Chondromyxoid Fibroma of the Clavicle: A Case Report of a Rare Clinical Entity

Diogo Soares, Francisco Bernardes, Nuno Vieira Silva, M. Silva, Daniel Lopes
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Abstract

Introduction: Chondromyxoid fibroma is a rare benign cartilaginous tumor that accounts for less than 1% of all bone tumors and involves long bones of the lower extremities more frequently. Therefore, the clavicle is a rare location of involvement for this entity. Case Presentation: The authors report a case of a diaphyseal chondromyxoid fibroma of the right clavicle in a 30-year-old male that was submitted to en bloc resection of the lesion and reconstruction with an autologous tricortical graft from the iliac crest. The post-operative period was uneventful, and the patient had regained excellent function of this right shoulder. At 2 years of follow-up, there was no evidence of a recurrence of the disease. Conclusion: Chondromyxoid fibroma of the clavicle should be included in the differential diagnosis of an indolent growing mass in this anatomic location.
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锁骨软骨样纤维瘤:罕见临床病例报告
导言软骨样纤维瘤是一种罕见的良性软骨肿瘤,占所有骨肿瘤的 1%以下,多累及下肢长骨。因此,锁骨是罕见的受累部位。病例介绍:作者报告了一例 30 岁男性右锁骨软骨样纤维瘤病例,患者接受了病灶整体切除术,并用髂嵴的自体三皮质移植进行了重建。患者术后恢复顺利,右肩功能恢复良好。随访两年后,没有发现疾病复发的迹象。结论锁骨软骨样纤维瘤应列入该解剖位置生长性肿块的鉴别诊断中。
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Chondromyxoid Fibroma of the Clavicle: A Case Report of a Rare Clinical Entity Chondromyxoid Fibroma of the Clavicle: A Case Report of a Rare Clinical Entity Acknowledgement to Reviewers
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