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Fungal hepatic abscess formation postlaparoscopic cholecystectomy. 腹腔镜胆囊切除术后形成真菌性肝脓肿。
IF 0.4 Q4 SURGERY Pub Date : 2024-12-21 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjae802
Dana AlNuaimi, Ghufran Saeed, Shareefa Abdulghaffar, Reem AlKetbi, Essa M Aleassa, Numan Cem Balci

Laparoscopic cholecystectomy is the preferred method for treating acute cholecystitis. Although the incidence of postoperative infections in laparoscopic cholecystectomy is low, serious postoperative surgical site infections are still reported. Hepatic abscesses, particularly fungal, can occur post-cholecystectomy leading to significant mortality and morbidity. We report a case of a 58-year-old female who underwent laparoscopic cholecystectomy and subsequently developed fever, jaundice, and right upper quadrant pain. Laboratory results showed deranged liver function tests with raised inflammatory markers. Radiographic investigations, including CT and MRI, revealed an irregular hilar lesion with periportal changes suggestive of an abscess with portal vein thrombosis. Histopathological examination of the biopsy obtained from the hilar lesion showed a fungal hepatic infection, and particularly conidiobolomycosis. To our best knowledge, this is the first case that reports this fungal infection as a complication of laparoscopic cholecystectomy. The patient was managed with a combination of intravenous antibiotics and antifungals, which yielded mild improvement. Unfortunately, the patient decided to leave the hospital against medical advice, limiting the information on the disease course.

腹腔镜胆囊切除术是治疗急性胆囊炎的首选方法。虽然腹腔镜胆囊切除术术后感染的发生率较低,但仍有严重的术后手术部位感染的报道。肝脓肿,尤其是真菌性,可在胆囊切除术后发生,导致显著的死亡率和发病率。我们报告一例58岁的女性,她接受了腹腔镜胆囊切除术,随后出现发烧、黄疸和右上腹疼痛。实验室结果显示肝功能异常炎症标志物升高影像学检查,包括CT和MRI,显示不规则的门静脉病变,门静脉周围改变提示脓肿合并门静脉血栓形成。肝门病变活检的组织病理学检查显示真菌性肝脏感染,特别是分生孢子菌病。据我们所知,这是第一例报道这种真菌感染作为腹腔镜胆囊切除术的并发症。患者接受静脉注射抗生素和抗真菌药物的联合治疗,病情得到轻微改善。不幸的是,病人不顾医嘱决定离开医院,限制了对病情的了解。
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引用次数: 0
Diffuse large B-cell lymphoma mimicking the cervical epidural hematoma in a patient who underwent spinal manipulation therapy: a case report and literature review. 弥漫性大b细胞淋巴瘤模拟宫颈硬膜外血肿的病人接受脊柱推拿治疗:一个病例报告和文献复习。
IF 0.4 Q4 SURGERY Pub Date : 2024-12-21 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjae807
Klaudia Kokot, Oskar Chasles, Michał Krakowiak, Rami Yuser, Jarosław Dzierżanowski, Tomasz Szmuda, Aleksandra Maj, Jacek Nacewicz, Piotr Zieliński

The diffuse large B-cell lymphoma (DLBCL) mimicking an epidural hematoma in the cervical spine is an extremely unique case. We present a case of a 42-year-old man, who presented to the emergency department with symptoms of tetraparesis after a session of spinal manipulation therapy. magnetic resonance imaging visualized a lesion located at C3-C7 causing spinal cord compression with surrounding soft tissue edema suggesting epidural hematoma. The patient was admitted to the Neurosurgery Department and emergent laminectomy was performed. Intraoperatively, an infiltrating tumor was found, which was partially resected and sent for post-op histopathological examination, determining it to be a DLBCL. Our work aims to increase awareness of such cases, which may make it easier to make the proper diagnosis.

弥漫大b细胞淋巴瘤(DLBCL)模拟硬膜外血肿在颈椎是一个非常独特的情况。我们提出一个病例,42岁的男子,谁提出了四部曲的症状后,脊柱推拿治疗后的急诊科。磁共振成像显示位于C3-C7的病变导致脊髓受压,周围软组织水肿提示硬膜外血肿。患者被送往神经外科,并进行了紧急椎板切除术。术中发现浸润性肿瘤,部分切除并送术后组织病理学检查,确定为DLBCL。我们的工作旨在提高人们对这类病例的认识,从而更容易做出正确的诊断。
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引用次数: 0
Thoracic endovascular aortic repair (TEVAR) in a combined penetrating thoracic aortic and spinal cord injury. 合并穿透性胸主动脉和脊髓损伤的胸腔内血管主动脉修复术(TEVAR)。
IF 0.4 Q4 SURGERY Pub Date : 2024-12-21 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjae771
Jacqueline Amm, Estelle Laney, Rubinette Robbertze, Maeyane Moeng

Endovascular repair of aortic injuries secondary to blunt trauma has been widely described. However, literature on endovascular management in penetrating aortic injuries is scarce. The patient in this case report, a victim of penetrating thoracic aortic trauma, presented 5 days after injury with Brown-Sequard syndrome and a contained aortic injury (pseudoaneurysm) and was haemodynamically stable. Therefore, thoracic endovascular aortic repair was an option in this case. Endovascular repair carries a lower peri-operative morbidity and mortality rate than open repair. However, because most cases of penetrating thoracic vascular injury have haemodynamic instability, open surgery is considered the standard of care. This case demonstrates successful management of an aortic injury with a minimally invasive procedure.

钝性外伤继发主动脉损伤的血管内修复已被广泛报道。然而,关于穿透性主动脉损伤的血管内处理的文献很少。本病例报告的患者是一名穿透性胸主动脉创伤的患者,在伤后5天出现了Brown-Sequard综合征和包含性主动脉损伤(假性动脉瘤),血流动力学稳定。因此,在这种情况下,胸腔血管内主动脉修复是一种选择。血管内修复术的围手术期发病率和死亡率低于开放修复术。然而,由于大多数穿透性胸血管损伤病例存在血流动力学不稳定,开放手术被认为是标准的治疗方法。本病例展示了微创手术对主动脉损伤的成功治疗。
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引用次数: 0
VACStent closure of oesophageal defects by covered stent and endoscopic vacuum therapy: initial use and clinical outcomes. 覆盖支架和内镜真空治疗食管缺损的VACStent闭合:初始使用和临床结果。
IF 0.4 Q4 SURGERY Pub Date : 2024-12-21 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjae804
Kristali Ylli, Jowhara AlQahtani, Ihab Hraishawi, Thomas Murphy

Endoscopic management of transmural oesophageal defects following esophagectomy or spontaneous perforations, such as Boerhaave's syndrome, is often complicated by stent migration and luminal occlusion [1]. The Vacuum-Assisted Closure (VAC) stent, which integrates a covered stent with endoscopic vacuum therapy, aims to address these issues by providing functional drainage and promoting wound healing [2]. This case series presents our initial experience with VACStent therapy in four patients treated between February 2023 and April 2024. Two patients had staple line defects post-esophagectomy, and two had Boerhaave's syndrome. Treatment involved stent placement under general anaesthesia, followed by evaluations and scheduled stent exchanges every 6 days. All patients achieved successful defect closure, with no procedural complications noted. Three patients required one stent application, while one needed two applications. VACStent therapy appears to be a safe and effective treatment for transmural oesophageal defects, potentially establishing a new standard of care.

内镜下治疗食管切除术或自发性穿孔后的经壁食管缺损,如Boerhaave综合征,常并发支架移位和管腔阻塞[1]。真空辅助闭合(VAC)支架将覆盖支架与内窥镜真空治疗相结合,旨在通过提供功能性引流和促进伤口愈合来解决这些问题。本病例系列介绍了我们在2023年2月至2024年4月期间接受VACStent治疗的4例患者的初步经验。2例患者食管切除术后出现钉线缺损,2例患者出现布尔哈夫综合征。治疗包括在全身麻醉下放置支架,随后每6天进行评估和安排支架更换。所有患者均成功完成缺损闭合,无手术并发症。3例患者需要一次支架应用,1例患者需要两次。血管内支架治疗似乎是一种安全有效的治疗跨壁食道缺陷的方法,有可能建立一种新的护理标准。
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引用次数: 0
Complex perianal abscess: a case report of shooting from the hip. 复杂肛周脓肿:髋部射伤1例。
IF 0.4 Q4 SURGERY Pub Date : 2024-12-21 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjae801
Peter Tilleard, Kate Swift, Daniel Tani, Ju Yong Cheong

The perianal abscess is a common emergency surgical presentation. While in most cases simple drainage suffices, occasionally the abscess can track deeply presenting a management challenge. We describe the case of a complex circumferential horseshoe ischioanal abscess with extension below the levator ani through the greater sciatic notch and into the left gluteal region, with the collection involving the intergluteal space and gluteus maximus. The complex nature of the abscess warranted a novel joint approach by Colorectal surgery and Orthopaedic surgery teams. This case highlights the importance of maintaining a high degree of suspicion for, early recognition and imaging of deeper anorectal abscess extension.

肛周脓肿是一种常见的急诊手术表现。虽然在大多数情况下,简单的引流就足够了,但偶尔脓肿可以深入追踪,给管理带来挑战。我们描述了一个复杂的环形马蹄形坐骨肛门脓肿的病例,其延伸至提肛肌以下,穿过坐骨大切迹并进入左臀区,其集合涉及臀间隙和臀大肌。脓肿的复杂性质保证了结直肠外科和矫形外科团队采用一种新的联合方法。本病例强调了保持高度怀疑,早期识别和成像的重要性更深的肛门直肠脓肿延伸。
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引用次数: 0
Above knee amputation following periprosthetic joint infection after total knee arthroplasty: a fatal outcome. 全膝关节置换术后假体周围关节感染后的膝上截肢:一个致命的结果。
IF 0.4 Q4 SURGERY Pub Date : 2024-12-21 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjae806
Catherine Purcell, Rajkumar Gangadharan, George Ampat

Primary total knee arthroplasty (TKA) is a successful and cost-effective procedure for which demand is increasing annually. Outcomes are generally good with satisfaction rates of 70%, so the procedure is commonly used in osteoarthritis management to improve mobility and alleviate pain. Above knee amputation (AKA) is a devastating complication of TKA. AKA is associated with high mortality, phantom pain, and non-ambulatory disability. In the US, the incidence of AKAs due to periprosthetic joint infection (PJI) is rising drastically, with the proportion of AKAs performed due to PJI having almost quadrupled from 1998 to 2013. We present the case of a patient who developed severe uncontrolled infection following routine TKA, resulting in an above-knee amputation and ultimately death. Due to the extremity of the outcome and the rising incidence of the complication involved, this is an important case to discuss.

原发性全膝关节置换术(TKA)是一种成功且具有成本效益的手术,其需求每年都在增加。结果通常很好,满意率为70%,因此该手术通常用于骨关节炎治疗,以改善活动能力和减轻疼痛。膝上截肢(AKA)是TKA的致命并发症。AKA与高死亡率、幻肢痛和非行动性残疾有关。在美国,假体周围关节感染(PJI)导致的AKAs发生率急剧上升,从1998年到2013年,由于PJI而进行的AKAs的比例几乎翻了两番。我们提出了一个病例的病人谁发展严重的不受控制的感染后,常规TKA,导致膝盖以上截肢和最终死亡。由于结果的极端和并发症的发生率上升,这是一个重要的病例讨论。
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引用次数: 0
Constricting colonic lipoma causing acute intestinal obstruction. 收缩性结肠脂肪瘤,引起急性肠梗阻。
IF 0.4 Q4 SURGERY Pub Date : 2024-12-21 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjae798
Jay Lodhia, Atiyya Hussein, Alex Mremi

Colon lipomas are rare benign, nonepithelial tumors that are often asymptomatic. However, when symptoms do occur, they vary depending on the size and location of the lipoma and are generally nonspecific. Diagnosis is confirmed through histopathological analysis. Lipomas smaller than 2.5 cm can typically be observed without intervention, but larger or symptomatic lipomas require resection, which can be performed endoscopically or surgically. This case presents a rare phenomenon of synchronous left colonic lipoma leading to intestinal obstruction. Despite their benign nature, colonic lipomas can sometimes mimic malignant lesions, making histopathological analysis crucial for confirming the diagnosis.

结肠脂肪瘤是一种罕见的良性非上皮性肿瘤,通常无症状。然而,当症状确实出现时,它们因脂肪瘤的大小和位置而异,通常是非特异性的。通过组织病理学分析确诊。小于2.5 cm的脂肪瘤通常无需干预即可观察到,但较大或有症状的脂肪瘤需要切除,可通过内窥镜或手术进行。本病例呈现罕见的左结肠同步脂肪瘤导致肠梗阻的现象。尽管它们是良性的,但结肠脂肪瘤有时可以模仿恶性病变,因此组织病理学分析对于确认诊断至关重要。
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引用次数: 0
Incidental finding of duplication of vas deferens in inguinal hernia: a case report of rare anomaly. 腹股沟疝偶发输精管重复:一例罕见异常报告。
IF 0.4 Q4 SURGERY Pub Date : 2024-12-20 eCollection Date: 2024-12-01 DOI: 10.1093/jscr/rjae782
Bibek Shrestha, Krishna Yadav, Grishma Kandel, Pratibha Yadav, Sachet Subedi

Duplication of the vas deferens is a rare congenital anomaly, with an incidence of ~0.05% in the general population. It is typically discovered incidentally during surgeries involving the spermatic cord, such as inguinal hernia repair. This case report presents a 33-year-old male who underwent left inguinal hernioplasty, during which duplication of the vas deferens was incidentally identified. The patient had presented with left-sided inguinal swelling, painful testis, and a small left testis. Preoperative ultrasound suggested an inguinal hernia, but the vas deferens anomaly was only detected intraoperatively. The patient successfully underwent hernioplasty without postoperative complications. This case emphasizes the importance of recognizing rare anatomical variations like vas deferens duplication to prevent surgical complications.

输精管重复是一种罕见的先天性异常,在一般人群中的发病率约为0.05%。它通常在涉及精索的手术中偶然发现,如腹股沟疝修补术。这个病例报告提出了一个33岁的男性谁接受左腹股沟疝成形术,在此期间,重复输精管偶然发现。患者表现为左侧腹股沟肿胀,睾丸疼痛,左侧睾丸小。术前超声提示腹股沟疝,术中发现输精管异常。患者成功行疝成形术,无术后并发症。这个病例强调了识别罕见的解剖变异如输精管重复的重要性,以防止手术并发症。
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引用次数: 0
Management of recurrent intussusception after Roux-en-Y gastric bypass. Roux-en-Y胃旁路术后复发性肠套叠的处理。
IF 0.4 Q4 SURGERY Pub Date : 2024-12-19 eCollection Date: 2024-12-01 DOI: 10.1093/jscr/rjae778
Ankur Makani, Andrew Hendrix, Gunnar Orcutt, Christopher Stephenson, Thomas Crafton, David Moffatt

While intussusception is a well described complication of Roux-en-Y gastric bypass (RYGB), cases of recurrent intussusception after lead point resection and reconstruction are described much less frequently. We present a case of a 28-year-old female with triple recurrent intussusception all of which were treated with surgical resection and reconstruction of her RYGB anastomoses. There is currently limited evidence to direct management in the setting of recurrent intussusception. This case highlights the importance of considering intussusception in the RYGB patient with abdominal pain as well as demonstrates a need for further investigation into pathomechanisms which may lead to recurrence.

虽然肠套叠是Roux-en-Y胃旁路术(RYGB)的并发症,但导点切除和重建后复发的肠套叠病例的描述要少得多。我们报告一位28岁女性三重复发性肠套叠的病例,所有这些病例都通过手术切除和重建她的RYGB吻合器进行治疗。目前对复发性肠套叠的直接治疗证据有限。该病例强调了考虑RYGB患者伴有腹痛的肠套叠的重要性,并表明需要进一步研究可能导致复发的病理机制。
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引用次数: 0
Perforated anterior tenia coli-type appendicitis in a case of vermiform appendix duplex in a toddler: a case report. 幼儿蚓状双阑尾穿孔型结肠炎1例。
IF 0.4 Q4 SURGERY Pub Date : 2024-12-19 eCollection Date: 2024-12-01 DOI: 10.1093/jscr/rjae784
Zlatan Zvizdic, Melika Bukvic, Nermina Ibisevic, Alena Firdus, Asmir Jonuzi, Semir Vranic

Duplication of the vermiform appendix is a rare anomaly observed in patients undergoing appendectomy. A 27-month-old male toddler presented with a 9-day history of abdominal pain, vomiting, and diarrhea, progressing to an acute abdomen with signs of severe peritonitis. Intraoperative findings revealed a periappendicular infiltrate from a perforated vermiform appendix of the tenia coli type. A second, inflamed appendix was incidentally discovered in its typical location during the procedure. Vermiform appendix duplication presents a clinical challenge due to its rarity and potential for complications. According to the Cave-Wallbridge classification, this case represents Type B2, or the tenia coli variant, characterized by a perforated appendix originating at the tenia coli convergence and a smaller, secondary appendix in a retrocecal position. This case emphasizes the importance of thorough distal and proximal exploration during initial appendectomy when this anomaly is suspected, particularly in cases of Type B2.

蚓状阑尾重复是阑尾切除术中罕见的异常。一位27个月大的男婴以腹痛、呕吐和腹泻9天的病史出现,并发展为急性腹部,伴有严重腹膜炎的症状。术中发现大肠杆菌型穿孔蚓状阑尾有阑尾周围浸润。第二个发炎的阑尾在手术过程中偶然发现在它的典型位置。由于其罕见性和潜在的并发症,蚓状阑尾重复呈现临床挑战。根据Cave-Wallbridge分类,该病例为B2型,即大肠杆菌变种,其特征是阑尾穿孔起源于大肠杆菌会聚处,阑尾较小,位于盲肠后位置。本病例强调了当怀疑阑尾异常时,特别是B2型病例,在阑尾切除术初期进行彻底的远端和近端检查的重要性。
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引用次数: 0
期刊
Journal of Surgical Case Reports
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