Guidance on Imaging for Invasive Pulmonary Aspergillosis and Mucormycosis: From the Imaging Working Group for the Revision and Update of the Consensus Definitions of Fungal Disease from the EORTC/MSGERC

晕征 医学 曲菌病 毛霉病 放射科 疾病 医学物理学 病理 计算机断层摄影术 免疫学
作者
Barbara D. Alexander,Frédéric Lamoth,Claus Peter Heußel,Cornelia Schaefer Prokop,Sujal R. Desai,C. Orla Morrissey,John W. Baddley
出处
期刊:Clinical Infectious Diseases [Oxford University Press]
卷期号:72 (Supplement_2): S79-S88 被引量:64
标识
DOI:10.1093/cid/ciaa1855
摘要

Abstract Background Clinical imaging in suspected invasive fungal disease (IFD) has a significant role in early detection of disease and helps direct further testing and treatment. Revised definitions of IFD from the EORTC/MSGERC were recently published and provide clarity on the role of imaging for the definition of IFD. Here, we provide evidence to support these revised diagnostic guidelines. Methods We reviewed data on imaging modalities and techniques used to characterize IFDs. Results Volumetric high-resolution computed tomography (CT) is the method of choice for lung imaging. Although no CT radiologic pattern is pathognomonic of IFD, the halo sign, in the appropriate clinical setting, is highly suggestive of invasive pulmonary aspergillosis (IPA) and associated with specific stages of the disease. The ACS is not specific for IFD and occurs in the later stages of infection. By contrast, the reversed halo sign and the hypodense sign are typical of pulmonary mucormycosis but occur less frequently. In noncancer populations, both invasive pulmonary aspergillosis and mucormycosis are associated with “atypical” nonnodular presentations, including consolidation and ground-glass opacities. Conclusions A uniform definition of IFD could improve the quality of clinical studies and aid in differentiating IFD from other pathology in clinical practice. Radiologic assessment of the lung is an important component of the diagnostic work-up and management of IFD. Periodic review of imaging studies that characterize findings in patients with IFD will inform future diagnostic guidelines.
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