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A successful complete resection for multidrug-resistant giant gastrointestinal stromal tumor invading the transverse colon with multiple liver metastases in a young female: a case report. 一名年轻女性成功完全切除了侵犯横结肠并伴有多处肝转移的耐多药巨型胃肠道间质瘤:病例报告。
IF 0.8 Pub Date : 2024-06-14 DOI: 10.1186/s40792-024-01947-1
Kenta Aso, Nobuyuki Takemura, Yuhi Yoshizaki, Fuminori Mihara, Fuyuki Inagaki, Kazuhiko Yamada, Norihiro Kokudo

Background: Gastrointestinal stromal tumors (GISTs) are rare in young people and are often detected after becoming symptomatic or at an advanced stage. Herein, we report a case of complete reduction surgery for a substantially large malignant gastric GIST with multiple liver metastases in a young woman who successfully resulted in R0 surgery.

Case presentation: An 18-year-old woman presented to our hospital with anorexia and vomiting, and was diagnosed with a 17 cm gastric GIST with transverse colon invasion and multiple liver metastases. Due to being considered unresectable, tyrosine and multi-kinase inhibitor therapy were administered up to the fourth line yielding no response. After careful discussion at a multidisciplinary team conference, pancreatoduodenectomy or distal gastrectomy, transverse colectomy, and resection of the liver metastases were planned. Consequently, distal gastrectomy, transverse colectomy, resection of the liver metastases, and incidental peritoneal metastases were performed. Although the primary goal of the surgery was to reduce the volume of the tumor as much as possible, the results revealed that the complete removal of all detectable tumors was achieved. No recurrence was observed after surgery for 27 months with long-term adjuvant imatinib therapy.

Conclusions: Even for highly advanced GISTs, aggressive surgery followed by adjuvant drug therapy may prolong survival in young patients.

背景:胃肠道间质瘤(GIST)在年轻人中非常罕见,通常在出现症状或晚期才被发现。在此,我们报告了一例为一名年轻女性实施的完全减瘤手术,该女性患有伴有多发性肝转移的巨大恶性胃间质瘤,并成功实现了 R0 手术:一名 18 岁女性因厌食和呕吐来我院就诊,被诊断为 17 厘米胃 GIST,伴横结肠侵犯和多发性肝转移。由于被认为无法切除,她接受了酪氨酸和多激酶抑制剂治疗,直至第四线治疗,均无反应。经过多学科团队会议的仔细讨论,计划进行胰十二指肠切除术或远端胃切除术、横结肠切除术和肝转移灶切除术。最终,患者接受了远端胃切除术、横结肠切除术、肝转移灶切除术和腹膜转移灶切除术。虽然手术的主要目的是尽可能缩小肿瘤体积,但结果显示,所有可检测到的肿瘤都被完全切除。术后接受伊马替尼长期辅助治疗27个月未见复发:结论:即使是晚期GIST,积极的手术治疗和辅助药物治疗也能延长年轻患者的生存期。
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引用次数: 0
Appendiceal neoplasms derived from appendiceal tip remnants following appendectomy: a report of two cases. 阑尾切除术后阑尾尖端残留物引发的阑尾肿瘤:两例报告。
IF 0.8 Pub Date : 2024-06-13 DOI: 10.1186/s40792-024-01936-4
Yusuke Fujii, Koya Hida, Akihiko Sugimoto, Ryohei Nishijima, Masakazu Fujimoto, Nobuaki Hoshino, Hisatsugu Maekawa, Ryosuke Okamura, Yoshiro Itatani, Kazutaka Obama

Background: Neoplasms derived from remnant appendix are rarely described, with most cases arising from the appendiceal "stump". Here, we present two surgical cases of appendiceal neoplasms derived from appendiceal "tip" remnants.

Case presentation: The first patient was a 71-year-old man who had undergone laparoscopic appendectomy for acute appendicitis 12 years prior. During appendectomy, the appendiceal root was ligated, but the appendix was not completely removed due to severe inflammation. At the most recent presentation, computed tomography (CT) was performed to examine choledocholithiasis, which incidentally revealed a cystic lesion of approximately 90 mm adjacent to the cecum. A retrospective review revealed that the cystic lesion had increased in size over time, and laparoscopic ileocecal resection was performed. Pathology revealed no continuity from the appendiceal orifice to the cyst, and a diagnosis of low-grade appendiceal mucinous neoplasm (LAMN) was made from the appendiceal tip remnant. The patient was discharged without complications. The second patient was a 65-year-old man who had undergone surgery for peritonitis due to severe appendicitis 21 years prior. During this operation, the appendix could not be clearly identified due to severe inflammation; consequently, cecal resection was performed. He was referred to our department with a chief complaint of general fatigue and loss of appetite and a cystic lesion of approximately 85 mm close to the cecum that had increased over time. CT showed irregular wall thickening, and malignancy could not be ruled out; therefore, laparoscopic ileocecal resection with D3 lymph node dissection was performed. The pathological diagnosis revealed mucinous adenocarcinoma (TXN0M0) arising from the remnant appendiceal tip. The patient is undergoing follow-up without postoperative adjuvant chemotherapy, with no evidence of pseudomyxoma peritonei or cancer recurrence for 32 months postoperatively.

Conclusions: If appendicitis-associated inflammation is sufficiently severe that accurate identification of the appendix is difficult, it may remain on the apical side of the appendix, even if the root of the appendix is ligated and removed. If the appendectomy is terminated incompletely, it is necessary to check for the presence of a residual appendix postoperatively and provide appropriate follow-up.

背景:由阑尾残端引起的肿瘤很少见,大多数病例都是由阑尾 "残端 "引起的。在此,我们介绍两例由阑尾 "蒂部 "残留物引发阑尾肿瘤的手术病例:第一例患者是一名 71 岁的男性,12 年前曾因急性阑尾炎接受腹腔镜阑尾切除术。阑尾切除术中结扎了阑尾根部,但由于炎症严重,阑尾没有完全切除。最近一次就诊时,患者接受了计算机断层扫描(CT)检查胆总管结石,结果意外发现盲肠附近有一个约 90 毫米的囊性病变。回顾性复查显示,随着时间的推移,囊性病变的体积不断增大,于是进行了腹腔镜回盲肠切除术。病理结果显示,阑尾口与囊肿之间没有连续性,根据阑尾顶端残留物诊断为低级别阑尾粘液瘤(LAMN)。患者出院后未出现并发症。第二名患者是一名 65 岁的男性,21 年前曾因严重阑尾炎导致腹膜炎而接受过手术。在这次手术中,由于炎症严重,阑尾无法清晰辨认,因此进行了盲肠切除术。他因主诉全身乏力、食欲不振以及盲肠附近有一个约 85 毫米的囊性病变并随着时间推移而增大而被转到我科。CT 显示肠壁不规则增厚,无法排除恶性肿瘤的可能性,因此,我们为他实施了腹腔镜回盲部切除术,并进行了 D3 淋巴结清扫。病理诊断显示,残余阑尾顶端发生粘液腺癌(TXN0M0)。患者目前正在接受随访,术后未进行辅助化疗,术后 32 个月未发现假性腹膜瘤或癌症复发的迹象:结论:如果阑尾炎相关炎症严重到难以准确识别阑尾,即使结扎并切除阑尾根部,阑尾仍可能残留在阑尾顶端一侧。如果阑尾切除术未完全结束,则有必要在术后检查是否存在残留阑尾,并提供适当的随访。
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引用次数: 0
Minimally invasive elective gastrectomy after preoperative chemotherapy in a patient with frailty who presented with locally far advanced-stage gastric cancer: a case report. 一名局部远期胃癌患者在接受术前化疗后进行微创择期胃切除术:病例报告。
IF 0.8 Pub Date : 2024-06-13 DOI: 10.1186/s40792-024-01942-6
Naoto Shirakami, Shingo Kanaji, Atsushi Shimada, Tomosuke Mukoyama, Ryuichiro Sawada, Hitoshi Harada, Tomonori Tanaka, Naoki Urakawa, Hironobu Goto, Hiroshi Hasegawa, Kimihiro Yamashita, Takeru Matsuda, Yoshihiro Kakeji

Background: Herein, we report a case of gastric antrum cancer with multiple invasions to other organs that was completely cured with laparoscopic distal gastrectomy after preoperative chemotherapy in a patient with poor general condition.

Case presentation: An 80-year-old male patient was diagnosed with anemia during follow-up for cerebral lacunar infarction at another hospital. He was diagnosed with advanced-stage gastric antrum cancer and was referred to our hospital. On esophagogastroduodenoscopy, type 2 advanced-stage gastric cancer was detected at the greater curvature of the antrum, and the biopsy results revealed tubular adenocarcinoma. Contrast-enhanced computed tomography scan revealed multiple invasions to other organs, thick gastric wall with contrast effect, and superior mesenteric vein tumor thrombus. However, there was no evidence of distant metastasis on positron emission tomography/computed tomography scan. The clinical diagnosis was stage IVA gastric cancer. Pancreatoduodenectomy with portal vein resection could be important at this point. However, preoperative chemotherapy with S-1 and oxaliplatin was administered instead of performing extended surgery because the patient had poor general condition (performance status score of 3). The patient received three cycles of preoperative chemotherapy at the hospital along with rehabilitation and nutritional management with oral nutritional supplements. After treatment, the performance status score of the patient improved from 3 to 1. Furthermore, in terms of clinical therapeutic effect, the patient achieved partial response. Hence, laparoscopic distal gastrectomy with D2 lymph node dissection and partial transverse colectomy was performed. After surgery, the patient was admitted for oral intake on postoperative day 6 and was discharged on postoperative day 21. Based on the histopathological examination, gastric cancer had disappeared, and there were no evident malignant findings. Therefore, gastric cancer was classified as grade 3 according to the histological treatment efficacy criteria. The patient did not present with recurrence at 2 years after surgery.

Conclusions: By actively administering preoperative chemotherapy, minimally invasive radical surgery with maximum preservation of the surrounding organs can be performed for locally far advanced-stage gastric cancer in older patients with poor general condition.

背景:在此,我们报告了一例全身状况不佳的胃癌患者,在术前化疗后,通过腹腔镜远端胃切除术完全治愈了伴有其他器官多发浸润的胃癌:一名 80 岁的男性患者在另一家医院接受脑腔隙性梗死随访时被诊断为贫血。他被诊断为晚期胃窦癌,并被转诊至我院。食管胃十二指肠镜检查发现胃窦大弯处有 2 型晚期胃癌,活检结果显示为管状腺癌。造影剂增强计算机断层扫描显示胃癌多处侵犯其他器官,胃壁厚且有造影剂效应,肠系膜上静脉有瘤栓。但是,正电子发射断层扫描/计算机断层扫描没有发现远处转移的迹象。临床诊断为 IVA 期胃癌。此时,胰十二指肠切除术和门静脉切除术可能很重要。然而,由于患者全身状况不佳(表现状态评分为 3 分),因此采用了 S-1 和奥沙利铂术前化疗,而不是进行扩大手术。患者在医院接受了三个周期的术前化疗,同时进行了康复治疗和口服营养补充剂的营养管理。治疗后,患者的表现状态评分从 3 分提高到了 1 分。此外,从临床治疗效果来看,患者获得了部分应答。因此,患者接受了腹腔镜远端胃切除术、D2淋巴结清扫术和部分横结肠切除术。术后,患者于术后第 6 天入院口服,并于术后第 21 天出院。根据组织病理学检查,胃癌已经消失,没有明显的恶性发现。因此,根据组织学疗效标准,胃癌被定为 3 级。患者术后两年未出现复发:结论:通过积极的术前化疗,微创根治术可以最大限度地保留周围器官,适用于全身状况较差的老年晚期胃癌患者。
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引用次数: 0
Repair of a right coronary artery rupture with perforated right ventricle following spontaneous pseudoaneurysm: a case report. 自发性假性动脉瘤导致右冠状动脉破裂并右心室穿孔的修复术:病例报告。
IF 0.8 Pub Date : 2024-06-12 DOI: 10.1186/s40792-024-01941-7
Masato Furui, Hitoshi Matsumura, Yoshio Hayashida, Go Kuwahara, Masayuki Shimizu, Yuichi Morita, Yuta Matsuoka, Chihaya Ito, Masato Hayama, Kayo Wakamatsu, Hideichi Wada

Background: Following the rupture of a coronary artery, a patient's condition usually deteriorates rapidly due to cardiac tamponade. A pseudoaneurysm due to a coronary artery rupture is rare; however, when a spontaneous coronary artery pseudoaneurysm occurs without tamponade, it creates a fistula in the right ventricle, often requiring surgical repair.

Case presentation: This report describes the case of a 68-year-old man who presented with chest discomfort after a 12-day course of antibiotic treatment for bacteremia. Following coronary angiography, echocardiography, and enhanced computed tomography, he was diagnosed with a right coronary artery pseudoaneurysm accompanied with perforation of the right ventricle. Severe adhesions were observed during emergency surgery surrounding the entire heart. The patient presented with risk factors for coronary artery disease, including hypertension and smoking history. His coronary artery was severely calcified due to end-stage renal failure requiring dialysis; thus, a covered stent could not fit inside the arterial lumen. Consequently, coronary artery bypass grafting to the right coronary artery and right ventricle repair were performed. Unfortunately, the patient died postoperatively due to sepsis from intestinal translocation. This rare development was hypothesized to be an incidental result of the combination of severe post-inflammatory adhesions, extensive coronary artery calcification, and rupture of the calcification crevices.

Conclusions: In the case of a severe post-inflammatory response, shock without cardiac tamponade may require further scrutiny by assuming the possibility of inward rupture. For patients in poor condition, two-stage surgical treatment might be considered after stabilization with a covered stent.

背景:冠状动脉破裂后,患者的病情通常会因心脏填塞而迅速恶化。冠状动脉破裂导致的假性动脉瘤非常罕见;但是,当自发性冠状动脉假性动脉瘤发生时,如果没有出现心肌填塞,就会在右心室形成瘘管,通常需要进行手术修补:本报告描述了一名 68 岁男性的病例,他在接受了为期 12 天的菌血症抗生素治疗后出现胸部不适。经过冠状动脉造影、超声心动图和增强型计算机断层扫描,他被诊断为右冠状动脉假性动脉瘤,并伴有右心室穿孔。紧急手术中发现整个心脏周围有严重粘连。患者具有冠状动脉疾病的危险因素,包括高血压和吸烟史。他的冠状动脉因终末期肾衰竭而严重钙化,需要进行透析治疗;因此,有盖支架无法放入动脉管腔内。因此,他接受了右冠状动脉搭桥术和右心室修补术。不幸的是,患者术后死于肠易位引起的败血症。据推测,这种罕见的病变是严重炎症后粘连、冠状动脉广泛钙化和钙化缝隙破裂共同作用的偶然结果:结论:在出现严重炎症后反应的情况下,没有心脏填塞的休克可能需要进一步检查,假设有向内破裂的可能性。对于病情较差的患者,在使用覆盖支架稳定病情后,可考虑两阶段手术治疗。
{"title":"Repair of a right coronary artery rupture with perforated right ventricle following spontaneous pseudoaneurysm: a case report.","authors":"Masato Furui, Hitoshi Matsumura, Yoshio Hayashida, Go Kuwahara, Masayuki Shimizu, Yuichi Morita, Yuta Matsuoka, Chihaya Ito, Masato Hayama, Kayo Wakamatsu, Hideichi Wada","doi":"10.1186/s40792-024-01941-7","DOIUrl":"10.1186/s40792-024-01941-7","url":null,"abstract":"<p><strong>Background: </strong>Following the rupture of a coronary artery, a patient's condition usually deteriorates rapidly due to cardiac tamponade. A pseudoaneurysm due to a coronary artery rupture is rare; however, when a spontaneous coronary artery pseudoaneurysm occurs without tamponade, it creates a fistula in the right ventricle, often requiring surgical repair.</p><p><strong>Case presentation: </strong>This report describes the case of a 68-year-old man who presented with chest discomfort after a 12-day course of antibiotic treatment for bacteremia. Following coronary angiography, echocardiography, and enhanced computed tomography, he was diagnosed with a right coronary artery pseudoaneurysm accompanied with perforation of the right ventricle. Severe adhesions were observed during emergency surgery surrounding the entire heart. The patient presented with risk factors for coronary artery disease, including hypertension and smoking history. His coronary artery was severely calcified due to end-stage renal failure requiring dialysis; thus, a covered stent could not fit inside the arterial lumen. Consequently, coronary artery bypass grafting to the right coronary artery and right ventricle repair were performed. Unfortunately, the patient died postoperatively due to sepsis from intestinal translocation. This rare development was hypothesized to be an incidental result of the combination of severe post-inflammatory adhesions, extensive coronary artery calcification, and rupture of the calcification crevices.</p><p><strong>Conclusions: </strong>In the case of a severe post-inflammatory response, shock without cardiac tamponade may require further scrutiny by assuming the possibility of inward rupture. For patients in poor condition, two-stage surgical treatment might be considered after stabilization with a covered stent.</p>","PeriodicalId":22096,"journal":{"name":"Surgical Case Reports","volume":null,"pages":null},"PeriodicalIF":0.8,"publicationDate":"2024-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11169172/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141306891","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
Migrated tubal sterilisation clip presenting as a subcutaneous gluteal foreign body 24 years later: a case report and literature review. 输卵管绝育夹移位 24 年后出现臀部皮下异物:病例报告和文献综述。
IF 0.8 Pub Date : 2024-06-12 DOI: 10.1186/s40792-024-01937-3
Adil S Lakha, Andrew Ang, Sarmad Mohammed Salih, Christopher Lewis

Background: The incidence of sterilisation clip migration is reportedly 25%. However, less than 1% of those who experience clip migration will present with pain, an abscess, or spontaneous extrusion. Here we present a rare case of sterilisation clip migration through the entire pelvic floor.

Case presentation: A 66-year-old female was referred from community to the Surgical Emergency Unit with a possible metallic foreign body under the skin following an attempted routine gluteal cyst excision. The patient first noticed a lump under the skin 2 years ago which gradually became more apparent and tender over the previous 2 months. The patient denied recent trauma, had no co-morbidities and had a sterilisation procedure 24 years prior. Examination revealed a non-mobile solid structure just beneath the skin 5 cm laterally from the anal verge. Inflammatory markers were normal and an ultrasound confirmed a 15 × 7 mm foreign body in the subcutaneous tissues. The foreign body was excised easily under local anaesthesia, revealing a closed Filshie sterilisation clip. The wound was closed primarily, and recovery was uncomplicated.

Conclusions: This was a case of sterilisation clip migration to the subcutaneous gluteal region. A literature review revealed 34 case reports of sterilisation clip migration, mostly to the bladder. Patients with a previous sterilisation procedure and suspected subcutaneous foreign body without trauma should elicit a high index of suspicion for migrated sterilisation clips. These clips can migrate through multiple layers of muscle and fascia, including the pelvic floor.

背景:据报道,绝育夹移位的发生率为 25%。然而,只有不到 1%的绝育夹移位患者会出现疼痛、脓肿或自发性脱出。在此,我们介绍一例绝育夹移位至整个盆底的罕见病例:病例介绍:一名 66 岁的女性从社区转诊至外科急诊室,她在尝试常规臀部囊肿切除术后发现皮下可能有金属异物。患者于 2 年前首次发现皮下有肿块,2 个月后肿块逐渐增大并有触痛。患者否认近期有外伤,没有并发症,24 年前曾做过绝育手术。检查发现,在距离肛门边缘横向 5 厘米处的皮肤下有一个不可移动的固体结构。炎症指标正常,超声波检查证实皮下组织中有一个 15 × 7 毫米的异物。在局部麻醉下,异物很容易就被切除了,露出了一个封闭的 Filshie 消毒夹。伤口基本闭合,恢复过程并不复杂:这是一例消毒夹移位到臀部皮下区域的病例。文献回顾显示,有 34 例绝育夹移位的病例报告,其中大部分移位至膀胱。既往接受过绝育手术、怀疑皮下异物且无外伤的患者应高度怀疑绝育夹移位。这些夹子可以穿过多层肌肉和筋膜,包括盆底。
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引用次数: 0
Laparoscopic left hepatectomy for a patient with an absence of portal bifurcation using real-time imaging: a case report. 利用实时成像为一名没有肝门分叉的患者实施腹腔镜左肝切除术:病例报告。
IF 0.8 Pub Date : 2024-06-11 DOI: 10.1186/s40792-024-01945-3
Shugo Mizuno, Yusuke Iizawa, Akihiro Tanemura, Benson Kaluba, Daisuke Noguchi, Takahiro Ito, Aoi Hayasaki, Takehiro Fujii, Yasuhiro Murata, Naohisa Kuriyama, Masashi Kishiwada

Background: Absence of portal bifurcation is an extremely rare anomaly that should be recognized preoperatively, especially prior to a major hepatectomy.

Case presentation: A 45-year-old woman presented with abdominal pain, and abdominal computed tomography (CT) revealed dilatation of both the common bile duct (CBD) and intrahepatic bile duct (IHBD). Endoscopic retrograde cholangiopancreatography (ERCP) showed CBD and IHBD stones (B2 and B4). The CBD stones were removed, but the IHBD stones could not be, yet there was no evidence of malignancy at the site of IHBD stenosis. Enhanced CT revealed a dilated IHBD, while three-dimensional CT images showed the left portal vein running through the ventral side of the middle hepatic vein, which was diagnosed as the absence of portal vein bifurcation (APB). Laparoscopic left hepatectomy was successfully performed using real-time indocyanine green (ICG) fluorescence imaging.

Conclusion: Surgeons should be aware of the possibility of APB, a rare portal vein anomaly, before performing major hepatectomy. Real-time ICG fluorescence imaging may be helpful to ensure the precise anatomy of the liver during laparoscopic surgery.

背景:门静脉分叉缺失是一种极为罕见的异常现象,应该在术前,尤其是在进行肝脏大部切除术之前加以识别:一名 45 岁女性因腹痛就诊,腹部计算机断层扫描(CT)显示总胆管(CBD)和肝内胆管(IHBD)均有扩张。内镜逆行胰胆管造影术(ERCP)显示总胆管(CBD)和肝内胆管(IHBD)结石(B2 和 B4)。CBD结石被取出,但IHBD结石未能取出,但IHBD狭窄部位没有恶性肿瘤的证据。增强 CT 显示 IHBD 扩张,而三维 CT 图像显示左侧门静脉穿过肝中静脉腹侧,诊断为门静脉分叉(APB)缺失。利用实时吲哚青绿(ICG)荧光成像技术,成功实施了腹腔镜左肝切除术:结论:外科医生在进行肝脏大部切除术前应了解 APB 这种罕见门静脉异常的可能性。实时 ICG 荧光成像可能有助于确保腹腔镜手术中肝脏的精确解剖。
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引用次数: 0
Totally thoracoscopic atrial fibrillation surgery following massive small bowel resection due to superior mesenteric artery embolization: report of two cases. 肠系膜上动脉栓塞导致大量小肠切除术后的全胸腔镜心房颤动手术:两例病例报告。
IF 0.8 Pub Date : 2024-06-11 DOI: 10.1186/s40792-024-01938-2
Taisuke Nakayama, Yoshitsugu Nakamura, Kusumi Niitsuma, Masaki Ushijima, Yuto Yasumoto, Miho Kuroda, Kosuke Nakamae, Naoshi Minamidate, Yujiro Hayashi, Ryo Tsuruta, Yujiro Ito, Akira Furutachi, Hiroaki Yusa

Background: Thromboembolic occlusion of the superior mesenteric artery (SMA) is a grave complication in individuals diagnosed with atrial fibrillation (AF). This condition often necessitates extensive bowel resection, culminating in short bowel syndrome, which presents challenges for anticoagulant administration and/or antiarrhythmic therapy.

Case presentation: Presented here are findings of two patients, aged 78 and 72 years, respectively, who underwent comprehensive thoracoscopic AF surgery subsequent to extensive small bowel resection following SMA embolization. In each, onset of AF precipitated an embolic event, while the concurrent presence of short bowel syndrome complicated anticoagulation management. Total thoracoscopic AF surgery, comprised stapler-closure of the left atrial appendage (LAA) and bilateral epicardial clamp-isolation of the pulmonary veins, an operative modality aimed at addressing AF rhythm control and mitigating embolic events such as cerebral infarction, led to favorable outcomes in both cases. Additionally, computed tomography (CT) conducted one month post-surgery revealed the absence of residual tissue in the LAA, with the left atrium demonstrating a well-rounded, spherical shape. At the time of writing, the patients have remained asymptomatic following surgery regarding thromboembolic and arrhythmic manifestations for 29 and 10 months, respectively, notwithstanding the absence of anticoagulant or antiarrhythmic pharmacotherapy. Additionally, electrocardiographic surveillance has revealed persistent sinus rhythm.

Conclusions: The present findings underscore the feasibility and efficacy of a total thoracoscopic AF surgery procedure for patients presented with short bowel syndrome complicating SMA embolization, thus warranting consideration for its broader clinical application.

背景:肠系膜上动脉(SMA)血栓栓塞是心房颤动(AF)患者的一种严重并发症。这种情况往往需要进行大范围的肠道切除,最终导致短肠综合征,给抗凝剂管理和/或抗心律失常治疗带来挑战:本文介绍了两名患者的病例,他们的年龄分别为 78 岁和 72 岁,在 SMA 栓塞术后接受了广泛的小肠切除术,随后又接受了综合胸腔镜房颤手术。在这两名患者中,房颤的发生都是栓塞事件的诱因,而同时存在的短肠综合征使抗凝治疗变得复杂。全胸腔镜房颤手术包括用订书机关闭左心房阑尾(LAA)和双侧心外膜钳夹隔离肺静脉,这种手术方式旨在控制房颤节律和减轻脑梗塞等栓塞事件,为两例患者带来了良好的治疗效果。此外,手术后一个月进行的计算机断层扫描(CT)显示 LAA 中没有残留组织,左心房呈现出圆润的球形。在撰写本报告时,尽管没有进行抗凝或抗心律失常药物治疗,但患者在术后 29 个月和 10 个月分别没有出现血栓栓塞和心律失常症状。此外,心电图监测显示窦性心律持续存在:本研究结果强调了全胸腔镜房颤手术治疗 SMA 栓塞并发短肠综合征患者的可行性和有效性,因此值得考虑将其广泛应用于临床。
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引用次数: 0
A case of pseudo-Kaposi sarcoma with chronic limb-threatening ischemia. 一例伴有慢性肢体缺血的假性卡波西肉瘤。
IF 0.8 Pub Date : 2024-06-06 DOI: 10.1186/s40792-024-01933-7
Yuya Tamaru, Shinsuke Kikuchi, Takayuki Uramoto, Kazuki Takahashi, Keisuke Kamada, Yuri Yoshida, Daiki Uchida, Takuya Nishio, Takeshi Yamao, Shunta Ishitoya, Mari Kishibe, Masashi Inaba, Toshihiko Hayashi, Akemi Ishida-Yamamoto, Nobuyoshi Azuma

Background: Pseudo-Kaposi sarcoma (PKS) is a rare vascular proliferative disease, caused by arteriovenous malformation (AVM) and chronic venous insufficiency. The lesions are characterized by purple or reddish-brownish papules, plaques, and nodules. Although benign, it is clinically similar to Kaposi's sarcoma (KS), a malignant disease, and must be differentiated by histopathological examination. We report a rare case of PKS with chronic limb-threatening ischemia (CLTI).

Case presentation: An 83-year-old man with diabetes mellitus (DM) presented to a local dermatology department with a complaint of a right second toe ulcer and was, thereby, referred to our department due to arterial bleeding during skin biopsy to exclude malignant diseases. Although the pulsation of dorsalis pedis artery of the affected limb was palpable, the skin perfusion pressure was only 20 and 30 mmHg on the dorsum and planter surface, respectively, indicating severe ischemia of toe and forefoot. Ultrasonography and computed tomography revealed an AVM around the right second metatarsophalangeal joint and occlusion of the right dorsalis pedis artery in the middle, indicating CLTI in the background. Pathological findings of the skin biopsy found capillary blood vessel proliferation, hemosiderin deposition, and extravascular red blood cell leakage in the dermal layer, which could be found in KS. However, CD34 was normally stained in the vascular endothelium, and human herpesvirus-8 staining was negative, resulting in the pathological diagnosis of PKS, a proliferative vascular lesion associated with AVM. The ulcer was spontaneously epithelialized, but 2 years later the ulcer recurred and infection developed, necessitating treatment for abnormal blood flow. Transarterial embolization using N-butyl 2-cyanoacrylate for the AVM controlled abnormal perfusion once; however, the procedure exacerbated perfusion of the toe, resulting in foot ulcer progression. Forefoot amputation with surgical excision of AVM was performed, and thereby, wound healing was achieved.

Conclusion: This is a rare case of PKS with CLTI complicated with AVM. As there is currently no established consensus on the treatment of PKS, the approach to treatment strategy should be tailored to the specific condition of each patient.

背景:假性卡波西肉瘤(PKS)是一种罕见的血管增生性疾病,由动静脉畸形(AVM)和慢性静脉功能不全引起。病变特征为紫色或红褐色丘疹、斑块和结节。这种病虽然是良性的,但在临床上与恶性疾病卡波西肉瘤(KS)相似,必须通过组织病理学检查加以鉴别。我们报告了一例罕见的伴有慢性肢体缺血(CLTI)的 PKS 病例:病例介绍:一名83岁的男性糖尿病患者因右第二脚趾溃疡到当地皮肤科就诊,在进行皮肤活检以排除恶性疾病时发现动脉出血,遂被转诊至我科。虽然患肢足背动脉搏动清晰可触,但足背和足跖面的皮肤灌注压分别只有 20 和 30 mmHg,表明脚趾和前足严重缺血。超声波检查和计算机断层扫描显示,右侧第二跖趾关节周围有一个动静脉畸形,右侧足背动脉中部闭塞,表明背景为CLTI。皮肤活检的病理结果发现,真皮层有毛细血管增生、血色素沉积和血管外红细胞渗漏,这些在 KS 中都能发现。然而,血管内皮的 CD34 染色正常,人类疱疹病毒-8 染色阴性,因此病理诊断为 PKS,一种与 AVM 相关的增生性血管病变。溃疡自发上皮化,但 2 年后溃疡复发并出现感染,需要对异常血流进行治疗。使用 2-氰基丙烯酸 N-丁酯对 AVM 进行经动脉栓塞治疗,一度控制了异常血流灌注;但该手术加剧了脚趾的血流灌注,导致足部溃疡恶化。在手术切除 AVM 的同时进行了前足截肢,从而实现了伤口愈合:这是一例罕见的 PKS 伴 CLTI 并发 AVM 病例。结论:这是一例罕见的 PKS 伴 CLTI 并发 AVM 病例。由于目前尚未就 PKS 的治疗达成共识,因此应根据每位患者的具体病情制定治疗策略。
{"title":"A case of pseudo-Kaposi sarcoma with chronic limb-threatening ischemia.","authors":"Yuya Tamaru, Shinsuke Kikuchi, Takayuki Uramoto, Kazuki Takahashi, Keisuke Kamada, Yuri Yoshida, Daiki Uchida, Takuya Nishio, Takeshi Yamao, Shunta Ishitoya, Mari Kishibe, Masashi Inaba, Toshihiko Hayashi, Akemi Ishida-Yamamoto, Nobuyoshi Azuma","doi":"10.1186/s40792-024-01933-7","DOIUrl":"10.1186/s40792-024-01933-7","url":null,"abstract":"<p><strong>Background: </strong>Pseudo-Kaposi sarcoma (PKS) is a rare vascular proliferative disease, caused by arteriovenous malformation (AVM) and chronic venous insufficiency. The lesions are characterized by purple or reddish-brownish papules, plaques, and nodules. Although benign, it is clinically similar to Kaposi's sarcoma (KS), a malignant disease, and must be differentiated by histopathological examination. We report a rare case of PKS with chronic limb-threatening ischemia (CLTI).</p><p><strong>Case presentation: </strong>An 83-year-old man with diabetes mellitus (DM) presented to a local dermatology department with a complaint of a right second toe ulcer and was, thereby, referred to our department due to arterial bleeding during skin biopsy to exclude malignant diseases. Although the pulsation of dorsalis pedis artery of the affected limb was palpable, the skin perfusion pressure was only 20 and 30 mmHg on the dorsum and planter surface, respectively, indicating severe ischemia of toe and forefoot. Ultrasonography and computed tomography revealed an AVM around the right second metatarsophalangeal joint and occlusion of the right dorsalis pedis artery in the middle, indicating CLTI in the background. Pathological findings of the skin biopsy found capillary blood vessel proliferation, hemosiderin deposition, and extravascular red blood cell leakage in the dermal layer, which could be found in KS. However, CD34 was normally stained in the vascular endothelium, and human herpesvirus-8 staining was negative, resulting in the pathological diagnosis of PKS, a proliferative vascular lesion associated with AVM. The ulcer was spontaneously epithelialized, but 2 years later the ulcer recurred and infection developed, necessitating treatment for abnormal blood flow. Transarterial embolization using N-butyl 2-cyanoacrylate for the AVM controlled abnormal perfusion once; however, the procedure exacerbated perfusion of the toe, resulting in foot ulcer progression. Forefoot amputation with surgical excision of AVM was performed, and thereby, wound healing was achieved.</p><p><strong>Conclusion: </strong>This is a rare case of PKS with CLTI complicated with AVM. As there is currently no established consensus on the treatment of PKS, the approach to treatment strategy should be tailored to the specific condition of each patient.</p>","PeriodicalId":22096,"journal":{"name":"Surgical Case Reports","volume":null,"pages":null},"PeriodicalIF":0.8,"publicationDate":"2024-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11156619/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141262895","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
Successful R0 resection after chemotherapy, including nivolumab, for gastric cancer with liver metastases: three case reports. 化疗(包括 nivolumab)后成功 R0 切除伴肝转移的胃癌:三份病例报告。
IF 0.8 Pub Date : 2024-06-05 DOI: 10.1186/s40792-024-01929-3
Junpei Kawai, Itaru Yasufuku, Masahiro Fukada, Ryuichi Asai, Yuta Sato, Yu Jesse Tajima, Chiemi Saigo, Shigeru Kiyama, Akitaka Makiyama, Yoshihiro Tanaka, Naoki Okumura, Katsutoshi Murase, Tatsuhiko Miyazaki, Nobuhisa Matsuhashi

Background: Advances in chemotherapy have increased clinical experience with conversion surgery for inoperable advanced gastric cancer. This report describes three patients with unresectable gastric cancer accompanied by multiple liver metastases. In all three patients, nivolumab resolved the liver metastases and subsequent conversion surgery achieved a pathological complete response.

Case presentation: In Case 1, a 68-year-old man with clinical Stage IVB gastric cancer and multiple liver metastases initiated first-line therapy with SOX plus nivolumab. The patient completed 13 cycles; however, only nivolumab was continued for 3 cycles because of adverse events. Distal gastrectomy and partial hepatic resection were performed because of a significant reduction in the size of the liver metastases as observed on magnetic resonance imaging (MRI). In Case 2, a 72-year-old man with clinical Stage IVB gastric cancer and multiple liver metastases initiated first-line therapy with SOX. Because of the subsequent emergence of new liver metastases, the patient transitioned to ramucirumab plus paclitaxel as second-line therapy. Third-line therapy with nivolumab was initiated because of side effects. MRI revealed necrosis within the liver metastasis, and the patient underwent proximal gastrectomy and partial hepatectomy. In Case 3, a 51-year-old woman with clinical Stage IVB gastric cancer accompanied by multiple metastases of the liver and para-aortic lymph nodes began first-line therapy with SOX plus nivolumab. The patient completed 10 cycles; however, only nivolumab was continued for 5 cycles because of adverse events. Computed tomography showed a significant decrease in the size of the para-aortic lymph nodes, while MRI indicated the presence of a singular liver metastasis. Distal gastrectomy and partial hepatic resection were subsequently performed. In all three cases, MRI revealed the presence of liver metastases; however, pathological examination showed no viable tumor cells.

Conclusions: We herein present three cases in which chemotherapy, including nivolumab, elicited a response in patients with multiple unresectable liver metastases, ultimately culminating in R0 resection through conversion surgery. Although MRI showed liver metastases, pathological analysis revealed no cancer, underscoring the beneficial impact of chemotherapy.

背景:化疗的进步增加了对无法手术的晚期胃癌进行转化手术的临床经验。本报告介绍了三例伴有多发性肝转移的不可切除胃癌患者。在这三位患者中,nivolumab 解决了肝转移问题,随后的转换手术获得了病理完全反应:在病例 1 中,一名 68 岁的男性患者患有临床 IVB 期胃癌和多发性肝转移,开始接受 SOX 加 nivolumab 的一线治疗。患者完成了 13 个周期的治疗,但由于不良反应,只继续使用了 3 个周期的 nivolumab。由于在磁共振成像(MRI)上观察到肝转移灶的大小明显缩小,患者接受了远端胃切除术和肝部分切除术。在病例 2 中,一名 72 岁的男性患者患有临床 IVB 期胃癌和多发性肝转移,开始接受 SOX 的一线治疗。由于随后出现了新的肝转移灶,患者转而接受拉莫单抗加紫杉醇的二线治疗。由于副作用,患者开始接受尼妥珠单抗的三线治疗。核磁共振成像显示肝转移灶内出现坏死,患者接受了近端胃切除术和肝部分切除术。在病例 3 中,一名 51 岁的女性患者患有临床 IVB 期胃癌,并伴有肝脏和主动脉旁淋巴结的多发转移,她开始接受 SOX 加 nivolumab 的一线治疗。患者完成了 10 个周期的治疗,但由于不良反应,只继续使用了 5 个周期的 nivolumab。计算机断层扫描显示主动脉旁淋巴结明显缩小,而核磁共振成像显示存在单发肝转移灶。随后进行了远端胃切除术和肝部分切除术。在所有三个病例中,磁共振成像均显示存在肝转移灶;但病理检查显示没有存活的肿瘤细胞:我们在此介绍了三例化疗(包括 nivolumab)对多发性不可切除肝转移瘤患者产生反应的病例,最终通过转化手术实现了 R0 切除。虽然磁共振成像显示有肝转移,但病理分析却未发现癌症,这凸显了化疗的益处。
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引用次数: 0
A case of surgical treatment for recurrence of right ventricular metastasis due to renal cell carcinoma after molecular targeted therapy. 一例肾细胞癌分子靶向治疗后右心室转移复发的手术治疗病例。
IF 0.8 Pub Date : 2024-06-04 DOI: 10.1186/s40792-024-01940-8
Keita Sasaki, Naritomo Nishioka, Mika Yamamoto, Kenichi Kato, Ryo Matsumoto, Takahiko Masuda, Ryushi Maruyama, Yoshihiko Kurimoto, Akira Yamada, Shuichi Naraoka

Background: Cardiac metastasis including the right ventricle from renal cell carcinoma is rare. No standard treatment for cardiac metastasis and recurrence in renal cell carcinoma has been established.

Case presentation: We present the case of a 61-year-old man who underwent the resection of recurrent right ventricular metastasis caused by renal cell carcinoma following molecular targeted therapy. The first cardiac operation was performed for right ventricular metastasis due to renal cell carcinoma. The patient had a good postoperative course. Two years after the first operation, however, follow-up computed tomography revealed the recurrence of the right ventricular tumor and metastases in both lungs. Molecular targeted therapy was carried out and effectively controlled the lung metastasis but the right ventricular lesion remained unchanged, leading to reoperation. The recurrent right ventricular tumor was completely resected through a redo median sternotomy assisted by cardiopulmonary bypass. The patient had an uneventful postoperative course and was discharged on the 13th postoperative day. Follow-ups at 2 years showed no cardiac recurrence.

Conclusion: Surgical intervention was considered useful in managing the recurrence of right ventricular metastasis from renal cell carcinoma after molecular targeted therapy.

背景:肾细胞癌包括右心室在内的心脏转移非常罕见。目前还没有针对肾细胞癌心脏转移和复发的标准治疗方法:本病例是一名 61 岁的男性,在接受分子靶向治疗后,他接受了由肾细胞癌引起的复发性右心室转移瘤切除术。第一次心脏手术是因肾细胞癌导致的右心室转移而进行的。患者术后恢复良好。然而,第一次手术两年后,随访的计算机断层扫描显示右心室肿瘤复发,并出现双肺转移。患者接受了分子靶向治疗,有效控制了肺部转移,但右心室病灶仍未改变,因此需要再次手术。在心肺旁路辅助下,通过重新进行的胸骨正中切口手术完全切除了复发的右心室肿瘤。患者术后恢复顺利,于术后第13天出院。2年的随访显示,患者的心脏没有复发:结论:手术干预被认为是治疗肾细胞癌分子靶向治疗后右心室转移复发的有效方法。
{"title":"A case of surgical treatment for recurrence of right ventricular metastasis due to renal cell carcinoma after molecular targeted therapy.","authors":"Keita Sasaki, Naritomo Nishioka, Mika Yamamoto, Kenichi Kato, Ryo Matsumoto, Takahiko Masuda, Ryushi Maruyama, Yoshihiko Kurimoto, Akira Yamada, Shuichi Naraoka","doi":"10.1186/s40792-024-01940-8","DOIUrl":"10.1186/s40792-024-01940-8","url":null,"abstract":"<p><strong>Background: </strong>Cardiac metastasis including the right ventricle from renal cell carcinoma is rare. No standard treatment for cardiac metastasis and recurrence in renal cell carcinoma has been established.</p><p><strong>Case presentation: </strong>We present the case of a 61-year-old man who underwent the resection of recurrent right ventricular metastasis caused by renal cell carcinoma following molecular targeted therapy. The first cardiac operation was performed for right ventricular metastasis due to renal cell carcinoma. The patient had a good postoperative course. Two years after the first operation, however, follow-up computed tomography revealed the recurrence of the right ventricular tumor and metastases in both lungs. Molecular targeted therapy was carried out and effectively controlled the lung metastasis but the right ventricular lesion remained unchanged, leading to reoperation. The recurrent right ventricular tumor was completely resected through a redo median sternotomy assisted by cardiopulmonary bypass. The patient had an uneventful postoperative course and was discharged on the 13th postoperative day. Follow-ups at 2 years showed no cardiac recurrence.</p><p><strong>Conclusion: </strong>Surgical intervention was considered useful in managing the recurrence of right ventricular metastasis from renal cell carcinoma after molecular targeted therapy.</p>","PeriodicalId":22096,"journal":{"name":"Surgical Case Reports","volume":null,"pages":null},"PeriodicalIF":0.8,"publicationDate":"2024-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11150214/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141238061","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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Surgical Case Reports
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