Wessel Lauren E, Christ Alexander B, Athanasian Edward A
Department of Orthopaedic Surgery, University of California Los Angeles, Los Angeles, CA.
Department of Orthopaedic Surgery, Keck Hospital of University of Southern California, Los Angeles, CA.
J Hand Surg Am. 2023 May;48(5):512.e1-512.e7. doi: 10.1016/j.jhsa.2021.11.027. Epub 2022 Jan 31.
The approach to the treatment of enchondromas of the hand is varied, and there is no clear consensus on graft source, fixation, or need for intraoperative adjuvant therapy. We reviewed a cohort of patients who underwent curettage and bone grafting with cancellous allograft chips without internal fixation or adjuvant therapy and reported on postoperative range of motion (ROM) and recurrence rates.
We performed a retrospective review of patients who underwent surgical treatment for hand enchondroma over a 23-year period. We collected information on demographics and presenting enchondroma characteristics, including Takigawa classification and presence of pathologic fracture or associated syndromes. Patients were treated with open biopsy with curettage and grafting with cancellous allograft chips. Postoperative ROM, complications, and recurrences were recorded.
Our series included 111 enchondromas in 104 patients. Seventeen of 104 patients (16%) had a diagnosis of Ollier disease. Average length of follow-up was 3.1 years. Eighty-one percent of patients achieved full ROM. Treatment of patients who presented with preoperative pathologic fracture resulted in a greater frequency of reduced postoperative ROM at 28% (9/32) compared to 15% (11/72) of those patients who did not present with preoperative pathologic fracture. Local recurrence developed in 5 of 50 (10%) patients with a minimum of 2 years of follow-up. Local recurrence occurred at higher-than-average rates in patients with giant form Takigawa classification (43%, 3/7) and Ollier disease (23%, 3/13).
Treatment of enchondromas with biopsy, curettage, and allograft results in full ROM in 81% of patients. Patients with preoperative pathologic fracture should be advised of a greater risk of postoperative extension deficit. Recurrence remains rare and is associated with syndromic presentation and giant form lesions.
TYPE OF STUDY/LEVEL OF EVIDENCE: Therapeutic IV.
手部内生软骨瘤的治疗方法多样,在移植来源、固定方式或术中辅助治疗的必要性方面尚无明确共识。我们回顾了一组接受刮除术及松质骨同种异体骨碎片植骨且未进行内固定或辅助治疗的患者,并报告了术后活动范围(ROM)及复发率。
我们对23年间接受手部内生软骨瘤手术治疗的患者进行了回顾性研究。收集了人口统计学信息及内生软骨瘤的特征,包括Takigawa分类以及病理性骨折或相关综合征的情况。患者接受了开放活检、刮除术及松质骨同种异体骨碎片植骨。记录术后ROM、并发症及复发情况。
我们的系列研究包括104例患者的111个内生软骨瘤。104例患者中有17例(16%)诊断为Ollier病。平均随访时间为3.1年。81%的患者实现了完全ROM。术前出现病理性骨折的患者术后ROM降低的频率更高,为28%(9/32),而术前未出现病理性骨折的患者这一比例为15%(11/72)。50例至少随访2年的患者中有5例(10%)出现局部复发。Takigawa分类为巨大型的患者(43%,3/7)及Ollier病患者(23%,3/13)的局部复发率高于平均水平。
活检、刮除术及同种异体骨移植治疗内生软骨瘤可使81%的患者实现完全ROM。应告知术前出现病理性骨折的患者术后活动度受限风险更高。复发仍然少见,且与综合征表现及巨大型病变相关。
研究类型/证据水平:治疗性IV级。