Qutbi Mohsen, Ghanbari Sajad, Asli Isa Neshandar, Shafiei Babak
Department of Nuclear Medicine, Taleghani Educational Hospital, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
World J Nucl Med. 2019 Apr-Jun;18(2):189-191. doi: 10.4103/wjnm.WJNM_21_18.
Jaffe-Campanacci syndrome (JCS) is a rare clinical disorder with almost unknown etiology. The main feature of this syndrome is skeletal involvement as nonossifying fibroma which may cause severe morbidity to these patients. X-ray imaging is the widely available modality for evaluation of skeleton, but radionuclide imaging modalities may have a role in workup. Herein, we present a case of JCS evaluated with Tc-methylene diphosphonate bone and Tc-octreotide scans for the extent of skeletal involvement. To the best of our knowledge, from over than 30 cases reported in the literature, no evaluation with radionuclide imaging has been done.
贾菲-坎帕纳奇综合征（JCS）是一种病因几乎不明的罕见临床疾病。该综合征的主要特征是骨骼受累，表现为非骨化性纤维瘤，这可能给这些患者带来严重的发病率。X线成像是评估骨骼的广泛可用方式，但放射性核素成像方式可能在检查中发挥作用。在此，我们报告一例通过锝-亚甲基二膦酸盐骨扫描和锝-奥曲肽扫描评估骨骼受累程度的JCS病例。据我们所知，在文献报道的30多例病例中，尚未进行放射性核素成像评估。
