首页 > 最新文献

JBJS case connector最新文献

英文 中文
"Baby" Jefferson Fractures Through the C1 Synchondrosis: A Report of 3 Cases. “婴儿”杰弗逊骨折经C1关节联合:附3例报告。
Q4 Medicine Pub Date : 2025-12-04 eCollection Date: 2025-10-01 DOI: 10.2106/JBJS.CC.25.00336
Kyung Jin Park, Zaid Elsabbagh, Paul D Sponseller

Case: We describe the clinical presentation, management, and outcomes of 3 patients, aged 1.5 to 4 years, with C1 synchondrosis ("Jefferson") fractures treated nonoperatively. Minimally widened anterior arch fractures were identified on computed tomography that were not visible on conventional radiographs. Serial imaging showed fracture healing in all patients at minimum 1-year follow-up.

Conclusion: These cases highlight the susceptibility of preschool-aged children to "baby Jefferson" fractures through the anterior synchondroses, the importance of early computed tomography imaging when conventional radiographs are inconclusive, and the favorable outcomes of nonoperative treatment with cervical immobilization of stable, nondisplaced pediatric C1 fractures.

病例:我们描述了3例患者的临床表现、治疗和结果,年龄1.5至4岁,患有C1软骨联合症(“杰弗逊”)骨折的非手术治疗。在计算机断层扫描上发现了常规x线片上看不到的前弓轻度增宽骨折。随访至少1年,影像学显示所有患者骨折愈合。结论:这些病例强调了学龄前儿童通过前联合软骨发生“婴儿杰弗逊”骨折的易感,在常规x线片不确定的情况下早期计算机断层成像的重要性,以及颈椎固定非手术治疗稳定、非移位的儿童C1骨折的良好效果。
{"title":"\"Baby\" Jefferson Fractures Through the C1 Synchondrosis: A Report of 3 Cases.","authors":"Kyung Jin Park, Zaid Elsabbagh, Paul D Sponseller","doi":"10.2106/JBJS.CC.25.00336","DOIUrl":"https://doi.org/10.2106/JBJS.CC.25.00336","url":null,"abstract":"<p><strong>Case: </strong>We describe the clinical presentation, management, and outcomes of 3 patients, aged 1.5 to 4 years, with C1 synchondrosis (\"Jefferson\") fractures treated nonoperatively. Minimally widened anterior arch fractures were identified on computed tomography that were not visible on conventional radiographs. Serial imaging showed fracture healing in all patients at minimum 1-year follow-up.</p><p><strong>Conclusion: </strong>These cases highlight the susceptibility of preschool-aged children to \"baby Jefferson\" fractures through the anterior synchondroses, the importance of early computed tomography imaging when conventional radiographs are inconclusive, and the favorable outcomes of nonoperative treatment with cervical immobilization of stable, nondisplaced pediatric C1 fractures.</p>","PeriodicalId":14748,"journal":{"name":"JBJS case connector","volume":"15 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146142507","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Delayed Presentation of Pediatric Atlantoaxial Subluxation with Cervical Myelopathy After Clavicle Fracture: A Case Report. 锁骨骨折后小儿寰枢椎半脱位伴颈椎病的延迟表现:1例报告。
Q4 Medicine Pub Date : 2025-12-04 eCollection Date: 2025-10-01 DOI: 10.2106/JBJS.CC.25.00357
Sang Bum Kim, Hyung-Jin Chung, Seung Hoo Lee

Case: A 10-year-old girl developed persistent torticollis after surgery for a clavicular fracture. This condition was initially misattributed to muscle spasms and hardware irritation, leading to a delayed diagnosis. Eventually, the patient developed cervical myelopathy, and subsequent evaluation revealed atlantoaxial rotatory subluxation (AARS) equivalent to Fielding and Hawkins type III, ultimately requiring emergency surgical fusion.

Conclusion: Persistent torticollis after pediatric clavicle fractures warrants careful evaluation for possible AARS. Awareness of this rare coexistence and timely imaging are essential to avoid invasive surgery and serious complications.

病例:一名10岁女孩锁骨骨折手术后出现持续性斜颈。这种情况最初被误认为是肌肉痉挛和硬件刺激,导致延迟诊断。最终,患者发展为颈髓病,随后的评估显示寰枢旋转半脱位(AARS)相当于Fielding和Hawkins III型,最终需要紧急手术融合。结论:小儿锁骨骨折后的持续性斜颈需要仔细评估可能的AARS。意识到这种罕见的共存和及时的影像学检查对于避免侵入性手术和严重的并发症至关重要。
{"title":"Delayed Presentation of Pediatric Atlantoaxial Subluxation with Cervical Myelopathy After Clavicle Fracture: A Case Report.","authors":"Sang Bum Kim, Hyung-Jin Chung, Seung Hoo Lee","doi":"10.2106/JBJS.CC.25.00357","DOIUrl":"https://doi.org/10.2106/JBJS.CC.25.00357","url":null,"abstract":"<p><strong>Case: </strong>A 10-year-old girl developed persistent torticollis after surgery for a clavicular fracture. This condition was initially misattributed to muscle spasms and hardware irritation, leading to a delayed diagnosis. Eventually, the patient developed cervical myelopathy, and subsequent evaluation revealed atlantoaxial rotatory subluxation (AARS) equivalent to Fielding and Hawkins type III, ultimately requiring emergency surgical fusion.</p><p><strong>Conclusion: </strong>Persistent torticollis after pediatric clavicle fractures warrants careful evaluation for possible AARS. Awareness of this rare coexistence and timely imaging are essential to avoid invasive surgery and serious complications.</p>","PeriodicalId":14748,"journal":{"name":"JBJS case connector","volume":"15 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145677592","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Long-Term Outcomes on Bone Growth Following Reconstruction of the Distal Fibula Using a Pedicled Second Metatarsal Osteomyocutaneous Flap in Children: A Case Report. 带蒂第二跖骨肌皮瓣重建儿童腓骨远端骨生长的长期疗效:1例报告。
Q4 Medicine Pub Date : 2025-12-04 eCollection Date: 2025-10-01 DOI: 10.2106/JBJS.CC.25.00244
Thomas Yvonnet, Wyçal Saraoui, Bernard Fraisse, Weiguo Hu

Case report: This report describes a 22-year-old man who sustained a severe left ankle injury caused by a lawnmower at the age of 4 years, resulting in loss of the lateral malleolus. He was treated with a pedicled composite flap using the ipsilateral second metatarsal and was followed until skeletal maturity. A favorable functional outcome was maintained for 15 years.

Conclusion: At final follow-up after growth completion, no limb length discrepancy was observed. The ankle was stable, painless, and preserved good range of motion, with no significant donor site morbidity. This surgical technique represents a technically simpler alternative with lower morbidity compared with vascularized proximal fibular epiphyseal transfer for lateral malleolus reconstruction in growing children.

病例报告:本报告描述了一名22岁的男子,他在4岁时被割草机造成严重的左脚踝损伤,导致外踝丢失。患者采用同侧第二跖骨带蒂复合皮瓣治疗,并随访至骨骼成熟。良好的功能结果维持了15年。结论:在生长完成后的最后随访中,未观察到肢体长度差异。踝关节稳定,无痛,保持良好的活动范围,无明显的供体部位发病率。与带血管的腓骨近端骨骺移植相比,该手术技术在技术上更简单,发病率更低,可用于生长中的儿童外踝重建。
{"title":"Long-Term Outcomes on Bone Growth Following Reconstruction of the Distal Fibula Using a Pedicled Second Metatarsal Osteomyocutaneous Flap in Children: A Case Report.","authors":"Thomas Yvonnet, Wyçal Saraoui, Bernard Fraisse, Weiguo Hu","doi":"10.2106/JBJS.CC.25.00244","DOIUrl":"https://doi.org/10.2106/JBJS.CC.25.00244","url":null,"abstract":"<p><strong>Case report: </strong>This report describes a 22-year-old man who sustained a severe left ankle injury caused by a lawnmower at the age of 4 years, resulting in loss of the lateral malleolus. He was treated with a pedicled composite flap using the ipsilateral second metatarsal and was followed until skeletal maturity. A favorable functional outcome was maintained for 15 years.</p><p><strong>Conclusion: </strong>At final follow-up after growth completion, no limb length discrepancy was observed. The ankle was stable, painless, and preserved good range of motion, with no significant donor site morbidity. This surgical technique represents a technically simpler alternative with lower morbidity compared with vascularized proximal fibular epiphyseal transfer for lateral malleolus reconstruction in growing children.</p>","PeriodicalId":14748,"journal":{"name":"JBJS case connector","volume":"15 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145677634","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Opioid Hypermetabolism in a Multiextremity Spine Trauma Patient: A Case Report. 阿片类药物高代谢在多肢脊柱创伤患者:1例报告。
Q4 Medicine Pub Date : 2025-12-04 eCollection Date: 2025-10-01 DOI: 10.2106/JBJS.CC.25.00430
Stephen Fanous, Zach Denton, Nicolette Saddler, Anne Stuedemann, John T Anderson, K Aaron Shaw

Case: A 17-year-old man presented with an unstable C5 flexion-compression injury and bilateral comminuted distal radius fractures after a motorcycle collision. Despite standard opioid therapy, he experienced difficulty with pain control during and after treatment. Genetic testing revealed a polymorphism in the cytochrome P450 2D6 (CYP2D6) gene, resulting in ultrarapid metabolism.

Conclusion: Genetic mutations in CYP2D6 can result in impaired opioid metabolism and impaired pain control. Impaired pain control in musculoskeletal trauma patients should raise concern for a potential CYP2D6 mutation. A proper understanding of this condition and adjustments in pain management can guide optimal care for these patients.

病例:一名17岁男子在摩托车碰撞后出现不稳定C5屈曲压缩损伤和双侧粉碎性桡骨远端骨折。尽管有标准的阿片类药物治疗,但他在治疗期间和治疗后都难以控制疼痛。基因检测显示细胞色素P450 2D6 (CYP2D6)基因多态性,导致超快速代谢。结论:CYP2D6基因突变可导致阿片类物质代谢受损和疼痛控制受损。肌肉骨骼创伤患者疼痛控制受损应引起对潜在CYP2D6突变的关注。正确理解这种情况和调整疼痛管理可以指导这些患者的最佳护理。
{"title":"Opioid Hypermetabolism in a Multiextremity Spine Trauma Patient: A Case Report.","authors":"Stephen Fanous, Zach Denton, Nicolette Saddler, Anne Stuedemann, John T Anderson, K Aaron Shaw","doi":"10.2106/JBJS.CC.25.00430","DOIUrl":"10.2106/JBJS.CC.25.00430","url":null,"abstract":"<p><strong>Case: </strong>A 17-year-old man presented with an unstable C5 flexion-compression injury and bilateral comminuted distal radius fractures after a motorcycle collision. Despite standard opioid therapy, he experienced difficulty with pain control during and after treatment. Genetic testing revealed a polymorphism in the cytochrome P450 2D6 (CYP2D6) gene, resulting in ultrarapid metabolism.</p><p><strong>Conclusion: </strong>Genetic mutations in CYP2D6 can result in impaired opioid metabolism and impaired pain control. Impaired pain control in musculoskeletal trauma patients should raise concern for a potential CYP2D6 mutation. A proper understanding of this condition and adjustments in pain management can guide optimal care for these patients.</p>","PeriodicalId":14748,"journal":{"name":"JBJS case connector","volume":"15 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145677656","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Novel Approach to the Treatment of Familial Expansile Osteolysis: A Rare Genetic Bone Pathology: A Case Report. 一种治疗家族性扩张性骨溶解的新方法:一种罕见的遗传骨病理:1例报告。
Q4 Medicine Pub Date : 2025-11-20 eCollection Date: 2025-10-01 DOI: 10.2106/JBJS.CC.25.00353
Stephanie Lennon, Phil Allen, Luke Johnson

Case: Familial expansile osteolysis (FEO) is a rare inherited autosomal dominant condition causing the development of painful lytic bone lesions. We present the case of a 54-year-old man with FEO who was treated with denosumab. The patient's progress was monitored with radiographs, magnetic resonance imaging, bone turnover markers, pain, and functional scores.

Conclusion: The use of denosumab for FEO displays improvement in radiological appearances of the affected bone, increased quality of life and may prevent the development of further lesions. It is a safe treatment modality for patients with FEO that allows for limb salvage surgery rather than amputation.

病例:家族性扩张性骨溶解症(FEO)是一种罕见的遗传常染色体显性遗传病,引起疼痛的溶解性骨病变。我们报告一例54岁的FEO患者,接受denosumab治疗。通过x线片、磁共振成像、骨转换标志物、疼痛和功能评分来监测患者的进展。结论:使用denosumab治疗FEO可改善受影响骨的影像学表现,提高生活质量,并可防止进一步病变的发展。对于FEO患者来说,它是一种安全的治疗方式,允许肢体保留手术而不是截肢。
{"title":"A Novel Approach to the Treatment of Familial Expansile Osteolysis: A Rare Genetic Bone Pathology: A Case Report.","authors":"Stephanie Lennon, Phil Allen, Luke Johnson","doi":"10.2106/JBJS.CC.25.00353","DOIUrl":"https://doi.org/10.2106/JBJS.CC.25.00353","url":null,"abstract":"<p><strong>Case: </strong>Familial expansile osteolysis (FEO) is a rare inherited autosomal dominant condition causing the development of painful lytic bone lesions. We present the case of a 54-year-old man with FEO who was treated with denosumab. The patient's progress was monitored with radiographs, magnetic resonance imaging, bone turnover markers, pain, and functional scores.</p><p><strong>Conclusion: </strong>The use of denosumab for FEO displays improvement in radiological appearances of the affected bone, increased quality of life and may prevent the development of further lesions. It is a safe treatment modality for patients with FEO that allows for limb salvage surgery rather than amputation.</p>","PeriodicalId":14748,"journal":{"name":"JBJS case connector","volume":"15 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145564045","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Periprosthetic Solitary Fibrous Tumor of the Proximal Femur: A Case Report. 股骨近端假体周围孤立性纤维性肿瘤1例。
Q4 Medicine Pub Date : 2025-11-20 eCollection Date: 2025-10-01 DOI: 10.2106/JBJS.CC.25.00087
Dev Laungani, Bhargavi Maheshwer, Alessandra Nascimento, Brandon Jonard

Case: A 77-year-old man with myelodysplastic syndrome presented with a dedifferentiated solitary fibrous tumor (SFT) of the proximal femur in the setting of a prior total hip arthroplasty. Diagnosis involved biopsy, NAB2::STAT6 gene fusion identification, and imaging. Management included wide resection, revision arthroplasty, and postoperative infection control. Despite local control, metastatic lung disease developed, and the patient opted for hospice care.

Conclusion: This case underscores the aggressive potential of dedifferentiated SFTs and highlights the diagnostic role of NAB2::STAT6 fusion. It emphasizes the importance of multidisciplinary care in managing rare, high-risk tumors of the bone.

病例:一名患有骨髓增生异常综合征的77岁男性,在之前的全髋关节置换术中表现为股骨近端去分化孤立纤维性肿瘤(SFT)。诊断包括活检、NAB2::STAT6基因融合鉴定和影像学检查。治疗包括广泛切除、关节翻修成形术和术后感染控制。尽管局部控制,转移性肺疾病发展,病人选择临终关怀。结论:该病例强调了去分化SFTs的侵袭潜力,并强调了NAB2::STAT6融合的诊断作用。它强调多学科护理在管理罕见的,高风险的骨肿瘤的重要性。
{"title":"Periprosthetic Solitary Fibrous Tumor of the Proximal Femur: A Case Report.","authors":"Dev Laungani, Bhargavi Maheshwer, Alessandra Nascimento, Brandon Jonard","doi":"10.2106/JBJS.CC.25.00087","DOIUrl":"https://doi.org/10.2106/JBJS.CC.25.00087","url":null,"abstract":"<p><strong>Case: </strong>A 77-year-old man with myelodysplastic syndrome presented with a dedifferentiated solitary fibrous tumor (SFT) of the proximal femur in the setting of a prior total hip arthroplasty. Diagnosis involved biopsy, NAB2::STAT6 gene fusion identification, and imaging. Management included wide resection, revision arthroplasty, and postoperative infection control. Despite local control, metastatic lung disease developed, and the patient opted for hospice care.</p><p><strong>Conclusion: </strong>This case underscores the aggressive potential of dedifferentiated SFTs and highlights the diagnostic role of NAB2::STAT6 fusion. It emphasizes the importance of multidisciplinary care in managing rare, high-risk tumors of the bone.</p>","PeriodicalId":14748,"journal":{"name":"JBJS case connector","volume":"15 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145892679","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Treatment of Persistent Pectoralis Minor Hyperactivity and Compensatory Trapezius Hypertrophy Using Arthroscopic Release: A Case Report. 关节镜下松解治疗持续性胸小肌亢进和代偿性斜方肌肥大1例。
Q4 Medicine Pub Date : 2025-11-20 eCollection Date: 2025-10-01 DOI: 10.2106/JBJS.CC.25.00391
Tobias Gruber, Verena Edler, Markus Scheibel

Case: We report on a 20-year-old male patient with shoulder pain and severely altered scapulothoracic kinematics due to pectoralis minor muscle hyperactivity and compensatory trapezius hypertrophy. After failed conservative treatment, an isolated arthroscopic release of the pectoralis minor tendon was performed, resulting in substantial pain relief and improved range of motion in the 6-week follow-up and sustained benefits 6 years later.

Conclusion: Persistent pectoralis minor hyperactivity may be the cause of altered scapulothoracic movement, resulting in pronounced hypertrophy of the trapezius muscle. It can be safely treated with an isolated arthroscopic detachment of the pectoralis minor tendon.

病例:我们报告了一位20岁的男性患者,由于胸小肌过度活跃和代偿性斜方肌肥大,导致肩部疼痛和肩胸运动严重改变。保守治疗失败后,进行了孤立的关节镜下胸小肌肌腱松解术,在6周的随访中疼痛得到了明显缓解,活动范围得到了改善,并在6年后持续获益。结论:持续的胸小肌过度活动可能是导致肩胸运动改变的原因,导致斜方肌明显肥大。它可以通过孤立的关节镜下胸小肌肌腱脱离安全治疗。
{"title":"Treatment of Persistent Pectoralis Minor Hyperactivity and Compensatory Trapezius Hypertrophy Using Arthroscopic Release: A Case Report.","authors":"Tobias Gruber, Verena Edler, Markus Scheibel","doi":"10.2106/JBJS.CC.25.00391","DOIUrl":"10.2106/JBJS.CC.25.00391","url":null,"abstract":"<p><strong>Case: </strong>We report on a 20-year-old male patient with shoulder pain and severely altered scapulothoracic kinematics due to pectoralis minor muscle hyperactivity and compensatory trapezius hypertrophy. After failed conservative treatment, an isolated arthroscopic release of the pectoralis minor tendon was performed, resulting in substantial pain relief and improved range of motion in the 6-week follow-up and sustained benefits 6 years later.</p><p><strong>Conclusion: </strong>Persistent pectoralis minor hyperactivity may be the cause of altered scapulothoracic movement, resulting in pronounced hypertrophy of the trapezius muscle. It can be safely treated with an isolated arthroscopic detachment of the pectoralis minor tendon.</p>","PeriodicalId":14748,"journal":{"name":"JBJS case connector","volume":"15 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145563999","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Devil is in the Details-Near-Miss Wrong-Level Thoracic Spine Surgery Despite Robotic Navigation: A Case Report. 细节决定成败——尽管有机器人导航,但胸椎手术差点出错:一个病例报告。
Q4 Medicine Pub Date : 2025-11-19 eCollection Date: 2025-10-01 DOI: 10.2106/JBJS.CC.25.00259
Michael Lim, Lawal Labaran, Ved A Vengsarkar, Li Jin, Xudong Li

Case: A 67-year-old woman who presented with left-sided upper back pain, upper trunk paresthesia, and CT-identified left neural foraminal stenosis at T7 to T8 was planned for posterior spinal fusion and decompression using a robotic system. T7 to T8 was labelled with manual sacral counting. T7 to T8 level was registered robotically, but the arm was sent to the T5 to T6 level. T7 to T12 was re-registered, and the robot successfully targeted the correct site.

Conclusion: Technology is still fraught with error and is still in its nascency. It is important to use traditional methods with intraoperative verification to prevent errors in wrong-level thoracic spinal surgery.

病例:一名67岁女性,表现为左侧上背部疼痛,上躯干感觉异常,ct识别为T7至T8处左侧神经孔狭窄,计划使用机器人系统进行后路脊柱融合减压。T7至T8进行人工骶骨计数标记。机器人注册T7到T8级,但手臂被发送到T5到T6级。重新注册T7到T12,机器人成功定位到正确的位置。结论:技术仍然充满了错误,仍然处于起步阶段。在胸椎错位手术中,采用传统方法并进行术中验证是防止错误发生的重要措施。
{"title":"The Devil is in the Details-Near-Miss Wrong-Level Thoracic Spine Surgery Despite Robotic Navigation: A Case Report.","authors":"Michael Lim, Lawal Labaran, Ved A Vengsarkar, Li Jin, Xudong Li","doi":"10.2106/JBJS.CC.25.00259","DOIUrl":"https://doi.org/10.2106/JBJS.CC.25.00259","url":null,"abstract":"<p><strong>Case: </strong>A 67-year-old woman who presented with left-sided upper back pain, upper trunk paresthesia, and CT-identified left neural foraminal stenosis at T7 to T8 was planned for posterior spinal fusion and decompression using a robotic system. T7 to T8 was labelled with manual sacral counting. T7 to T8 level was registered robotically, but the arm was sent to the T5 to T6 level. T7 to T12 was re-registered, and the robot successfully targeted the correct site.</p><p><strong>Conclusion: </strong>Technology is still fraught with error and is still in its nascency. It is important to use traditional methods with intraoperative verification to prevent errors in wrong-level thoracic spinal surgery.</p>","PeriodicalId":14748,"journal":{"name":"JBJS case connector","volume":"15 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145633762","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Pediatric Coronoid-Deficient Elbow Reconstruction with Iliac Crest Allograft: A Case Report. 髂骨异体移植重建小儿冠状缺损肘1例。
Q4 Medicine Pub Date : 2025-11-17 eCollection Date: 2025-10-01 DOI: 10.2106/JBJS.CC.25.00378
Christian Shigley, Jonathan T Yamaguchi, Lara Shefelbine, Douglas Hanel, Mike Tretiakov

Case: A 5-year-old boy sustained a right elbow fracture dislocation with an associated displaced comminuted coronoid fracture. Acute closed reduction as well as an initial attempt at open repair and fixation failed. This case was salvaged 8 weeks after injury with coronoid reconstruction using an iliac crest allograft.

Conclusion: This is the first reported case of coronoid reconstruction using iliac crest allograft in a pediatric patient. 2.5 years after reconstruction, the elbow joint is stable, pain free, and demonstrates elbow motion well within the range for full function.

病例:一名5岁男孩右肘骨折脱位伴伴移位粉碎性冠状骨骨折。急性闭合复位以及最初的开放修复和固定尝试都失败了。本病例在损伤后8周采用髂骨异体移植重建冠状骨。结论:这是首次报道的应用同种异体髂骨移植重建小儿冠状动脉的病例。重建后2.5年,肘关节稳定,无疼痛,肘关节活动范围良好,功能齐全。
{"title":"Pediatric Coronoid-Deficient Elbow Reconstruction with Iliac Crest Allograft: A Case Report.","authors":"Christian Shigley, Jonathan T Yamaguchi, Lara Shefelbine, Douglas Hanel, Mike Tretiakov","doi":"10.2106/JBJS.CC.25.00378","DOIUrl":"10.2106/JBJS.CC.25.00378","url":null,"abstract":"<p><strong>Case: </strong>A 5-year-old boy sustained a right elbow fracture dislocation with an associated displaced comminuted coronoid fracture. Acute closed reduction as well as an initial attempt at open repair and fixation failed. This case was salvaged 8 weeks after injury with coronoid reconstruction using an iliac crest allograft.</p><p><strong>Conclusion: </strong>This is the first reported case of coronoid reconstruction using iliac crest allograft in a pediatric patient. 2.5 years after reconstruction, the elbow joint is stable, pain free, and demonstrates elbow motion well within the range for full function.</p>","PeriodicalId":14748,"journal":{"name":"JBJS case connector","volume":"15 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12610896/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145540787","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
Distal Femur Fracture Above a High Below-The-Knee Amputation Managed With Lateral Locking Plate: A Case Report. 外侧锁定钢板治疗膝下高位截肢股骨远端骨折1例。
Q4 Medicine Pub Date : 2025-11-13 eCollection Date: 2025-10-01 DOI: 10.2106/JBJS.CC.25.00351
Catherine M Call, Andrew D Lachance, Matthew R Camuso

Case: We report the case of a patient with a below-the-knee amputation who sustained a complex femur fracture ipsilateral to his residual limb after a fall from height. His fracture was managed with a lateral locking plate of the distal femur for fixation. He was followed for 16 months; at 7 months, he demonstrated return to pretrauma functional status.

Conclusion: Fixation of the distal femur with a lateral locking plate did not interfere with the patient's ability to wear a prosthesis and should be considered for managing "periprosthetic" femur fractures in those with a below-the-knee amputation to maintain prosthetic usage.

病例:我们报告的情况下,病人膝下截肢谁维持一个复杂的股骨骨折同侧他的残肢从高处坠落后。骨折采用股骨远端外侧锁定钢板固定。他被跟踪了16个月;7个月时,患者恢复到创伤前的功能状态。结论:外侧锁定钢板固定股骨远端不会影响患者佩戴假体的能力,对于膝下截肢的患者,应考虑对“假体周围”股骨骨折进行治疗,以维持假体的使用。
{"title":"Distal Femur Fracture Above a High Below-The-Knee Amputation Managed With Lateral Locking Plate: A Case Report.","authors":"Catherine M Call, Andrew D Lachance, Matthew R Camuso","doi":"10.2106/JBJS.CC.25.00351","DOIUrl":"10.2106/JBJS.CC.25.00351","url":null,"abstract":"<p><strong>Case: </strong>We report the case of a patient with a below-the-knee amputation who sustained a complex femur fracture ipsilateral to his residual limb after a fall from height. His fracture was managed with a lateral locking plate of the distal femur for fixation. He was followed for 16 months; at 7 months, he demonstrated return to pretrauma functional status.</p><p><strong>Conclusion: </strong>Fixation of the distal femur with a lateral locking plate did not interfere with the patient's ability to wear a prosthesis and should be considered for managing \"periprosthetic\" femur fractures in those with a below-the-knee amputation to maintain prosthetic usage.</p>","PeriodicalId":14748,"journal":{"name":"JBJS case connector","volume":"15 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145512947","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
JBJS case connector
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1