Sanket Karangutkar, Athar Haroon, Ahmed Abdalla Ahmed Elramadi
{"title":"<sup>18</sup>F-NaF PET/CT Versus <sup>18</sup>F-FDG PET/CT for Baseline Mapping in Ollier Disease: A Pediatric Case.","authors":"Sanket Karangutkar, Athar Haroon, Ahmed Abdalla Ahmed Elramadi","doi":"10.2967/jnmt.126.272370","DOIUrl":null,"url":null,"abstract":"<p><p>Ollier disease is a rare skeletal dysplasia characterized by multifocal enchondromas and a 5%-50% lifetime risk of malignant transformation to chondrosarcoma. Whole-body mapping is essential for surveillance. <sup>18</sup>F-FDG PET/CT shows limited sensitivity because of low glycolytic activity and physiologic uptake. This case highlights the superior performance of <sup>18</sup>F-NaF PET/CT for osteoblastic lesion detection and anatomic delineation in a pediatric patient with <i>IDH1</i>-mutated Ollier disease.</p>","PeriodicalId":16548,"journal":{"name":"Journal of nuclear medicine technology","volume":" ","pages":""},"PeriodicalIF":1.5000,"publicationDate":"2026-06-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of nuclear medicine technology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2967/jnmt.126.272370","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING","Score":null,"Total":0}
引用次数: 0
Abstract
Ollier disease is a rare skeletal dysplasia characterized by multifocal enchondromas and a 5%-50% lifetime risk of malignant transformation to chondrosarcoma. Whole-body mapping is essential for surveillance. 18F-FDG PET/CT shows limited sensitivity because of low glycolytic activity and physiologic uptake. This case highlights the superior performance of 18F-NaF PET/CT for osteoblastic lesion detection and anatomic delineation in a pediatric patient with IDH1-mutated Ollier disease.