 62 years, of which 33 (47.8%) were men and 36 (52.2%) women. Biopsies were obtained by transbronchial biopsy in 49 (71%) cases and surgical biopsy in 19 (27.5%) cases. In terms of etiology, 37 (53.6%) of them were considered cryptogenic, 12 (17.4%) secondary to the use of medication / drugs and 11 (15.9%) cases associated with connective tissue disease. Regarding treatment, 36 (52.2%) patients received oral steroids and 10 (14.5%) were treated with a mix of corticosteroids and immunosuppressors. In the long-term follow-up, there were 23 deaths in just over 6 years.

Conclusions: The reported series has similar characteristics to those reported in the literature. Most of the cases described in this series were classified as COP. The most common underlying etiologies were connective tissue diseases and medications. The most used treatment was corticosteroid alone or mixed with immunosuppressors.

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