Aneurysmal bone cyst arising in iliopubic chondromyxoid fibroma – a case report

J. Vale, S. Diniz, F. Rodrigues, A. Ribau, A. Coelho, Vânia Oliveira, P. Cardoso
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Abstract

Chondromyxoid fibroma is rare cartilaginous tumor, accounting for 0.5% of all primary bone tumors and 2% of benign bone tumors. Areas of aneurysmal bone cysts (ABC) may be found within CMF in 8.6% of cases. A 20-year-old man presents pain due to a mass on iliopubic ramus that was diagnosed as an aneurysmal bone cyst arising from a chondromyxoid fibroma. This case confirms the rare association between aneurysmal bone cyst and chondromyxoid fibroma. Although aneurysmal bone cyst is more frequently associated with highly vascularized tumors, it is important to consider the diagnosis in the presence of chondromyxoid fibroma. Keywords: Chondromyxoid fibroma; scecondary aneurysmal bone cyst; iliopubic ramus
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髂耻骨软骨粘液样纤维瘤并发动脉瘤样骨囊肿1例
软骨粘液样纤维瘤是一种罕见的软骨肿瘤,占所有原发性骨肿瘤的0.5%,占良性骨肿瘤的2%。8.6%的病例可在CMF内发现动脉瘤性骨囊肿(ABC)。一位20岁的男性,因髂耻支肿块而疼痛,该肿块被诊断为由软骨粘液样纤维瘤引起的动脉瘤性骨囊肿。本病例证实动脉瘤性骨囊肿与软骨粘液样纤维瘤之间的罕见关联。虽然动脉瘤性骨囊肿更常与高度血管化的肿瘤相关,但在存在软骨粘液样纤维瘤时考虑诊断是很重要的。关键词:软骨粘液样纤维瘤;继发性动脉瘤性骨囊肿;髂耻支
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