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Robotic-assisted excision of left para-aortic paraganglioma: a novel approach. 机器人辅助切除左主动脉旁副神经节瘤:一种新方法。
IF 0.4 Q4 SURGERY Pub Date : 2025-01-21 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjae842
Jack Kang Tan, Jason Ramsingh

Paragangliomas, a type of extra-adrenal tumour, albeit rare, are dangerous due to their high metastatic potential and risk of hypertensive crisis from massive catecholamine release. It typically presents with sympathetic overdrive symptoms such as diaphoresis, headache, and palpitation, accompanied by substantially high plasma metanephrines level and mass on contrasted computed tomography abdomen and pelvis, whilst some are found incidentally. In this report, we discuss a case of an extra-adrenal lesion located near susceptible major structures with extensive vascularisation, in a patient with near-death experience. Complete excision of the pulsatile mass with minimal bleeding and no complications, was made possible utilizing the da Vinci Robotic System. Robotic surgery, being a part of a multidisciplinary approach, leads to better patient outcomes and shorter hospitalisations. Moreover, it offers enhanced dexterity and improved depth perception compared to conventional methods. However, further studies are needed to validate its application in standard practice.

副神经节瘤是肾上腺外肿瘤的一种,虽然罕见,但由于其高转移潜力和大量儿茶酚胺释放引起高血压危象的风险,是危险的。典型表现为交感神经亢进症状,如出汗、头痛和心悸,伴有血浆肾上腺素水平明显升高,腹部和骨盆ct上可见肿块,但也有一些是偶然发现的。在这个报告中,我们讨论了一个病例的肾上腺外病变位于附近的易感大结构与广泛的血管化,在病人的濒死经验。使用达芬奇机器人系统完全切除搏动性肿块,出血最少,无并发症。作为多学科方法的一部分,机器人手术可以带来更好的患者治疗效果和更短的住院时间。此外,与传统方法相比,它提供了更高的灵活性和深度感知能力。然而,需要进一步的研究来验证其在标准实践中的应用。
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引用次数: 0
First full intracorporeal robotic cystectomy and neobladder in a renal transplant recipient. 肾移植受者首次全体内机器人膀胱切除术和新膀胱。
IF 0.4 Q4 SURGERY Pub Date : 2025-01-20 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjaf009
Xavier Tillou, Lisa Le Bloa, Vanja Courteille, Clemence Bechade, Thibaut Waeckel

The literature regarding robotic-assisted radical cystectomy in kidney transplant recipients is limited. We present the first reported case of robotic-assisted radical cystectomy with a full intracorporeal orthotopic neobladder in a kidney transplant recipient. A 36-year-old man was diagnosed with muscle-invasive urothelial carcinoma 12 years after kidney transplantation. His immunosuppressive regimen consisted of everolimus, mycophenolate mofetil, and prednisolone. After cystectomy and left lymph node dissection, we used a U-shaped neobladder technique slightly modified to adapt to the fixed position of the renal transplant ureter. The surgical time was 305 min, and the blood loss was 200 ml. The patient was discharged 16 days after hospitalization with no surgical complications. Histological analysis revealed no UC (pT0N0) with disseminated carcinoma in situ. Seven months after the surgery, no signs of recurrence or distant/lymph node metastasis were observed. No urinary leakage with complete bladder emptying was reported. Serum creatinine clearance rate was 51 ml/min. Immunosuppressive regimen was not modified after surgery.

关于肾移植受者机器人辅助根治性膀胱切除术的文献是有限的。我们提出了第一例报道的机器人辅助根治性膀胱切除术与全体内原位新膀胱在肾移植受者。一名36岁的男性在肾移植12年后被诊断为肌肉侵袭性尿路上皮癌。他的免疫抑制方案包括依维莫司、霉酚酸酯和强的松龙。在膀胱切除术和左侧淋巴结清扫后,我们采用稍作修改的u型新膀胱技术,以适应肾移植输尿管的固定位置。手术时间305 min,出血量200 ml。患者住院16天后出院,无手术并发症。组织学分析未发现UC (pT0N0)伴播散性原位癌。术后7个月,未发现复发或远处/淋巴结转移的迹象。没有漏尿和膀胱完全排空的报道。血清肌酐清除率为51 ml/min。术后未改变免疫抑制方案。
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引用次数: 0
Perianal abscess complicated by histiocytic necrotizing lymphadenitis postoperatively: a case report. 术后肛周脓肿并发组织细胞坏死性淋巴结炎1例。
IF 0.4 Q4 SURGERY Pub Date : 2025-01-20 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjaf007
Liman Zhang, Jie Yang, Lili Wang, Tianpeng Zhang, Fei Ju, Yanjang Wu

Histiocytic necrotizing lymphadenitis (HNL) is a rare condition presenting with lymphadenopathy and fever. We report a case of a 61-year-old male with a history of perianal abscess surgery who developed HNL postoperatively. The patient was treated with corticosteroids, leading to resolution of fever and alleviation of symptoms. This case emphasizes the need for clinical vigilance for HNL in patients with a history of perianal abscess surgery and postoperative fever with lymph node enlargement.

组织细胞坏死性淋巴结炎(HNL)是一种罕见的疾病,表现为淋巴结病变和发烧。我们报告一例61岁男性肛周脓肿手术史,术后发展为HNL。患者接受皮质类固醇治疗,发热消退,症状减轻。本病例强调有肛周脓肿手术史和术后发热伴淋巴结肿大的HNL患者需要临床警惕。
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引用次数: 0
Long-term survival of stage 4 gallbladder cancer after extended radical surgery plus limited chemotherapy: a case report. 延长根治性手术加有限化疗后4期胆囊癌的长期生存:1例报告。
IF 0.4 Q4 SURGERY Pub Date : 2025-01-20 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjaf010
Zhengbin Huang, Jian Sun, Changsong Li, Sheng Chen, Tian Jin, Zhengqi Wu

Gallbladder cancers (GBC) are insidious, malignant, and associated with poor prognosis, with a 5-year survival rate of 5%. Long-term survival in advanced GBC is rare. Here, we report a case of a 45-year-old female who presented with intermittent right upper quadrant pain for 1 month. A gallbladder mass and two liver masses were identified on a computed tomography (CT) scan of the abdomen and pelvis with intravenous contrast, which was highly suspicious for GBC. The patient underwent extended radical surgery, and a low to moderately differentiated gallbladder adenocarcinoma was diagnosed through pathology. Postoperatively, the patient received chemotherapy with gemcitabine and cisplatin but only tolerated one cycle. The patient has been disease-free for over 7 years, representing an unusually long survival.

胆囊癌(GBC)隐匿,恶性,预后差,5年生存率为5%。晚期GBC的长期存活是罕见的。在这里,我们报告一例45岁的女性谁提出间歇性右上腹部疼痛1个月。腹部和骨盆经静脉造影剂CT扫描发现胆囊肿块和两个肝脏肿块,高度怀疑为GBC。患者接受了广泛的根治性手术,病理诊断为低分化至中分化胆囊腺癌。术后,患者接受吉西他滨和顺铂化疗,但仅耐受一个周期。患者已无病7年多,生存时间异常长。
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引用次数: 0
Intracranial neurenteric cyst in the cerebellopontine angle: a case report. 脑桥小脑角颅内神经直肠囊肿1例。
IF 0.4 Q4 SURGERY Pub Date : 2025-01-15 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjae840
Nyoman Golden, Steven Awyono, Christopher Lauren, Dicky T Prakoso

Neurenteric cysts, rare benign tumors, are most often found in the cervical or thoracic spinal cord, with intracranial occurrences being extremely uncommon. This case report describes a 52-year-old female with a neurenteric cyst in the cerebellopontine angle, presenting with headaches and balance disturbances. Magnetic resonance imaging (MRI) revealed a cystic lesion causing hydrocephalus, and surgical removal was performed using a retrosigmoid approach. Histopathological analysis confirmed the cyst as Type A neurenteric, characterized by ciliated columnar epithelium and goblet cells. Postoperatively, the patient showed significant improvement with resolved symptoms. Neurenteric cysts can mimic other cystic lesions radiologically, complicating diagnosis. Management typically involves surgical excision, although complete removal is often challenging due to cyst adherence to nearby structures. Recurrence rates remain high, necessitating long-term follow-up. This case highlights the importance of differential diagnosis and careful surgical planning in managing neurenteric cysts to optimize patient outcomes.

神经肠囊肿是一种罕见的良性肿瘤,常见于颈或胸脊髓,颅内发生极为罕见。本病例报告描述了一名52岁女性脑桥小脑角神经系统囊肿,表现为头痛和平衡障碍。磁共振成像(MRI)显示囊性病变引起脑积水,手术切除采用乙状结肠后入路。组织病理学分析证实该囊肿为A型神经肠,以纤毛柱状上皮和杯状细胞为特征。术后,患者症状明显改善。神经肠囊肿在影像学上可与其他囊性病变相似,使诊断复杂化。治疗通常包括手术切除,但由于囊肿粘附在附近的结构上,完全切除通常具有挑战性。复发率仍然很高,需要长期随访。本病例强调了鉴别诊断和精心的手术计划在处理神经肠囊肿以优化患者预后的重要性。
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引用次数: 0
A rare case of endo-bronchial lipoma presenting with vague cardiac symptoms. 一例罕见的支气管内脂肪瘤,表现为模糊的心脏症状。
IF 0.4 Q4 SURGERY Pub Date : 2025-01-15 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjae703
Zoha Asghar, Muhammad Mehdi Irfani, Alizeh Fatimi, Abdul Ahad Sohail, Saulat Hasnain Fatimi

Endobronchial lipoma is an extremely rare benign tumor, accounting for 0.1%-0.5% of all lung tumors. This case report presents a patient diagnosed with endobronchial lipoma, a condition that can lead to significant bronchial obstruction and subsequent parenchymal damage. Patients usually exhibit symptoms including cough, dyspnea, and recurrent respiratory infections, which initially mimic more common pulmonary conditions such as chronic obstructive pulmonary disease. However, in our case patient presented with non-specific cardiac symptoms. Diagnosis was confirmed through bronchoscopy, revealing a well-circumscribed mass obstructing the bronchus. Due to severe parenchymal inflammation, treatment involved left-sided thoracotomy and upper lobectomy which successfully relieved the obstruction and alleviated the patient's symptoms. Histopathological examination identified the tumor as a lipoma. This case underscores the importance of considering endobronchial lipoma in differential diagnoses for patients with unexplained cardiac or respiratory symptoms, as early detection and treatment can prevent significant complications.

支气管内脂肪瘤是一种极为罕见的良性肿瘤,约占所有肺部肿瘤的0.1%-0.5%。这个病例报告了一个诊断为支气管内脂肪瘤的病人,这种情况可以导致严重的支气管阻塞和随后的实质损害。患者通常表现出咳嗽、呼吸困难和反复呼吸道感染等症状,这些症状最初类似于更常见的肺部疾病,如慢性阻塞性肺病。然而,在我们的病例中,患者表现出非特异性心脏症状。通过支气管镜检查确诊,发现一个界限清晰的肿块阻塞了支气管。由于严重的实质炎症,治疗包括左侧开胸和上肺叶切除术,成功地解除了阻塞,缓解了患者的症状。组织病理学检查证实该肿瘤为脂肪瘤。这个病例强调了在鉴别诊断中考虑支气管内脂肪瘤对于无法解释的心脏或呼吸系统症状的重要性,因为早期发现和治疗可以预防严重的并发症。
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引用次数: 0
Acute thoracic disc herniation with severe spinal cord compression: a case report. 急性胸椎间盘突出伴严重脊髓压迫1例。
IF 0.4 Q4 SURGERY Pub Date : 2025-01-15 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjaf001
Mario Cahueque, Andres Cobar, Santiago Montenegro

This case report highlights the rare presentation of an acute thoracic disc herniation in a 27-year-old male. Thoracic disc herniations are uncommon, accounting for less than 1% of all disc herniations, and acute presentations have scantly been recorded in literature. The patient, a mechanic, presented with a sudden onset of dorsal pain and bilateral lower limb weakness after lifting heavy equipment, leading to a sudden cease of most motor functions in the patient's lower limbs. Magnetic resonance imaging revealed a severe T9/T10 herniation with significant spinal cord compression. Emergency surgical decompression via a right-sided transpedicular thoracic approach was performed, resulting in progressive neurological recovery. This case underscores the importance of early diagnosis, timely surgical intervention, and multidisciplinary management in achieving favorable outcomes for this rare condition.

这个病例报告强调了一个罕见的急性胸椎间盘突出症的表现在一个27岁的男性。胸椎间盘突出并不常见,占所有椎间盘突出的不到1%,在文献中很少有急性表现的记录。患者是一名机械师,在搬运重型设备后突然出现背部疼痛和双侧下肢无力,导致患者下肢大部分运动功能突然停止。磁共振成像显示严重的T9/T10疝伴明显的脊髓压迫。通过右侧经椎弓根胸入路进行紧急手术减压,导致神经系统渐进式恢复。这个病例强调了早期诊断、及时手术干预和多学科管理对这种罕见疾病取得良好结果的重要性。
{"title":"Acute thoracic disc herniation with severe spinal cord compression: a case report.","authors":"Mario Cahueque, Andres Cobar, Santiago Montenegro","doi":"10.1093/jscr/rjaf001","DOIUrl":"10.1093/jscr/rjaf001","url":null,"abstract":"<p><p>This case report highlights the rare presentation of an acute thoracic disc herniation in a 27-year-old male. Thoracic disc herniations are uncommon, accounting for less than 1% of all disc herniations, and acute presentations have scantly been recorded in literature. The patient, a mechanic, presented with a sudden onset of dorsal pain and bilateral lower limb weakness after lifting heavy equipment, leading to a sudden cease of most motor functions in the patient's lower limbs. Magnetic resonance imaging revealed a severe T9/T10 herniation with significant spinal cord compression. Emergency surgical decompression via a right-sided transpedicular thoracic approach was performed, resulting in progressive neurological recovery. This case underscores the importance of early diagnosis, timely surgical intervention, and multidisciplinary management in achieving favorable outcomes for this rare condition.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2025 1","pages":"rjaf001"},"PeriodicalIF":0.4,"publicationDate":"2025-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11733772/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143014121","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
Case report of the successful treatment of pemphigus vulgaris using ovine forestomach matrix graft. 使用绵羊林胃基质移植成功治疗寻常性丘疹痤疮的病例报告。
IF 0.4 Q4 SURGERY Pub Date : 2025-01-14 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjae848
William A Kokal, Jessica Simon

Pemphigus vulgaris (PV) is a subtype of pemphigus and life-altering disorder that results in the formation of intraepithelial blisters in mucosa and skin. Though the etiology is not well understood, it is an autoimmune disorder resulting in acantholytic blisters due to auto-antibodies targeting proteins of keratinocyte adhesion. Rapid diagnosis and restoration of the epidermal layer is imperative for patients with PV as widespread epidermal damage can lead to high morbidity and mortality rates. This case report presents the treatment of PV in a 53-year-old female who presented after 9 months of worsening symptoms and 30% total body surface area blistering. Most of the lesion was re-epithelialized in 1 week, with complete healing in 4 weeks following a single application of ovine forestomach matrix (OFM) graft. This case represents the first report of the use of OFM to aid regeneration of epithelial lesions resulting from an autoimmune bullous disease.

寻常型天疱疮(Pemphigus vulgaris, PV)是天疱疮和改变生活的疾病的一种亚型,导致粘膜和皮肤上皮内水疱的形成。虽然病因尚不清楚,但它是一种自身免疫性疾病,由于自身抗体靶向角质细胞粘附蛋白而导致棘溶性水泡。快速诊断和修复表皮层对PV患者至关重要,因为广泛的表皮损伤可导致高发病率和死亡率。本病例报告介绍了一名53岁女性的PV治疗,她在症状恶化9个月后出现30%的体表面积水泡。大部分病变在1周内重新上皮化,在单次应用羊前胃基质(OFM)移植后4周内完全愈合。本病例是首次报道使用OFM来帮助自身免疫性大疱病引起的上皮病变再生。
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引用次数: 0
Staged surgery for the treatment of carotid aneurysm. 分期手术治疗颈动脉瘤。
IF 0.4 Q4 SURGERY Pub Date : 2025-01-14 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjae849
Shiyi Zhao, Dejie Chen

Extracranial carotid artery aneurysm (ECAA) is a relatively rare vascular lesion of the neck, and is usually found incidentally and is usually asymptomatic. Surgery is currently the first choice for symptomatic or growing ECAA, including open resection of the entire aneurysm, with or without arterial replacement and insertion of grafts. Ischemic stroke is the most serious complication after resection of ECAA. The preoperative Matas test facilitates the collateral circulation through the circle of Willis, which allows the brain to adapt to the hypoxic situation and effectively reduces ischemic stroke. We report a case of a young patient who underwent a staged surgery to treat it (the first stage was prophylactic carotid artery blockade, so called open Matas test), and achieved good results.

颅外颈动脉动脉瘤(ECAA)是一种相对罕见的颈部血管病变,通常是偶然发现的,通常无症状。手术是目前治疗有症状或正在生长的ECAA的首选方法,包括切开切除整个动脉瘤,伴或不伴动脉置换和移植物植入。缺血性脑卒中是ECAA术后最严重的并发症。术前Matas试验通过威利斯环促进侧支循环,使大脑适应缺氧情况,有效减少缺血性卒中。我们报告一例年轻患者分期手术治疗此病(第一期为预防性颈动脉阻断,即开放Matas试验),并取得良好效果。
{"title":"Staged surgery for the treatment of carotid aneurysm.","authors":"Shiyi Zhao, Dejie Chen","doi":"10.1093/jscr/rjae849","DOIUrl":"10.1093/jscr/rjae849","url":null,"abstract":"<p><p>Extracranial carotid artery aneurysm (ECAA) is a relatively rare vascular lesion of the neck, and is usually found incidentally and is usually asymptomatic. Surgery is currently the first choice for symptomatic or growing ECAA, including open resection of the entire aneurysm, with or without arterial replacement and insertion of grafts. Ischemic stroke is the most serious complication after resection of ECAA. The preoperative Matas test facilitates the collateral circulation through the circle of Willis, which allows the brain to adapt to the hypoxic situation and effectively reduces ischemic stroke. We report a case of a young patient who underwent a staged surgery to treat it (the first stage was prophylactic carotid artery blockade, so called open Matas test), and achieved good results.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2025 1","pages":"rjae849"},"PeriodicalIF":0.4,"publicationDate":"2025-01-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11731181/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142985022","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
Case presentation of a robot-assisted bilateral benign tonsillectomy using the da Vinci SP system. 使用达芬奇 SP 系统进行机器人辅助双侧良性扁桃体切除术的病例介绍。
IF 0.4 Q4 SURGERY Pub Date : 2025-01-13 eCollection Date: 2025-01-01 DOI: 10.1093/jscr/rjae631
Christopher Seifen, Christoph Matthias, Harishanker Jeyarajan, Tilman Huppertz
{"title":"Case presentation of a robot-assisted bilateral benign tonsillectomy using the da Vinci SP system.","authors":"Christopher Seifen, Christoph Matthias, Harishanker Jeyarajan, Tilman Huppertz","doi":"10.1093/jscr/rjae631","DOIUrl":"10.1093/jscr/rjae631","url":null,"abstract":"","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2025 1","pages":"rjae631"},"PeriodicalIF":0.4,"publicationDate":"2025-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11729732/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142984924","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
期刊
Journal of Surgical Case Reports
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