文章摘要

18F-FDG-PET/CT 在肺结核诊断及疗效评估中的应用

作者: 1王毅翔
1 香港中文大学医学院影像及介入放射科,香港 999077
通讯: 王毅翔 Email: yixiang_wang@cuhk.edu.hk
DOI: 10.3978/j.issn.2095-6959.2019.07.027

摘要

结核病仍为目前世界上传染病死亡的第一诱因。人体对结核分枝杆菌的免疫反应可导致非 常不同的临床表现, 因此临床和影像学评估常常有困难。18F 标记脱氧葡萄糖(f l u o r i n e - 1 8 fluorodeoxyglucose,18F-FDG)正电子发射断层扫描(positron emission tomography,PET)/CT可以进 行全身成像并提供感染病变的代谢图,从而有效地评估疾病严重程度。18F-FDG-PET/CT扫描尤其 适用于检出未知部位的结核感染,为选择最合适的活检部位提供指导。18F-FDG-PET/CT在评估结 核病变对治疗的早期反应也非常有用,这点尤其在无法获得常规微生物学检查结果的患者以及耐 多药结核或肺外结核病的疗效评估特别有帮助。值得注意的是,结核患者临床治愈后及部分陈旧 肺结核病灶仍然可以表现18F-FDG摄取增高,但这些代谢活跃的部位不一定代表活动性疾病,更可 能是反映宿主免疫反应与结核菌复制之间的平衡,但也同时代表结核病发展的风险增加。另外,18F-FDG-PET/CT常常不能可靠地区分活动性结核病变与恶性肿瘤,且其他感染或炎症状况也可以 引起类似的18F-FDG-PET高摄取。18F-FDG-PET也无法区分淋巴结结核和淋巴结转移性肿瘤。缺乏 特异性是18F-FDG-PET/CT临床应用中的一个缺陷,因此在解释18F-FDG-PET/CT结果时必须密切 参考其他临床资料。
关键词: 结核;18F标记脱氧葡萄糖;治疗反应;正电子发射断层扫描

Clinical application of 18F-FDG-PET/CT for tuberculosis evaluation and therapeutic monitoring

Authors: 1WANG Yixiang
1 Department of Imaging and Interventional Radiology, Faculty of Medicine, Chinese University of Hong Kong, Hong Kong 999077, China

CorrespondingAuthor: WANG Yixiang Email: yixiang_wang@cuhk.edu.hk

DOI: 10.3978/j.issn.2095-6959.2019.07.027

Abstract

Tuberculosis (TB) is currently the world’s leading cause of infectious mortality. The complex immune response of the human body to mycobacterium tuberculosis results in a wide array of clinical manifestations, thus the clinical and radiological diagnosis are challenging. 18F-FDG-PET/CT images the whole body and provides a metabolic map of the infection, enabling clinicians to assess the disease burden. 18F-FDG-PET/CT scan is particularly useful in detecting the disease in previously unknown sites, and allows the most appropriate site of biopsy to be selected. 18F-FDG-PET/CT is also very valuable in assessing early disease response to therapy, and play an important role in cases where conventional microbiological methods are unavailable and for monitoring response to therapy in cases of undecided treatment duration such as multidrug-resistant TB or in extrapulmonary TB. High 18F-FDG up-taking focus can also be seen in clinically cured patients and in old fibrotic scarring. Thus, high uptake of 18F-FDG by PET may both represent ongoing active disease, or simply the host immune system activity that will ultimately prevail. 18F-FDG-PET/CT cannot reliably differentiate active TB lesion from malignant lesions and false positives can also be due to other infective or inflammatory conditions. 18F-FDG PET is also unable to distinguish tuberculous lymphadenitis from metastatic lymph node involvement. The lack of specificity is a limitation for 18F-FDG-PET/CT in TB management. The interpretation of 18F-FDG-PET finding must be carefully correlated with clinical data.
Keywords: tuberculosis; fluorine-18 fluorodeoxyglucose; treatment response; positron emission tomography and computed tomography

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