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Long-term survival following serial pulmonary metastasectomies for uterine leiomyosarcoma: a case report. 子宫平滑肌肉瘤连续肺转移切除术后的长期生存:1例报告。
IF 0.1 Pub Date : 2025-11-11 DOI: 10.1186/s44215-025-00231-4
Ken Kodama, Toru Momozane, Hiroshi Takehara, Kazuaki Sato

Background: In patients with uterine leiomyosarcoma and multiple pulmonary metastases complicated by pneumothorax during chemotherapy, repeated metastasectomy may contribute to long-term survival.

Case presentation: A 45-year-old woman underwent total hysterectomy for uterine leiomyosarcoma. She subsequently developed multiple pulmonary metastases and was treated with gemcitabine plus docetaxel (GD) chemotherapy. During the course of chemotherapy, she developed a pneumothorax, possibly as a consequence of tumor necrosis induced by treatment. Due to a rapidly declining in the performance status (PS), right lower lobectomy was performed to manage the pneumothorax and reduce the tumor burden. GD chemotherapy was resumed postoperatively but discontinued after a total of 14 cycles due to adverse events. As anticipated, the pulmonary metastases regrew. However, no evidence of extrathoracic disease was identified, and her respiratory function was deemed sufficient for surgery. She subsequently underwent one-stage partial bilateral lung resections, during which a total of 12 metastatic nodules were removed. Two years later, two additional metastatic lesions were resected. Since that time, 5 years and 8 months have passed without any recurrence or additional treatment. At the time of reporting, the patient had remained disease-free, 16 years after the initial hysterectomy, with PS of 0.

Conclusion: Uterine leiomyosarcoma is an aggressive tumor; however, in selected cases, long-term survival may be achieved through multimodal treatment approaches, including surgical resection of metastatic lesions.

背景:在化疗期间子宫平滑肌肉瘤合并多发性肺转移并气胸的患者中,反复转移切除可能有助于长期生存。病例介绍:一名45岁女性因子宫平滑肌肉瘤接受全子宫切除术。她随后出现多发性肺转移,并接受吉西他滨加多西紫杉醇(GD)化疗。在化疗过程中,她出现气胸,可能是治疗引起的肿瘤坏死的结果。由于表现状态(PS)迅速下降,我们行右下肺叶切除术以控制气胸并减轻肿瘤负担。术后恢复GD化疗,但由于不良事件共14个周期后停止。正如预期的那样,肺转移瘤重新生长。然而,没有发现胸外疾病的证据,她的呼吸功能被认为足以进行手术。随后,她接受了一期双侧部分肺切除术,期间共切除了12个转移性结节。两年后,又切除了两个转移性病灶。从那时起,5年零8个月过去了,没有任何复发或额外的治疗。在报告时,患者在首次子宫切除术16年后仍无疾病,PS为0。结论:子宫平滑肌肉瘤是一种侵袭性肿瘤;然而,在选定的病例中,长期生存可以通过多种治疗方法实现,包括手术切除转移灶。
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引用次数: 0
Boerhaave syndrome complicated by ruptured esophageal varices: a case report. 布尔哈夫综合征并发食管静脉曲张破裂1例。
IF 0.1 Pub Date : 2025-11-07 DOI: 10.1186/s44215-025-00226-1
Kosei Uehara, Makoto Sohda, Kengo Kuriyama, Akiharu Kimura, Akihiko Sano, Makoto Sakai, Ken Shirabe, Hiroshi Saeki

Background: Boerhaave syndrome is a life-threatening condition caused by a spontaneous full-thickness rupture of the esophagus, typically following forceful vomiting. Esophageal variceal rupture is another potentially fatal condition commonly observed in patients with liver cirrhosis. These two conditions are usually reported independently, and their coexistence is extremely rare. Managing this combination is particularly challenging because of the need for both infection control and hemostasis in the presence of portal hypertension.

Case presentation: We report the case of a 51-year-old man with liver cirrhosis (Child-Pugh Grade B) and a history of endoscopic variceal ligation, who presented with hematemesis followed by vomiting. He had not consumed any alcohol at that time and exhibited no signs of melena. Computed tomography revealed mediastinal emphysema, right-sided hemopneumothorax, and esophageal perforation. Endoscopy confirmed a lower esophageal tear with active variceal bleeding. Emergency surgery was performed via a right thoracotomy. A 35-mm longitudinal tear in the lower esophagus was identified and sutured; however, owing to tissue fragility and signs of infection, a T-tube was placed at the perforation site. The patient had an uneventful postoperative course, resumed oral intake on postoperative day 17, and was discharged without any complications on day 46.

Conclusions: This was a rare case of Boerhaave syndrome complicated by ruptured esophageal varices. Surgical management with T-tube drainage was effective in controlling both infection and bleeding. Patients with esophageal varices may be at an increased risk of esophageal rupture, especially following vomiting. Awareness of this association is essential for timely diagnosis and management.

背景:Boerhaave综合征是一种由自发性食管全层破裂引起的危及生命的疾病,通常在强烈呕吐后发生。食管静脉曲张破裂是肝硬化患者常见的另一种潜在的致命性疾病。这两种情况通常是独立报道的,它们的共存是极其罕见的。管理这种组合是特别具有挑战性的,因为需要感染控制和止血存在门脉高压。病例介绍:我们报告一例51岁男性肝硬化患者(Child-Pugh分级B级),有内窥镜下静脉曲张结扎史,表现为呕血伴呕吐。他当时没有喝任何酒,也没有表现出黑肠病的迹象。电脑断层显示纵隔肺气肿、右侧血气胸及食道穿孔。内窥镜证实食管下部撕裂伴活动性静脉曲张出血。紧急手术通过右开胸进行。发现食管下段纵裂35mm并缝合;然而,由于组织脆弱和感染的迹象,在穿孔部位放置了t管。患者术后过程平稳,术后第17天恢复口服,第46天无并发症出院。结论:这是一例罕见的布尔哈夫综合征并发食管静脉曲张破裂的病例。t管引流术能有效控制感染和出血。食管静脉曲张患者发生食管破裂的风险增加,尤其是在呕吐后。意识到这种关联对于及时诊断和管理至关重要。
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引用次数: 0
A case of impending paradoxical embolism. 一个即将发生的矛盾栓塞的病例。
IF 0.1 Pub Date : 2025-10-21 DOI: 10.1186/s44215-025-00229-y
Hideaki Kanda, Kazuhisa Matsumoto, Akira Hiwatashi, Yoshiharu Soga

Background: Impending paradoxical embolism (IPDE) is a rare condition characterized by the presence of a thrombus in a patent foramen ovale. We were able to image a thrombus lodged in a patent foramen ovale and remove the thrombus before it could result in arterial embolism.

Case presentation: A 24-year-old woman was admitted to our hospital with chest pain and dyspnea. Pulmonary embolism was diagnosed via computed tomography. Additionally, transesophageal echocardiography revealed a thrombus lodged in a patent foramen ovale and fluttering in both atria, leading to a diagnosis of IPDE. Rather than incurring the risk associated with embolization by thrombolytic treatment, we elected to remove the incarcerated thrombus and close the patent foramen ovale under cardiopulmonary bypass.

Conclusions: We successfully treated a case of IPDE by removing the thrombus under cardiopulmonary bypass, before arterial thrombosis could occur.

背景:即将发生的矛盾栓塞(IPDE)是一种罕见的情况,其特征是在卵圆孔未闭处存在血栓。我们能够成像在未闭卵圆孔内的血栓,并在血栓可能导致动脉栓塞之前将其移除。病例介绍:一名24岁女性因胸痛和呼吸困难入院。通过计算机断层扫描诊断肺栓塞。此外,经食管超声心动图显示血栓位于卵圆孔未闭内,双心房颤动,诊断为IPDE。为了避免溶栓治疗带来的栓塞风险,我们选择在体外循环下切除嵌顿血栓并关闭卵圆孔未闭。结论:我们成功地在动脉血栓形成之前通过体外循环去除血栓治疗了一例IPDE。
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引用次数: 0
Surgical management for catheter-induced pulmonary artery injury during cardiac surgery: a case report. 心脏手术中导管性肺动脉损伤的外科处理:1例报告。
IF 0.1 Pub Date : 2025-10-21 DOI: 10.1186/s44215-025-00227-0
Harunobu Sasanuma, Masaaki Nagano, Mamoru Muto, Tatsuo Maeyashiki, Nobuyuki Inoue, Satoshi Nagasaka

Background: A pulmonary artery catheter (PAC) is widely used to manage various health conditions during cardiac surgery. However, it can cause rare but life-threatening complications such as pulmonary artery injury. Although surgical treatment is often required for pulmonary artery injury caused by a PAC, detailed reports of the surgical management of this complication are lacking. We present a case of PAC-induced pulmonary artery injury that occurred during cardiac surgery and was successfully managed with surgical treatment without pulmonary resection.

Case presentation: A 76-year-old woman with severe heart valve disease underwent replacement of the aortic and mitral valves and surgical repair of the tricuspid valve using a PAC. Massive bleeding into the airway occurred during withdrawal from cardiopulmonary bypass. Fluoroscopic contrast injection through the PAC identified a PAC-induced tear in the left pulmonary artery as the cause of the bleeding. Opening of the left fourth intercostal space was performed without changing the supine position of the patient. Bleeding was successfully controlled by ligating the damaged branch of the pulmonary artery (A6c) and suturing the roots of the peripheral pulmonary arteries (A9 and A10) without performing lung resection. The patient recovered without complications and was discharged in good condition.

Conclusions: Although PAC-induced pulmonary artery injury is associated with a high mortality rate, the patient survived cardiac surgery with lung preservation in the supine position.

背景:肺动脉导管(PAC)被广泛应用于心脏手术期间的各种健康状况。然而,它会引起罕见但危及生命的并发症,如肺动脉损伤。虽然PAC引起的肺动脉损伤通常需要手术治疗,但缺乏这种并发症的手术治疗的详细报告。我们报告了一例在心脏手术中发生的pac引起的肺动脉损伤,并成功地通过手术治疗而不切除肺。病例介绍:一名患有严重心脏瓣膜疾病的76岁女性接受了主动脉瓣和二尖瓣的置换术和三尖瓣的手术修复,在体外循环退出时发生了大量的气道出血。通过PAC的透视造影剂注射确定PAC引起的左肺动脉撕裂是出血的原因。在不改变患者仰卧位的情况下开放左侧第四肋间隙。在不切除肺的情况下,结扎受损肺动脉分支(A6c),缝合周围肺动脉根(A9和A10),成功地控制了出血。患者康复无并发症,出院情况良好。结论:尽管pac引起的肺动脉损伤与高死亡率相关,但患者在仰卧位下保留肺存活。
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引用次数: 0
Fatal outcome after self-expanding transcatheter aortic valve replacement of the bicuspid valve due to infolding: a case report. 自扩张经导管主动脉瓣置换术后因二尖瓣内折导致的死亡结果:1例报告。
IF 0.1 Pub Date : 2025-10-14 DOI: 10.1186/s44215-025-00224-3
Nagi Hayashi, Junji Yunoki, Keijiro Shigetomi, Kouhei Baba, Masahide Shichijo, Koki Jinnouchi, Hiroyuki Morokuma, Manabu Itoh, Keiji Kamohara

Background: Infolding is a rare but potentially life-threatening complication of self-expanding transcatheter aortic valve replacement (TAVR).

Case presentation: We describe the case of an 80-year-old man who was referred for the treatment of severe aortic stenosis complicated by heart failure. Transthoracic echocardiography revealed the following: peak velocity, 6.1 m/s; mean pressure gradient, 102 mmHg; and aortic valve area, 0.26 cm2. Computed tomography (CT) showed a bicuspid aortic valve with a R-L raphe, an annular area of 529 mm2, and a perimeter of 83.4 mm. Considering the patient's severe emphysema, transfemoral TAVR was performed with the patient under deep sedation. A 34-mm Evolut FX valve was implanted after predilation with a 20-mm Inoue balloon. During deployment up to the point of no recapture, hypotension occurred without improvement, and mild infolding was suspected. However, full deployment was performed, as valve optimization was considered likely to stabilize hemodynamics. Post-deployment balloon dilation was performed; however, valve under-expansion and moderate aortic regurgitation persisted. Initial hemodynamics were stabilized; however, the patient gradually developed respiratory distress. Follow-up CT confirmed substantial valve infolding. Pulmonary hypertension, alveolar hemorrhage, and disseminated intravascular coagulation developed. Surgical aortic valve replacement with a 21-mm valve was performed 15 days post-TAVR. The explanted TAVR valve exhibited marked structural deformation. Although the patient's circulatory status improved postoperatively, he died of respiratory failure due to pneumonia.

Conclusion: This case highlights the importance of comprehensive preoperative anatomical assessment and intraoperative decision making in high-risk patients, particularly those with bicuspid valves. Valve selection (considering the valve type and size) must be meticulously tailored to the anatomical features surrounding the annulus. In addition, upon its recognition, substantial infolding should be promptly addressed by recapturing the valve, adjusting the valve size, or redeploying the valve with additional balloon aortic valvuloplasty.

背景:内折叠是经导管自我扩张主动脉瓣置换术(TAVR)中一种罕见但可能危及生命的并发症。病例介绍:我们描述的情况下,一个80岁的男子谁是转诊治疗严重主动脉瓣狭窄合并心力衰竭。经胸超声心动图显示:峰值速度6.1 m/s;平均压力梯度102 mmHg;主动脉瓣面积,0.26平方厘米。计算机断层扫描(CT)显示二尖瓣主动脉瓣呈R-L切面,环形面积529mm2,周长83.4 mm。考虑到患者严重的肺气肿,在患者深度镇静的情况下进行经股TAVR。20mm的Inoue球囊预扩张后植入34mm Evolut FX瓣膜。在部署期间,没有再发作,低血压没有改善,并怀疑轻度内折叠。然而,由于瓣膜优化可能稳定血流动力学,因此进行了全部署。部署后进行球囊扩张;然而,瓣膜扩张不足和中度主动脉反流持续存在。初始血流动力学稳定;然而,患者逐渐出现呼吸窘迫。随访CT证实大量瓣膜内折。并发肺动脉高压、肺泡出血和弥散性血管内凝血。tavr术后15天行21毫米主动脉瓣置换术。移植后的TAVR瓣膜出现明显的结构变形。虽然术后患者的循环状况有所改善,但他死于肺炎引起的呼吸衰竭。结论:本病例强调了高危患者术前解剖评估和术中决策的重要性,特别是双尖瓣患者。瓣膜的选择(考虑瓣膜的类型和尺寸)必须根据环周围的解剖特征精心定制。此外,一旦发现,应立即通过重新捕获瓣膜,调整瓣膜大小或通过额外的球囊主动脉瓣成形术重新放置瓣膜来解决严重的内折叠。
{"title":"Fatal outcome after self-expanding transcatheter aortic valve replacement of the bicuspid valve due to infolding: a case report.","authors":"Nagi Hayashi, Junji Yunoki, Keijiro Shigetomi, Kouhei Baba, Masahide Shichijo, Koki Jinnouchi, Hiroyuki Morokuma, Manabu Itoh, Keiji Kamohara","doi":"10.1186/s44215-025-00224-3","DOIUrl":"10.1186/s44215-025-00224-3","url":null,"abstract":"<p><strong>Background: </strong>Infolding is a rare but potentially life-threatening complication of self-expanding transcatheter aortic valve replacement (TAVR).</p><p><strong>Case presentation: </strong>We describe the case of an 80-year-old man who was referred for the treatment of severe aortic stenosis complicated by heart failure. Transthoracic echocardiography revealed the following: peak velocity, 6.1 m/s; mean pressure gradient, 102 mmHg; and aortic valve area, 0.26 cm<sup>2</sup>. Computed tomography (CT) showed a bicuspid aortic valve with a R-L raphe, an annular area of 529 mm<sup>2</sup>, and a perimeter of 83.4 mm. Considering the patient's severe emphysema, transfemoral TAVR was performed with the patient under deep sedation. A 34-mm Evolut FX valve was implanted after predilation with a 20-mm Inoue balloon. During deployment up to the point of no recapture, hypotension occurred without improvement, and mild infolding was suspected. However, full deployment was performed, as valve optimization was considered likely to stabilize hemodynamics. Post-deployment balloon dilation was performed; however, valve under-expansion and moderate aortic regurgitation persisted. Initial hemodynamics were stabilized; however, the patient gradually developed respiratory distress. Follow-up CT confirmed substantial valve infolding. Pulmonary hypertension, alveolar hemorrhage, and disseminated intravascular coagulation developed. Surgical aortic valve replacement with a 21-mm valve was performed 15 days post-TAVR. The explanted TAVR valve exhibited marked structural deformation. Although the patient's circulatory status improved postoperatively, he died of respiratory failure due to pneumonia.</p><p><strong>Conclusion: </strong>This case highlights the importance of comprehensive preoperative anatomical assessment and intraoperative decision making in high-risk patients, particularly those with bicuspid valves. Valve selection (considering the valve type and size) must be meticulously tailored to the anatomical features surrounding the annulus. In addition, upon its recognition, substantial infolding should be promptly addressed by recapturing the valve, adjusting the valve size, or redeploying the valve with additional balloon aortic valvuloplasty.</p>","PeriodicalId":520286,"journal":{"name":"General Thoracic and Cardiovascular Surgery Cases","volume":"4 1","pages":"39"},"PeriodicalIF":0.1,"publicationDate":"2025-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12522575/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145294900","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
Unanticipated stenosis of the distal edge of frozen elephant trunk caused by retrograde perfusion: A case report. 逆行灌注致冷冻象鼻远端意外狭窄1例。
IF 0.1 Pub Date : 2025-10-14 DOI: 10.1186/s44215-025-00223-4
Taiki Niki, Jiro Esaki

Background: Total arch replacement with frozen elephant trunk (FET) has been reported to be associated with favorable aortic remodeling when used for aortic dissection. However, several complications associated with FET have been reported, including distal stent graft-induced new entry (dSINE), which potentially results in aortic rupture and late mortality. Frozenix Partial ET (Japan Lifeline Inc., Tokyo, Japan) is a unique FET device that has a non-stent zone at the distal 2 cm end to decrease the radial force to lower the incidence of dSINE. Owing to its novelty, there are few preceding literatures regarding its efficacy and complications. In this report, we present a case of an unanticipated complication arising from the use of Frozenix Partial ET subsequent to the initiation of extracorporeal membrane oxygenation (ECMO).

Case presentation: A 54-year-old male diagnosed with Stanford type A acute aortic dissection underwent emergency total aortic arch replacement, frozen elephant trunk with Frozenix partial ET (Japan Lifeline Inc., Tokyo, Japan), the Bentall procedure, and coronary artery bypass grafting. The patient developed cardiogenic shock, requiring extracorporeal membrane oxygenation with left common femoral artery and vein cannulation on postoperative day 1. Despite adequate ECMO flow, high doses of catecholamines were required to maintain blood pressure measured at the right radial artery. Transesophageal echocardiography revealed stenosis of the distal part of the FET presumably due to retrograde perfusion from the femoral artery. The addition of left axillary artery cannulation improved systemic circulation, reducing the dose of catecholamine.

Conclusion: Although designed to reduce the risk of dSINE, Frozenix Partial ET may induce unforeseen complications. Particularly, its non-stent distal part can become stenotic under conditions of retrograde perfusion. Surgeons should carefully choose where to cannulate in patients with this device requiring redo surgery or ECMO support.

背景:冷冻象鼻全弓置换术(FET)被报道用于主动脉夹层时有利于主动脉重塑。然而,一些与FET相关的并发症已被报道,包括远端支架移植诱导的新进入(dsin),这可能导致主动脉破裂和晚期死亡。Frozenix Partial ET (Japan Lifeline Inc., Tokyo, Japan)是一种独特的FET装置,在远端2cm处有一个非支架区域,以减少径向力,降低dsin的发生率。由于其新颖性,关于其疗效和并发症的文献很少。在这个报告中,我们提出了一个意外并发症的情况下,使用Frozenix部分ET后,开始体外膜氧合(ECMO)。病例介绍:一名54岁男性,诊断为Stanford A型急性主动脉夹层,接受了紧急全主动脉弓置换术、冷冻象鼻与Frozenix部分ET(日本生命线公司,东京,日本)、Bentall手术和冠状动脉旁路移植术。患者发生心源性休克,术后第1天需要体外膜氧合并左股总动脉和静脉插管。尽管有足够的ECMO流量,仍然需要大剂量的儿茶酚胺来维持右桡动脉的血压。经食管超声心动图显示FET远端狭窄,可能是由于股动脉逆行灌注所致。左腋窝动脉插管改善体循环,减少儿茶酚胺剂量。结论:虽然旨在降低dsin的风险,但Frozenix部分ET可能会引起不可预见的并发症。特别是在逆行灌注的情况下,其非支架远端部分可能变得狭窄。对于需要重做手术或ECMO支持的患者,外科医生应仔细选择插管位置。
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引用次数: 0
Delayed aortic injury following multiple rib fractures: a case report. 多发肋骨骨折后迟发性主动脉损伤1例。
IF 0.1 Pub Date : 2025-10-14 DOI: 10.1186/s44215-025-00225-2
Kei Nakano, Tomohiko Matsuzaki, Shota Fujino, Masaya Ohara, Takashi Ishihara, Kazuhiro Matsuo, Tomoki Higeta, Kie Maita, Hiroto Onozawa, Takaaki Tsuboi, Atsushi Wada, Naohiro Aruga, Tomoki Nakagawa, Ryota Masuda

Background: Delayed hemothorax due to aortic injury is rare, and its delayed diagnosis can be fatal. Herein, we report a case of delayed hemothorax owing to aortic injury following blunt chest trauma, which was successfully treated through emergency surgery.

Case presentation: A woman in her 70s fell on an escalator at a train station and was brought to our emergency department. Initial evaluation with computed tomography (CT) imaging revealed a thoracic vertebral fracture, bilateral lower rib fractures, and a right-sided hemothorax. She was admitted for observation and supportive care, and her condition remained stable for days. On day 9 of hospitalization, the patient suddenly experienced cardiac arrest. A plain chest X-ray showed a massive pleural effusion on the left side, prompting the insertion of a chest tube. The drainage was hemorrhagic, and laboratory tests showed a significant decline in the hemoglobin level to 4.9 g/dL. Following successful cardiopulmonary resuscitation and the return of spontaneous circulation, a contrast-enhanced CT scan of the chest was performed. However, no active extravasation or apparent source of bleeding was observed. Owing to ongoing hemodynamic instability and the substantial volume of hemothorax, emergency surgery was conducted to identify and control the source of hemorrhage. Intraoperatively, after evacuating a large hematoma from the left thoracic cavity, a small ulcerated hole was identified in the descending thoracic aorta, which appeared tortuous. Pulsatile bleeding was observed from this site. Manual compression was applied to achieve temporary homeostasis. Intraoperative ultrasound showed no evidence of aortic dissection. The bleeding site was sutured directly, and hemostasis was achieved. No additional significant intrathoracic injuries were identified. The aortic injury had resulted from mechanical irritation or penetration by the adjacent fractured lower rib. This represented a case of delayed hemothorax secondary to traumatic aortic injury, a rare but potentially fatal complication.

Conclusions: In cases of delayed hemothorax following blunt thoracic trauma-particularly with fractures of the lower left posterior ribs, clinicians should maintain a high index of suspicion for aortic injury. Prompt recognition and surgical intervention are critical for patient survival in such cases.

背景:主动脉损伤引起的迟发性血胸是罕见的,其延误诊断可能是致命的。在此,我们报告一例钝性胸外伤后主动脉损伤导致的迟发性血胸,并通过紧急手术成功治疗。病例介绍:一名70多岁的妇女在火车站的自动扶梯上摔倒,被送到急诊科。计算机断层扫描(CT)的初步评估显示胸部椎体骨折,双侧下肋骨骨折和右侧血胸。她入院接受观察和支持性护理,几天来病情保持稳定。住院第9天,患者突然出现心脏骤停。胸部x光平片显示左侧有大量胸腔积液,需要插入胸管。引流液出血性,实验室检查显示血红蛋白水平显著下降至4.9 g/dL。在心肺复苏成功并恢复自主循环后,进行了胸部CT增强扫描。然而,没有观察到活动性外渗或明显的出血来源。由于持续的血流动力学不稳定和大量血胸,急诊手术以确定和控制出血的来源。术中,从左胸腔排出大血肿后,发现胸降主动脉有一个小的溃疡洞,呈弯曲状。在该部位观察到搏动性出血。手动压缩以达到暂时的内稳态。术中超声未见主动脉夹层。直接缝合出血部位,完成止血。未发现其他明显的胸内损伤。主动脉损伤是由于机械刺激或邻近的下肋骨骨折穿透造成的。这是一例继发于外伤性主动脉损伤的迟发性血胸,这是一种罕见但可能致命的并发症。结论:对于钝性胸外伤后迟发性血胸,特别是左下后肋骨骨折,临床医生应高度怀疑主动脉损伤。在这种情况下,及时识别和手术干预对患者的生存至关重要。
{"title":"Delayed aortic injury following multiple rib fractures: a case report.","authors":"Kei Nakano, Tomohiko Matsuzaki, Shota Fujino, Masaya Ohara, Takashi Ishihara, Kazuhiro Matsuo, Tomoki Higeta, Kie Maita, Hiroto Onozawa, Takaaki Tsuboi, Atsushi Wada, Naohiro Aruga, Tomoki Nakagawa, Ryota Masuda","doi":"10.1186/s44215-025-00225-2","DOIUrl":"10.1186/s44215-025-00225-2","url":null,"abstract":"<p><strong>Background: </strong>Delayed hemothorax due to aortic injury is rare, and its delayed diagnosis can be fatal. Herein, we report a case of delayed hemothorax owing to aortic injury following blunt chest trauma, which was successfully treated through emergency surgery.</p><p><strong>Case presentation: </strong>A woman in her 70s fell on an escalator at a train station and was brought to our emergency department. Initial evaluation with computed tomography (CT) imaging revealed a thoracic vertebral fracture, bilateral lower rib fractures, and a right-sided hemothorax. She was admitted for observation and supportive care, and her condition remained stable for days. On day 9 of hospitalization, the patient suddenly experienced cardiac arrest. A plain chest X-ray showed a massive pleural effusion on the left side, prompting the insertion of a chest tube. The drainage was hemorrhagic, and laboratory tests showed a significant decline in the hemoglobin level to 4.9 g/dL. Following successful cardiopulmonary resuscitation and the return of spontaneous circulation, a contrast-enhanced CT scan of the chest was performed. However, no active extravasation or apparent source of bleeding was observed. Owing to ongoing hemodynamic instability and the substantial volume of hemothorax, emergency surgery was conducted to identify and control the source of hemorrhage. Intraoperatively, after evacuating a large hematoma from the left thoracic cavity, a small ulcerated hole was identified in the descending thoracic aorta, which appeared tortuous. Pulsatile bleeding was observed from this site. Manual compression was applied to achieve temporary homeostasis. Intraoperative ultrasound showed no evidence of aortic dissection. The bleeding site was sutured directly, and hemostasis was achieved. No additional significant intrathoracic injuries were identified. The aortic injury had resulted from mechanical irritation or penetration by the adjacent fractured lower rib. This represented a case of delayed hemothorax secondary to traumatic aortic injury, a rare but potentially fatal complication.</p><p><strong>Conclusions: </strong>In cases of delayed hemothorax following blunt thoracic trauma-particularly with fractures of the lower left posterior ribs, clinicians should maintain a high index of suspicion for aortic injury. Prompt recognition and surgical intervention are critical for patient survival in such cases.</p>","PeriodicalId":520286,"journal":{"name":"General Thoracic and Cardiovascular Surgery Cases","volume":"4 1","pages":"42"},"PeriodicalIF":0.1,"publicationDate":"2025-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12522982/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145294876","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
Complete thoracoscopic resection for TXN2aM0 primary lung cancer: a case series with 5-year follow-up. TXN2aM0型原发性肺癌全胸腔镜切除5年随访1例
IF 0.1 Pub Date : 2025-10-14 DOI: 10.1186/s44215-025-00228-z
Daiki Yoshikawa, Takeshi Kawaguchi, Ryo Miyata, Keiji Yamanashi, Maiko Takeda, Akihiko Yoshizawa, Takao Osa, Kazuya Tanimura, Shigeto Hontsu, Shigeo Muro, Sachiko Miura, Mitsuharu Hosono, Masatsugu Hamaji

Management of resectable TXN2aM0 primary lung cancer is controversial, and data regarding the long-term outcomes and guideline recommendations for such cases are lacking. We present the characteristics and long-term outcomes of four patients who underwent complete thoracoscopic resection of TXN2aM0 primary lung cancer. All patients experienced an uneventful postoperative course and survived for 5 to 10 years postoperatively; however, one patient experienced local recurrence at 2 years postoperatively and one patient experienced local recurrence at 5 years postoperatively. Our limited experience suggested that long-term survival may be achieved with complete resection of TXN2aM0; however, late recurrence and local recurrence are possible.

可切除的TXN2aM0原发性肺癌的治疗是有争议的,并且缺乏关于此类病例的长期结果和指南建议的数据。我们报告了4例接受胸腔镜完全切除TXN2aM0原发性肺癌的患者的特点和长期预后。所有患者均经历了平稳的术后过程,术后存活5至10年;然而,1例患者术后2年出现局部复发,1例患者术后5年出现局部复发。我们有限的经验表明,完全切除TXN2aM0可以实现长期生存;然而,晚期复发和局部复发是可能的。
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引用次数: 0
Successful Commando procedure using the superior transseptal approach in a high-risk case. 在高危病例中成功使用上隔入路行突击手术。
IF 0.1 Pub Date : 2025-09-02 DOI: 10.1186/s44215-025-00220-7
Hiroki Moriuchi, Mamoru Orii, Takayuki Fujii, Kohei Narayama, Nobuhiro Shimabukuro, Akihiko Yamauchi

Background: The Commando procedure, which involves replacement of both the aortic and mitral valves along with reconstruction of the intervalvular fibrous body, is technically demanding. Commando procedure typically performed via an incision extending from the ascending aorta to the roof of the left atrium. However, in patients with extensive adhesions due to prior cardiac surgery, adding a superior transseptal incision can provide good exposure and reduce the risk of surrounding tissue injury.

Case presentation: A 48-year-old woman with end-stage kidney disease on dialysis, diabetes mellitus, bilateral leg amputations from critical limb ischemia, and chronic steroid use presented in cardiogenic and septic shock. The patient had undergone mitral valve repair and coronary bypass surgery using saphenous vein grafts. Echocardiography revealed severe aortic and mitral valves stenosis. Given the extensive adhesions and complex anatomy, the Commando procedure was performed using a superior transseptal approach. A 25-mm MITRIS was implanted in the mitral position, and a 25-mm INSPIRIS in the aortic position. A tailored oval-shaped patch made of bovine pericardium was used to reconstruct the intervalvular fibrous body. The patient recovered without major complications.

Conclusion: The superior transseptal approach provided excellent exposure and a stable operative field, facilitating standardized surgical maneuvers throughout the Commando procedure.

背景:Commando手术包括主动脉瓣和二尖瓣的置换以及瓣间纤维体的重建,在技术上要求很高。突击手术通常通过从升主动脉延伸到左心房顶部的切口进行。然而,对于先前心脏手术导致广泛粘连的患者,增加上隔切口可以提供良好的暴露,降低周围组织损伤的风险。病例介绍:一名48岁女性,终末期肾病透析,糖尿病,严重肢体缺血导致双侧腿截肢,慢性使用类固醇,表现为心源性和感染性休克。患者接受了二尖瓣修复和隐静脉移植冠状动脉搭桥手术。超声心动图显示主动脉瓣和二尖瓣严重狭窄。鉴于广泛的粘连和复杂的解剖结构,突击队手术采用上隔入路进行。在二尖瓣位置植入25mm MITRIS,在主动脉位置植入25mm INSPIRIS。用牛心包订制的椭圆形补片重建瓣间纤维体。病人康复后无重大并发症。结论:上隔入路提供了良好的暴露和稳定的手术视野,促进了整个突击队手术过程中标准化的手术操作。
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引用次数: 0
Primary pulmonary artery sarcoma treated with simultaneous pulmonary valve replacement, artificial vessel replacement, and total right pneumonectomy: a case report. 同时行肺动脉瓣置换术、人工血管置换术及右全肺切除术治疗原发性肺动脉肉瘤1例。
IF 0.1 Pub Date : 2025-08-27 DOI: 10.1186/s44215-025-00221-6
Kento Fujii, Hideki Morita, Hiroshi Nagano, Hiroyuki Kawaura, Hidetaka Kariya, Minoru Kowada, Takehiro Shirasugi

Background: Primary pulmonary artery sarcoma progresses extremely rapidly and has a poor prognosis. This condition is managed with surgical resection and multimodality therapy. However, standardized treatment is not available.

Case presentation: A 54-year-old woman was brought to the emergency department because of chest pain and worsening dyspnea that had developed in the past month. Contrast-enhanced computed tomography scan revealed severe stenosis extending from the pulmonary artery trunk to the right pulmonary artery due to an embolic substance. Because primary pulmonary artery sarcoma was suspected, emergency surgery was performed to improve the patient's symptoms. In addition to maximal tumor resection, pulmonary artery valve replacement, artificial vessel replacement, and right total pneumonectomy were performed. Based on the assessment performed using the specimen collected perioperatively, a pathological diagnosis of angiosarcoma of the right pulmonary artery was made. The patient was discharged on postoperative day 17 with a good postoperative course. However, because of dyspnea, she was readmitted to the hospital on day 85. Tumor recurrence was noted, and chemotherapy was initiated. The patient developed cardiac failure and died on postoperative day 119. A pathological postmortem examination was performed. Metastatic lesions were found in the pericardial sac, left lung, right chest wall and pleura, and mediastinum.

Conclusions: In the present case, postoperative recurrence was observed despite maximal resection of the surrounding tissues with tumor invasion and simultaneous reconstruction. Chemotherapy was initiated but was ineffective. Gene panel testing can help identify novel treatment options for patients with neoplastic diseases without standardized treatment. In addition, preparations should be made before surgery.

背景:原发性肺动脉肉瘤进展极快,预后差。这种情况是通过手术切除和综合治疗来处理的。然而,目前还没有标准化的治疗方法。病例介绍:一名54岁女性因过去一个月出现的胸痛和呼吸困难加重而被送到急诊科。增强计算机断层扫描显示,由于栓塞物质,从肺动脉干延伸到右肺动脉严重狭窄。由于怀疑为原发性肺动脉肉瘤,急诊手术以改善患者症状。除最大肿瘤切除外,还行肺动脉瓣置换术、人工血管置换术和右侧全肺切除术。根据围手术期标本的评估,病理诊断为右肺血管肉瘤。患者术后第17天出院,术后病程良好。然而,由于呼吸困难,她于第85天再次入院。发现肿瘤复发,开始化疗。患者发生心力衰竭,于术后第119天死亡。进行病理尸检。转移病灶见于心包囊、左肺、右胸壁、胸膜和纵隔。结论:在本病例中,尽管对肿瘤浸润的周围组织进行了最大程度的切除并同时进行了重建,但术后仍出现复发。开始化疗,但无效。基因面板测试可以帮助没有标准化治疗的肿瘤疾病患者确定新的治疗方案。此外,术前应做好准备工作。
{"title":"Primary pulmonary artery sarcoma treated with simultaneous pulmonary valve replacement, artificial vessel replacement, and total right pneumonectomy: a case report.","authors":"Kento Fujii, Hideki Morita, Hiroshi Nagano, Hiroyuki Kawaura, Hidetaka Kariya, Minoru Kowada, Takehiro Shirasugi","doi":"10.1186/s44215-025-00221-6","DOIUrl":"10.1186/s44215-025-00221-6","url":null,"abstract":"<p><strong>Background: </strong>Primary pulmonary artery sarcoma progresses extremely rapidly and has a poor prognosis. This condition is managed with surgical resection and multimodality therapy. However, standardized treatment is not available.</p><p><strong>Case presentation: </strong>A 54-year-old woman was brought to the emergency department because of chest pain and worsening dyspnea that had developed in the past month. Contrast-enhanced computed tomography scan revealed severe stenosis extending from the pulmonary artery trunk to the right pulmonary artery due to an embolic substance. Because primary pulmonary artery sarcoma was suspected, emergency surgery was performed to improve the patient's symptoms. In addition to maximal tumor resection, pulmonary artery valve replacement, artificial vessel replacement, and right total pneumonectomy were performed. Based on the assessment performed using the specimen collected perioperatively, a pathological diagnosis of angiosarcoma of the right pulmonary artery was made. The patient was discharged on postoperative day 17 with a good postoperative course. However, because of dyspnea, she was readmitted to the hospital on day 85. Tumor recurrence was noted, and chemotherapy was initiated. The patient developed cardiac failure and died on postoperative day 119. A pathological postmortem examination was performed. Metastatic lesions were found in the pericardial sac, left lung, right chest wall and pleura, and mediastinum.</p><p><strong>Conclusions: </strong>In the present case, postoperative recurrence was observed despite maximal resection of the surrounding tissues with tumor invasion and simultaneous reconstruction. Chemotherapy was initiated but was ineffective. Gene panel testing can help identify novel treatment options for patients with neoplastic diseases without standardized treatment. In addition, preparations should be made before surgery.</p>","PeriodicalId":520286,"journal":{"name":"General Thoracic and Cardiovascular Surgery Cases","volume":"4 1","pages":"37"},"PeriodicalIF":0.1,"publicationDate":"2025-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12382254/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144985839","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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General Thoracic and Cardiovascular Surgery Cases
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