Pathologic fracture

病理性骨折
  • 文章类型: Case Reports
    包虫病,是一种在全球养羊地区普遍存在的人畜共患疾病。肌肉骨骼包虫病并不常见,通常长期无症状。肌肉骨骼包虫病的检测通常意味着骨髓腔内广泛的囊肿扩散,使治疗困难,复发率高。与传统的内脏包虫囊肿手术方法不同,治疗骨性包虫病需要类似于肿瘤治疗的策略。我们报告了一例罕见的原发性包虫病,该病例影响了一名58岁女性的尺骨和邻近的软组织。她表现出了六年来无痛的前臂肿块,伴有近期发作的压痛和肘关节活动受限。成像显示前臂有一个囊性肿块,尺骨内病变,鹰嘴骨折.根据临床发现和放射学影像学对肌肉骨骼包虫病进行了初步诊断。治疗包括切除尺骨近端2/3,并切除软组织包虫囊肿。肌肉骨骼包虫病的诊断对于有效的术前计划至关重要,因为内固定经常失败而不根除感染。治疗通常包括根治性手术,广泛切除受影响的骨骼和邻近的关节结构,加上化疗。流行地区的临床医生应在溶骨性病变和缓慢增长的囊性肿块的鉴别诊断中考虑肌肉骨骼包虫病。诊断依赖于临床,血清学,和放射学评估。
    Hydatidosis, is a zoonotic disease prevalent in sheep-raising regions globally. Musculoskeletal hydatidosis is uncommon and usually remains asymptomatic over a long period. The detection of musculoskeletal hydatidosis often signifies extensive cyst spread within the bone marrow cavity, making treatment difficult with a high recurrence rate. Unlike the conventional surgical approach for visceral hydatid cysts, treating osseous hydatidosis requires a strategy akin to oncologic therapy. We report a rare case of primary hydatidosis affecting the ulna and adjacent soft tissue in a 58-year-old woman. She presented with a painless forearm mass evolving over six years, accompanied by recent onset tenderness and restricted elbow joint mobility. Imaging revealed a cystic mass in the forearm, an intra-ulnar bone lesion, and an olecranon fracture. The primary diagnosis of musculoskeletal hydatidosis was made based on clinical findings and radiological imaging. Treatment involved resection of 2/3 of the proximal ulna and pericystectomy for the soft tissue hydatid cyst. Diagnosis of musculoskeletal hydatidosis is vital for effective preoperative planning, as internal fixation often fails without eradicating the infestation. Treatment typically involves radical operation with wide excision of the affected bone and adjacent joint structures, coupled with chemotherapy. Clinicians in endemic regions should consider musculoskeletal hydatidosis in the differential diagnosis of osteolytic lesions and slow-growing cystic masses. Diagnosis relies on clinical, serological, and radiological assessments.
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  • 文章类型: Case Reports
    病理性指骨骨折是指孤立性内软骨瘤的常见初始表现。中指骨的软骨瘤最常与术后运动范围缺陷相关。本报告描述了一个案例,其中在手术固定中指中内软骨瘤伴伸肌腱损伤的病理性骨折后,使用克氏针(K线)和同种异体骨修复手指运动。
    一名37岁的右手优势女子表现为左食指中指骨病理性骨折。患者选择进行手术干预,以稳定骨折并使近端指间关节(PIP)早期运动。手术固定术涉及肿瘤刮除术,用纵向K线进行断裂稳定和长度保持,具有硬化特性的同种异体骨填充骨缺损,和用于固定伸肌腱的背侧K线。术后11个月随访,同种异体移植几乎完全解决了,患者恢复了PIP90°屈曲和完全伸展。
    中指骨内生软骨瘤的病理性骨折容易因伸肌腱损伤和相关的术后运动丧失而发生并发症。植骨和克氏针固定可以早期动员手指运动,因此可能是治疗其他病理性骨折的有用技术。
    UNASSIGNED: Pathologic phalangeal fracture is a common initial presentation of solitary enchondroma of the finger. Enchondromas of the middle phalanx are most frequently associated with post-operative range of motion deficits. This report describes a case in which the use of Kirschner wires (K-wires) and allograft bone were used to salvage finger motion following surgical fixation of pathologic fracture of a middle phalanx enchondroma with extensor tendon injury.
    UNASSIGNED: A 37-year-old right hand dominant woman presents with pathologic fracture of the left index finger middle phalanx. The patient elected for surgical intervention to stabilize fracture and enable early motion at the proximal interphalangeal joint (PIP). Surgical fixation involved tumor curettage, fracture stabilization and length preservation with longitudinal K-wires, allograft bone with hardening properties to fill the bony defect, and dorsal K-wires for securing the extensor tendon. At follow-up 11 months postoperatively, the allograft had almost completely resolved, and the patient had regained PIP flexion of 90° and full extension.
    UNASSIGNED: Pathologic fracture of middle phalanx enchondroma is prone to complication by extensor tendon injury and associated post-operative loss of motion. Bone grafting and Kirschner wire fixation allowed for early mobilization of finger motion and thus may be a useful technique for use in treatment of other pathologic fractures.
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  • 文章类型: Case Reports
    免疫检查点抑制剂(ICIs)通过增强细胞毒性T细胞活性,在转移性癌症的不同亚型中与患者生存相关的肿瘤学结果显着增强。ICI相关的毒性通常被称为免疫相关的不良事件(irAE),并且发生在几乎每个器官系统中。然而,ICI对骨骼的影响研究不充分,只发表了几个案例系列。
    方法:一名37岁男子,在腹腔镜下根治性肾切除术治疗右肾细胞癌之后,在辅助pembrolizumab治疗期间出现右肱骨近端病理性骨折。
    ICI与几乎影响所有宿主组织的各种irAE有关,其中大多数已通过药物警戒分析得到了很好的描述。然而,到目前为止,很少有研究检查ICI对骨骼的影响。
    结论:泌尿科肿瘤学家和泌尿科医师应该意识到ICIs的罕见但可能致命的骨副作用。
    UNASSIGNED: Immune checkpoint inhibitors (ICIs) have noticeably enhanced oncologic outcomes associated with patient survival in different subtypes of metastatic cancer by enhancing cytotoxic T-cell activity. ICI-associated toxicities are often referred to as immune-related adverse events (irAEs) and occur in nearly every organ system. However, the effect of ICIs on the skeleton is poorly examined, and only a few case series have been published.
    METHODS: A 37-year-old man who presented with pathologic fractures of the right proximal humerus during adjuvant pembrolizumab therapy following laparoscopic radical nephrectomy for right renal cell carcinoma.
    UNASSIGNED: ICIs are associated with various irAEs virtually affecting all host tissues, most of which have been described well by pharmacovigilance analyses. However, to date, very few studies have examined the effects of ICI on the skeleton.
    CONCLUSIONS: Urologic oncologists and urologists should be aware of the rare but potentially fatal bone side effects of ICIs.
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  • 文章类型: Case Reports
    非骨化性纤维瘤(NOF)是一种良性纤维化病变,与功能异常骨化有关,是儿童时期最常见的良性骨肿瘤之一,在骨骼未成熟儿童中发病率为30-40%。
    一名25岁女性,过去2个月有左髋部疼痛,被保守地对待,臀部出现剧烈疼痛.X线显示股骨颈病理性骨折,并伴有潜在病变。MRI显示股骨颈溶骨性病变。用游离腓骨植骨对病灶进行刮除,并用动力髋螺钉和标本送病理。病理报告由NOF组成。命令进行8周无负重并进行身体康复,六个月后,患者进行了全方位的运动并愈合了骨折。
    这项研究表明,对于病理性股骨颈骨折和潜在的NOF,采用植骨的手术治疗可以快速恢复活动,并且可以充分固定以实现出色的术后恢复。
    UNASSIGNED: Nonossifying fibroma (NOF) is a benign fibrogenic lesion that is related to dysfunctional ossification and one of the most common benign bone tumors in childhood with incidence rate of 30-40% of skeletally immature children.
    UNASSIGNED: A 25-year-old female with left hip pain for the past 2 months, which was treated conservatively, presented with severe pain in the hip. X-ray showed a pathologic fracture in the neck of the femur with underlying lesion. MRI showed an osteolytic lesion in neck of the femur. Curettage of the lesion was done with free fibular bone graft and stabilized by Dynamic Hip Screw and specimen sent to pathology. The pathology report consisted with NOF. No-weight bearing for 8 weeks with physical rehabilitation were ordered and six months later the patient had a full range of motion and healed fracture.
    UNASSIGNED: This study revealed that the surgical treatment with bone graft for pathologic femoral neck fracture and underlying NOF allowed a quick return to mobility and can be fixed sufficiently to achieve excellent postoperative recovery.
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  • 文章类型: Case Reports
    肾和甲状腺癌等高血管肿瘤具有术中出血的重大风险。为了帮助减轻出血,传统上使用介入性术前栓塞;然而,成功是高度可变的。这是第一个病例报告,讨论使用可扩张球囊植入物与微创方法来实现骨折固定和填塞急性术中出血。
    一名48岁男性,患有透明细胞肾细胞癌,表现为左肱骨干病理性骨折。病人被安排接受开放活检,肿瘤刮治,用髓内装置固定骨折。术中,在开放活检和刮宫期间,出血快,在插入髓内光动力骨稳定植入物(IlluminOss)后停止。植入物的球囊扩张到肱骨的直径允许填塞,断裂稳定性,和微创方法。
    我们提出了一种可能的术中选择,通过部署光动力稳定装置来控制病理性长骨骨折的出血。所描述的方法可以在特定患者中应用,并且由于植入物在骨骼内产生填塞的能力,因此无需对高血管性肿瘤进行术前栓塞。
    UNASSIGNED: Hypervascular tumors such as renal and thyroid carcinoma have a significant risk of intraoperative bleeding. To help mitigate bleeding, interventional preoperative embolization is traditionally used; however, it is success is highly variable. This is the first case report to discuss using expandable balloon implants with a minimally invasive approach to achieve fracture fixation and tamponade acute intraoperative bleeding.
    UNASSIGNED: A 48-year-old male with clear-cell renal cell carcinoma presented with a left humeral shaft pathologic fracture. The patient was scheduled to undergo open biopsy, curettage of tumor, and fracture fixation with an intramedullary device. Intraoperatively, during open biopsy and curettage, brisk bleeding was encountered, which ceased after inserting an intramedullary photodynamic bone stabilization implant (IlluminOss). The implant\'s balloon expanded to the diameter of the humerus allowing for tamponade, fracture stability, and a minimally invasive approach.
    UNASSIGNED: We present a possible intraoperative option for achieving control of bleeding in pathologic long bone fractures by deploying a photodynamic stabilization device. The method described can have applications in specific patients and obviate the need for pre-operative embolization for highly vascular tumors due to the implant\'s ability to create tamponade within the bone.
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  • 文章类型: Case Reports
    Ollier病是一种罕见的骨骼发育不良,其特征是形成多个内生软骨瘤(内生软骨瘤病),通常在四肢的长骨中。这些肿瘤是良性的,但可能因病理性骨折的发展而变得复杂,肢体畸形,恶性转化为软骨肉瘤.Ollier疾病具有高度可变的表现,并且与一系列表现发现相关;然而,最常见的表现是病理性骨折。手术选择包括刮宫和移植内生瘤,当流离失所时,骨折复位固定。值得注意的是,这些骨折不用手术就会愈合.无论如何,所有患者都必须接受年度X光片常规监测,以便尽早发现恶性转化.在这份报告中,我们描述了一个11岁女性的案例,她在游泳池里玩耍后,向医生展示了她的右无名指和小指疼痛和肿胀,没有明显的创伤机制。例行公事,对她的手进行常规X线检查显示存在多发性内生软骨瘤病。我们希望利用这个案例来强调年轻的Ollier病患者的手术管理选择,并讨论可能不需要手术管理的情况。
    Ollier disease is a rare skeletal dysplasia characterized by the formation of multiple enchondromas (enchondromatosis), typically in the long bones of the extremities. These tumors are benign but can become complicated by the development of pathologic fractures, limb deformity, and malignant transformation to chondrosarcoma. Ollier disease has a highly variable presentation and is associated with a range of presenting findings; however, the most common presentation is a pathologic fracture. Surgical options include curettage and grafting of the enchondromas and, when displaced, fracture reduction and fixation. Of note, these fractures will heal without surgery. Regardless, all patients must be routinely monitored with yearly radiographs in order to detect malignant transformation as early as possible.  In this report, we describe the case of an 11-year-old female who presented to her physician with pain and swelling of her right ring and small fingers after playing in a swimming pool with no obvious mechanism of trauma. A routine, plain radiographic evaluation of her hand revealed the presence of multiple enchondromatosis. We hope to use this case to highlight the surgical management options for young patients with Ollier disease and discuss circumstances in which surgical management may not be indicated.
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    文章类型: Case Reports
    骨内肌纤维瘤是一种罕见的良性肿瘤,生长缓慢,低发病率。本文的目的是报告一例与青少年下颌骨肌纤维瘤的偶然诊断相关的病理性骨折。一名15岁女孩报告说,她在1个月前遭受了身体攻击,导致面部受伤,此后经历了严重的疼痛,错牙合,咀嚼困难。锥形束计算机断层扫描检查显示多种特征,提示病理性骨折与具有分叶状界限的低密度病变相关。以及左下颌骨皮质骨的扩张和变薄。病变的组织病理学诊断为肌纤维瘤。治疗包括病灶的摘除和刮除,骨折复位和内固定。18个月后,去除接骨板和受影响的下颌第三磨牙。与下颌骨骨折治疗相关的病灶刮除被证明对骨骼巩固和无复发均有效,同时恢复下颌骨功能。
    Intraosseous myofibroma is a rare tumor of benign nature, slow growth, and low morbidity. The aim of this article is to report a case of pathologic fracture associated with the incidental diagnosis of myofibroma in the mandible of an adolescent. A 15-year-old girl reported that she experienced a physical assault resulting in facial injuries 1 month previously and had since experienced severe pain, malocclusion, and chewing difficulty. The cone beam computed tomographic examination revealed multiple features suggestive of pathologic fracture associated with a hypodense lesion with lobulated limits, as well as expansion and thinning of the cortical bone in the left mandible. The histopathologic diagnosis of the lesion indicated myofibroma. Treatment consisted of enucleation and curettage of the lesion with reduction and internal fixation of the fracture. After 18 months, the osteosynthesis plates and an impacted mandibular third molar were removed. Curettage of the lesion in association with treatment of the mandibular fracture proved to be effective for both bone consolidation and absence of recurrence while restoring mandibular functionality.
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  • 文章类型: Case Reports
    背景:朗格汉斯细胞组织细胞增生症(LCH)是一种罕见的疾病。治疗方案取决于涉及的器官数量和疾病的广泛性。在这份报告中,介绍了一例LCH伴孤立的第6颈椎(C6)塌陷的病例。此病例采用前路椎体全切术和器械融合治疗,其次是局部放疗(RT),具有良好的临床效果,直到术后六个月。
    方法:这是一名47岁的女性患者,在咨询前两个月主诉颈部疼痛和双侧肩部疼痛。她最初是用镇痛药治疗的,但是疼痛是持续的。进一步的放射学评估显示C6椎体内有溶骨性病变,伴有病理性骨折。磁共振成像(MRI)与颈椎对比显示,C6椎体T1加权图像上弥散的低信号变化和T2加权图像上的高信号变化,具有显著的对比增强的浸润信号。此外,在正电子发射断层扫描-计算机断层扫描(PET-CT)中,局灶性高代谢和异常摄取信号仅见于C6椎体。该患者接受了颈椎前路切除术和器械融合。组织病理学结果证实了LCH的诊断。患者报告术后第一天疼痛明显缓解。此外,术后1个月接受局部RT治疗。直到术后六个月,没有疼痛和颈部活动恢复,取得了良好的临床结果。在最后一次随访中没有观察到复发的证据。
    结论:本病例报告描述了通过前路椎体切除术和器械融合治疗LCH的孤立性C6塌陷的治疗选择,其次是当地的RT,术后6个月临床疗效良好。需要更多的研究来阐明这种治疗策略是否优于手术或单独的RT。
    BACKGROUND: Langerhans cell histiocytosis (LCH) is a rare disorder. The treatment options vary depending on how many organs are involved and how extensive the disease is. In this report, a case of LCH with isolated 6th cervical vertebra (C6) collapse was presented. This case was treated with anterior corpectomy and instrumented fusion, followed by local radiotherapy (RT), with a good clinical outcome up to postoperative six months.
    METHODS: This was a 47-year-old female patient with a complaint of neck pain and bilateral shoulder pain for two months before consultation. She was initially treated with analgesics, but the pain was persistent. Further radiological evaluations revealed an osteolytic lesion within the C6 vertebral body with a pathological fracture. Magnetic resonance imaging (MRI) with contrast of the cervical spine revealed diffused hypointense signal changes on the T1-weighted images and hyperintense signal changes on the T2-weighted images in the C6 vertebral body, with significant contrast-enhanced infiltration signals. Furthermore, in positron emission tomography-computed tomography (PET-CT), focal hypermetabolism and abnormal uptake signals were seen only in the C6 vertebral body. The patient underwent an anterior cervical corpectomy with instrumented fusion. The histopathological results confirmed the diagnosis of LCH. The patient reported significant pain relief on postoperative day one. Moreover, she was treated by local RT at postoperative one month. Good clinical outcomes were achieved in the form of no pain and recovery in neck mobility up to postoperative six months. No evidence of recurrence was observed at the final follow-up.
    CONCLUSIONS: This case report describes a treatment option for a solitary C6 collapse with LCH managed by anterior corpectomy and instrumented fusion, followed by local RT, with a good clinical outcome at postoperative six months. More studies are needed to elucidate whether such a treatment strategy is superior to surgery or RT alone.
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  • 文章类型: Case Reports
    前列腺腺癌转移至骨并形成脆弱的母细胞性病变,术中可以表现为密集的障碍。关于外科医生在通过这些病变进行手术时所面临的挑战的报道有限。一名60岁的男性患有病理性股骨粗隆下骨折,存在母细胞性病变,并通过髓内(IM)固定成功治疗。由于转移性前列腺癌的生存能力提高,预计由爆发性骨病变引起的病理性骨折的患病率将增加。骨科医生,对这些骨折进行IM固定时,应准备使用附属设备,并应采用创造性的技术进行复位和固定。
    Prostate adenocarcinoma metastasizes to bone and forms fragile blastic lesions, which can present as dense obstacles intraoperatively. There are limited reports on the challenges surgeons face when operating through these lesions. A 60-year-old male with a pathologic subtrochanteric femur fracture in the presence of blastic lesions was successfully treated with intramedullary (IM) fixation. Pathologic fractures from blastic bone lesions are expected to increase in prevalence as survivability improves for metastatic prostate cancer. Orthopedic surgeons, when performing IM fixation for these fractures, should be prepared to utilize accessory equipment and should adopt creative techniques for reduction and fixation.
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  • 文章类型: Case Reports
    在良性或恶性病变的情况下,病理性骨折通常继发于骨骼生理异常。很少,病理性骨折可能发生在淋巴异常的情况下,如广泛性淋巴管瘤病。这种罕见的疾病的特点是在广泛的患者年龄范围内表现不同。通过了解广泛的淋巴异常对各种器官系统的影响,临床医生将能够更早和更确定地做出这一诊断.
    Pathologic fractures commonly occur secondary to abnormal skeletal physiology in the context of benign or malignant lesions. Rarely, pathologic fractures may occur in the context of a lymphatic abnormality, such as generalized lymphangiomatosis. This rare disorder is characterized by variable presentations in a broad age range of patients. By understanding the effect of widespread lymphatic anomalies on various organ systems, clinicians will be able to make this diagnosis earlier and with more certainty.
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