肺、胸膜、淋巴结活检肉芽肿性炎症的诊断分布:来自三级单中心胸外科医院的经验。

IF 1.4 4区 医学 Q4 RESPIRATORY SYSTEM Sarcoidosis, Vasculitis, and Diffuse Lung Diseases Pub Date : 2022-01-01 Epub Date: 2022-01-13 DOI:10.36141/svdld.v38i4.11914
Selma Aydogan Eroglu, Tekin Yildiz, Esin Sonkaya, Murat Kavas, Fatma Ozbaki, Lale Sertçelik, Aycim Sen, Tulin Sevim
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引用次数: 2

摘要

背景:肉芽肿性炎症广泛存在于多种疾病中,最常与结节病和结核病相关。肉芽肿在病理学上可分为两大类;坏死的和非坏死的。目的:本研究的目的是评估大量活检样本中肉芽肿患者的放射学、实验室和病理结果,以确定最终的诊断分布。方法:本研究采用回顾性、描述性、观察性、横断面研究。它是在肺、胸膜、纵隔、肺门和/或周围淋巴结活检中发现肉芽肿性炎症的患者进行的。通过医院的信息处理系统获取患者的人口统计信息、放射学、微生物学和实验室结果。记录的诊断由至少两名经验丰富的临床医生重新评估,并做出最终诊断分布。结果:共纳入392例患者。非坏死性炎症268例,坏死性肉芽肿性炎症124例。非坏死性炎症最常见的原因是结节病,坏死性炎症最常见的原因是结核。结节病患者有非坏死性炎症的占77.2%,肺结核患者有坏死性炎症的占54.3%。肉芽肿性炎症结节病的诊断分布分别为分枝杆菌感染(尤其是结核)、恶性肿瘤引起的结节反应、尘肺病、肉芽肿性多血管炎和超敏性肺炎。共有392名患者被诊断患有13种不同的疾病。15例患者(3.8%)没有明确的诊断。结论:在活检样本中发现肉芽肿性炎症的诊断对临床医生来说是常见的,在许多情况下鉴别诊断是困难的。应详细评估患者的临床表现、实验室结果和放射学表现,只有在多学科讨论后才能做出最终诊断。组织样本中坏死的单独存在并不是最终诊断的可靠发现。
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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Diagnosis distribution in cases with granulomatous inflammation in lung, pleura, and lymph node biopsies: an experience from a tertiary level single center chest diseases and thoracic surgery hospital.

Background: Granulomatous inflammation is found in a wide range of diseases, and most commonly associated with sarcoidosis and tuberculosis. Granulomas are pathologically classified into two main groups; necrotic and non-necrotic.

Objectives: The aim of this study was to evaluate the radiological, laboratory, and pathological findings of a large patient population with granuloma in biopsy samples, to determine the final diagnostic distribution.

Methods: This study was designed as a retrospective, descriptive, observational, cross-sectional study. It was conducted in patients with granulomatous inflammation detected in lung, pleural, mediastinal, hilar, and/or peripheral lymph node biopsies. Demographic information, radiological, microbiological, and laboratory results of the patients were obtained via the information processing system of the hospital. The diagnoses recorded were re-evaluated by at least two experienced clinicians and the final diagnosis distributions were made.

Results: A total of 392 patients were included in the study. Non-necrotizing inflammation was detected in 268 patients, and necrotizing granulomatous inflammation was found in 124 patients. The most common cause of non-necrotizing inflammation was sarcoidosis, and tuberculosis in the case of necrotizing inflammation. A total of 77.2% of sarcoidosis patients had non-necrotizing inflammation and 54.3% of the tuberculosis patients had necrotizing inflammation. In the diagnosis distribution of granulomatous inflammation sarcoidosis, mycobacterium infections (especially tuberculosis), sarcoid reaction due to malignancy, pneumoconiosis, granulomatosis with polyangiitis and hypersensitivity pneumonitis were detected, respectively. A total of 392 patients were diagnosed with 13 different diseases. In 15 patients (3.8%) no specific diagnosis could be made.

Conclusions: The diagnosis of granulomatous inflammation detected in biopsy samples is common for clinicians and a differential diagnosis is difficult in many cases. A patient's clinical findings, laboratory results, and radiological appearance, should be evaluated in detail and a final diagnosis only made following a multidisciplinary discussion. The presence of necrosis in tissue samples alone is not a reliable finding for a final diagnosis.

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来源期刊
CiteScore
2.20
自引率
6.20%
发文量
34
期刊介绍: Sarcoidosis Vasculitis and Diffuse Lung Disease is a quarterly journal founded in 1984 by G. Rizzato. Now directed by R. Baughman (Cincinnati), P. Rottoli (Siena) and S. Tomassetti (Forlì), is the oldest and most prestigious Italian journal in such field.
期刊最新文献
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