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Acupuncture gone awry: surgical management of a popliteal artery pseudoaneurysm with concurrent abdominal aortic aneurysm. 针刺出错:腘动脉假性动脉瘤并发腹主动脉瘤的手术治疗。
IF 0.4 Q4 SURGERY Pub Date : 2025-01-08 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjae837
Sebastian Asteguieta, Carlos Diaz Q, Luis P Jacobs, Kelly Villeda, Sebastian Estrada

Popliteal artery pseudoaneurysms are rare, especially from acupuncture-related trauma. We report a 67-year-old male with hypertension, diabetes, chronic kidney disease, and an abdominal aortic aneurysm (AAA), who developed a popliteal pseudoaneurysm after acupuncture. Imaging confirmed the pseudoaneurysm and a 55 mm AAA. Urgent surgical repair with a Gore-Tex graft led to a smooth recovery. This case emphasizes the vascular risks of acupuncture and the importance of early diagnosis, multidisciplinary care, and personalized follow-up in patients with complex comorbidities.

腘动脉假性动脉瘤是罕见的,特别是来自针灸相关的创伤。我们报告一位67岁男性,患有高血压、糖尿病、慢性肾脏疾病和腹主动脉瘤(AAA),在针灸后发展为腘动脉假性动脉瘤。影像学证实假性动脉瘤和55毫米AAA。紧急手术修复Gore-Tex移植物使患者顺利恢复。本病例强调了针灸的血管风险,以及对复杂合并症患者进行早期诊断、多学科治疗和个性化随访的重要性。
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引用次数: 0
Persistent ascending mesocolon: an unexpected content in a giant and complex paraumbilical hernia of a 48-year-old obese woman. 持续上升的肠系膜:一个巨大的和复杂的48岁肥胖妇女脐旁疝的意外内容。
IF 0.4 Q4 SURGERY Pub Date : 2025-01-07 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjae834
Nuhu N Naabo, Raymond S Maalman, Aishah F Adamu, Mohammed N Naabo, Samuel Mensah

Persistent ascending mesocolon (PAM) is a rare congenital anomaly in ⁓2%-4% of individuals. PAM is associated with various complications, including volvulus of the colon and caecum, bowel perforation, intestinal obstruction, and adhesions. This case is reported on a 48-year-old woman who reported to the Ho Teaching Hospital specialist clinic with a 13-year history of initial painless and reducible paraumbilical swelling. Management was based on a surgical approach. The content of the hernia sac was unusual with a viable appendix, caecum, ascending and transverse colons inclusive, and ascending mesocolon was persistent. The repair was done through an anterior component separation technique. An onlay mesh repair was fashioned with a 30 cm × 30 cm polypropylene mesh. This case report highlights the complexities of managing a giant paraumbilical hernia in a morbidly obese patient with a PAM, a rare congenital anomaly.

持续性升结肠系膜(PAM)是一种罕见的先天性异常,发病率为⁓2%-4%。PAM与多种并发症相关,包括结肠和盲肠扭转、肠穿孔、肠梗阻和粘连。本病例报告于一名48岁妇女,她到何氏教学医院专科诊所就诊,有13年的初始无痛和可减轻的脐旁肿胀史。治疗基于手术方法。疝囊内容物不寻常,有存活的阑尾、盲肠、升结肠和横结肠,升结肠肠系膜持续存在。通过前体分离技术进行修复。用30cm × 30cm聚丙烯网进行嵌板补片。本病例报告强调了管理一个巨大的脐旁疝在病态肥胖患者与PAM,一种罕见的先天性异常。
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引用次数: 0
Surgical management of an extensive nasal mass in an adolescent: insights from diagnostic imaging and histopathology. 青少年广泛鼻肿块的外科治疗:来自诊断成像和组织病理学的见解。
IF 0.4 Q4 SURGERY Pub Date : 2025-01-07 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjae831
Sebastian Asteguieta, Carlos Diaz, Javier Alarcon, Vanessa Godinez

A 17-year-old female presented with a mass in the right nasal fossa and eye protrusion. Imaging revealed a large osseous mass originating from the right turbinates, causing exophthalmos without tissue invasion. A partial resection via the Caldwell-Luc approach was performed, but hemodynamic instability halted the procedure, leaving a residual mass. Histopathology confirmed an osseous lesion with osteoblasts in a hypocellular stroma. The patient required blood transfusions postoperatively due to significant blood loss, but recovered well with antibiotics and supplements and was discharged after mild nausea was managed.

17岁女性,右鼻窝肿块及眼外突出。影像学显示一大块骨性肿块起源于右鼻甲,引起眼球突出,但无组织侵犯。通过Caldwell-Luc入路进行部分切除,但血流动力学不稳定导致手术停止,留下残留肿块。组织病理学证实一骨病变与成骨细胞在低细胞间质。患者术后因大量失血需要输血,但经抗生素和补品治疗恢复良好,轻度恶心处理后出院。
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引用次数: 0
Curative resection of multiple primary neuroendocrine tumors enabled by preoperative imaging: a case report. 术前影像学辅助治疗多发性原发性神经内分泌肿瘤1例。
IF 0.4 Q4 SURGERY Pub Date : 2025-01-07 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjae805
Hidetoshi Shidahara, Masakazu Hashimoto, Keiichi Mori, Shintaro Kuroda, Hiroyuki Tahara, Tsuyoshi Kobayashi, Hideki Ohdan

Neuroendocrine tumors (NENs) originate from neuroendocrine cells and predominantly occur in the gastrointestinal tract, lungs, and pancreas. Although the liver is commonly involved in NEN metastasis, primary hepatic neuroendocrine tumors (PHNETs) are rare. Herein, we report a case of a 52-year-old female who presented with slowly enlarging, cystic, multiple PHNETs. Two tumors in segments 6 (S6) and S7 were noted on computed tomography (CT), and an additional S7/8 tumor was found on magnetic resonance imaging. Additionally, CT during hepatic arteriography (CTHA) revealed a small tumor in S8. No other primary tumors were detected in other organs. Posterior segmentectomy and S8 partial resection were performed for the tumors. The postoperative pathological diagnosis was a grade 2 neuroendocrine tumor. The patient showed no recurrence of tumor 3 years postoperatively. In this study, CTHA was more effective than other examinations in detecting small tumors, which could be resected without any residual tumors.

神经内分泌肿瘤(NENs)起源于神经内分泌细胞,主要发生在胃肠道、肺和胰腺。虽然NEN转移通常涉及肝脏,但原发性肝神经内分泌肿瘤(PHNETs)是罕见的。在此,我们报告一例52岁女性,表现为缓慢增大,囊性,多发性PHNETs。计算机断层扫描(CT)发现6节段(S6)和S7两个肿瘤,磁共振成像发现另外一个S7/8肿瘤。此外,肝动脉造影(CTHA)期间的CT显示S8小肿瘤。其他脏器未发现其他原发肿瘤。对肿瘤行后节段切除术和S8部分切除术。术后病理诊断为2级神经内分泌肿瘤。术后3年未见肿瘤复发。在本研究中,CTHA在检测小肿瘤方面比其他检查更有效,可以切除无残留肿瘤。
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引用次数: 0
Gestational gigantomastia with pseudoangiomatous stromal hyperplasia - a case report of rare entities. 妊娠期巨乳瘤合并假性血管瘤间质增生1例。
IF 0.4 Q4 SURGERY Pub Date : 2025-01-07 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjae835
Sophia Moore, Carlos Neblett, Kenneth Appiah, Rory Thompson

Gestational gigantomastia (GG) is a rare and severe clinical complication of pregnancy. It is characterized by dramatic and uncontrolled growth of the breasts, often leading to physical discomfort, psychological distress and significant surgical complications. Its pathophysiology is poorly understood; management options include conservative pharmacological and surgical interventions. Pseudoangiomatous stromal hyperplasia of the breast is a very rare, incidental, and histological diagnosis seen predominantly in women aged 30-40 years old, with the management generally involving surgical excision. The authors herein discuss an unusual case of bilateral GG complicated by pseudoangiomatous stromal hyperplasia in a premenopausal Caribbean woman, which is the second reported case in this population, with the first reported by one of our authors.

妊娠期巨乳症(GG)是一种罕见而严重的妊娠并发症。它的特点是乳房急剧和不受控制的生长,经常导致身体不适,心理困扰和严重的手术并发症。其病理生理机制尚不清楚;治疗方案包括保守的药物和手术干预。乳腺假性血管瘤间质增生是一种非常罕见的、偶发的组织学诊断,主要见于30-40岁的女性,治疗通常涉及手术切除。作者在此讨论一个不寻常的病例双侧GG合并假性血管瘤间质增生在绝经前加勒比妇女,这是第二例报告的情况下,与第一个报告的作者之一。
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引用次数: 0
Metastatic multicentric epithelioid angiosarcoma of bone. A case report with pitfalls. Tumor seeding after percutaneous biopsy and hypercalcemia. 骨转移性多中心上皮样血管肉瘤。一份充满陷阱的案例报告。经皮活检和高钙血症后肿瘤播种。
IF 0.4 Q4 SURGERY Pub Date : 2025-01-07 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjae022
Jorge Fuentes-Sánchez, Eva Manuela Pena-Burgos, Mar Tapia-Viñe, Jose Juan Pozo-Kreilinger, Eduardo Jose Ortiz-Cruz

Angiosarcomas are a type of malignant tumor of vascular origin. They represent <1% of all primary bone tumors. The multicentric or metastatic does not differ in its high aggressiveness and poor prognosis. A 72-year-old male with bone angiosarcoma initially located in proximal femur. After biopsy in a non-expert sarcoma center, he presented tumor involvement in the needle trajectory and multicentric/metastatic involvement at the sacro-coccygeal level. He associated tumoral-hypercalcemia and was referred to our sarcoma center. He was treated by tumoral resection and tumor prosthesis. In the follow-up he presented pulmonary metastasis and new implants, dying 2 months later. Multicentric or metastatic bone involvement in angiosarcomas has only theoretical relevance for their management. Biopsy should be performed in sarcoma centers due to the risk of dissemination. Although hypercalcemia in sarcomas is uncommon, we highlight its investigation.

血管肉瘤是一种起源于血管的恶性肿瘤。他们代表
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引用次数: 0
CT navigation-assisted intraoral extraction of large submandibular gland stones: a minimally invasive approach. CT导航辅助下颌下腺结石的口腔内取出:一种微创方法。
IF 0.4 Q4 SURGERY Pub Date : 2025-01-07 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjae832
Utku Kubilay, Canberk Kertmen, Orçun Delice

Sialolithiasis is a common cause of salivary gland obstruction, leading to symptoms such as pain and swelling. In cases of intraparenchymal submandibular stones and proximal ductal stones larger than 7 mm, interventional sialendoscopy may fail, necessitating sialoadenectomy. As an alternative, intraoral stone extraction can be performed with CT-guided navigation. This case report describes a 52-year-old male with previous sialadenitis complaints. Imaging confirmed a fixed intraparenchymal stone measuring 21 × 18 mm. Using CT navigation, the stone was located and removed intraorally. Salivary flow resumed through Wharton's duct on the same day postoperatively and the patient was discharged without further complaints or new stone formation during a 1-year follow-up. This minimally invasive method, utilizing CT navigation, allows for the preservation and functional recovery of the submandibular gland, avoiding skin scarring and reducing the risk of nerve damage.

涎石症是唾液腺阻塞的常见原因,导致疼痛和肿胀等症状。对于实质内下颌下结石和近端导管结石大于7mm的病例,介入性涎腺内镜检查可能失败,需要行涎腺切除术。作为一种替代方法,可以在ct引导下进行口内结石取出。本病例报告描述一名52岁男性,既往有涎腺炎主诉。影像学证实肝实质内固定结石,尺寸为21 × 18 mm。利用CT导航定位结石并经口内取出。术后当天唾液通过沃顿氏管恢复流动,患者出院,随访1年,无进一步抱怨或新的结石形成。这种微创方法,利用CT导航,允许保存和功能恢复颌下腺,避免皮肤疤痕和降低神经损伤的风险。
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引用次数: 0
Perforated marginal ulceration in the setting of single anastomosis duodeno-ileal switch (SADI-S) with conversion to Roux-en-Y gastric bypass and literature review. 单吻合术十二指肠回肠开关(SADI-S)转Roux-en-Y胃旁路的穿孔边缘溃疡及文献复习。
IF 0.4 Q4 SURGERY Pub Date : 2025-01-04 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjae828
Vincent Marcucci, Amanda R Camarda, Veysel Embel, Seth Kipnis

The single anastomosis duodenal-ileal switch (SADI-S) has become a safe alternative to Roux-en-Y gastric bypass (RYGB) in the treatment for morbid obesity. A known complication after bariatric surgery is the development of marginal ulceration. The current literature demonstrates an overwhelmingly low incidence of ulceration in patients who underwent SADI-S. The management and prevention is an ongoing subject of debate with no clear algorithm. The conversation of SADI-S to RYGB has been accomplished; however, this procedure has not been previously reported for marginal ulceration.

单吻合术十二指肠回肠开关(SADI-S)已成为Roux-en-Y胃旁路术(RYGB)治疗病态肥胖的安全替代方法。减肥手术后已知的并发症是边缘溃疡的发展。目前的文献显示,在接受SADI-S的患者中,溃疡的发生率极低。管理和预防是一个持续争论的主题,没有明确的算法。SADI-S与RYGB的对话已经完成;然而,这种方法在治疗边缘溃疡方面尚未见报道。
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引用次数: 0
Thoracic approach for suspected internal mammary lymph node recurrence following mastectomy and implant-based reconstruction: a case report. 胸部入路治疗乳房切除术及假体重建后疑似内乳淋巴结复发1例。
IF 0.4 Q4 SURGERY Pub Date : 2025-01-04 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjae829
Daisuke Murayama, Ryosuke Hirano, Osamu Mishima, Toko Hashizume

The use of video-assisted thoracic surgery (VATS) has increased in recent years. We herein report a case wherein suspected intramammary lymph node (IM) recurrence of breast cancer was treated using the thoracic approach (VATS). A 53-year-old woman had undergone right total mastectomy, axillary lymph node dissection, and implant-based reconstruction for right breast cancer 19 years ago. Hormone therapy was commenced postoperatively. Positron emission tomography as health check up performed at another hospital 1 year prior to presentation revealed enlargement of the right IMs, suggesting recurrence of breast cancer. IM biopsy was performed using VATS to preserve the artificial breast implant. The operative time and blood loss were 157 min and 20 ml, respectively. The postoperative course was favourable. IM biopsy revealed reactive enlargement owing to inflammation. In conclusion, VATS is a safer approach that yields superior outcomes in terms of appearance care.

近年来,视频辅助胸外科手术(VATS)的使用有所增加。我们在此报告一例疑似乳腺癌乳腺内淋巴结(IM)复发的病例,采用胸部入路(VATS)治疗。一位53岁的女性在19年前接受了右侧乳房全切除术,腋窝淋巴结清扫和基于植入物的右侧乳腺癌重建。术后开始激素治疗。在发病前1年在另一家医院进行的健康检查中,正电子发射断层扫描显示右侧IMs增大,提示乳腺癌复发。采用VATS进行IM活检以保存人工乳房植入物。手术时间157 min,出血量20 ml。术后过程良好。IM活检显示炎症引起的反应性扩大。综上所述,VATS是一种更安全的方法,在外观护理方面效果更好。
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引用次数: 0
Two cases of giant mucinous cystadenomas in postmenopausal women. 绝经后妇女巨大粘液囊腺瘤2例。
IF 0.4 Q4 SURGERY Pub Date : 2025-01-03 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjae833
Shumarova Svetlana, Anatoli Semkov, Vesela Karamisheva

Mucinous ovarian cystadenomas are rare epithelial benign tumors that can reach significant sizes. They are often asymptomatic and are discovered incidentally during an ultrasound examination. We present two clinical cases of mucinous ovarian cystadenomas with abdominal distention. Complicated variants can mimic an acute surgical abdomen and often require the involvement of a multidisciplinary team in operative treatment. Timely diagnosis and treatment are of utmost importance to prevent complications and malignancy.

卵巢粘液囊腺瘤是一种罕见的上皮性良性肿瘤,可达到显著的大小。它们通常是无症状的,是在超声检查时偶然发现的。我们报告两例卵巢粘液性囊腺瘤伴腹胀的临床病例。复杂的变异可以模仿急性手术腹部,通常需要多学科团队参与手术治疗。及时诊断和治疗对预防并发症和恶性肿瘤至关重要。
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引用次数: 0
期刊
Journal of Surgical Case Reports
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