Golden Todd, Siordia Juan A
University of Arizona Medical Center, University of Arizona, 1501 N Campbell Ave., Tucson, AZ 85724, United States.
Department of Surgery, Baylor College of Medicine, Houston, TX, United States.
J Bone Oncol. 2016 Jul 12;5(4):194-197. doi: 10.1016/j.jbo.2016.07.002. eCollection 2016 Nov.
Osteochondromyxoma is an extremely rare bone tumor associated with 1% of Carney complex patients and constitutes one of its 11 diagnostic criteria. This narrative review of osteochondromyxoma is based on a search of all references to the topic in PubMed, Web Of Science, SCOPUS, ScienceDirect, and JSTOR databases. Special attention was focused on case reports, leading to a review encompassing the case reports to date, as well as related animal model studies. This review covers the current understanding of osteochondromyxoma, highlighting its variability while providing consensus on the most common clinical presentation, pathological findings, and genetic features of this rare bone tumor.
骨软骨黏液瘤是一种极其罕见的骨肿瘤，在1%的卡尼综合征患者中出现，是其11项诊断标准之一。本关于骨软骨黏液瘤的叙述性综述基于在PubMed、科学网、Scopus、ScienceDirect和JSTOR数据库中对该主题的所有参考文献进行的检索。特别关注病例报告，从而对迄今为止的病例报告以及相关动物模型研究进行了综述。本综述涵盖了目前对骨软骨黏液瘤的认识，突出了其变异性，同时就这种罕见骨肿瘤最常见的临床表现、病理发现和遗传特征达成了共识。
