Pub Date : 2026-01-12eCollection Date: 2025-01-01DOI: 10.3389/fsurg.2025.1737191
Zaichao Ma, Mengxue Guan, Maimaitiyibubaji Abudukadier, Xiaoping Han, Tao Huang, Zengqiang Yang, Biao Li, Yong Cui
Background: Suprascapular nerve entrapment is a cause of shoulder pain and dysfunction, often complicated by symptomatic overlap with other shoulder pathologies. Entrapment most commonly occurs at two anatomical constrictions: the suprascapular notch and the spinoglenoid notch. Compression of the nerve's inferior branch at the spinoglenoid notch by a paralabral cyst, leading to isolated infraspinatus weakness and atrophy, is a relatively common pattern. Diagnosis relies on a detailed physical examination, multimodal imaging evaluation including MRI and ultrasound, and confirmation by electromyography. For patients who do not respond to conservative management or who have definitive space-occupying compression, surgical decompression is an effective treatment option.
Case presentation: This is the case of a 27-year-old man presenting with progressive right shoulder weakness and pain over just one month, already demonstrating isolated infraspinatus atrophy. Imaging revealed the etiology to be a paralabral cyst that, notably, occupied both the suprascapular and spinoglenoid notches, creating a "double-crush" compression on the suprascapular nerve. This case clearly illustrates how a strategically located space-occupying lesion can lead to rapid and characteristic neurologic deficit, even within a short clinical course.
Conclusion: This case clearly illustrates the classic presentation of an isolated spinoglenoid notch cyst causing suprascapular nerve compression, underscoring that this diagnosis must be considered in patients with isolated external rotation weakness even without a clear traumatic etiology, and highlighting that early recognition and systematic evaluation are key to successful management and neurological recovery.
{"title":"Suprascapular nerve entrapment syndrome caused by a spinoglenoid notch cyst with a concomitant giant lipoma: a case report.","authors":"Zaichao Ma, Mengxue Guan, Maimaitiyibubaji Abudukadier, Xiaoping Han, Tao Huang, Zengqiang Yang, Biao Li, Yong Cui","doi":"10.3389/fsurg.2025.1737191","DOIUrl":"10.3389/fsurg.2025.1737191","url":null,"abstract":"<p><strong>Background: </strong>Suprascapular nerve entrapment is a cause of shoulder pain and dysfunction, often complicated by symptomatic overlap with other shoulder pathologies. Entrapment most commonly occurs at two anatomical constrictions: the suprascapular notch and the spinoglenoid notch. Compression of the nerve's inferior branch at the spinoglenoid notch by a paralabral cyst, leading to isolated infraspinatus weakness and atrophy, is a relatively common pattern. Diagnosis relies on a detailed physical examination, multimodal imaging evaluation including MRI and ultrasound, and confirmation by electromyography. For patients who do not respond to conservative management or who have definitive space-occupying compression, surgical decompression is an effective treatment option.</p><p><strong>Case presentation: </strong>This is the case of a 27-year-old man presenting with progressive right shoulder weakness and pain over just one month, already demonstrating isolated infraspinatus atrophy. Imaging revealed the etiology to be a paralabral cyst that, notably, occupied both the suprascapular and spinoglenoid notches, creating a \"double-crush\" compression on the suprascapular nerve. This case clearly illustrates how a strategically located space-occupying lesion can lead to rapid and characteristic neurologic deficit, even within a short clinical course.</p><p><strong>Conclusion: </strong>This case clearly illustrates the classic presentation of an isolated spinoglenoid notch cyst causing suprascapular nerve compression, underscoring that this diagnosis must be considered in patients with isolated external rotation weakness even without a clear traumatic etiology, and highlighting that early recognition and systematic evaluation are key to successful management and neurological recovery.</p>","PeriodicalId":12564,"journal":{"name":"Frontiers in Surgery","volume":"12 ","pages":"1737191"},"PeriodicalIF":1.6,"publicationDate":"2026-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12833322/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146062071","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-12eCollection Date: 2025-01-01DOI: 10.3389/fsurg.2025.1726163
Xi Chen, Ting Jiang, Yonghai Peng, Ruizi Shi, Chuan Qin, Hua Luo, Xintao Zeng, Pei Yang, Jianjun Wang
Background: To evaluate the feasibility, safety, and short-term clinical outcomes of robot-assisted partial splenectomy (RAPS) in the treatment of benign splenic lesions (BSLs).
Methods: A retrospective analysis was conducted on nine patients with BSLs who underwent RAPS in the Department of Hepatobiliary, Pancreatic, and Splenic Surgery at Mianyang Central Hospital between January 2024 and September 2025. Clinical data, including demographic characteristics, lesion features, intraoperative parameters, postoperative recovery, and complications, were collected. All patients underwent preoperative contrast-enhanced abdominal computed tomography, magnetic resonance imaging, and three-dimensional (3D) reconstruction to delineate the anatomical relationship between the lesion and splenic vasculature. All procedures were performed by the same surgical team.
Results: All nine procedures were successfully completed without conversion to open surgery. The cohort comprised three men and six women, with a mean age of 49.0 ± 10.3 years. Lesions were located in the lower pole in seven cases and in the upper pole in two, with a mean diameter of 4.34 ± 0.8 cm. The mean operative time was 179.4 ± 15.5 min, the mean intraoperative blood loss was 71.1 ± 19.6 mL, and the mean postoperative hospital stay was 6.4 ± 0.9 days. No cases of splenic infarction, pancreatic fistula, hemorrhage, or severe infection were observed. Pathological diagnoses included splenic hemangioma (n = 3), non-parasitic splenic cyst (n = 5), and splenic lymphangioma (n = 1). During follow-up, no recurrence, new lesions, or splenic dysfunction were detected, and hematologic parameters remained within normal ranges.
Conclusion: RAPS is a safe, feasible, and minimally invasive spleen-preserving procedure. Preoperative 3D reconstruction facilitates precise surgical planning, and when combined with the high-precision maneuverability of robotic technology, enables complete lesion removal while preserving functional splenic tissue. This approach aligns with the principles of modern precision and minimally invasive surgery.
{"title":"Feasibility and outcomes of robot-assisted partial splenectomy for benign splenic lesions: a single-center experience.","authors":"Xi Chen, Ting Jiang, Yonghai Peng, Ruizi Shi, Chuan Qin, Hua Luo, Xintao Zeng, Pei Yang, Jianjun Wang","doi":"10.3389/fsurg.2025.1726163","DOIUrl":"10.3389/fsurg.2025.1726163","url":null,"abstract":"<p><strong>Background: </strong>To evaluate the feasibility, safety, and short-term clinical outcomes of robot-assisted partial splenectomy (RAPS) in the treatment of benign splenic lesions (BSLs).</p><p><strong>Methods: </strong>A retrospective analysis was conducted on nine patients with BSLs who underwent RAPS in the Department of Hepatobiliary, Pancreatic, and Splenic Surgery at Mianyang Central Hospital between January 2024 and September 2025. Clinical data, including demographic characteristics, lesion features, intraoperative parameters, postoperative recovery, and complications, were collected. All patients underwent preoperative contrast-enhanced abdominal computed tomography, magnetic resonance imaging, and three-dimensional (3D) reconstruction to delineate the anatomical relationship between the lesion and splenic vasculature. All procedures were performed by the same surgical team.</p><p><strong>Results: </strong>All nine procedures were successfully completed without conversion to open surgery. The cohort comprised three men and six women, with a mean age of 49.0 ± 10.3 years. Lesions were located in the lower pole in seven cases and in the upper pole in two, with a mean diameter of 4.34 ± 0.8 cm. The mean operative time was 179.4 ± 15.5 min, the mean intraoperative blood loss was 71.1 ± 19.6 mL, and the mean postoperative hospital stay was 6.4 ± 0.9 days. No cases of splenic infarction, pancreatic fistula, hemorrhage, or severe infection were observed. Pathological diagnoses included splenic hemangioma (<i>n</i> = 3), non-parasitic splenic cyst (<i>n</i> = 5), and splenic lymphangioma (<i>n</i> = 1). During follow-up, no recurrence, new lesions, or splenic dysfunction were detected, and hematologic parameters remained within normal ranges.</p><p><strong>Conclusion: </strong>RAPS is a safe, feasible, and minimally invasive spleen-preserving procedure. Preoperative 3D reconstruction facilitates precise surgical planning, and when combined with the high-precision maneuverability of robotic technology, enables complete lesion removal while preserving functional splenic tissue. This approach aligns with the principles of modern precision and minimally invasive surgery.</p>","PeriodicalId":12564,"journal":{"name":"Frontiers in Surgery","volume":"12 ","pages":"1726163"},"PeriodicalIF":1.6,"publicationDate":"2026-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12832720/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146062100","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-12eCollection Date: 2025-01-01DOI: 10.3389/fsurg.2025.1742042
Li Yongjun, Wu Weinian
Objective: This study aimed to systematically identify independent risk factors for chronic postsurgical pain (CPSP) in patients undergoing minimally invasive pulmonary surgery, thereby providing an evidence-based foundation for the early identification of high-risk patients and the development of targeted preventive strategies.
Methods: A case-control study design was employed. A total of 280 patients who underwent minimally invasive thoracic surgery between January 2022 and June 2024 were enrolled and categorized into a CPSP group (n = 48) and a non-CPSP group (n = 232) based on the presence of CPSP at 3 months postoperatively. Baseline characteristics, surgical features, and perioperative pain indicators-including visual analog scale (VAS) scores for pain at rest, during coughing, and during shoulder abduction assessed daily from postoperative day 1 to day 6-were prospectively collected. The occurrence of CPSP was evaluated at the 3-month follow-up. Univariate and multivariate logistic regression analyses were used to screen for independent factors influencing CPSP, and the predictive performance of these factors was assessed using receiver operating characteristic (ROC) curve analysis.
Results: Univariate analysis revealed that preoperative anxiety, preoperative pain, surgical approach, intercostal suture, scar length, and postoperative shoulder abduction pain were significantly associated with CPSP development (P < 0.05). Multivariate logistic regression analysis ultimately identified postoperative shoulder abduction pain (OR = 1.893, 95% CI: 1.432-2.502, P < 0.001), scar length (OR = 1.240, 95% CI: 1.049-1.466, P = 0.011), and preoperative anxiety (OR = 3.089, 95% CI: 1.201-7.943, P = 0.019) as independent risk factors for CPSP, while intercostal suture (OR = 0.234, 95% CI: 0.074-0.736, P = 0.013) was an independent protective factor. Predictive performance analysis showed that postoperative shoulder abduction pain had the best predictive value [Area Under the Curve (AUC) = 0.821], with an optimal cut-off value of >3.5 points.
Conclusion: For patients undergoing minimally invasive thoracic surgery, higher early postoperative (within 6 days) shoulder abduction pain scores, greater scar length, and the presence of preoperative anxiety are significant independent risk factors for developing CPSP at 3 months, whereas the use of the intercostal suture technique demonstrates a protective effect. Clinical practice should emphasize enhanced monitoring and management of postoperative shoulder abduction pain, the proactive adoption of protective surgical techniques, and attention to patients' preoperative psychological state to effectively reduce the risk of CPSP.
目的:本研究旨在系统识别微创肺手术患者慢性术后疼痛(CPSP)的独立危险因素,为早期识别高危患者和制定有针对性的预防策略提供循证依据。方法:采用病例-对照研究设计。在2022年1月至2024年6月期间,共有280例患者接受了微创胸外科手术,并根据术后3个月CPSP的存在分为CPSP组(n = 48)和非CPSP组(n = 232)。前瞻性收集基线特征、手术特征和围手术期疼痛指标,包括从术后第1天到第6天每天评估的静息、咳嗽和肩外展疼痛的视觉模拟评分(VAS)。随访3个月评估CPSP的发生情况。采用单因素和多因素logistic回归分析筛选影响CPSP的独立因素,并采用受试者工作特征(ROC)曲线分析评估这些因素的预测效果。结果:单因素分析显示,术前焦虑、术前疼痛、手术入路、肋间缝合、疤痕长度、术后肩外展疼痛与CPSP的发生有显著相关性(P P P = 0.011),术前焦虑(OR = 3.089, 95% CI: 1.201 ~ 7.943, P = 0.019)是CPSP的独立危险因素,肋间缝合(OR = 0.234, 95% CI: 0.074 ~ 0.736, P = 0.013)是CPSP的独立保护因素。预测性能分析显示,术后肩外展痛具有最佳的预测价值[曲线下面积(Area Under the Curve, AUC) = 0.821],最佳截断值为>3.5分。结论:微创胸外科手术患者术后早期(6天内)肩外展痛评分较高、瘢痕长度较大、术前存在焦虑是3个月发生CPSP的重要独立危险因素,而肋间缝合技术的使用具有保护作用。临床应加强对术后肩外展疼痛的监测和管理,积极采用保护性手术技术,重视患者术前心理状态,有效降低CPSP发生的风险。
{"title":"Risk factors for chronic postsurgical pain following minimally invasive thoracic surgery.","authors":"Li Yongjun, Wu Weinian","doi":"10.3389/fsurg.2025.1742042","DOIUrl":"10.3389/fsurg.2025.1742042","url":null,"abstract":"<p><strong>Objective: </strong>This study aimed to systematically identify independent risk factors for chronic postsurgical pain (CPSP) in patients undergoing minimally invasive pulmonary surgery, thereby providing an evidence-based foundation for the early identification of high-risk patients and the development of targeted preventive strategies.</p><p><strong>Methods: </strong>A case-control study design was employed. A total of 280 patients who underwent minimally invasive thoracic surgery between January 2022 and June 2024 were enrolled and categorized into a CPSP group (<i>n</i> = 48) and a non-CPSP group (<i>n</i> = 232) based on the presence of CPSP at 3 months postoperatively. Baseline characteristics, surgical features, and perioperative pain indicators-including visual analog scale (VAS) scores for pain at rest, during coughing, and during shoulder abduction assessed daily from postoperative day 1 to day 6-were prospectively collected. The occurrence of CPSP was evaluated at the 3-month follow-up. Univariate and multivariate logistic regression analyses were used to screen for independent factors influencing CPSP, and the predictive performance of these factors was assessed using receiver operating characteristic (ROC) curve analysis.</p><p><strong>Results: </strong>Univariate analysis revealed that preoperative anxiety, preoperative pain, surgical approach, intercostal suture, scar length, and postoperative shoulder abduction pain were significantly associated with CPSP development (<i>P</i> < 0.05). Multivariate logistic regression analysis ultimately identified postoperative shoulder abduction pain (OR = 1.893, 95% CI: 1.432-2.502, <i>P</i> < 0.001), scar length (OR = 1.240, 95% CI: 1.049-1.466, <i>P</i> = 0.011), and preoperative anxiety (OR = 3.089, 95% CI: 1.201-7.943, <i>P</i> = 0.019) as independent risk factors for CPSP, while intercostal suture (OR = 0.234, 95% CI: 0.074-0.736, <i>P</i> = 0.013) was an independent protective factor. Predictive performance analysis showed that postoperative shoulder abduction pain had the best predictive value [Area Under the Curve (AUC) = 0.821], with an optimal cut-off value of >3.5 points.</p><p><strong>Conclusion: </strong>For patients undergoing minimally invasive thoracic surgery, higher early postoperative (within 6 days) shoulder abduction pain scores, greater scar length, and the presence of preoperative anxiety are significant independent risk factors for developing CPSP at 3 months, whereas the use of the intercostal suture technique demonstrates a protective effect. Clinical practice should emphasize enhanced monitoring and management of postoperative shoulder abduction pain, the proactive adoption of protective surgical techniques, and attention to patients' preoperative psychological state to effectively reduce the risk of CPSP.</p>","PeriodicalId":12564,"journal":{"name":"Frontiers in Surgery","volume":"12 ","pages":"1742042"},"PeriodicalIF":1.6,"publicationDate":"2026-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12805442/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145997782","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-12eCollection Date: 2025-01-01DOI: 10.3389/fsurg.2025.1714640
Fuyong Zhu, Chengjun Wang
Purpose: To compare the perioperative efficacy and safety of ultramini-percutaneous nephrolithotomy (ultramini-PCNL) combined with flexible ureteroscopic lithotripsy (FURL) vs. standard-channel PCNL in patients with complex renal calculi, with a focus on evaluating the impacts of the two procedures on postoperative oxidative stress responses, inflammatory factor levels, and renal hemodynamic parameters.
Methods: A retrospective analysis was conducted on the clinical data of 135 patients with complex renal calculi admitted to our hospital from January 2023 to December 2024. According to different surgical approaches, the patients were divided into a study group (SG, n = 72) and a control group (CG, n = 63). The CG underwent standard-channel PCNL, while the SG received ultramini-PCNL combined with FURL. Surgical parameters, pain conditions, stone-free rate, oxidative stress markers, inflammatory factors, renal function, renal blood flow levels before and after surgery, as well as postoperative complications, were compared between the two groups.
Results: Compared with the CG, perioperative blood volume, time to out of bed activity and hospital stay were shorter in the SG (P < 0.05); Postoperative pain scores were lower in the SG than in CG at 12 h, 24 h and 72 h (P < 0.05), postoperative stone-free rate was higher in the SG (P < 0.05); Postoperative Cor and MDA levels were lower while SOD levels were higher in SG (P < 0.05); Postoperative CRP, IL-6 and the complication rate were lower in SG than in CG (P < 0.05). Postoperatively, compared with the preoperative values, both groups showed slight fluctuations in serum urea and creatinine (Cr) levels; however, the differences were not statistically significant (P > 0.05). After surgery, the renal artery Vmax in the SG was significantly higher than that in the CG (P < 0.05). No significant differences were observed between the two groups regarding the RI index (P > 0.05).
Conclusion: Ultramini-PCNL combined with FURL demonstrates superior efficacy in the treatment of complex renal calculi. This approach effectively improves stone-free rate, reduces stress responses, ameliorates inflammatory factor levels, and provides a high level of safety, supporting its broader clinical application.
目的:比较微创经皮肾镜取石术(ultra -PCNL)联合输尿管镜柔性碎石术(FURL)与标准通道PCNL在复杂肾结石患者围手术期的疗效和安全性,重点评价两种手术方式对术后氧化应激反应、炎症因子水平和肾脏血流动力学参数的影响。方法:回顾性分析我院2023年1月至2024年12月收治的135例复杂肾结石患者的临床资料。根据手术入路不同,将患者分为研究组(SG, n = 72)和对照组(CG, n = 63)。CG行标准通道PCNL, SG行超微通道PCNL联合FURL。比较两组患者手术参数、疼痛情况、无结石率、氧化应激指标、炎症因子、肾功能、术后肾血流量水平及术后并发症。结果:SG组围手术期血容量、下床活动时间、住院时间较CG组短(P P P P P > 0.05)。术后SG组肾动脉Vmax明显高于CG组(P < 0.05)。结论:超微量pcnl联合FURL治疗复杂性肾结石疗效显著。这种方法有效地提高了结石的游离率,减少了应激反应,改善了炎症因子水平,并提供了高水平的安全性,支持其更广泛的临床应用。
{"title":"Ultramini-percutaneous nephrolithotomy combined with flexible ureteroscopic lithotripsy for the treatment of complex renal calculi: a clinical study.","authors":"Fuyong Zhu, Chengjun Wang","doi":"10.3389/fsurg.2025.1714640","DOIUrl":"10.3389/fsurg.2025.1714640","url":null,"abstract":"<p><strong>Purpose: </strong>To compare the perioperative efficacy and safety of ultramini-percutaneous nephrolithotomy (ultramini-PCNL) combined with flexible ureteroscopic lithotripsy (FURL) vs. standard-channel PCNL in patients with complex renal calculi, with a focus on evaluating the impacts of the two procedures on postoperative oxidative stress responses, inflammatory factor levels, and renal hemodynamic parameters.</p><p><strong>Methods: </strong>A retrospective analysis was conducted on the clinical data of 135 patients with complex renal calculi admitted to our hospital from January 2023 to December 2024. According to different surgical approaches, the patients were divided into a study group (SG, <i>n</i> = 72) and a control group (CG, <i>n</i> = 63). The CG underwent standard-channel PCNL, while the SG received ultramini-PCNL combined with FURL. Surgical parameters, pain conditions, stone-free rate, oxidative stress markers, inflammatory factors, renal function, renal blood flow levels before and after surgery, as well as postoperative complications, were compared between the two groups.</p><p><strong>Results: </strong>Compared with the CG, perioperative blood volume, time to out of bed activity and hospital stay were shorter in the SG (<i>P</i> < 0.05); Postoperative pain scores were lower in the SG than in CG at 12 h, 24 h and 72 h (<i>P</i> < 0.05), postoperative stone-free rate was higher in the SG (<i>P</i> < 0.05); Postoperative Cor and MDA levels were lower while SOD levels were higher in SG (<i>P</i> < 0.05); Postoperative CRP, IL-6 and the complication rate were lower in SG than in CG (<i>P</i> < 0.05). Postoperatively, compared with the preoperative values, both groups showed slight fluctuations in serum urea and creatinine (Cr) levels; however, the differences were not statistically significant (<i>P</i> > 0.05). After surgery, the renal artery Vmax in the SG was significantly higher than that in the CG (<i>P</i> < 0.05). No significant differences were observed between the two groups regarding the RI index (<i>P</i> > 0.05).</p><p><strong>Conclusion: </strong>Ultramini-PCNL combined with FURL demonstrates superior efficacy in the treatment of complex renal calculi. This approach effectively improves stone-free rate, reduces stress responses, ameliorates inflammatory factor levels, and provides a high level of safety, supporting its broader clinical application<b>.</b></p>","PeriodicalId":12564,"journal":{"name":"Frontiers in Surgery","volume":"12 ","pages":"1714640"},"PeriodicalIF":1.6,"publicationDate":"2026-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12833387/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146062075","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-12eCollection Date: 2025-01-01DOI: 10.3389/fsurg.2025.1728951
Yu Wang, Chang-Zhi Zhao, Kai-Long Zhang, Yi-Xiao Chen, Ao Li, Jie Yin, Fei Long, Qi-Hong Wang
Objective: This study aimed to compare the outcomes of direct suturing (Method 1) and pericranium-assisted suturing (Method 2) for U-shaped dural incisions, with a specific focus on site-specific differences in cerebrospinal fluid (CSF) leak and postoperative infection.
Methods: In this retrospective cohort, 172 patients undergoing repair of U-shaped dural incisions were analyzed. Based on intraoperative feasibility, patients underwent either Method 1 (n = 94) or Method 2 (n = 78). Primary and secondary outcomes were CSF leak and postoperative infection rates, respectively. Subgroup analyses were stratified by surgical site (supratentorial vs. infratentorial).
Results: The incidence of CSF leak was low and comparable between the two methods, regardless of surgical site (Method 1: 7.14% supratentorial vs. 7.69% infratentorial, P = 1.00; Method 2: 4.17% vs. 3.33%, P = 1.00). Re-repair rates were similarly low across all groups. However, Method 2 was associated with a significantly higher overall infection rate in the infratentorial compartment compared to supratentorial surgeries (23.33% vs. 6.25%, P = 0.039). Sub-analysis revealed this was primarily driven by a higher incidence of incision infection/delayed healing in the infratentorial group (16.67% vs. 2.08%, P = 0.028), whereas meningitis rates were comparable. Multivariable analysis confirmed the surgical site itself was not an independent risk factor for infection.
Conclusion: Both direct and pericranium-assisted suturing are effective in preventing CSF leak for U-shaped dural incisions. However, the pericranium-assisted technique carries a significantly increased risk of incision-related infections in the infratentorial region. Clinical decision-making must therefore balance the reliable sealing capability of pericranium-assisted repair against its site-specific infection profile, particularly in complex posterior fossa surgeries.
目的:比较u型硬脑膜切口直接缝合(方法1)和包膜辅助缝合(方法2)的效果,特别关注脑脊液(CSF)泄漏和术后感染的部位特异性差异。方法:回顾性分析172例硬膜u型切口修补术患者的资料。根据术中可行性,患者采用方法1 (n = 94)或方法2 (n = 78)。主要和次要结果分别是脑脊液泄漏和术后感染率。亚组分析按手术部位(幕上和幕下)分层。结果:无论手术部位如何,两种方法的脑脊液漏发生率均较低且具有可比性(方法1:幕上7.14% vs.幕下7.69%,P = 1.00;方法2:4.17% vs. 3.33%, P = 1.00)。所有组的再修复率都很低。然而,方法2与幕上手术相比,幕下腔室的总感染率明显更高(23.33% vs. 6.25%, P = 0.039)。亚分析显示,这主要是由于幕下组较高的切口感染/延迟愈合发生率(16.67%对2.08%,P = 0.028),而脑膜炎发生率相当。多变量分析证实手术部位本身不是感染的独立危险因素。结论:u型硬脑膜切口直接缝合和包膜辅助缝合均可有效预防脑脊液漏。然而,包皮辅助技术明显增加幕下区域切口相关感染的风险。因此,临床决策必须在包皮辅助修复的可靠密封能力与其部位特异性感染特征之间取得平衡,特别是在复杂的后窝手术中。
{"title":"Comparative evaluation of two dural closure techniques for U-shaped incisions: sealing efficacy vs. site-specific infection risk.","authors":"Yu Wang, Chang-Zhi Zhao, Kai-Long Zhang, Yi-Xiao Chen, Ao Li, Jie Yin, Fei Long, Qi-Hong Wang","doi":"10.3389/fsurg.2025.1728951","DOIUrl":"10.3389/fsurg.2025.1728951","url":null,"abstract":"<p><strong>Objective: </strong>This study aimed to compare the outcomes of direct suturing (Method 1) and pericranium-assisted suturing (Method 2) for U-shaped dural incisions, with a specific focus on site-specific differences in cerebrospinal fluid (CSF) leak and postoperative infection.</p><p><strong>Methods: </strong>In this retrospective cohort, 172 patients undergoing repair of U-shaped dural incisions were analyzed. Based on intraoperative feasibility, patients underwent either Method 1 (<i>n</i> = 94) or Method 2 (<i>n</i> = 78). Primary and secondary outcomes were CSF leak and postoperative infection rates, respectively. Subgroup analyses were stratified by surgical site (supratentorial vs. infratentorial).</p><p><strong>Results: </strong>The incidence of CSF leak was low and comparable between the two methods, regardless of surgical site (Method 1: 7.14% supratentorial vs. 7.69% infratentorial, <i>P</i> = 1.00; Method 2: 4.17% vs. 3.33%, <i>P</i> = 1.00). Re-repair rates were similarly low across all groups. However, Method 2 was associated with a significantly higher overall infection rate in the infratentorial compartment compared to supratentorial surgeries (23.33% vs. 6.25%, <i>P</i> = 0.039). Sub-analysis revealed this was primarily driven by a higher incidence of incision infection/delayed healing in the infratentorial group (16.67% vs. 2.08%, <i>P</i> = 0.028), whereas meningitis rates were comparable. Multivariable analysis confirmed the surgical site itself was not an independent risk factor for infection.</p><p><strong>Conclusion: </strong>Both direct and pericranium-assisted suturing are effective in preventing CSF leak for U-shaped dural incisions. However, the pericranium-assisted technique carries a significantly increased risk of incision-related infections in the infratentorial region. Clinical decision-making must therefore balance the reliable sealing capability of pericranium-assisted repair against its site-specific infection profile, particularly in complex posterior fossa surgeries.</p>","PeriodicalId":12564,"journal":{"name":"Frontiers in Surgery","volume":"12 ","pages":"1728951"},"PeriodicalIF":1.6,"publicationDate":"2026-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12832958/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146062082","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-12eCollection Date: 2025-01-01DOI: 10.3389/fsurg.2025.1727578
Ning Ma, Xinghua Chen, Chenshuai Pan, Zonggang Xie
Purpose: Rotator cuff tears (RCTs) are a prevalent source of shoulder disability, frequently accompanied by pathologies of the long head of the biceps tendon (LHBT). While both tenotomy and tenodesis are established procedures for managing LHBT lesions during rotator cuff repair, their comparative efficacy remains a subject of debate. This study aimed to compare the clinical outcomes of isolated tenotomy vs. tenotomy with tenodesis in patients undergoing arthroscopic RCTs in a retrospective study.
Methods: All surgical procedures involved arthroscopic rotator cuff repair performed by a single surgeon. Patients were divided into isolated biceps tenotomy and tenotomy with tenodesis using a suture anchor. Postoperative rehabilitation was standardized. Outcomes were assessed preoperatively and at 3, 6, 12 months, and final follow-up using ASES and Constant-Murley scores, VAS pain scale, operative time, and complications.
Results: A total of 63 patients (mean age 67.3 years) were retrospectively reviewed and divided into two groups: isolated tenotomy (n = 28) and tenotomy with tenodesis (n = 35). Preoperative demographics and functional scores (ASES, Constant-Murley, VAS) were comparable between groups. Both techniques resulted in significant and sustained improvements in all functional and pain outcomes at 3, 6, and 12 months postoperatively compared to baseline. In the early postoperative period (3 months), the tenotomy group demonstrated a statistically superior improvement in VAS pain scores. However, these differences in functional and pain scores between the two groups were no longer significant at the 6 and 12-month follow-ups. The operative time was significantly shorter for the tenotomy group. The only significant complication difference was the occurrence of Popeye deformity in two patients (14%) in the tenotomy group, with no cases in the tenodesis group.
Conclusion: In conclusion, both isolated tenotomy and tenodesis provide equivalent, excellent functional improvements and pain relief at the 12-month follow-up. Tenotomy offers the advantages of a shorter operative time and better early pain control, at the cost of a higher risk of Popeye deformity. Tenodesis effectively prevents this cosmetic complication but requires a longer surgery.
{"title":"Comparison of isolated tenotomy vs. tenotomy with tenodesis for long head of biceps tendon in middle-aged and elderly patients undergoing rotator cuff repair: a retrospective study.","authors":"Ning Ma, Xinghua Chen, Chenshuai Pan, Zonggang Xie","doi":"10.3389/fsurg.2025.1727578","DOIUrl":"10.3389/fsurg.2025.1727578","url":null,"abstract":"<p><strong>Purpose: </strong>Rotator cuff tears (RCTs) are a prevalent source of shoulder disability, frequently accompanied by pathologies of the long head of the biceps tendon (LHBT). While both tenotomy and tenodesis are established procedures for managing LHBT lesions during rotator cuff repair, their comparative efficacy remains a subject of debate. This study aimed to compare the clinical outcomes of isolated tenotomy vs. tenotomy with tenodesis in patients undergoing arthroscopic RCTs in a retrospective study.</p><p><strong>Methods: </strong>All surgical procedures involved arthroscopic rotator cuff repair performed by a single surgeon. Patients were divided into isolated biceps tenotomy and tenotomy with tenodesis using a suture anchor. Postoperative rehabilitation was standardized. Outcomes were assessed preoperatively and at 3, 6, 12 months, and final follow-up using ASES and Constant-Murley scores, VAS pain scale, operative time, and complications.</p><p><strong>Results: </strong>A total of 63 patients (mean age 67.3 years) were retrospectively reviewed and divided into two groups: isolated tenotomy (<i>n</i> = 28) and tenotomy with tenodesis (<i>n</i> = 35). Preoperative demographics and functional scores (ASES, Constant-Murley, VAS) were comparable between groups. Both techniques resulted in significant and sustained improvements in all functional and pain outcomes at 3, 6, and 12 months postoperatively compared to baseline. In the early postoperative period (3 months), the tenotomy group demonstrated a statistically superior improvement in VAS pain scores. However, these differences in functional and pain scores between the two groups were no longer significant at the 6 and 12-month follow-ups. The operative time was significantly shorter for the tenotomy group. The only significant complication difference was the occurrence of Popeye deformity in two patients (14%) in the tenotomy group, with no cases in the tenodesis group.</p><p><strong>Conclusion: </strong>In conclusion, both isolated tenotomy and tenodesis provide equivalent, excellent functional improvements and pain relief at the 12-month follow-up. Tenotomy offers the advantages of a shorter operative time and better early pain control, at the cost of a higher risk of Popeye deformity. Tenodesis effectively prevents this cosmetic complication but requires a longer surgery.</p>","PeriodicalId":12564,"journal":{"name":"Frontiers in Surgery","volume":"12 ","pages":"1727578"},"PeriodicalIF":1.6,"publicationDate":"2026-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12833041/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146062103","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Aim: The adrenal gland is a vital endocrine organ responsible for maintaining physiological homeostasis. Bilateral adrenalectomy results in adrenal insufficiency, requiring lifelong hormone replacement therapy. This study aimed to establish a reproducible experimental model for vascularized adrenal gland transplantation in rats.
Materials and methods: Twenty male Wistar Albino rats (180-220 g) were randomly assigned into two equal groups (n = 10 each): control and transplantation. The control group underwent bilateral total adrenalectomy. In the transplantation group, vascularized adrenal grafts-including the adrenal artery and vein with attached aortic and inferior vena cava segments-were anastomosed end-to-side to the recipient's femoral artery and vein using 10-0 nylon sutures under general anesthesia. On postoperative day 15, all recipients underwent bilateral adrenalectomy. On day 100, animals were sacrificed for macroscopic and histopathological evaluation of graft viability.
Results: All control rats died within 15 days, whereas all transplanted rats survived throughout the 100-day observation period. Macroscopic inspection revealed viable grafts without vascular compromise. Histopathological analysis demonstrated preserved cortical and medullary architecture, confirming the long-term viability of the transplanted adrenal glands.
Conclusion: This study presents a technically feasible and reproducible model for vascularized adrenal gland transplantation in rats. The model provides a reliable experimental platform for future research on adrenal physiology and transplantation surgery.
{"title":"Development of an experimental model for vascularized adrenal gland transplantation in rats.","authors":"Cumhur Ozcan, Selcuk Mevlut Hazinedaroglu, Tugbay Tug","doi":"10.3389/fsurg.2025.1749069","DOIUrl":"10.3389/fsurg.2025.1749069","url":null,"abstract":"<p><strong>Aim: </strong>The adrenal gland is a vital endocrine organ responsible for maintaining physiological homeostasis. Bilateral adrenalectomy results in adrenal insufficiency, requiring lifelong hormone replacement therapy. This study aimed to establish a reproducible experimental model for vascularized adrenal gland transplantation in rats.</p><p><strong>Materials and methods: </strong>Twenty male Wistar Albino rats (180-220 g) were randomly assigned into two equal groups (<i>n</i> = 10 each): control and transplantation. The control group underwent bilateral total adrenalectomy. In the transplantation group, vascularized adrenal grafts-including the adrenal artery and vein with attached aortic and inferior vena cava segments-were anastomosed end-to-side to the recipient's femoral artery and vein using 10-0 nylon sutures under general anesthesia. On postoperative day 15, all recipients underwent bilateral adrenalectomy. On day 100, animals were sacrificed for macroscopic and histopathological evaluation of graft viability.</p><p><strong>Results: </strong>All control rats died within 15 days, whereas all transplanted rats survived throughout the 100-day observation period. Macroscopic inspection revealed viable grafts without vascular compromise. Histopathological analysis demonstrated preserved cortical and medullary architecture, confirming the long-term viability of the transplanted adrenal glands.</p><p><strong>Conclusion: </strong>This study presents a technically feasible and reproducible model for vascularized adrenal gland transplantation in rats. The model provides a reliable experimental platform for future research on adrenal physiology and transplantation surgery.</p>","PeriodicalId":12564,"journal":{"name":"Frontiers in Surgery","volume":"12 ","pages":"1749069"},"PeriodicalIF":1.6,"publicationDate":"2026-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12833046/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146062079","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Hemophilic pseudotumor is a rare complication of hemophilia in which a chronic, expanding hemorrhagic mass erodes adjacent bone; intracranial presentations are exceedingly uncommon and can mimic neoplasms. We describe a 36-year-old man with severe hemophilia A who developed a five-year, progressively enlarging left frontoparietal swelling with worsening right-sided hemiparesis. MRI demonstrated a heterogeneously enhancing extra-axial lesion destroying the left cranial vault with "mushroom-like" extracranial extension, marked mass effect, and midline shift, initially interpreted as a possible meningioma. Given progressive deficits, the patient underwent resection under intensive factor VIII replacement. Intraoperatively, a 10 × 10 × 5 cm encapsulated lesion containing organizing clot and fibrous tissue was excised en bloc; the skull defect was reconstructed in a staged procedure. Histopathology confirmed hemophilic pseudotumor. Postoperatively, hemiparesis improved markedly; a small epidural hematoma was managed conservatively. At 12 months, MRI showed no recurrence and the patient remained neurologically intact on prophylactic factor VIII. This case highlights the need to include hemophilic pseudotumor in the differential diagnosis of skull lesions in patients with hemophilia and underscores the value of early recognition and multidisciplinary management-particularly meticulous perioperative hemostatic support-to enable safe resection and excellent outcomes.
{"title":"Case Report: Intracranial hemophilic pseudotumor mimicking an aggressive neoplasm: a rare skull-invasive presentation.","authors":"Moksada Regmi, Junyi Liu, Shikun Liu, Ying Xiong, Zihan Zhao, Xu Zhang, Chenlong Yang","doi":"10.3389/fsurg.2025.1709321","DOIUrl":"10.3389/fsurg.2025.1709321","url":null,"abstract":"<p><p>Hemophilic pseudotumor is a rare complication of hemophilia in which a chronic, expanding hemorrhagic mass erodes adjacent bone; intracranial presentations are exceedingly uncommon and can mimic neoplasms. We describe a 36-year-old man with severe hemophilia A who developed a five-year, progressively enlarging left frontoparietal swelling with worsening right-sided hemiparesis. MRI demonstrated a heterogeneously enhancing extra-axial lesion destroying the left cranial vault with \"mushroom-like\" extracranial extension, marked mass effect, and midline shift, initially interpreted as a possible meningioma. Given progressive deficits, the patient underwent resection under intensive factor VIII replacement. Intraoperatively, a 10 × 10 × 5 cm encapsulated lesion containing organizing clot and fibrous tissue was excised <i>en bloc</i>; the skull defect was reconstructed in a staged procedure. Histopathology confirmed hemophilic pseudotumor. Postoperatively, hemiparesis improved markedly; a small epidural hematoma was managed conservatively. At 12 months, MRI showed no recurrence and the patient remained neurologically intact on prophylactic factor VIII. This case highlights the need to include hemophilic pseudotumor in the differential diagnosis of skull lesions in patients with hemophilia and underscores the value of early recognition and multidisciplinary management-particularly meticulous perioperative hemostatic support-to enable safe resection and excellent outcomes.</p>","PeriodicalId":12564,"journal":{"name":"Frontiers in Surgery","volume":"12 ","pages":"1709321"},"PeriodicalIF":1.6,"publicationDate":"2026-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12832656/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146062097","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Objective: Recurrence of trigeminal neuralgia (TN) after microvascular decompression (MVD) poses a challenge for neurosurgeons. This study aimed to investigate the effect of repeat posterior fossa exploration (RPFE) and external neurolysis for TN recurrence following MVD.
Methods: Totally, 38 TN patients who experienced recurrence after MVD were included. All patients underwent RPFE and limited neurolysis. The Barrow Neurological Institute Pain Intensity Scale were utilized to evaluate preoperative pain and postoperative outcomes.
Results: The median follow-up period was 63.8 months (range: 5-112 months). Thirty-three out of the 38 patients achieved excellent outcomes, 4 had good outcomes, and 1 experienced failure. The rates of complete pain relief was 92% immediately post-surgery and 86.8% at the final follow-up. Re-exploration revealed Teflon adhesion in almost all patients (92%). Complications included new facial numbness (n = 5), temporary facial weakness (n = 3), hearing loss and tinnitus (n = 1), wound infection (n = 1), and postoperative hemorrhage (n = 1).
Conclusions: Teflon adhesion was frequently observed upon re-exploration. A substantial majority of TN patients experiencing recurrence post-MVD achieved positive outcomes via RPFE and neurolysis. Complications, particularly facial numbness attributed to premature excessive Teflon dislodgement, continue to pose challenges. However, limited neurolysis, have proven effective in minimizing these complications.
{"title":"Repeat posterior fossa exploration and external neurolysis for recurrent trigeminal neuralgia following microvascular decompression.","authors":"Zhong Liu, Jiao Xu, Ming-Liang Ren, Min-Hui Xu, Sha Chen, Xu-Zhi He, Xu-Hui Wang","doi":"10.3389/fsurg.2025.1694389","DOIUrl":"10.3389/fsurg.2025.1694389","url":null,"abstract":"<p><strong>Objective: </strong>Recurrence of trigeminal neuralgia (TN) after microvascular decompression (MVD) poses a challenge for neurosurgeons. This study aimed to investigate the effect of repeat posterior fossa exploration (RPFE) and external neurolysis for TN recurrence following MVD.</p><p><strong>Methods: </strong>Totally, 38 TN patients who experienced recurrence after MVD were included. All patients underwent RPFE and limited neurolysis. The Barrow Neurological Institute Pain Intensity Scale were utilized to evaluate preoperative pain and postoperative outcomes.</p><p><strong>Results: </strong>The median follow-up period was 63.8 months (range: 5-112 months). Thirty-three out of the 38 patients achieved excellent outcomes, 4 had good outcomes, and 1 experienced failure. The rates of complete pain relief was 92% immediately post-surgery and 86.8% at the final follow-up. Re-exploration revealed Teflon adhesion in almost all patients (92%). Complications included new facial numbness (<i>n</i> = 5), temporary facial weakness (<i>n</i> = 3), hearing loss and tinnitus (<i>n</i> = 1), wound infection (<i>n</i> = 1), and postoperative hemorrhage (<i>n</i> = 1).</p><p><strong>Conclusions: </strong>Teflon adhesion was frequently observed upon re-exploration. A substantial majority of TN patients experiencing recurrence post-MVD achieved positive outcomes via RPFE and neurolysis. Complications, particularly facial numbness attributed to premature excessive Teflon dislodgement, continue to pose challenges. However, limited neurolysis, have proven effective in minimizing these complications.</p>","PeriodicalId":12564,"journal":{"name":"Frontiers in Surgery","volume":"12 ","pages":"1694389"},"PeriodicalIF":1.6,"publicationDate":"2026-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12833354/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146062040","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-12eCollection Date: 2025-01-01DOI: 10.3389/fsurg.2025.1710878
Jun Li, He Shang, Tao Ma, Tianxiang Yang, Yi Wang, Xueqi Liu, Xing He, Yumei Ding, Jinpeng Liang, Yinbin Wang, Desheng Chen
Background: Total joint arthroplasty is an effective treatment for end-stage joint diseases, with approximately 1.5 million procedures performed globally annually and a 25%-30% annual growth rate in China. However, 10%-15% of patients develop prosthetic loosening or subsidence within 15-20 years postoperatively, predominantly due to aseptic loosening (incidence >10%) caused by wear particle-induced aseptic inflammatory osteolysis. The role of autophagy in this pathogenesis remains incompletely understood.
Methods: A 61-year-old female patient developed aseptic loosening 11 months after left total knee arthroplasty. Comprehensive management included preoperative screening (including synovial cell count, differential, and alpha-defensin detection), revision surgery (debridement of necrotic/inflammatory tissue/residual cement and implantation of a new prosthesis with vancomycin-impregnated cement), synovial HE staining, quantitative immunohistochemistry (IHC; Ki67, CD3, CD20, CD68, P62, LC3II, and Beclin1), and postoperative rehabilitation.
Results: Postoperatively, pain was relieved: the patient ambulated with crutches at 3 days, achieved 90° knee flexion at 1 week, and full pain-free weight-bearing (110° flexion) at 2 months. Postoperative infection markers (C-reactive protein and erythrocyte sedimentation rate) were temporarily elevated due to surgical trauma and returned to normal during follow-up. Imaging showed a stable prosthesis without infection or recurrent loosening. Synovial HE staining revealed extensive inflammatory infiltration; quantitative IHC showed high expression of inflammatory markers and low expression of autophagy-related markers. Clinical outcomes were favorable with validated patient-reported outcome measures (Knee injury and Osteoarthritis Outcome Score: 85 points; Western Ontario and McMaster Universities Osteoarthritis Index score: 20 points) at 6 months post-revision.
Conclusion: The integrated protocol effectively treated aseptic loosening. Wear particle-induced chronic synovitis and altered autophagy-related marker expression may be involved in the pathogenesis, providing preliminary clinical and pathological evidence for further research.
{"title":"Case Report: Prosthetic revision due to aseptic loosening following total knee arthroplasty: a clinical management and pathological mechanism investigation.","authors":"Jun Li, He Shang, Tao Ma, Tianxiang Yang, Yi Wang, Xueqi Liu, Xing He, Yumei Ding, Jinpeng Liang, Yinbin Wang, Desheng Chen","doi":"10.3389/fsurg.2025.1710878","DOIUrl":"10.3389/fsurg.2025.1710878","url":null,"abstract":"<p><strong>Background: </strong>Total joint arthroplasty is an effective treatment for end-stage joint diseases, with approximately 1.5 million procedures performed globally annually and a 25%-30% annual growth rate in China. However, 10%-15% of patients develop prosthetic loosening or subsidence within 15-20 years postoperatively, predominantly due to aseptic loosening (incidence >10%) caused by wear particle-induced aseptic inflammatory osteolysis. The role of autophagy in this pathogenesis remains incompletely understood.</p><p><strong>Methods: </strong>A 61-year-old female patient developed aseptic loosening 11 months after left total knee arthroplasty. Comprehensive management included preoperative screening (including synovial cell count, differential, and alpha-defensin detection), revision surgery (debridement of necrotic/inflammatory tissue/residual cement and implantation of a new prosthesis with vancomycin-impregnated cement), synovial HE staining, quantitative immunohistochemistry (IHC; Ki67, CD3, CD20, CD68, P62, LC3II, and Beclin1), and postoperative rehabilitation.</p><p><strong>Results: </strong>Postoperatively, pain was relieved: the patient ambulated with crutches at 3 days, achieved 90° knee flexion at 1 week, and full pain-free weight-bearing (110° flexion) at 2 months. Postoperative infection markers (C-reactive protein and erythrocyte sedimentation rate) were temporarily elevated due to surgical trauma and returned to normal during follow-up. Imaging showed a stable prosthesis without infection or recurrent loosening. Synovial HE staining revealed extensive inflammatory infiltration; quantitative IHC showed high expression of inflammatory markers and low expression of autophagy-related markers. Clinical outcomes were favorable with validated patient-reported outcome measures (Knee injury and Osteoarthritis Outcome Score: 85 points; Western Ontario and McMaster Universities Osteoarthritis Index score: 20 points) at 6 months post-revision.</p><p><strong>Conclusion: </strong>The integrated protocol effectively treated aseptic loosening. Wear particle-induced chronic synovitis and altered autophagy-related marker expression may be involved in the pathogenesis, providing preliminary clinical and pathological evidence for further research.</p>","PeriodicalId":12564,"journal":{"name":"Frontiers in Surgery","volume":"12 ","pages":"1710878"},"PeriodicalIF":1.6,"publicationDate":"2026-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12832683/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146062119","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}