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Transjugular Tricuspid Valve Implantation of Valve-in-Ring Bioprosthesis: Feasibility in a Preclinical, Pilot Trial. 经颈静脉三尖瓣环形瓣膜植入生物假体:临床前试验的可行性。
Lishan Zhong, Qiuji Wang, Shuo Xiao, Junfei Zhao, Yingjie Ke, Zhaolong Zhang, Huanlei Huang

This preclinical study in a porcine model of recurrent regurgitation following tricuspid valvuloplasty aims to confirm the feasibility and safety of a novel transjugular tricuspid valve (TV) replacement device and to optimize the implantation procedure prior to first-in-human study. The novel device was implanted via a transjugular approach in a large white pig model (n = 2). No perivalvular leakage (PVL) or central tricuspid regurgitation (TR) was observed on post-operative echocardiography. The mean transvalvular gradient at 3 months follow-up was 1.69 ± 0.7 mmHg with mild central TR but no PVL. There was no right ventricular outflow tract obstruction, III atrioventricular block, device malposition, pericardial effusion, coronary artery compression, or myocardial infarction. This technique may be a promising option for patients after TV valvuloplasty and is ideal for high-risk patients undergoing open-heart surgery.

本研究在猪三尖瓣成形术后复发性返流模型中进行临床前研究,旨在证实一种新型经颈静脉三尖瓣(TV)置换装置的可行性和安全性,并在首次人体研究之前优化植入程序。该新型装置经颈静脉入路植入一只大白猪模型(n = 2)。术后超声心动图未观察到瓣膜周围渗漏(PVL)或中央三尖瓣反流(TR)。随访3个月时,平均经瓣梯度为1.69±0.7 mmHg,伴有轻度中枢性TR,无PVL。无右心室流出道梗阻、房室传导阻滞、器械错位、心包积液、冠状动脉受压、心肌梗死。该技术可能是电视瓣膜成形术后患者的一种有希望的选择,也是接受心脏直视手术的高危患者的理想选择。
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引用次数: 0
Stapler-Less Uniportal Video-Assisted Thoracoscopic Surgery: A Case Series and Review of the Literature. 无订书机单门静脉电视胸腔镜手术:病例系列及文献回顾。
Rawan F Ayyad, Alaa Ayyad, Raghad Sweity, Mayar Idkedek, Firas Abu Akar

Purpose: Video-assisted thoracoscopic surgery (VATS) is a minimally invasive approach widely used for lung resections. However, reliance on staplers increases costs, limiting its adoption in resource-constrained settings. This study evaluates the feasibility, safety, and cost-effectiveness of uniportal stapler-less VATS lobectomies and segmentectomies.

Methods: A retrospective analysis of 7 stapler-less uniportal VATS surgeries performed between March 2021 and February 2022 was conducted. Data on operative time, blood loss, postoperative outcomes, and complications were collected from patient records.

Results: Seven procedures were completed with an average operative time of 80 min (range: 48-118 min). Estimated blood loss was minimal (10-100 mL) in 6 cases. One patient required conversion to open thoracotomy due to vessel injury. Postoperatively, all patients were stable with no major complications.

Conclusion: Stapler-less VATS is a viable, cost-effective alternative to conventional techniques, offering comparable safety and outcomes. This approach supports broader adoption of minimally invasive surgery, particularly in low-income settings, where reducing procedural costs is critical.

目的:视频胸腔镜手术(VATS)是一种广泛应用于肺切除术的微创方法。然而,对订书机的依赖增加了成本,限制了在资源有限的环境中采用订书机。本研究评估无单门静脉吻合器的VATS肺叶和节段切除术的可行性、安全性和成本效益。方法:回顾性分析2021年3月至2022年2月间进行的7例无吻合器单门VATS手术。从患者记录中收集手术时间、出血量、术后结果和并发症的数据。结果:7例手术完成,平均手术时间80 min(范围48 ~ 118 min)。6例出血量最小(10-100 mL)。1例患者因血管损伤需转开胸。术后所有患者病情稳定,无重大并发症。结论:无订书机VATS是一种可行的、经济有效的替代传统技术,具有相当的安全性和效果。这种方法支持更广泛地采用微创手术,特别是在降低手术成本至关重要的低收入环境中。
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引用次数: 0
Total Robot-Assisted Minimally Invasive Esophagectomy for De Novo Esophageal Cancer after Liver Transplantation: The Potential of Robotic Surgery in a Complex Posttransplant Case. 全机器人辅助微创食管切除术治疗肝移植后新生食管癌:机器人手术在复杂移植后病例中的潜力。
Toshikatsu Tsuji, Noriyuki Inaki, Jun Kinoshita, Hideki Moriyama, Daisuke Yamamoto, Hiroto Saito, Kenta Doden

The malignancy risk has increased following improvements in the long-term survival rates after liver transplantation. Reports show a 23.4-fold increase in the risk of de novo esophageal cancer after liver transplantation compared to the general population. We report the case of a 47-year-old female diagnosed with early esophageal cancer after liver transplantation. Endoscopic submucosal dissection was performed; however, due to it being a noncurative resection, additional treatment was required. Total robot-assisted minimally invasive esophagectomy (RAMIE) was performed using a robot for thoracic and abdominal procedures. Although extensive adhesions were observed after liver transplantation, precise surgery using the robot did not damage any vital organs, such as the graft blood vessels. The patient was discharged without postoperative complications. Total RAMIE for esophageal cancer after liver transplantation is a feasible and safe option following careful evaluation of the patient's condition, and expands the possibilities of successful complex posttransplant surgeries through robotic precision.

随着肝移植术后长期生存率的提高,恶性肿瘤的风险也随之增加。报告显示,与普通人群相比,肝移植术后新发食管癌的风险增加了23.4倍。我们报告一位47岁女性,在肝移植后被诊断为早期食管癌。内镜下粘膜夹层;然而,由于它是一个不可治愈的切除,需要额外的治疗。全机器人辅助微创食管切除术(RAMIE)由机器人进行胸部和腹部手术。尽管肝移植后观察到广泛的粘连,但使用机器人进行的精确手术并未损害任何重要器官,如移植血管。患者出院,无术后并发症。在仔细评估患者病情后,全RAMIE治疗食管癌肝移植术后是一种可行且安全的选择,并通过机器人精度扩大了复杂移植后手术成功的可能性。
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引用次数: 0
Long-Term Outcomes of Concomitant Modified Cox-Maze and Mitral Surgery. 改良Cox-Maze联合二尖瓣手术的远期疗效。
Choosak Kasemsarn, Pramote Porapakkham, Sahaporn Wathanawanichakun, Piyawat Lerdsomboon, Krisulang Chanpa

Purpose: There are limited data on outcomes of combined Maze and mitral valve procedures beyond 10 years. This study analyzed the efficacy of this operation.

Methods: Between June 2004 and December 2022, 406 patients underwent mitral surgery concomitant with Maze procedure were evaluated. Rhythm outcomes, predictors of recurrence, and survival were assessed.

Results: The median follow-up period was 100 months. Rheumatic disease was present in 58%. Mitral valve repair was performed in 57.1%. Freedom from atrial fibrillation (AF) at 5, 10, and 15 years was 82.5%, 70.8%, and 52.7%, respectively. Overall survival rates were not different between patients in sinus rhythm (SR) and those who remained in AF (p = 0.172). However, patients in SR experienced fewer neurological complication (p = 0.001). Predictors of AF recurrence included preoperative AF duration (p = 0.005), left atrial diameter (LAD) >50 mm (p <0.001), concomitant tricuspid valve surgery (p = 0.049), and the presence of AF on postoperative day 7 (p <0.001). Factors influencing survival were age >60 years (p <0.001) and a postoperative left ventricular ejection fraction <40% (p <0.001).

Conclusions: The combined Maze and mitral valve surgery provides significant benefits in managing AF with mitral disease. Predictors of recurrence included AF duration, LAD size >50 mm, associated tricuspid valve disease, and AF on day 7. SR patients had fewer neurological complications.

目的:关于迷宫和二尖瓣联合手术超过10年的结果数据有限。本研究分析了该手术的疗效。方法:2004年6月至2022年12月,对406例二尖瓣手术合并Maze手术患者进行评估。评估心律结果、复发预测因素和生存率。结果:中位随访时间为100个月。58%的患者有风湿病。二尖瓣修复率为57.1%。5年、10年和15年无房颤(AF)者分别为82.5%、70.8%和52.7%。窦性心律(SR)患者与房颤患者的总生存率无显著差异(p = 0.172)。然而,SR患者的神经系统并发症较少(p = 0.001)。房颤复发的预测因素包括术前房颤持续时间(p = 0.005)、左房径(LAD) bbb50 mm (p = 60年)。结论:迷宫联合二尖瓣手术治疗房颤合并二尖瓣疾病有显著的疗效。复发的预测因素包括房颤持续时间、LAD大小bbb50 mm、相关三尖瓣疾病和房颤第7天。SR患者神经系统并发症较少。
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引用次数: 0
Lobectomy Increases Postoperative Pulmonary Artery Enlargement to a Greater Extent than Segmentectomy. 肺叶切除术比节段切除术在更大程度上增加术后肺动脉扩张。
Megumi Nishikubo, Yugo Tanaka, Shinya Tane, Daisuke Hokka, Yoshimasa Maniwa

Purpose: The underlying mechanism why segmentectomy has demonstrated the non-inferiority to lobectomy in several randomized trials remains unclear. Computed tomography (CT)-measured pulmonary artery (PA) enlargement reflects PA pressure and predicts the prognosis of certain respiratory diseases. We compared the preoperative and postoperative PA diameter to the ascending aorta diameter (PA/A) ratio, investigating its impact on right ventricular function in lung resection.

Methods: This retrospective study was conducted in patients with lower-lobe lung tumors who underwent anatomical lung resection between 2017 and 2022. The PA diameter at the bifurcation and the ascending aorta diameter at the same CT image slice were measured preoperatively and postoperatively. We calculated the enlargement of PA/A ratio (PA/A change) and compared lobectomy and segmentectomy.

Results: This analysis included 279 patients (235 with lobectomy and 44 with segmentectomy). The PA/A change was significantly greater in patients with lobectomy than segmentectomy (104% vs. 102%, P = 0.02). In the multivariable analysis, airflow obstruction (yes, P = 0.04) and the type of surgery (segmentectomy, P = 0.04) were independent prognostic factors for PA/A change.

Conclusions: The PA/A change was greater in lobectomy than in segmentectomy. This change could reflect a burden on right ventricular function after lobectomy.

目的:在几项随机试验中,节段切除术优于肺叶切除术的潜在机制尚不清楚。计算机断层扫描(CT)测量肺动脉(PA)扩大反映PA压力和预测某些呼吸系统疾病的预后。我们比较了术前和术后升主动脉直径(PA/A)比,探讨其对肺切除术中右心室功能的影响。方法:回顾性研究2017 - 2022年行解剖性肺切除术的肺下叶肿瘤患者。术前、术后分别测量分叉处的主动脉直径和同一CT图像切片上的升主动脉直径。我们计算PA/A比值的增大(PA/A变化),并比较肺叶切除术和节段切除术。结果:本分析纳入279例患者(肺叶切除术235例,节段切除术44例)。肺叶切除术患者的PA/A变化明显大于节段切除术患者(104% vs 102%, P = 0.02)。在多变量分析中,气流阻塞(是,P = 0.04)和手术类型(节段切除术,P = 0.04)是PA/A变化的独立预后因素。结论:肺叶切除术的PA/A变化大于节段切除术。这种变化可能反映了肺叶切除术后右心室功能的负担。
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引用次数: 0
Kartagener Syndrome Complicated by Middle and Lower Lobar Mucinous Adenocarcinoma in the Left Lung. 卡塔格纳综合征并发左肺中下叶黏液腺癌。
Guang-Yuan Shao, Cheng-De Wang, Dong Wang, Si-Yuan Sun, Bao-Kai Wang, Xiao-Nu Peng, Wen-Quan Yu

Introduction: Kartagener syndrome (KS), a distinct subtype of primary ciliary dyskinesia, is linked to progressive lung disease; concurrent pulmonary mucinous adenocarcinoma mimicking pneumonia is rarely reported and easily misdiagnosed.

Case presentation: A 64-year-old female presented with years of recurrent cough and sputum. Chest computed tomography (CT) revealed bilateral chronic inflammation, interstitial changes, a left lower lobe mass-like shadow, partial bronchiectasis, and dextrocardia. Bronchoscopy showed chronic mucosal inflammation in the left lower lobe base segment; sputum culture was negative. Symptoms improved with antibiotics/expectorants. Two months later, worsening symptoms prompted re-evaluation. Extensive diagnostic tests (tumor markers, bacteriological/mycological, immunological, viral) were largely negative. CT-guided percutaneous lung biopsy confirmed invasive mucinous adenocarcinoma. Preoperative evaluation revealed situs inversus totalis, chronic sinusitis, and bronchiectasis, confirming concurrent KS. Following multidisciplinary discussion, she underwent thoracoscopic left middle and lower lobectomy with uncomplicated recovery; pathology confirmed R0 resection. She completed 5 cycles of adjuvant pemetrexed/platinum chemotherapy and remains recurrence-free on follow-up.

Conclusions: This represents the first documented case of KS coexisting with pulmonary invasive mucinous adenocarcinoma, to some extent expanding the clinical spectrum of ciliopathy-associated lung malignancies. It suggests that clinicians and radiologists should consider the possibility of concurrent mucinous adenocarcinoma in KS patients.

简介:Kartagener综合征(KS)是原发性纤毛运动障碍的一种独特亚型,与进行性肺病有关;并发肺黏液腺癌模拟肺炎是罕见的报告和容易误诊。病例介绍:一名64岁女性,常年咳嗽和痰。胸部计算机断层扫描(CT)显示双侧慢性炎症,间质改变,左下叶肿块样影,部分支气管扩张和右心。支气管镜检查显示左下肺叶基底段慢性黏膜炎症;痰培养阴性。使用抗生素/祛痰剂后症状有所改善。两个月后,症状恶化促使重新评估。广泛的诊断试验(肿瘤标志物、细菌学/真菌学、免疫学、病毒学)基本上呈阴性。ct引导下经皮肺活检证实浸润性粘液腺癌。术前评估显示完全性倒位,慢性鼻窦炎和支气管扩张,确认并发KS。经过多学科的讨论,她接受了胸腔镜下的左中下肺叶切除术,并没有复杂的恢复;病理证实R0切除。她完成了5个周期的培美曲塞/铂辅助化疗,随访时无复发。结论:这是第一例有文献记载的KS与肺浸润性粘液腺癌共存的病例,在一定程度上扩大了纤毛病相关肺部恶性肿瘤的临床范围。提示临床医生和放射科医生应考虑KS患者并发粘液腺癌的可能性。
{"title":"Kartagener Syndrome Complicated by Middle and Lower Lobar Mucinous Adenocarcinoma in the Left Lung.","authors":"Guang-Yuan Shao, Cheng-De Wang, Dong Wang, Si-Yuan Sun, Bao-Kai Wang, Xiao-Nu Peng, Wen-Quan Yu","doi":"10.5761/atcs.cr.25-00150","DOIUrl":"10.5761/atcs.cr.25-00150","url":null,"abstract":"<p><strong>Introduction: </strong>Kartagener syndrome (KS), a distinct subtype of primary ciliary dyskinesia, is linked to progressive lung disease; concurrent pulmonary mucinous adenocarcinoma mimicking pneumonia is rarely reported and easily misdiagnosed.</p><p><strong>Case presentation: </strong>A 64-year-old female presented with years of recurrent cough and sputum. Chest computed tomography (CT) revealed bilateral chronic inflammation, interstitial changes, a left lower lobe mass-like shadow, partial bronchiectasis, and dextrocardia. Bronchoscopy showed chronic mucosal inflammation in the left lower lobe base segment; sputum culture was negative. Symptoms improved with antibiotics/expectorants. Two months later, worsening symptoms prompted re-evaluation. Extensive diagnostic tests (tumor markers, bacteriological/mycological, immunological, viral) were largely negative. CT-guided percutaneous lung biopsy confirmed invasive mucinous adenocarcinoma. Preoperative evaluation revealed situs inversus totalis, chronic sinusitis, and bronchiectasis, confirming concurrent KS. Following multidisciplinary discussion, she underwent thoracoscopic left middle and lower lobectomy with uncomplicated recovery; pathology confirmed R0 resection. She completed 5 cycles of adjuvant pemetrexed/platinum chemotherapy and remains recurrence-free on follow-up.</p><p><strong>Conclusions: </strong>This represents the first documented case of KS coexisting with pulmonary invasive mucinous adenocarcinoma, to some extent expanding the clinical spectrum of ciliopathy-associated lung malignancies. It suggests that clinicians and radiologists should consider the possibility of concurrent mucinous adenocarcinoma in KS patients.</p>","PeriodicalId":93877,"journal":{"name":"Annals of thoracic and cardiovascular surgery : official journal of the Association of Thoracic and Cardiovascular Surgeons of Asia","volume":"31 1","pages":""},"PeriodicalIF":1.3,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12575073/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145402829","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
Machine Learning-Based Random Forest to Predict 3-Year Survival after Endovascular Aneurysm Repair. 基于机器学习的随机森林预测血管内动脉瘤修复后3年生存率。
Toshiya Nishibe, Tsuyoshi Iwasa, Seiji Matsuda, Masaki Kano, Shinobu Akiyama, Shoji Fukuda, Masayasu Nishibe

Purpose: Endovascular aneurysm repair (EVAR) is widely used to treat abdominal aortic aneurysms (AAAs), but mid-term survival remains a concern. This study aims to develop a machine learning-based random forest model to predict 3-year survival after EVAR.

Methods: A random forest model was trained using data from 176 EVAR patients, of whom 169 patients were retained for analysis, incorporating 23 preoperative and perioperative variables. Model performance was evaluated using 5-fold cross-validation.

Results: The model achieved an area under the receiver-operating characteristic curve (AUC) of 0.91, with an accuracy of 81.1%, a sensitivity of 81.6%, a specificity of 80.9%, and an F1 score of 0.66. Feature importance analysis identified poor nutritional status (geriatric nutritional risk index <101.4), compromised immunity (neutrophil-to-lymphocyte ratio >3.19), chronic kidney disease (CKD), octogenarian status, chronic obstructive pulmonary disease (COPD), small aneurysm size, and statin use as the top predictors of 3-year mortality. The average values of the AUC, accuracy, sensitivity, specificity, and F1 score across the 5-folds were 0.76 ± 0.10, 73.9 ± 5.8%, 60.4 ± 1.9%, 77.8 ± 0.7%, and 0.59 ± 0.17, indicating consistent performance across different data subsets.

Conclusions: The random forest model effectively predicts 3-year survival after EVAR, indicating key factors such as poor nutritional status, compromised immunity, CKD, octogenarian status, COPD, small aneurysm size, and statin use.

目的:血管内动脉瘤修复(EVAR)被广泛应用于腹主动脉瘤(AAAs)的治疗,但中期生存仍然是一个问题。本研究旨在开发一种基于机器学习的随机森林模型来预测EVAR后的3年生存率。方法:使用176例EVAR患者的数据训练随机森林模型,其中保留169例患者进行分析,包括23个术前和围手术期变量。采用5倍交叉验证评估模型性能。结果:该模型的受者工作特征曲线下面积(AUC)为0.91,准确率为81.1%,灵敏度为81.6%,特异性为80.9%,F1评分为0.66。特征重要性分析发现营养状况不良(老年营养风险指数3.19)、慢性肾脏疾病(CKD)、八旬状态、慢性阻塞性肺疾病(COPD)、小动脉瘤和他汀类药物使用是3年死亡率的主要预测因素。5组的AUC、准确度、灵敏度、特异性和F1评分的平均值分别为0.76±0.10、73.9±5.8%、60.4±1.9%、77.8±0.7%和0.59±0.17,表明在不同的数据子集中表现一致。结论:随机森林模型可有效预测EVAR后3年生存率,提示营养状况不良、免疫力低下、CKD、老年状态、COPD、小动脉瘤大小和他汀类药物使用等关键因素。
{"title":"Machine Learning-Based Random Forest to Predict 3-Year Survival after Endovascular Aneurysm Repair.","authors":"Toshiya Nishibe, Tsuyoshi Iwasa, Seiji Matsuda, Masaki Kano, Shinobu Akiyama, Shoji Fukuda, Masayasu Nishibe","doi":"10.5761/atcs.oa.25-00036","DOIUrl":"10.5761/atcs.oa.25-00036","url":null,"abstract":"<p><strong>Purpose: </strong>Endovascular aneurysm repair (EVAR) is widely used to treat abdominal aortic aneurysms (AAAs), but mid-term survival remains a concern. This study aims to develop a machine learning-based random forest model to predict 3-year survival after EVAR.</p><p><strong>Methods: </strong>A random forest model was trained using data from 176 EVAR patients, of whom 169 patients were retained for analysis, incorporating 23 preoperative and perioperative variables. Model performance was evaluated using 5-fold cross-validation.</p><p><strong>Results: </strong>The model achieved an area under the receiver-operating characteristic curve (AUC) of 0.91, with an accuracy of 81.1%, a sensitivity of 81.6%, a specificity of 80.9%, and an F1 score of 0.66. Feature importance analysis identified poor nutritional status (geriatric nutritional risk index <101.4), compromised immunity (neutrophil-to-lymphocyte ratio >3.19), chronic kidney disease (CKD), octogenarian status, chronic obstructive pulmonary disease (COPD), small aneurysm size, and statin use as the top predictors of 3-year mortality. The average values of the AUC, accuracy, sensitivity, specificity, and F1 score across the 5-folds were 0.76 ± 0.10, 73.9 ± 5.8%, 60.4 ± 1.9%, 77.8 ± 0.7%, and 0.59 ± 0.17, indicating consistent performance across different data subsets.</p><p><strong>Conclusions: </strong>The random forest model effectively predicts 3-year survival after EVAR, indicating key factors such as poor nutritional status, compromised immunity, CKD, octogenarian status, COPD, small aneurysm size, and statin use.</p>","PeriodicalId":93877,"journal":{"name":"Annals of thoracic and cardiovascular surgery : official journal of the Association of Thoracic and Cardiovascular Surgeons of Asia","volume":"31 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12086006/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144082776","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
Peribronchial Arteriovenous Malformation with Cowden Syndrome: A Rare Case Report. 支气管周围动静脉畸形伴考登综合征1例报告。
Shuta Sumitomo, Gouji Toyokawa, Yue Cong, Takatoshi Kubo, Hiroyuki Saigusa, Masaaki Sato

Cowden syndrome (CS) is a rare hereditary disorder caused by a germline variant of the phosphatase and tensin homolog, associated with multiple hamartomatous lesions occurring in various organs. Additionally, although rare, arteriovenous malformations (AVMs) with CS are found in the skin, brain, and spinal cord; however, peribronchial AVMs have not been previously reported. Herein, we report a rare case of a peribronchial AVM in a 30-year-old man with CS who presented with hemoptysis. Computed tomography (CT) revealed an AVM around the left upper bronchus, which was mainly fed by the left bronchial artery and drained into the left inferior pulmonary vein. Under video-assisted thoracic surgery, ligation of the feeding and draining vessels was performed. The AVM remarkably decreased in size one month after the surgery. This case highlights the need for whole-body contrast-enhanced CT to screen for AVMs and the importance of identifying feeding and draining vessels for optimal treatment methods.

考登综合征(CS)是一种罕见的遗传性疾病,由磷酸酶和紧张素同源物的种系变异引起,与多种器官发生的多种错构瘤病变有关。此外,虽然罕见,动静脉畸形(AVMs)与CS发现在皮肤,大脑和脊髓;然而,支气管周围动静脉畸形以前未见报道。在此,我们报告一个罕见的病例支气管周围AVM在一个30岁的男子与CS谁提出了咯血。CT示左上支气管周围AVM,主要由左支气管动脉供血,引流至左下肺静脉。在视频辅助胸外科手术下,结扎喂养和引流血管。手术后一个月,AVM的大小明显减小。该病例强调了采用全身增强CT筛查avm的必要性,以及识别供血和引流血管以获得最佳治疗方法的重要性。
{"title":"Peribronchial Arteriovenous Malformation with Cowden Syndrome: A Rare Case Report.","authors":"Shuta Sumitomo, Gouji Toyokawa, Yue Cong, Takatoshi Kubo, Hiroyuki Saigusa, Masaaki Sato","doi":"10.5761/atcs.cr.25-00171","DOIUrl":"10.5761/atcs.cr.25-00171","url":null,"abstract":"<p><p>Cowden syndrome (CS) is a rare hereditary disorder caused by a germline variant of the phosphatase and tensin homolog, associated with multiple hamartomatous lesions occurring in various organs. Additionally, although rare, arteriovenous malformations (AVMs) with CS are found in the skin, brain, and spinal cord; however, peribronchial AVMs have not been previously reported. Herein, we report a rare case of a peribronchial AVM in a 30-year-old man with CS who presented with hemoptysis. Computed tomography (CT) revealed an AVM around the left upper bronchus, which was mainly fed by the left bronchial artery and drained into the left inferior pulmonary vein. Under video-assisted thoracic surgery, ligation of the feeding and draining vessels was performed. The AVM remarkably decreased in size one month after the surgery. This case highlights the need for whole-body contrast-enhanced CT to screen for AVMs and the importance of identifying feeding and draining vessels for optimal treatment methods.</p>","PeriodicalId":93877,"journal":{"name":"Annals of thoracic and cardiovascular surgery : official journal of the Association of Thoracic and Cardiovascular Surgeons of Asia","volume":"31 1","pages":""},"PeriodicalIF":1.3,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12714414/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145776554","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
Patient Outcomes after Introduction of Novel Myocardial Protection Protocol for Prolonged Aortic Cross-Clamping. 采用新型心肌保护方案治疗延长主动脉交叉夹紧后的患者预后。
Masahide Komagamine, Takuma Fukunishi, Yoshiki Yamasaki, Masahiro Tomita, Satoshi Kinebuchi, Daijun Tomimoto, Kan Nawata

Purpose: Cardioplegia directly affects patient outcomes after cardiac surgery with prolonged aortic cross-clamping. Our hospital revised its myocardial protection protocol in April 2021 and compared the clinical outcomes of patients with prolonged aortic cross-clamping before versus after the revision.

Methods: This study included 36 patients who underwent cardiac surgery via a median sternotomy and prolonged aortic cross-clamping for >4 h at our hospital from 2018 to 2024. Patients treated between 2018 and March 2021 (before the protocol revision) were designated as Group 1, while those treated from April 2021 to 2024 (after the revision) were designated as Group 2.

Results: Groups 1 and 2 comprised 17 and 19 patients, respectively. The mean creatine kinase level immediately postoperative was significantly lower in Group 2 versus Group 1 (P = 0.018). The mean hospital stay was also significantly shorter in Group 2 versus Group 1 (P = 0.017). Regarding new postoperative right-ventricular dysfunction, there were 3 cases (15.8%) in Group 2 versus 5 cases (29.4%) in Group 1, but the difference was not statistically significant.

Conclusion: These findings suggest that our hospital's revised myocardial protection protocol, which requires no alteration of the solution itself, achieves safe and favorable surgical results, even in cardiac surgeries requiring prolonged aortic cross-clamping.

目的:心脏停跳直接影响心脏手术后主动脉交叉夹持时间延长患者的预后。我院于2021年4月修订心肌保护方案,比较修订前后主动脉交叉夹持时间延长患者的临床结局。方法:本研究纳入我院2018年至2024年36例经胸骨正中切开术并延长主动脉交叉夹持时间bbbb4 h的心脏手术患者。2018年至2021年3月(方案修订前)治疗的患者被指定为1组,2021年4月至2024年(方案修订后)治疗的患者被指定为2组。结果:1组17例,2组19例。术后即刻肌酸激酶的平均水平2组明显低于1组(P = 0.018)。2组的平均住院时间也明显短于1组(P = 0.017)。术后新发右室功能障碍2组3例(15.8%),1组5例(29.4%),差异无统计学意义。结论:我院修改后的心肌保护方案无需改变溶液本身,即使在需要长时间主动脉交叉夹持的心脏手术中也能获得安全、良好的手术效果。
{"title":"Patient Outcomes after Introduction of Novel Myocardial Protection Protocol for Prolonged Aortic Cross-Clamping.","authors":"Masahide Komagamine, Takuma Fukunishi, Yoshiki Yamasaki, Masahiro Tomita, Satoshi Kinebuchi, Daijun Tomimoto, Kan Nawata","doi":"10.5761/atcs.oa.25-00079","DOIUrl":"10.5761/atcs.oa.25-00079","url":null,"abstract":"<p><strong>Purpose: </strong>Cardioplegia directly affects patient outcomes after cardiac surgery with prolonged aortic cross-clamping. Our hospital revised its myocardial protection protocol in April 2021 and compared the clinical outcomes of patients with prolonged aortic cross-clamping before versus after the revision.</p><p><strong>Methods: </strong>This study included 36 patients who underwent cardiac surgery via a median sternotomy and prolonged aortic cross-clamping for >4 h at our hospital from 2018 to 2024. Patients treated between 2018 and March 2021 (before the protocol revision) were designated as Group 1, while those treated from April 2021 to 2024 (after the revision) were designated as Group 2.</p><p><strong>Results: </strong>Groups 1 and 2 comprised 17 and 19 patients, respectively. The mean creatine kinase level immediately postoperative was significantly lower in Group 2 versus Group 1 (P = 0.018). The mean hospital stay was also significantly shorter in Group 2 versus Group 1 (P = 0.017). Regarding new postoperative right-ventricular dysfunction, there were 3 cases (15.8%) in Group 2 versus 5 cases (29.4%) in Group 1, but the difference was not statistically significant.</p><p><strong>Conclusion: </strong>These findings suggest that our hospital's revised myocardial protection protocol, which requires no alteration of the solution itself, achieves safe and favorable surgical results, even in cardiac surgeries requiring prolonged aortic cross-clamping.</p>","PeriodicalId":93877,"journal":{"name":"Annals of thoracic and cardiovascular surgery : official journal of the Association of Thoracic and Cardiovascular Surgeons of Asia","volume":"31 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12169755/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144277008","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
Thymoma without Myasthenia Gravis Showing Size Fluctuation in Parallel to Alopecia Areata Activity: A Case Report. 胸腺瘤无重症肌无力,大小波动与斑秃平行1例。
Keisuke Fujimoto, Koichiro Kenzaki, Takako Kubo, Toru Sawada, Shoko Norimura, Kazumasa Miura, Akiyoshi Yamamoto

Thymomas are commonly associated with autoimmune diseases such as myasthenia gravis (MG), pure red cell aplasia, and hypogammaglobulinemia, while those associated solely with alopecia areata (AA) are extremely rare. A 55-year-old woman with AA underwent chest computed tomography, which revealed a 33-mm anterior mediastinal cystic mass with fluctuating size. She was referred to our department for evaluation of a suspected cystic thymoma. The patient underwent thoracoscopic tumor resection under general anesthesia with isolated lung ventilation in the left lateral decubitus position. The operation lasted 81 minutes with minimal blood loss, and her postoperative course was uneventful. Histopathology confirmed a type B2-dominant thymoma. Notably, the patient's AA improved rapidly after surgery and did not recur for at least 3 years. This case strongly suggests a potential immunological relationship between AA and thymoma, though further research is needed to confirm this relationship.

胸腺瘤通常与自身免疫性疾病相关,如重症肌无力(MG)、纯红细胞发育不全和低γ -球蛋白血症,而仅与斑秃(AA)相关的胸腺瘤极为罕见。一名55岁女性AA患者接受胸部计算机断层扫描,发现一个33毫米大小波动的前纵隔囊性肿块。她因疑似囊性胸腺瘤被转介到我科进行评估。患者在全麻下行胸腔镜肿瘤切除术,左侧卧位孤立肺通气。手术持续了81分钟,出血量最小,术后过程平稳。组织病理学证实为b2型胸腺瘤。值得注意的是,患者的AA在手术后迅速改善,至少3年内没有复发。该病例强烈提示AA和胸腺瘤之间存在潜在的免疫学关系,尽管需要进一步的研究来证实这种关系。
{"title":"Thymoma without Myasthenia Gravis Showing Size Fluctuation in Parallel to Alopecia Areata Activity: A Case Report.","authors":"Keisuke Fujimoto, Koichiro Kenzaki, Takako Kubo, Toru Sawada, Shoko Norimura, Kazumasa Miura, Akiyoshi Yamamoto","doi":"10.5761/atcs.cr.25-00082","DOIUrl":"10.5761/atcs.cr.25-00082","url":null,"abstract":"<p><p>Thymomas are commonly associated with autoimmune diseases such as myasthenia gravis (MG), pure red cell aplasia, and hypogammaglobulinemia, while those associated solely with alopecia areata (AA) are extremely rare. A 55-year-old woman with AA underwent chest computed tomography, which revealed a 33-mm anterior mediastinal cystic mass with fluctuating size. She was referred to our department for evaluation of a suspected cystic thymoma. The patient underwent thoracoscopic tumor resection under general anesthesia with isolated lung ventilation in the left lateral decubitus position. The operation lasted 81 minutes with minimal blood loss, and her postoperative course was uneventful. Histopathology confirmed a type B2-dominant thymoma. Notably, the patient's AA improved rapidly after surgery and did not recur for at least 3 years. This case strongly suggests a potential immunological relationship between AA and thymoma, though further research is needed to confirm this relationship.</p>","PeriodicalId":93877,"journal":{"name":"Annals of thoracic and cardiovascular surgery : official journal of the Association of Thoracic and Cardiovascular Surgeons of Asia","volume":"31 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12266934/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144651423","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
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Annals of thoracic and cardiovascular surgery : official journal of the Association of Thoracic and Cardiovascular Surgeons of Asia
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