From the Department of Nuclear Medicine, Marmara University Pendik Training and Research Hospital, Istanbul, Turkey.
Clin Nucl Med. 2021 Jul 1;46(7):e387-e388. doi: 10.1097/RLU.0000000000003531.
Erdheim-Chester disease is an uncommon non-Langerhans cell histiocytosis. The diagnosis depends on imaging and histological criteria. The most common presentation is the multiple bone lesions with involvement of at least 1 more organ. We present the FDG PET/CT findings of a 19-year-old man who presented with central nervous system symptoms such as progressive polyuria, polydipsia, gait disturbances, and eye pain and was later diagnosed with Erdheim-Chester disease.
额颞叶骨嗜酸性肉芽肿病是一种罕见的非朗格汉斯细胞组织细胞增生症。诊断依赖于影像学和组织学标准。最常见的表现是多骨病变,至少有 1 个以上器官受累。我们介绍了一名 19 岁男性的 FDG PET/CT 表现,他以中枢神经系统症状就诊,如进行性多尿、多饮、步态障碍和眼痛,后来被诊断为额颞叶骨嗜酸性肉芽肿病。