ATYPICAL FEMUR FRACTURE

不典型股骨骨折
  • 文章类型: Journal Article
    非典型股骨骨折(AFFs)是长期双膦酸盐(BP)治疗的公认并发症,但其发病机制尚不完全清楚。尽管许多长期BP治疗的患者骨转换(SSBT)受到严重抑制,并不是所有这样的病人都会经历AFF,尽管SSBT是AFF的主要贡献者。因此,我们对12名女性(年龄和种族相匹配的6名和6名无AFF患者)使用经髂骨活检标本的纳米划痕试验评估了组织水平特性.使用混合模型ANOVA分析纳米划痕数据,其中体积归一化划痕能作为AFF的函数(是或否),区域(骨膜或内膜),以及区域和AFF之间的一阶相互作用。对刮擦能量的最小平方平均值的差异进行了Tukey事后分析,如果p<0.05,则报告为显着。AFF患者的体积归一化划痕能量比非AFF患者高10.6%(p=.003),骨膜比骨内区高17.9%(p=.004)。标准化划痕能量的差异提示长期BP治疗后骨组织的硬度更高。这项研究的结果与文献中的其他研究一致,并证明了使用Nano-Scratch技术评估表现出SSBT和AFF的骨组织的有效性。使用纳米划痕的进一步研究可能有助于量化和阐明AFF发病机理的潜在机制。
    Atypical femur fractures (AFFs) are a well-established complication of long-term bisphosphonate (BP) therapy, but their pathogenesis is not fully understood. Although many patients on long-term BP therapy have severe suppression of bone turnover (SSBT), not all such patients experience AFF, even though SSBT is a major contributor to AFF. Accordingly, we evaluated tissue level properties using nano-scratch testing of trans-iliac bone biopsy specimens in 12 women (6 with and 6 without AFF matched for age and race). Nano-scratch data were analyzed using a mixed-model ANOVA with volume-normalized scratch energy as a function of AFF (Yes or No), region (periosteal or endosteal), and a first-order interaction between region and AFF. Tukey post hoc analyses of the differences of least squared means of scratch energy were performed and reported as significant if p<.05. The volume-normalized scratch energy was 10.6% higher in AFF than in non-AFF patients (p=.003) and 17.9 % higher in the periosteal than in the endosteal region (p=.004). The differences in normalized scratch energy are suggestive of a higher hardness of the bone tissue after long-term BP therapy. The results of this study are consistent with other studies in the literature and demonstrate the efficacy of using Nano-Scratch technique to evaluate bone tissue that exhibits SSBT and AFF. Further studies using nano-scratch may help quantify and elucidate underlying mechanisms for the pathogenesis of AFF.
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  • 文章类型: Journal Article
    尽管非典型股骨骨折(AFF)的影像学诊断标准明确,漏诊和延误诊断很常见.AFF诊断软件可以提供及时的AFF检测以防止对侧AFF的不完全进展或发展。在这项研究中,我们研究了基于人工智能(AI)的应用程序的能力,使用深度学习模型(DLM),特别是卷积神经网络(CNN),从股骨X光片检测AFF。澳大利亚术前完整AFF(cAFF)的标记数据集,不完整的AFF(iAFF),典型股骨干骨折(TFF),和前后视图中的非骨折股骨(NFF)X射线图像用于训练(分别为N=213、49、394、1359)。AFFnet模型是使用预训练(ImageNet数据集)ResNet-50骨干开发的,和一个新颖的框注意指南(BAG)模块,以指导模型的扫描模式,以增强其学习。所有图像都用于训练和内部测试模型,使用5倍交叉验证方法,并通过外部数据集进一步验证。在包括733个TFF和290个AFF图像的瑞典数据集上进行模型性能的外部验证。Precision,灵敏度,特异性,在AFFnet和使用ResNet-50的全球方法之间测量并比较F1评分和AUC。在两个模型中都记录了出色的诊断性能(所有AUC>0.97),然而,AFFnet记录的预测误差较低,和改进的灵敏度,在内部和外部测试中与ResNet-50相比,F1评分和精度。AFFnet检测iAFF的灵敏度高于ResNet-50(82%vs56%)。总之,AFFnet在内部和外部验证中实现了出色的诊断性能,这优于预先存在的模型。准确的基于AI的AFF诊断软件有可能改善AFF诊断,减少放射科医生的错误,并允许紧急干预,从而改善患者的预后。
    Despite well-defined criteria for radiographic diagnosis of atypical femur fractures (AFFs), missed and delayed diagnosis is common. An AFF diagnostic software could provide timely AFF detection to prevent progression of incomplete or development of contralateral AFFs. In this study, we investigated the ability for an artificial intelligence (AI)-based application, using deep learning models (DLMs), particularly convolutional neural networks (CNNs), to detect AFFs from femoral radiographs. A labelled Australian dataset of pre-operative complete AFF (cAFF), incomplete AFF (iAFF), typical femoral shaft fracture (TFF), and non-fractured femoral (NFF) X-ray images in anterior-posterior view were used for training (N = 213, 49, 394, 1359, respectively). An AFFnet model was developed using a pretrained (ImageNet dataset) ResNet-50 backbone, and a novel Box Attention Guide (BAG) module to guide the model\'s scanning patterns to enhance its learning. All images were used to train and internally test the model using a 5-fold cross validation approach, and further validated by an external dataset. External validation of the model\'s performance was conducted on a Sweden dataset comprising 733 TFF and 290 AFF images. Precision, sensitivity, specificity, F1-score and AUC were measured and compared between AFFnet and a global approach with ResNet-50. Excellent diagnostic performance was recorded in both models (all AUC >0.97), however AFFnet recorded lower number of prediction errors, and improved sensitivity, F1-score and precision compared to ResNet-50 in both internal and external testing. Sensitivity in the detection of iAFF was higher for AFFnet than ResNet-50 (82 % vs 56 %). In conclusion, AFFnet achieved excellent diagnostic performance on internal and external validation, which was superior to a pre-existing model. Accurate AI-based AFF diagnostic software has the potential to improve AFF diagnosis, reduce radiologist error, and allow urgent intervention, thus improving patient outcomes.
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  • 文章类型: Case Reports
    背景:石骨症是一种罕见的遗传性疾病,可以通过常染色体隐性遗传或常染色体显性遗传传播。
    方法:这里,我们报告了一个18岁男孩的股骨转子骨折病例,该病例带有解剖钢板。在最后一次随访中,手术后24个月,骨折愈合良好,患者活动不受限制。
    结论:石骨病是一种罕见的骨疾病,主要由破骨细胞功能障碍引起。它是由导致骨骼过度矿化的重塑缺陷引起的,导致骨骼脆弱。手术和非手术治疗各有优缺点。因此,切开复位和解剖钢板内固定仍然是治疗骨结石患者股骨转子骨折的有效方法。
    结论:对于我们的患者,如文献中所述,随着骨质疏松性骨折的巩固,一些原则得到尊重,并发症发生率降低。
    BACKGROUND: Osteopetrosis is a rare hereditary disease that can be transmitted in an autosomal recessive or autosomal dominant.
    METHODS: Here, we report a case of trochanteric fracture in an 18-year-old boy with an anatomical plate. At the last follow-up, 24 months after surgery, the fracture had healed well, and the patient was not restricted in his activities.
    CONCLUSIONS: Osteopetrosis is a rare bone disease that is mainly caused by osteoclast dysfunction. It results from a remodelling defect that leads to hypermineralization of the skeleton, resulting in bone fragility. Both surgical and nonsurgical management have advantages and disadvantages. Thus, open reduction and anatomic plate fixation remain effective management modalities for trochanteric fractures in osteopetrosis patients.
    CONCLUSIONS: For our patient and as described in the literature, the complication rate decreases as some principles are respected with better consolidation of the osteoporotic fracture.
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  • 文章类型: Journal Article
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  • 文章类型: Journal Article
    不完全的非典型股骨骨折(iAFF)与长期使用抗吸收疗法有关。尽管X射线通常用于筛选iAFF,来自双能X射线吸收法(DXA)的图像提供了检测iAFF的替代方法。尽管存在关于这一主题的2019年ISCD官方立场,我们的工作组旨在更新文献综述,并就可能在DXA图像上观察到的与iAFF相关的报告结果提出建议.工作组建议DXA的全长股骨成像(FFI)可用作iAFF的筛查工具。应报告局灶性外侧皮质增厚和横向透明的存在,如果在FFI上识别。这个工作组提出了一个分类系统来确定iAFF的可能性,根据FFI上的射线照相特征。最后,特别工作组建议,FFI评估不需要对前驱症状(疼痛)进行临床评估.
    Incomplete atypical femur fractures (iAFFs) are associated with the long-term use of anti-resorptive therapies. Although X-rays are typically used to screen for iAFFs, images from dual-energy X-ray absorptiometry (DXA) offer an alternate method for detecting iAFFs. Although a previous 2019 ISCD Official Position on this subject exists, our task force aimed to update the literature review and to propose recommendations on reporting findings related to iAFFs that may be observed on DXA images. The task force recommended that full-length femur imaging (FFI) from DXA can be used as a screening tool for iAFFs. The presence of focal lateral cortical thickening and transverse lucencies should be reported, if identified on the FFI. This task force proposed a classification system to determine the likelihood of an iAFF, based on radiographic features seen on the FFI. Lastly, the task force recommended that the clinical assessment of prodromal symptoms (pain) is not required for the assessment of FFI.
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  • 文章类型: Case Reports
    双膦酸盐已被接受为绝经后骨质疏松症的一线治疗。非典型股骨干骨折是长期双膦酸盐治疗的副作用之一。这种非典型骨折的主要治疗方法是双膦酸盐停止和内固定稳定。我们正在报告一例罕见的病例,该病例是在一名85岁的印度女士手术中发现的,该女士患有与五年阿仑膦酸盐治疗有关的非典型股骨干骨折。我们发现在闭合方法中,导丝难以穿过骨折部位,这使得切开复位来管理闭塞的髓内管。应强调术中改变决策的重要性,以避免进一步的并发症。我们在临床随访期间实现了骨折愈合。
    Bisphosphonates have been accepted as the first-line treatment for postmenopausal osteoporosis. Atypical femoral shaft fracture is one of the side effects of long-term bisphosphonate therapy. The mainstay treatment of this atypical fracture is bisphosphonates cessation and stabilization with internal fixation. We are reporting a rare case of a blocked intramedullary femoral canal found during surgery of an 85-year-old Indian lady with an atypical femoral shaft fracture related to her five-year alendronate therapy. We found difficulty in passing the guidewire through the fracture site during the closed method, which renders open reduction to manage the obliterated intramedullary canal. The importance of changing decisions intraoperatively should be highlighted to avoid further complications. Fracture union is achieved during our follow-up in the clinic.
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  • 文章类型: Case Reports
    非典型股骨骨折(AFF)是由低能量创伤或无创伤引起的应力或功能不全骨折,经常与长期的双膦酸盐治疗相关。诊断遵循主要和次要标准,最初由美国骨骼和矿物研究学会工作组于2010年描述,并于2014年更新。然而,报告中AFF的定义排除了假体周围骨折.当假体植入物附近发生非典型骨折时,情况变得危急,手术治疗通常是脱模性的,并得到药物治疗的支持。此外,急性ORIF作为一线治疗经常负担高失败率,通常需要茎翻修作为二线治疗。愈合过程漫长而困难,功能效果不佳,结果受损。我们介绍了一个在我们机构接受治疗的78岁女性,有股骨非典型假体周围骨折史,因多次手术翻修而复杂化。其艰巨的管理反映了这些类型的骨折可能给外科医生带来的所有困难,而其良好的最终结果可能会教会我们如何以正确的方式接近它们。
    Atypical femoral fractures (AFF) are stress or insufficiency fractures induced by low energy trauma or no trauma, frequently correlated with prolonged bisphosphonate therapy. The diagnosis follows major and minor criteria, originally described by the Task Force of the American Society for Bone and Mineral Research in 2010 and updated in 2014. However, the definition of AFFs in the report excluded periprosthetic fractures. When atypical fractures occur close to a prosthetic implant the situation become critical, the surgical treatment is often demolitive and supported by medical treatment. Moreover, acute ORIF as a first line treatment is frequently burdened by a high failure rate , and often a stem revision is required as second line treatment. The healing process is long and difficult with poor functional results and impairing outcomes. We present a case treated at our institution of a 78 year old woman with a history of a femoral atypical periprosthetic fracture, complicated by multiple surgical revisions. Its arduous management reflects all the difficulties that these type of fractures could present to the surgeon, while its good final result may teach us how to approach them in a correct way.
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  • 文章类型: Case Reports
    非典型股骨骨折(AFFs)是抗吸收治疗的罕见并发症。毁灭受影响的个人,它们引起公众健康关注,因为由于患者的关注,骨质疏松症的有效治疗方法减少了。与欧洲人相比,亚洲种族患者的AFF风险增加了六到七倍。遗传因素可能是AFF表型的基础。鉴于AFF的稀有性,研究家族性AFF病例对于提供对任何遗传易感性的见解很有价值。我们介绍两个新加坡家庭,一个包括母亲(1-a)和女儿(1-b),另一个包括两个姐妹(2-a和2-b)。所有四例均表现为双膦酸盐相关AFF。对1-b进行全外显子组测序(WES),2-a,2-b1-a的DNA不可用。使用候选基因方法检查变体,该方法包括文献中先前与AFF相关的基因列表。以及使用基于显性和/或隐性继承模式的无偏过滤。使用候选基因方法,未发现3例病例共有的罕见变异.TMEM25中的一种罕见变体,由两姐妹(2-a和2-b)共享,已确定。在AFF(1-b)的子病例中存在罕见的杂合PLOD2变体,但不是姐妹。在对两个姐妹(2-a和2-b)进行变异过滤和注释分析后,确定了AFF的潜在遗传变异列表,包括TRAF4中的Gly35Arg变体,这是正常骨骼发育所需的基因。虽然这个基因分析的结果没有定论,AFFs的家族聚集提示AFF发病机制中的遗传成分。我们提供了在这些AFF家族病例中发现的罕见变异的完整列表,以帮助未来的遗传研究。©2022作者JBMRPlus由WileyPeriodicalsLLC代表美国骨骼和矿物研究学会出版。
    Atypical femur fractures (AFFs) are rare complications of anti-resorptive therapy. Devastating to the affected individual, they pose a public health concern because of reduced uptake of an effective treatment for osteoporosis due to patient concern. The risk of AFF is increased sixfold to sevenfold in patients of Asian ethnicity compared with Europeans. Genetic factors may underlie the AFF phenotype. Given the rarity of AFFs, studying familial AFF cases is valuable in providing insights into any genetic predisposition. We present two Singaporean families, one comprising a mother (1-a) and a daughter (1-b), and the other comprising two sisters (2-a and 2-b). All four cases presented with bisphosphonate-associated AFF. Whole-exome sequencing (WES) was performed on 1-b, 2-a, and 2-b. DNA for 1-a was not available. Variants were examined using a candidate gene approach comprising a list of genes previously associated with AFF in the literature, as well as using unbiased filtering based on dominant and/or recessive inheritance patterns. Using a candidate gene approach, rare variants shared between all three cases were not identified. A rare variant in TMEM25, shared by the two sisters (2-a and 2-b), was identified. A rare heterozygous PLOD2 variant was present in the daughter case with AFF (1-b), but not in the sisters. A list of potential genetic variants for AFF was identified after variant filtering and annotation analysis of the two sisters (2-a and 2-b), including a Gly35Arg variant in TRAF4, a gene required for normal skeletal development. Although the findings from this genetic analysis are inconclusive, a familial aggregation of AFFs is suggestive of a genetic component in AFF pathogenesis. We provide a comprehensive list of rare variants identified in these AFF familial cases to aid future genetic studies. © 2022 The Authors. JBMR Plus published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research.
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  • 文章类型: Case Reports
    骨巨细胞瘤(GCTB)是一种局部侵袭性肿瘤,手术通常可以治愈。然而,它很少会引起远处转移。目前,不可切除的GCTB的唯一有效治疗选择是denosumab,一种抗RANKL单克隆抗体,可以抑制这种疾病中常见的侵袭性骨质溶解。对于晚期/转移性GCTB,denosumab应该终身持续,虽然它通常是很好的耐受性,该药物的长期安全性可能会出现重要问题。事实上,不常见但严重的毒性可能发生,并最终导致denosumab停药,如股骨非典型骨折(AFF)。与治疗相关的AFF的最佳管理是一个有争议的问题,到目前为止,目前尚不清楚在疾病进展时重新引入denosumab是否是临床上可行的选择,因为到目前为止还没有提供任何报告。下文中,我们介绍了一例转移性GCTB患者,该患者经过几年的denosumab治疗后患有AFF;我们描述了临床特征,骨科治疗,和肿瘤的结果,最后提供第一个证据表明,在GCTB进展时,在AFF发生后的denosumab再激发可能是一个安全可行的选择.
    Giant cell tumor of the bone (GCTB) is a locally aggressive neoplasm where surgery is often curative. However, it can rarely give rise to distant metastases. Currently, the only available active therapeutic option for unresectable GCTB is denosumab, an anti-RANKL monoclonal antibody that dampens the aggressive osteolysis typically seen in this disease. For advanced/metastatic GCTB, denosumab should be continued lifelong, and although it is usually well tolerated, important questions may arise about the long-term safety of this drug. In fact, uncommon but severe toxicities can occur and eventually lead to denosumab discontinuation, such as atypical fracture of the femur (AFF). The optimal management of treatment-related AFF is a matter of debate, and to date, it is unknown whether reintroduction of denosumab at disease progression is a clinically feasible option, as no reports have been provided so far. Hereinafter, we present a case of a patient with metastatic GCTB who suffered from AFF after several years of denosumab; we describe the clinical features, orthopedic treatment, and oncological outcomes, finally providing the first evidence that denosumab rechallenge after AFF occurrence may be a safe and viable option at GCTB progression.
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  • 文章类型: Case Reports
    随着患者寿命的不断提高,随着患者植入物的寿命延长,下肢翻修关节置换术的比率将继续增加。随着持续的骨质流失和稳定性降低,可以执行的修订操作的数量有限制。全股骨置换术(TFA)是一种越来越受欢迎的保肢替代方法,可以恢复患者一定程度的日常功能。本报告介绍了一名73岁的男性,在过去22年中发生了两次极端的摩托车事故后,进行了多次右下肢手术。由于多次全膝关节置换术(TKA)后持续疼痛和股骨量差,进行了TFA。尽管在立即康复方面遇到了挫折,该程序还是成功的,并且满足了术后的期望。总的来说,TFA是一种有效的替代下肢截肢在无菌设置,多次膝关节翻修后的非肿瘤性骨丢失。然而,谨慎的管理对于降低感染和其他并发症的风险是必要的.
    As patient longevity continues to improve, the rate of lower limb revision arthroplasties will continue to increase as patients outlive the expiration of their implants. With continued bone loss and reduced stability, there is a limit to the number of revision operations that can be performed. Total femoral arthroplasty (TFA) is an increasingly popular limb-salvaging alternative that can restore some degree of daily function to patients. This report presents a 73-year-old male with multiple right lower-limb operations following two extreme motorcycle accidents in the last 22 years. Due to continued pain and poor femoral bone stock following multiple total knee arthroplasty (TKA) revisions, a TFA was performed. The procedure was successful and post-operative expectations were met despite setbacks in immediate rehabilitation. Overall, TFA is an effective alternative to lower limb amputation in the setting of aseptic, non-oncologic bone loss following multiple knee revisions. However, careful management is necessary to reduce the risk of infection and other complications.
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