骶骨软骨母细胞瘤——罕见的发病部位，罕见的病理类型：一例病例报告及文献复习
Sacral chondroblastoma - a rare location, a rare pathology: A case report and review of literature.
作者信息
Zheng Bo-Wen, Niu Hua-Qing, Wang Xiao-Bin, Li Jing
机构信息
Department of Spine Surgery, The Second Xiangya Hospital, Central South University, Changsha 410011, Hunan Province, China.
Department of Orthopedics Surgery, General Hospital of the Central Theater Command, Wuhan 430061, Hubei Province, China.
出版信息
World J Clin Cases. 2021 Jul 16;9(20):5709-5716. doi: 10.12998/wjcc.v9.i20.5709.
BACKGROUND
Chondroblastoma (CB) is an intermediate tumor of cartilage origin. CB involving the sacrum is a very rare pathology.
CASE SUMMARY
A 17-year-old male with sacral CB was diagnosed as CB during the first surgery, and 18 mo later, the tumor recurred and a second surgery was performed with the same pathology result of CB.
CONCLUSION
We recommend complete removal of the tumor in a timely manner, provided that surgical conditions are met. At the same time, other diseases should be carefully differentiated in terms of imaging or pathological features so as to avoid erroneous diagnostic conclusions.
背景
软骨母细胞瘤（CB）是一种起源于软骨的中间型肿瘤。累及骶骨的CB是一种非常罕见的病理情况。
病例摘要
一名患有骶骨CB的17岁男性在首次手术时被诊断为CB，18个月后肿瘤复发，进行了第二次手术，病理结果同为CB。
结论
我们建议在满足手术条件的情况下及时彻底切除肿瘤。同时，应根据影像学或病理特征仔细鉴别其他疾病，以避免错误的诊断结论。
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