Malignant Transformation of Multiple Hand Enchondromas Secondary to Ollier Disease: A Case Report.

IF 0.5 Q4 SURGERY
Daniela Kristina Carolino, Keiichi Muramatsu, Yasuhiro Tani, Masaya Ueda
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引用次数: 0

Abstract

Enchondromatosis secondary to Ollier disease (OD) is rare, with secondary chondrosarcomas (CS) accounting for only 1% of malignant osseous tumours. This is one of only two reports documenting four enchondromas of different bones of the same hand developing malignant transformation, with long-term follow-up. This is a 72-year-old female with histologically proven CS from multiple enchondromas of the index finger metacarpal and proximal phalanx, and middle finger proximal and middle phalanges. Six years following curettage and bone grafting, she showed no recurrence or metastases from CS. While CS of the hand behaves aggressively, they rarely metastasise and show good 5-year survival rates. Due to good prognosis, function-sparing surgical options are acceptable over amputation, accompanied by close surveillance. Level of Evidence: Level V (Therapeutic).

继发于肝脏疾病的多发性手内生纤维瘤恶性转化1例报告。
继发于肝脏疾病(OD)的内生软骨瘤病是罕见的,继发软骨肉瘤(CS)仅占恶性骨性肿瘤的1%。这是仅有的两份报告之一,记录了同一只手不同骨骼的四个内生纤维瘤发展为恶性转化,并进行了长期随访。这是一名72岁的女性,组织学证实其CS来自于食指掌骨和近端指骨以及中指近端和中指骨的多发内生性瘤。刮除和植骨6年后,她没有出现CS复发或转移。虽然手部CS具有侵袭性,但很少转移,5年生存率较高。由于预后良好,保留功能的手术选择比截肢可接受,并伴有密切监测。证据等级:V级(治疗性)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.90
自引率
0.00%
发文量
304
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