K. Jamshidi, A. Bagherifard, A. Mirzaei, Bone and Joint Reconstruction Research Center, Shafa Orthopedic Hospital, Iran University of Medical Sciences, Tehran, Iran.
H. H. Al-Baseesee, College of Medicine, University of Al-Kufa, Kufa, Najaf, Iraq.
Clin Orthop Relat Res. 2021 May 1;479(5):1134-1143. doi: 10.1097/CORR.0000000000001539.
Heterotopic ossification (HO) is common after total joint arthroplasty and usually does not cause diagnostic problems. However, the occurrence of HO after oncologic prostheses implantation can be troublesome as it may mimic a locally recurrent tumor. Because this distinction could have a profound impact on the surgeon and patient, it is important to distinguish the two entities; to our knowledge, no study has evaluated this after oncologic endoprosthetic reconstruction around the knee after tumor resection.
QUESTIONS/PURPOSES: (1) How common is the occurrence of HO compared with local recurrence (LR) after resection of bone sarcoma and the use of an oncologic knee prosthesis? (2) Are there any factors associated with the development of HO after limb salvage procedures with an endoprosthesis? (3) What features allow the surgeon to differentiate HO from a locally recurrent tumor in this setting?
Between 2002 and 2018, we performed 409 resections of primary bone tumors followed by reconstructions with oncologic endoprostheses. Of these, 17% (71 of 409) died before 2 years and did not have HO at that time, 2% (8 of 409) were lost to follow-up before 2 years, and another 2% (10 of 409) did not have radiographs available at a minimum of 2 years after surgery (and had not developed HO before then), and so could not be analyzed, leaving 320 patients for analysis in this retrospective study. Forty-two patients were excluded; 2% (5 of 320) for a history of failed allograft reconstruction, 3% (8 of 320) for pathologic fracture at presentation, 2% (6 of 320) for inadequate or complicated biopsy, 1% (2 of 320) for stem fractures, 2% (7 of 320) for stem loosening, and 4% (14 of 320) for extracortical bone bridging, leaving 278 patients for final evaluation. Two observers analyzed AP and lateral radiographs for signs of HO at a mean follow-up of 63 ± 33 months after surgery. We defined HO as extraskeletal bone formation in soft tissues. The primary study endpoint was survivorship free from HO, as ascertained by a competing-risks estimator. To identify factors associated with HO appearance, the demographic, radiographic, clinical, pathologic, and surgical characteristics were compared between patients with HO and those who had no lesion. Characteristic features were also compared between patients with HO and those with LR to help their differentiation. Univariate analysis was used for all statistical evaluations.
HO developed in 8% (21 of 278) of patients in whom oncologic knee prosthesis was implanted. LR developed in 10% (28 of 278) of the patients. According to survivorship estimates, the HO-free survival rate was not different from the LR-free survival rate at 2 years after oncologic knee reconstruction (76 ± 5% [95% CI 63 to 87] versus 74 ± 5% [95% CI 62 to 88]; p = 0.19). History of infection was more common in patients with HO than in patients with no lesion (19% [4 of 21] versus 5% [12 of 229], Odds ratio [OR] 6 [95% CI 2 to 17]; p < 0.001). The male sex was more common in the HO group as well (76% [16 of 21] versus 55% [128 of 229], OR 2 [95% CI 1 to 5]; p = 0.03). The Modular Universal Tumor and Revision System prosthesis was more frequently used in patients with HO (67% [14 of 21]) compared to those with no lesions (40% [92 of 229]; OR 2 [95% CI 1 to 5]; p = 0.02). The lesion border in radiographs was ill-defined in 19% (4 of 21) of patients with HO and 100% (28 of 28) of patients with LR (OR 8 [95% CI 3 to 20]; p < 0.001). The median time to the appearance of HO was shorter than the time to LR (8 months [3 to 13] versus 16 months [11 to 21], [95% CI 10 to 13]; p < 0.001). Pain at presentation was more frequent in patients with LR than in those with HO (86% [24 of 28] versus 14% [3 of 21], OR 36 [95% CI 7 to 181]; p < 0.001).
HO may occur after the use of oncologic knee prostheses for reconstruction after tumor resection. In most patients, HO could be differentiated from local recurrence through identifying a well-defined border on radiographs. Otherwise, factors such as an earlier time of presentation and absence of pain could suggest an HO, rather than an LR.
Level III, therapeutic study.
在全关节置换术后,异位骨化(HO)很常见,通常不会引起诊断问题。然而,由于它可能模仿局部复发性肿瘤,因此在肿瘤假体植入后发生的 HO 可能会带来麻烦。由于这种区别可能对外科医生和患者产生深远的影响,因此区分这两种实体非常重要;据我们所知,尚无研究评估过切除肿瘤后使用肿瘤膝关节假体重建膝关节周围肿瘤切除后的 HO。
问题/目的:(1)与骨肉瘤切除和使用肿瘤膝关节假体后局部复发(LR)相比,HO 的发生频率如何?(2)是否存在与保肢手术后发生 HO 相关的任何因素?(3)在这种情况下,有哪些特征可以让外科医生区分 HO 与局部复发性肿瘤?
在 2002 年至 2018 年间,我们对 409 例原发性骨肿瘤进行了切除,并用肿瘤假体进行了重建。其中,71 例(71/409)在 2 年内死亡,当时没有 HO;8 例(8/409)在 2 年内失访;另外 2%(10/409)在手术后至少 2 年时没有 X 线片可供分析(并且在此之前没有发生 HO),因此无法进行分析,在这项回顾性研究中,320 例患者被纳入分析。42 例患者被排除在外;2%(5/320)是因为同种异体移植重建失败史,3%(8/320)是因为初次就诊时发生病理性骨折,2%(6/320)是因为活检不充分或复杂,1%(2/320)是因为干骺端骨折,2%(7/320)是因为干骺端松动,4%(14/320)是因为皮质外骨桥接,最终有 278 例患者接受了最终评估。两名观察者在手术后平均 63 ± 33 个月时对 AP 和侧位 X 线片进行分析,以确定 HO 的存在。我们将 HO 定义为软组织中额外的骨形成。主要研究终点是通过竞争风险估计确定的无 HO 存活。为了确定 HO 出现的相关因素,比较了 HO 患者和无病变患者的人口统计学、影像学、临床、病理学和手术特征。还比较了 HO 患者和 LR 患者的特征,以帮助他们进行区分。所有统计评估均采用单变量分析。
在接受肿瘤膝关节假体植入的患者中,有 8%(21/278)发生 HO。在 278 例患者中,有 10%(28/278)发生 LR。根据生存估计,HO 无生存患者的 2 年 LR 无生存率无差异(76 ± 5%[95%CI 63 至 87]与 74 ± 5%[95%CI 62 至 88];p = 0.19)。HO 患者的感染史较无病变患者更常见(19%[4/21]与 5%[12/229],比值比[OR]6[95%CI 2 至 17];p < 0.001)。HO 组男性比例也较高(76%[16/21]与 55%[128/229],OR 2[95%CI 1 至 5];p = 0.03)。HO 患者更常使用模块化通用肿瘤和修复系统假体(67%[14/21]),而无病变患者则更常使用通用型假体(40%[92/229];OR 2[95%CI 1 至 5];p = 0.02)。HO 患者的病变边界在 X 线片中的定义不明确(19%[4/21]),LR 患者的边界则是明确的(100%[28/28];OR 8[95%CI 3 至 20];p < 0.001)。HO 出现的时间比 LR 短(8 个月[3 至 13]与 16 个月[11 至 21],[95%CI 10 至 13];p < 0.001)。LR 患者的疼痛发生率高于 HO 患者(86%[24/28]与 14%[3/21],OR 36[95%CI 7 至 181];p < 0.001)。
HO 可能发生在肿瘤切除后使用肿瘤膝关节假体进行重建之后。在大多数患者中,通过在 X 线片上识别明确的边界,可以将 HO 与 LR 区分开来。否则,如出现较早的发病时间和无疼痛等因素,可能提示为 HO,而非 LR。
III 级,治疗性研究。