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A Case of Fixation Using Poly-L-Lactic Acid Pins for Chronic Juvenile Massive Osteochondritis Dissecans of the Knee. 聚l -乳酸钉固定治疗慢性幼年性大块性膝关节夹层性骨软骨炎1例。
Pub Date : 2026-02-01 DOI: 10.13107/jocr.2026.v16.i02.6780
Ken Ichikawa, Akira Maeyama, Tetsuro Ishimatsu, Taiki Matsunaga, Shizuhide Nakayama, Takuaki Yamamoto

Introduction: Chronic juvenile massive osteochondritis dissecans (OCD) presents significant therapeutic challenges due to the lack of established treatments. We herein report a case of chronic juvenile massive OCD treated with poly-L-lactic acid pin fixation.

Case report: A 13-year-old boy presented to another hospital with right knee pain after playing football. Initially, no significant abnormalities were noted, and he was placed under observation. However, the pain later worsened, and he was referred to our hospital with a diagnosis of OCD. An X-ray revealed a defect posterior to the lateral femoral condyle and a loose body in the suprapatellar bursa. Magnetic resonance imaging indicated the presence of a lateral discoid meniscus. Three months after the onset of symptoms, osteochondral fragment fixation and saucerization of the lateral meniscus were performed. One year postoperatively, the patient showed a good outcome with no recurrence of symptoms.

Conclusion: Chronic juvenile massive OCD may achieve fusion with fixation, even when bone fragments consist only of cartilage.

由于缺乏成熟的治疗方法,慢性青少年大块性夹层骨软骨炎(OCD)呈现出显著的治疗挑战。我们在此报告一例用聚乳酸针固定治疗慢性青少年大量强迫症。病例报告:一名13岁男孩因踢足球后右膝疼痛到另一家医院就诊。最初,没有发现明显的异常,他被置于观察之下。然而,后来疼痛加剧,他被诊断为强迫症,被转介到我们医院。x线显示股骨外侧髁后方有缺损,髌上滑囊内有疏松体。磁共振成像显示有外侧盘状半月板。症状出现3个月后,行外侧半月板骨软骨碎片固定和碟状固定术。术后1年,患者预后良好,无症状复发。结论:慢性青少年块状强迫症可实现骨融合固定,即使骨碎片仅由软骨组成。
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引用次数: 0
Addressing Bilateral Post-traumatic Distal Radius Growth Arrest with Positive Ulnar Variance with Acute Ulnar Shortening Osteotomy and Distal Radioulnar Joint Fixation in a 13-Year-Old Child: A Case Report. 治疗双侧创伤后桡骨远端生长停止伴尺侧正变异的一例13岁儿童:急性尺侧缩短截骨和尺桡远端关节固定。
Pub Date : 2026-02-01 DOI: 10.13107/jocr.2026.v16.i02.6746
Ahmed Khalaf Alanazi, Ali Mubarak Aldossari, Faisal Fahad Almalilk, Khaled Mohammed Alshehri

Introduction: Pediatric forearm fractures are very common. The distal radius growth physis contributes the majority of the radial length and nearly half of the entire upper extremity. Although growth arrest associated with physeal fractures is rare but the sequelae can be very detrimental and challenging. Partial or complete distal radius physis arrest can lead to radial shortening, alteration of radial tilt or inclination, distal radioulnar joint (DRUJ) incongruity, ulnocarpal abutment syndrome, and injury to the triangular fibrocartilage complex. Post-traumatic distal radius physis arrest is a serious complication that can lead to several disabilities. These disabilities could be devastating as it is related to the functional status of the wrist. In the literature, there are few studies reported post-traumatic distal radius growth arrest. Our case is bilateral post-traumatic distal radius growth arrest with positive ulnar variance that is limiting the patient's wrist function.

Case report: A 13-year-old boy presented to the outpatient department with bilateral wrists pain and deformities, 6 years after sustaining bilateral distal radius fractures, which was managed conservatively at that time. On examination, the patient had obvious bilateral wrists deformities and limitation of range of motion (ROM). Radiographic investigations showed: Bilateral central distal radius physeal osseous bar in the background of positive ulnar variance and dorsal subluxation of the DRUJ. After discussing treatment options with his parents, the patient was treated surgically, starting with the left side by ulnar shortening osteotomy and temporary DRUJ fixation. After 8 weeks from the surgical operation, the patient was referred for physiotherapy for gradual supervised sessions to regain full ROM and strength. One year follow-up, the patient showed near normal wrists activity with satisfactory outcome for him and his family, so the same surgical operation was done to the right side.

Conclusion: The treatment of these types of injuries is highly controversial. Options could vary from case to case. We do believe that ulnar shortening osteotomy with temporary DRUJ fixation should be considered in treating late presenting distal radius physeal injury in adolescent patients, aiming for an absolute great outcome.

儿童前臂骨折是非常常见的。桡骨远端生长体占桡骨长度的大部分,几乎占整个上肢的一半。虽然生长停滞与骨骺骨折是罕见的,但后遗症可能是非常有害的和具有挑战性的。部分或完全桡骨远端物理停止可导致桡骨缩短、桡骨倾斜或倾斜度改变、远端桡尺关节(DRUJ)不一致、尺腕关节基台综合征和三角纤维软骨复合体损伤。创伤后桡骨远端肢体停搏是一种严重的并发症,可导致多种残疾。这些残疾可能是毁灭性的,因为它与手腕的功能状态有关。在文献中,很少有研究报道创伤后桡骨远端生长停止。我们的病例是双侧创伤后桡骨远端生长停止,伴有尺侧正变异,限制了患者的手腕功能。病例报告:一名13岁男孩在双侧桡骨远端骨折6年后,因双侧手腕疼痛和畸形来到门诊,当时采取保守治疗。检查时,患者有明显的双侧手腕畸形和活动范围受限。x线检查显示:双侧中央桡骨远端骨性棒在尺侧变异阳性和DRUJ背侧半脱位的背景下。在与父母讨论治疗方案后,患者接受手术治疗,从左侧开始,通过尺侧截骨缩短和临时DRUJ固定。手术后8周,患者接受物理治疗,逐步进行监督治疗,以恢复完全的ROM和力量。随访1年,患者手腕活动接近正常,患者本人及其家人满意,因此对右侧进行了相同的手术。结论:这类损伤的治疗存在很大争议。选择可能因情况而异。我们认为,在治疗青少年晚期桡骨远端骨性损伤时,应考虑尺侧截骨短缩联合临时DRUJ固定,目的是获得绝对好的结果。
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引用次数: 0
A Humeral Shaft Non-union Treated With Proximal Tibia Cancellous Autograft and Fibular Strut Allograft: A Case Report. 胫骨近端自体松质骨和同种异体腓骨支架移植治疗肱骨骨不连1例。
Pub Date : 2026-02-01 DOI: 10.13107/jocr.2026.v16.i02.6764
P Tantone Ryan, SeHoon Park, Greco Victor

Introduction: Humeral shaft non-unions can pose a difficult challenge to orthopedic surgeons. There are various techniques to approach these injuries, but some require microsurgical techniques or staged procedures.

Case report: A 41-year-old woman presented with a 5-year-old humeral shaft non-union after previous open reduction and internal fixation complicated by infection. This was successfully treated surgically using a combination of proximal tibia cancellous autograft and structural allograft. Postoperatively, she had pain-free range of motion that was symmetric to her contralateral side.

Conclusion: Chronic humeral shaft non-unions may be successfully treated with a combination of tibial cancellous autograft and structural allograft.

肱骨不连是骨科医生面临的一大难题。有各种各样的技术来处理这些损伤,但有些需要显微外科技术或分阶段手术。病例报告:一名41岁女性在先前的切开复位和内固定并发感染后出现5年肱骨不愈合。手术成功地治疗了胫骨近端自体松质骨和同种异体结构骨的结合。术后,患者的活动范围与对侧对称,无痛。结论:自体胫骨松质骨与同种异体结构骨联合移植可成功治疗慢性肱骨不连。
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引用次数: 0
Iatrogenic Fibula Head Avulsion Fracture in Fixed Valgus Arthritic Knee During Total Knee Arthroplasty. 全膝关节置换术中固定外翻膝关节的医源性腓骨头撕脱骨折。
Pub Date : 2026-02-01 DOI: 10.13107/jocr.2026.v16.i02.6820
Vidya Sagar Reddy Chappidi, Palla Abhilash, Mantu Jain

Introduction: Total knee replacement in valgus knees is more challenging than in varus knees, which needs meticulous handling and decision-making from the surgical approach to the rehabilitation protocol. In this case, we report an iatrogenic fibula head fracture during total knee replacement for a valgus knee with no concomitant common peroneal nerve palsy. This is the first report of this kind in the literature.

Case report: We report a case of a 67-year-old male with fixed valgus and flexion deformity of the right knee, who underwent total knee arthroplasty by lateral para-patellar approach and sustained an iatrogenic fibula head fracture without common peroneal nerve palsy. The probable cause could be excess pressure exerted by the assistant holding the Hohmann retractor on the posterior aspect of the tibia and/or during the maneuvers to expose the posterolateral part of the tibia through the lateral para-patellar approach. He had no neurovascular defects postoperatively and has followed the regular rehabilitation protocol with good functional recovery and showing signs of radiological union in progress of the fracture at 2-month follow-up.

Conclusion: Gentle handling of rigid multiplanar deformity valgus arthritic knees is mandatory to prevent complications. A fibula head fracture could be one of the methods of lateral contracture release in rigid valgus knees.

引言:外翻膝关节的全膝关节置换术比内翻膝关节更具挑战性,需要从手术入路到康复方案的精心处理和决策。在这个病例中,我们报告了一例医源性腓骨头骨折,在全膝关节置换术中治疗外翻膝关节,没有伴随腓骨总神经麻痹。这在文献中尚属首次报道。病例报告:我们报告一例67岁男性右膝固定外翻和屈曲畸形,他接受了外侧髌骨旁入路全膝关节置换术,并持续了医源性腓骨头骨折,没有腓总神经麻痹。可能的原因是助手手持Hohmann牵开器对胫骨后侧和/或在通过外侧髌骨旁入路暴露胫骨后外侧时施加的压力过大。术后无神经血管缺损,术后遵循常规康复方案,功能恢复良好,随访2个月时骨折放射愈合。结论:软性多平面畸形外翻膝关节炎是预防并发症的必要措施。腓骨头骨折可作为刚性膝外翻侧缩松解的方法之一。
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引用次数: 0
Impaired Bone Healing and Fracture Complications during Limb Lengthening in a Neurofibromatosis Type 1 Patient Receiving Selumetinib: Case Report and Literature Review. 接受塞鲁美替尼的1型神经纤维瘤病患者肢体延长过程中骨愈合受损和骨折并发症:病例报告和文献回顾。
Pub Date : 2026-02-01 DOI: 10.13107/jocr.2026.v16.i02.6810
Zahra Safari, Maria Tirta, Ole Rahbek, Søren Kold

Introduction: Neurofibromatosis Type 1 (NF1) is a genetic disorder that may lead to the development of plexiform neurofibromas (Pns). Selumetinib, a selective mitogen-activated protein kinase (MEK1/2) inhibitor, has shown clinical benefit in shrinking inoperable PNs. However, its long-term effects on the skeleton remain unclear. This case describes impaired bone healing and pathological fractures following limb lengthening in a child with NF1 receiving prolonged selumetinib therapy.

Case report: A 5-year-old boy with genetically confirmed NF1 and left lower limb PN-induced overgrowth presented with a 4.5 cm limb length discrepancy. The patient had been receiving selumetinib (20 mg twice daily) without a clinically significant reduction in the size of the PNs. Lengthening was performed on a short healthy lower leg with an external fixator that did not include the femur. A distal femoral fracture occurred 3 weeks postoperatively on the same side as the lower leg lengthening was performed, and was treated with K-wire fixation. Despite healing, a refracture occurred 2 months later. In addition, delayed bone healing was observed for the tibial lengthening regenerate, and progressive valgus deformity and fibular migration developed. Selumetinib was discontinued due to adverse effects and suspected contribution to impaired bone healing.

Conclusion: In pediatric NF1 patients treated with selumetinib, fracture and impaired bone healing may be rare side effects, especially during limb lengthening. These findings highlight the importance of closely monitoring bone health in NF1 patients on MEK inhibitors, particularly when undergoing orthopedic procedures.

1型神经纤维瘤病(NF1)是一种遗传性疾病,可导致丛状神经纤维瘤(Pns)的发展。Selumetinib是一种选择性丝裂原活化蛋白激酶(MEK1/2)抑制剂,在缩小不能手术的PNs方面显示出临床益处。然而,它对骨骼的长期影响尚不清楚。本病例描述了一名儿童NF1患者接受长期塞鲁美替尼治疗后肢体延长后骨愈合受损和病理性骨折。病例报告:一名5岁男孩,遗传确诊为NF1,左下肢pn诱导过度生长,表现为4.5 cm肢体长度差异。患者一直接受selumetinib (20mg,每日两次)治疗,PNs的大小没有明显的临床减少。使用不包括股骨的外固定架对健康短小腿进行延长。术后3周同侧股骨远端骨折,行下肢延长术,采用k线固定。尽管愈合,2个月后再次发生骨折。此外,胫骨延长再生的骨愈合延迟,并出现进行性外翻畸形和腓骨移位。塞鲁美替尼因不良反应和疑似骨愈合受损而停用。结论:在接受selumetinib治疗的儿童NF1患者中,骨折和骨愈合受损可能是罕见的副作用,特别是在肢体延长期间。这些发现强调了密切监测使用MEK抑制剂的NF1患者骨骼健康的重要性,特别是在接受骨科手术时。
{"title":"Impaired Bone Healing and Fracture Complications during Limb Lengthening in a Neurofibromatosis Type 1 Patient Receiving Selumetinib: Case Report and Literature Review.","authors":"Zahra Safari, Maria Tirta, Ole Rahbek, Søren Kold","doi":"10.13107/jocr.2026.v16.i02.6810","DOIUrl":"https://doi.org/10.13107/jocr.2026.v16.i02.6810","url":null,"abstract":"<p><strong>Introduction: </strong>Neurofibromatosis Type 1 (NF1) is a genetic disorder that may lead to the development of plexiform neurofibromas (Pns). Selumetinib, a selective mitogen-activated protein kinase (MEK1/2) inhibitor, has shown clinical benefit in shrinking inoperable PNs. However, its long-term effects on the skeleton remain unclear. This case describes impaired bone healing and pathological fractures following limb lengthening in a child with NF1 receiving prolonged selumetinib therapy.</p><p><strong>Case report: </strong>A 5-year-old boy with genetically confirmed NF1 and left lower limb PN-induced overgrowth presented with a 4.5 cm limb length discrepancy. The patient had been receiving selumetinib (20 mg twice daily) without a clinically significant reduction in the size of the PNs. Lengthening was performed on a short healthy lower leg with an external fixator that did not include the femur. A distal femoral fracture occurred 3 weeks postoperatively on the same side as the lower leg lengthening was performed, and was treated with K-wire fixation. Despite healing, a refracture occurred 2 months later. In addition, delayed bone healing was observed for the tibial lengthening regenerate, and progressive valgus deformity and fibular migration developed. Selumetinib was discontinued due to adverse effects and suspected contribution to impaired bone healing.</p><p><strong>Conclusion: </strong>In pediatric NF1 patients treated with selumetinib, fracture and impaired bone healing may be rare side effects, especially during limb lengthening. These findings highlight the importance of closely monitoring bone health in NF1 patients on MEK inhibitors, particularly when undergoing orthopedic procedures.</p>","PeriodicalId":16647,"journal":{"name":"Journal of Orthopaedic Case Reports","volume":"16 2","pages":"221-227"},"PeriodicalIF":0.0,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12884274/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146157509","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Intra-articular Corrective Osteotomy for Bennett's Fracture Malunion: A Rare Case Report. 关节内矫正截骨术治疗Bennett骨折畸形愈合1例。
Pub Date : 2026-02-01 DOI: 10.13107/jocr.2026.v16.i02.6726
V S Kiran Raju, Avinash Rao

Introduction: Bennett's fracture is an intra-articular fracture-dislocation at the base of the first metacarpal. If inadequately treated, it may lead to malunion and subluxation of the carpometacarpal joint, resulting in pain, stiffness, and functional impairment.

Case report: We report the case of a 28-year-old male software professional who presented 7 months after sustaining a left thumb injury with persistent pain, stiffness, and difficulty in thumb use. Radiographs revealed a malunited intra-articular fracture of the first metacarpal base with joint subluxation. The patient underwent intra-articular corrective osteotomy with fixation using screws and a trans-articular K-wire to restore joint congruity. At 12 weeks, he achieved full, pain-free thumb movements, and at 10 months, radiographs confirmed fracture union with a Kapandji score of 10/10.

Conclusion: Intra-articular corrective osteotomy is a viable and effective treatment for symptomatic Bennett's fracture malunion, particularly when performed before the onset of degenerative changes, leading to excellent pain relief and restoration of thumb function.

Bennett骨折是发生在第一掌骨基部的关节内骨折脱位。如果治疗不当,可能导致腕掌关节畸形愈合和半脱位,导致疼痛、僵硬和功能损害。病例报告:我们报告一名28岁的男性软件专业人员,他在持续的左手拇指损伤7个月后出现持续疼痛,僵硬和拇指使用困难。x线片显示第一掌骨基部关节内骨折不愈合伴关节半脱位。患者接受关节内矫正截骨术,使用螺钉和经关节k针固定以恢复关节完整性。12周时,患者拇指完全无痛活动,10个月时,x线片证实骨折愈合,Kapandji评分为10/10。结论:关节内矫正截骨术是治疗症状性Bennett骨折不愈合的一种可行且有效的治疗方法,特别是在发生退行性改变之前进行,可显著缓解疼痛并恢复拇指功能。
{"title":"Intra-articular Corrective Osteotomy for Bennett's Fracture Malunion: A Rare Case Report.","authors":"V S Kiran Raju, Avinash Rao","doi":"10.13107/jocr.2026.v16.i02.6726","DOIUrl":"https://doi.org/10.13107/jocr.2026.v16.i02.6726","url":null,"abstract":"<p><strong>Introduction: </strong>Bennett's fracture is an intra-articular fracture-dislocation at the base of the first metacarpal. If inadequately treated, it may lead to malunion and subluxation of the carpometacarpal joint, resulting in pain, stiffness, and functional impairment.</p><p><strong>Case report: </strong>We report the case of a 28-year-old male software professional who presented 7 months after sustaining a left thumb injury with persistent pain, stiffness, and difficulty in thumb use. Radiographs revealed a malunited intra-articular fracture of the first metacarpal base with joint subluxation. The patient underwent intra-articular corrective osteotomy with fixation using screws and a trans-articular K-wire to restore joint congruity. At 12 weeks, he achieved full, pain-free thumb movements, and at 10 months, radiographs confirmed fracture union with a Kapandji score of 10/10.</p><p><strong>Conclusion: </strong>Intra-articular corrective osteotomy is a viable and effective treatment for symptomatic Bennett's fracture malunion, particularly when performed before the onset of degenerative changes, leading to excellent pain relief and restoration of thumb function.</p>","PeriodicalId":16647,"journal":{"name":"Journal of Orthopaedic Case Reports","volume":"16 2","pages":"11-15"},"PeriodicalIF":0.0,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12884151/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146157524","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Pediatric Tibial Plateau Fracture-Dislocation: A Case Report. 儿童胫骨平台骨折脱位1例报告。
Pub Date : 2026-02-01 DOI: 10.13107/jocr.2026.v16.i02.6776
Brian D Rust, Erin L Hofer, Marschall B Berkes

Introduction: Pediatric tibial plateau fracture-dislocations are extremely rare but can involve serious neurovascular and growth complications, requiring prompt evaluation, appropriate fixation, and long-term monitoring. This is the first case report of a tibial plateau fracture-dislocation in the pediatric population.

Case report: A 13-year-old male fell off a motorized scooter, sustaining a tibial plateau fracture-dislocation. He underwent urgent reduction and application of external fixator with subsequent extraphyseal fixation. He had an excellent outcome at both 1-year and 5-year follow-up.

Conclusion: This unusual injury pattern requires thoughtful and comprehensive evaluation, followed by appropriately timed open reduction and stable internal fixation to allow for the early joint range of motion and optimized function. The management of this case serves as an example of how to best approach a rare injury such as this. Patients should be followed until skeletal maturity for potential leg-length discrepancy or malalignment.

儿童胫骨平台骨折脱位极为罕见,但可能涉及严重的神经血管和生长并发症,需要及时评估、适当固定和长期监测。这是儿童人群中胫骨平台骨折脱位的第一例报告。病例报告:一名13岁男性从摩托车上摔下,维持胫骨平台骨折脱位。他接受了紧急复位和外固定架的应用,随后进行了骨干外固定。在1年和5年的随访中,他的预后都很好。结论:这种不寻常的损伤模式需要深思熟虑和全面的评估,其次是适当的时间切开复位和稳定的内固定,以允许早期关节活动范围和优化功能。这种情况下的管理作为一个例子,如何最好地接近一个罕见的伤害,如这。患者应随访至骨骼成熟,以发现潜在的腿长差异或错位。
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引用次数: 0
Conventional Total Knee Arthroplasty in Severe Anterolateral Femoral Bowing: Lateralized Femoral Entry Point to Approach Navigation Level Alignment - A Case Report. 常规全膝关节置换术治疗严重股骨前外侧弯曲:将股骨入口点外侧化以接近导航水平对准- 1例报告。
Pub Date : 2026-02-01 DOI: 10.13107/jocr.2026.v16.i02.6784
Pedro Rasteiro, João Pedro Nóbrega, João Rosado, João Gamelas, Joana Barreto, Nuno Marques

Introduction: Severe knee osteoarthritis associated with anterolateral femoral bowing presents unique challenges for achieving accurate alignment during total knee arthroplasty (TKA). Extra-articular deformity may prevent proper positioning of the femoral cutting block, increasing the risk of malalignment. This case is important because it illustrates a simple and accessible technique to manage substantial femoral bowing without relying on navigation or robotic technology.

Case report: We report the case of an 84-year-old woman with end-stage left knee osteoarthritis and marked anterolateral femoral bowing, treated with cemented posterior-stabilized TKA. A key technical adaptation was the use of a deliberately lateralized femoral intramedullary (IM) entry point, allowing alignment of the IM guide with the patient's mechanical axis despite the deformity. The patient recovered uneventfully and demonstrated progressive improvement. At 6 months, she walked independently without walking aids and had full functional recovery.

Conclusion: In cases of significant femoral bowing, intentional lateralization of the femoral entry point is crucial for achieving accurate mechanical alignment using conventional instrumentation. This technique is practical, reproducible, and particularly useful when advanced computer-assisted systems are unavailable.

导言:在全膝关节置换术(TKA)中,与股骨前外侧弯曲相关的严重膝骨关节炎提出了实现准确对齐的独特挑战。关节外畸形可能妨碍股骨截骨块的正确定位,增加不对准的风险。这个病例很重要,因为它说明了一种简单易行的技术来治疗严重的股骨弯曲,而不依赖于导航或机器人技术。病例报告:我们报告一例84岁女性终末期左膝骨关节炎和明显的股骨前外侧弯曲,采用骨水泥后稳定TKA治疗。一项关键的技术调整是故意使用偏侧的股骨髓内(IM)入口点,尽管存在畸形,但仍允许IM导具与患者的机械轴对齐。患者恢复平稳,并表现出进行性改善。6个月时,患者无需助行器即可独立行走,功能完全恢复。结论:在股骨明显弯曲的情况下,有意侧化股骨入点对于使用常规器械实现准确的机械对齐至关重要。这种技术是实用的、可重复的,在没有先进的计算机辅助系统时特别有用。
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引用次数: 0
Case Report on Steroid-induced Bilateral Femoral Head Osteonecrosis with Concomitant Hip Septic Arthritis in Primary Membranous Nephropathy. 原发性膜性肾病伴双侧股骨头坏死合并髋关节脓毒性关节炎1例报告。
Pub Date : 2026-02-01 DOI: 10.13107/jocr.2026.v16.i02.6750
James C George, Manish Tripathi, Jerry Jimmy Chiramel, Ranjana Jayan

Introduction: Concomitant femoral head osteonecrosis and hip joint septic arthritis is rare. Membranous nephropathy is an immune-mediated glomerular disease producing nephrotic syndrome in adults. Patients take glucocorticoids or immunosuppressants during treatment of this condition. We report the first case of a patient with nephrotic syndrome during treatment developing concomitant hip septic arthritis and femoral head osteonecrosis with an opportunistic pathogen seen in gastrointestinal tract.

Case report: A 37-year-old gentleman on treatment with high-dose prednisolone and mycophenolate for nephrotic syndrome developed bilateral hip pain and was diagnosed as osteonecrosis of femoral head. He underwent core decompression of both hips. Suspected concomitant septic arthritis noted in the magnetic resonance imaging was missed. Post decompression Citrobacter species was aspirated from the left hip and was then managed by debridement and antibiotics. Five years later, he developed secondary osteoarthritis with protrusio-acetabuli subsequent to septic sequelae and underwent total hip replacement without any reactivation till last follow-up.

Conclusion: Concomitant septic arthritis with femoral head osteonecrosis should be considered when treating patients on steroids or immunosuppressants. An elevated erythrocyte sedimentation rate and C-reactive protein in a patient with osteonecrosis warrants additional investigations, including ultrasound-guided aspiration and culture, before core decompression or any surgical intervention even in immunocompetent patients.

摘要股骨头坏死与髋关节脓毒性关节炎合并是罕见的。膜性肾病是一种免疫介导的肾小球疾病,在成人中产生肾病综合征。患者在治疗期间服用糖皮质激素或免疫抑制剂。我们报告第一例肾病综合征患者在治疗期间并发髋关节脓毒性关节炎和股骨头坏死与机会致病菌在胃肠道看到。病例报告:一位37岁的男士在接受大剂量强的松龙和霉酚酸盐治疗肾病综合征时,出现双侧髋关节疼痛,诊断为股骨头坏死。他接受了双髋核心减压术。在磁共振成像中发现的疑似脓毒性关节炎未被发现。减压后从左髋关节吸出柠檬酸杆菌,然后用清创和抗生素治疗。5年后,脓毒性后遗症导致继发性骨关节炎伴髋臼突,并行全髋关节置换术,直到最后一次随访均未复发。结论:在使用类固醇或免疫抑制剂治疗时应考虑脓毒性关节炎合并股骨头坏死。骨坏死患者的红细胞沉降率和c反应蛋白升高值得进一步调查,包括超声引导下的抽吸和培养,在核心减压或任何手术干预之前,即使是免疫功能正常的患者。
{"title":"Case Report on Steroid-induced Bilateral Femoral Head Osteonecrosis with Concomitant Hip Septic Arthritis in Primary Membranous Nephropathy.","authors":"James C George, Manish Tripathi, Jerry Jimmy Chiramel, Ranjana Jayan","doi":"10.13107/jocr.2026.v16.i02.6750","DOIUrl":"https://doi.org/10.13107/jocr.2026.v16.i02.6750","url":null,"abstract":"<p><strong>Introduction: </strong>Concomitant femoral head osteonecrosis and hip joint septic arthritis is rare. Membranous nephropathy is an immune-mediated glomerular disease producing nephrotic syndrome in adults. Patients take glucocorticoids or immunosuppressants during treatment of this condition. We report the first case of a patient with nephrotic syndrome during treatment developing concomitant hip septic arthritis and femoral head osteonecrosis with an opportunistic pathogen seen in gastrointestinal tract.</p><p><strong>Case report: </strong>A 37-year-old gentleman on treatment with high-dose prednisolone and mycophenolate for nephrotic syndrome developed bilateral hip pain and was diagnosed as osteonecrosis of femoral head. He underwent core decompression of both hips. Suspected concomitant septic arthritis noted in the magnetic resonance imaging was missed. Post decompression Citrobacter species was aspirated from the left hip and was then managed by debridement and antibiotics. Five years later, he developed secondary osteoarthritis with protrusio-acetabuli subsequent to septic sequelae and underwent total hip replacement without any reactivation till last follow-up.</p><p><strong>Conclusion: </strong>Concomitant septic arthritis with femoral head osteonecrosis should be considered when treating patients on steroids or immunosuppressants. An elevated erythrocyte sedimentation rate and C-reactive protein in a patient with osteonecrosis warrants additional investigations, including ultrasound-guided aspiration and culture, before core decompression or any surgical intervention even in immunocompetent patients.</p>","PeriodicalId":16647,"journal":{"name":"Journal of Orthopaedic Case Reports","volume":"16 2","pages":"75-79"},"PeriodicalIF":0.0,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12884318/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146157343","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Strength Recovery with Lateralized Reverse Total Shoulder Arthroplasty Combined with Pectoralis Major Transfer for Rotator Cuff Arthropathy with Internal Rotational Deficiency: A Case Report. 侧方反向全肩关节置换术联合胸大肌转移治疗内旋转缺陷的肩袖关节病:1例报告。
Pub Date : 2026-02-01 DOI: 10.13107/jocr.2026.v16.i02.6758
Chang Hee Baek, Bo Taek Kim, Jung Gon Kim

Introduction: Reverse total shoulder arthroplasty (RTSA) has shown promise as a solution for individuals with rotator cuff tear arthropathy (CTA). However, RTSA has demonstrated limited improvement in internal rotation (IR) range of motion (ROM) and strength, potentially affecting patients' ability to perform essential daily tasks such as toileting, a crucial factor that significantly influences overall patient satisfaction.

Case report: A 69-year-old female patient presented with a complaint of chronic pain and weakness in her right shoulder. The patient exhibited rotator CTA with irreparable subscapularis. As the owner of a fish restaurant, the patient underwent lateralized RTSA combined with pectoralis tendon transfer. By the post-operative 1 year 6 months, the patient's strengths of forward elevation (FE) and IR had improved from 14.2N to 20.2N and from 15.4 to 26.2N, respectively. The ROM increased from 80° to 150° for FE, from 70° to 150° for abduction, from 25° to 35° for external rotation, and from L5 to L1 for IR at the back. With no significant complications, the patient was able to return to her workplace.

Conclusion: Primary RTSA combined with pectoralis major tendon transfer could be a viable option for restoring both ROM and strength in FE and IR, particularly in cases of rotator CTA with irreparable subscapularis tears.

导言:反向全肩关节置换术(RTSA)已被证明是治疗肩袖撕裂性关节病(CTA)的有效方法。然而,RTSA对内旋(IR)活动范围(ROM)和力量的改善有限,可能影响患者执行基本日常任务的能力,如如厕,这是显著影响患者整体满意度的关键因素。病例报告:一名69岁的女性患者以右肩慢性疼痛和虚弱为主诉。患者表现为肩胛下肌不可修复的旋转CTA。作为一家鱼餐馆的老板,患者接受了侧化RTSA联合胸肌肌腱转移。术后1年6个月,患者的前抬高强度(FE)和IR分别从14.2N和15.4 n提高到20.2N。FE时ROM从80°增加到150°,外展时从70°增加到150°,外旋时从25°增加到35°,背部IR时从L5增加到L1。没有明显的并发症,病人能够回到她的工作场所。结论:原发性RTSA联合胸大肌肌腱转移是恢复FE和IR患者的ROM和力量的可行选择,特别是在肩胛下肌撕裂不可修复的旋转体CTA病例中。
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Journal of Orthopaedic Case Reports
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