罕见的黄色肉芽肿性病变——厄尔德海姆-切斯特病的正电子发射断层扫描/计算机断层扫描
Positron emission tomography/computed tomography of a rare xanthogranulomatous process: Erdheim-Chester disease.
作者信息
Pereira Neto Carlos Cunha, Roman Chris, Johnson Mahlon, Jagasia Madan, Martin William H, Delbeke Dominique
机构信息
Department of Radiology, Vanderbilt University Medical Center, Nashville, TN, USA.
出版信息
Mol Imaging Biol. 2004 Jan-Feb;6(1):63-7. doi: 10.1016/j.mibio.2004.01.023.
Erdheim-Chester disease (ECD) is a disseminated xanthogranulomatous infiltrative disease of unknown etiology due to infiltration of different organs and bones by foamy histiocytes. A 37-year-old male with cerebral and periorbital lesions was diagnosed with this rare disease and was evaluated with magnetic resonance imaging (MRI) and 2-deoxy-2-[(18)F]fluoro-D-glucose (FDG) with positron emission tomography/computed tomography (PET/CT) imaging at baseline and following therapy. FDG-PET imaging allowed accurate evaluation of the extent of the disease at baseline, as well as assessment of response to therapy.
厄尔德海姆-切斯特病（ECD）是一种病因不明的播散性黄瘤性浸润性疾病，由泡沫状组织细胞浸润不同器官和骨骼所致。一名患有脑部和眶周病变的37岁男性被诊断为这种罕见疾病，并在基线期和治疗后接受了磁共振成像（MRI）以及2-脱氧-2-[(18)F]氟代-D-葡萄糖（FDG）正电子发射断层扫描/计算机断层扫描（PET/CT）成像评估。FDG-PET成像能够在基线期准确评估疾病范围，并评估治疗反应。
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