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跟骨软骨黏液样纤维瘤。

Chondromyxoid fibroma of calcaneus.

机构信息

ShafaYahyaian Rehabilitation Center, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Foot Ankle Surg. 2013 Mar;19(1):48-52. doi: 10.1016/j.fas.2012.10.003. Epub 2012 Nov 7.

Abstract

BACKGROUND

Chondromyxoid fibroma is a rare benign primary bone tumor composed of immature myxoid mesenchymal and cartilaginous tissue. Its occurrence in calcaneus is very rare and few cases of calcaneal involvement have been reported in literature. We report five cases of CMF in calcaneus.

METHODS

Five cases, with the final diagnosis of chondromyxoid fibroma of the calcaneal bone are included in this report. Preoperative tumor workup was performed for our patients. We reviewed and recorded demographic data and the sign and symptoms of patients at presentation to our center. Mode of treatments, postoperative complications and recurrence were also studied. Curettage, high speed burring and bone grafting was performed in 4 of our patients and in the remaining case we only carried out curettage and burring.

RESULTS

Of the five patients, 3 were male and 2 were female. The mean age at presentation was 21. Two of our cases had previous surgery in other centers and had been referred to our clinic because of recurrence. The chief complaint in all of our patients was heel pain. The mean follow up period was 25.2 months. All of our patients had a delay in the diagnosis of tumor. We did not have any recurrence in our patients during follow up period.

CONCLUSIONS

This case series shows that chondromyxoid fibroma is not necessarily as exceedingly rare as generally reported in the current literature. This tumor should be considered in the differential diagnosis in patients with ankle and heel pain.

摘要

背景

软骨黏液样纤维瘤是一种罕见的良性原发性骨肿瘤,由未成熟的黏液样间充质和软骨组织组成。其发生在跟骨非常罕见,文献中报道的跟骨受累病例很少。我们报告了 5 例跟骨软骨黏液样纤维瘤。

方法

本报告包括 5 例最终诊断为跟骨软骨黏液样纤维瘤的病例。对我们的患者进行了术前肿瘤检查。我们回顾并记录了患者就诊时的人口统计学数据和症状。还研究了治疗方式、术后并发症和复发情况。我们对 4 例患者进行了刮除、高速打磨和植骨,而对另 1 例患者仅进行了刮除和打磨。

结果

5 例患者中,男性 3 例,女性 2 例。就诊时的平均年龄为 21 岁。我们的 2 例病例之前在其他中心接受过手术,并因复发而转诊至我们的诊所。所有患者的主要症状均为足跟痛。平均随访时间为 25.2 个月。我们所有患者的肿瘤诊断均有延迟。在随访期间,我们的患者均无复发。

结论

本病例系列表明,软骨黏液样纤维瘤并不像目前文献中普遍报道的那样罕见。在踝关节和足跟疼痛的患者中,应考虑将该肿瘤作为鉴别诊断。

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