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Transplant Ureter Inguinal Herniation Treated by Robotic Inguinal Hernia Repair. 应用机器人腹股沟疝修补术治疗移植性输尿管腹股沟疝。
Pub Date : 2023-09-22 eCollection Date: 2023-07-01 DOI: 10.4293/CRSLS.2023.00020
Diego Laurentino Lima, Valentina Viscarret, Raquel Nogueira, Kara Watts, Flavio Malcher

Introduction: We report the case of a transplanted ureter obstructed by an inguinal herniation treated by a robotic-assisted approach.

Case report: This is a case of a 63-year-old male who had a kidney transplant with a graft on the left pelvis in September 2014, and presented to the clinic for evaluation of bilateral inguinal hernia. On physical examination he had bilateral palpable inguinal hernias, with the right one larger and only partially reducible. Computed tomography scan showed portion of urinary bladder and transplant ureter in the left inguinal hernia and mild hydroureteronephrosis in the transplanted kidney. Patient underwent catheterization of the transplant ureter where indocyanine green was injected for proper transplant ureter identification with the Firefly filter and robotic assisted hernia repair. Surgery was uneventful and patient was discharged home the same day with no further complications.

Conclusion: The robotic approach using the Firefly filter was shown to be safe during the dissection to avoid injury to the transplant ureter.

引言:我们报告了一例因腹股沟疝而阻塞的移植输尿管,采用机器人辅助入路治疗。病例报告:这是一例63岁的男性病例,他于2014年9月接受了左骨盆移植物肾移植,并被送往诊所评估双侧腹股沟疝。体检时,他发现双侧腹股沟疝可触及,右侧腹股沟疝较大,只能部分缩小。计算机断层扫描显示左腹股沟疝的部分膀胱和移植输尿管,移植肾的轻度输尿管积水性肾病。患者接受了移植输尿管导管插入术,注射吲哚青绿,用萤火虫过滤器和机器人辅助疝修补术正确识别移植输尿管。手术很顺利,患者当天出院回家,没有出现任何并发症。结论:使用萤火虫过滤器的机器人入路在解剖过程中是安全的,可以避免对移植输尿管的损伤。
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引用次数: 0
Jejunal Intussusception Secondary to Pancreatic and Gastric Heterotopia in a 23-Year-Old. 一例23岁的胰腺和胃异位引起的空肠肠套叠。
Pub Date : 2023-09-04 eCollection Date: 2023-07-01 DOI: 10.4293/CRSLS.2023.00018
Caline McCarthy, Amendha Ware, Jay A Redan

Introduction: Pancreatic and gastric heterotopias are a rare presentation of pancreatic and gastric tissues located outside their expected location. The most common site of heterotopic pancreas is the gastric antrum, and the most common site of heterotopic gastric mucosa is the proximal esophagus. The two tissues rarely present simultaneously. Although lead-point intussusception secondary to simultaneous heterotypic gastric and pancreatic tissue is extremely rare, its management strategy is the same as other pathological lead-point intussusception.

Case description: This report presents a 23-year-old female who presented to the emergency department with abdominal pain, vomiting, and gastrointestinal bleeding. Computed tomography scan revealed features of distal small bowel intussusception secondary to a solid mass lead point. Following laparoscopic assisted small bowel resection and incidental appendectomy, histopathology evaluation confirmed the diagnosis of heterotopic pancreatic and gastric tissue as the lead point. The patient had an uneventful postoperative period and was discharged in stable condition, free of symptoms.

Discussion: Lead point intussusception of the jejunum in adults due to combined heterotopic tissue is extremely rare, with no reported cases in the literature. Prompt diagnosis and management are essential, with delays in treatments leading to a risk of perforation and mortality. If diagnosed, minimally invasive surgical approaches can treat obstruction and improve intraoperative and postoperative outcomes.

引言:胰腺和胃异位是一种罕见的胰腺和胃组织位于预期位置之外的表现。异位胰腺最常见的部位是胃窦,异位胃粘膜最常见的位置是食管近端。这两种组织很少同时存在。尽管继发于同时发生的非典型胃和胰腺组织的导点肠套叠极为罕见,但其处理策略与其他病理导点肠套叠相同。病例描述:本报告报告一名23岁女性,因腹痛、呕吐和胃肠道出血到急诊科就诊。计算机断层扫描显示远端小肠肠套叠的特征,继发于一个固体物质引导点。在腹腔镜辅助小肠切除术和附带阑尾切除术之后,组织病理学评估证实了异位胰腺和胃组织的诊断为指导点。患者术后平静,出院时情况稳定,没有任何症状。讨论:成人空肠联合异位组织引起的铅点肠套叠极为罕见,文献中尚无报道。及时诊断和管理至关重要,治疗延误会导致穿孔和死亡的风险。如果得到诊断,微创手术方法可以治疗梗阻并改善术中和术后结果。
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引用次数: 0
Swiss LithoClast® Trilogy Lithotripter for Use in Robotic Pyelolithotomy. 瑞士LithoClast®Trilogy碎石机,用于机器人Pyelolithotomy切开术。
Pub Date : 2023-09-04 eCollection Date: 2023-07-01 DOI: 10.4293/CRSLS.2023.00027
Micah Levy, Chih Peng Chin, Krishna T Ravivarapu, Osama Al-Alao, Francisca Larenas, Michael A Palese

Introduction: The Boston Scientific Swiss LithoClast® Trilogy lithotripter was intended for use in percutaneous nephrolithotomy. We performed, to our knowledge, the first two robotic pyelolithotomies using the Trilogy lithotripter for intracorporeal lithotripsy.

Case description: Two cases are presented involving a 65-year-old female with a complete left staghorn calculus and hydronephrosis secondary to a left ureteropelvic junction (UPJ) obstruction, and a 69-year-old male with a large left staghorn calculus and multiple large left sided simple renal cysts. In both cases, a robotic pyelolithotomy was scheduled for stone removal along with concurrent UPJ repair and cyst decortication respectively. Following pyeloplasty and cyst decortication respectively, and following stone visualization, the 2.4-mm Trilogy probe was inserted into the 12-mm assistant port and under direct visualization the stone was fragmented and removed using Trilogy's built-in mechanisms. Both patients were treated successfully without complications and were found to be stone-free on follow-up.

Conclusion: The Trilogy lithotripter may be an effective tool for stone management when introduced during robotic pyelolithotomy and provides additional optionality when manual extraction poses challenges.

简介:Boston Scientific Swiss LithoClast®Trilogy碎石机旨在用于经皮肾取石术。据我们所知,我们使用Trilogy碎石机进行了前两次机器人肾盂取石术。病例描述:两例病例涉及一名65岁女性,患有完全性左鹿角结石和继发于左肾盂输尿管连接处(UPJ)梗阻的肾积水,以及一名69岁男性,患有大的左鹿角结石,多个大的左侧单纯性肾囊肿。在这两种情况下,分别安排了机器人肾盂切开取石术,同时进行UPJ修复和囊肿剥脱术。分别在肾盂成形术和囊肿剥除术后,以及在结石显像后,将2.4mm的Trilogy探头插入12mm的辅助口,在直接显像下,使用Trilogy的内置机制将结石粉碎并取出。两名患者都得到了成功的治疗,没有并发症,并且在随访中发现没有结石。结论:Trilogy碎石机在机器人肾盂结石切开术中使用时可能是一种有效的结石管理工具,并在手动取石带来挑战时提供了额外的选择。
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引用次数: 0
Robotic-Assisted Repair of a Ureterosciatic Hernia with Combined Ureteral Stenting. 输尿管支架联合输尿管支架机器人辅助修复输尿管坐骨疝。
Pub Date : 2023-04-01 DOI: 10.4293/CRSLS.2023.00015
Jeremy Fridling, Brendan Gontarz, Joshua Stein, Vladimir Daoud

Pelvic floor hernias represent a rare type of hernia and a rare etiology of pelvic symptoms. The rarest type of pelvic floor hernias are sciatic hernias, which present with a variety of symptoms depending on the hernia contents and location. Many different treatment approaches are described in the literature. A 73-year-old female presented to our outpatient minimally invasive surgery (MIS) clinic with one year of colicky left flank pain. She had previously presented to an emergency department, at which time a computed tomography (CT) scan demonstrated left-sided hydronephrosis in the setting of a left-sided ureterosciatic hernia. She was asymptomatic and had no palpable hernia bulge. An operative repair was offered based on her prolonged symptoms. The patient was brought electively to the operating room with minimally invasive and urological surgeons. A left ureteral stent was placed over a guidewire. A robotic repair was performed with a round piece of biosynthetic mesh, secured in place with fibrin glue. Sciatic hernias are an extremely rare etiology of pelvic symptoms and require a high index of suspicion to identify. Obstructive and neuropathic symptoms may be intermittent, so diagnosis is often made using CT imaging. We report a successful treatment with pre-operative ureteral stenting followed by a robotic repair using biologic mesh secured with fibrin glue fixation. We believe this is a durable repair although acknowledge that longer follow-up is needed to establish the longevity of our treatment modality.

盆底疝是一种罕见的疝气类型,也是一种罕见的盆腔症状病因。最罕见的盆底疝类型是坐骨疝,它根据疝的内容物和位置表现出多种症状。文献中描述了许多不同的治疗方法。一位73岁的女性以一年的左腹绞痛就诊于我们的微创外科门诊。她之前曾到急诊室就诊,当时的计算机断层扫描(CT)显示左侧输尿管坐骨疝导致左侧肾积水。她无症状,没有可触及的疝隆起。根据她的症状延长,我们提供了手术修复。患者被选择性地带到了微创外科和泌尿外科的手术室。左侧输尿管支架放置在导丝上。机器人修复是用一个圆形的生物合成网片进行的,用纤维蛋白胶固定在适当的位置。坐骨疝是一种极其罕见的骨盆症状的病因,需要高度的怀疑指数来识别。梗阻性和神经性症状可能是间歇性的,因此通常使用CT成像进行诊断。我们报告了一个成功的治疗方法,术前输尿管支架置入,随后使用生物网状物与纤维蛋白胶固定固定的机器人修复。我们相信这是一个持久的修复,尽管我们承认需要更长的随访时间来确定我们的治疗方式的寿命。
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引用次数: 1
Incarcerated Epiploic Appendix in a Spigelian Hernia Treated by Robotic-Assisted Surgery. 机器人辅助手术治疗Spigelian疝嵌顿性网膜阑尾。
Pub Date : 2023-04-01 DOI: 10.4293/CRSLS.2023.00008
Diego L Lima, Analena Alcabes, Valentina Viscarret, Raquel Nogueira, Flavio Malcher

Introduction: We report a case of a patient who presented with incarceration of the epiploic appendix in a spigelian hernia, subsequently treated by a robotic-assisted surgical approach.

Case description: This is a case of a 52 year-old male patient who presented with nausea and two-week history of worsening left lower quadrant pain. On examination, the patient had an irreducible left lower quadrant mass. Computed tomography scan showed an epiploic appendagitis in a left Spigelian hernia. The patient underwent a robotic transabdominal preperitoneal hernia repair successfully and was discharged home the same day.

Conclusion: The robotic platform was a safe and effective approach to treating the patient with no postoperative complications.

简介:我们报告一个病例的病人谁提出了嵌顿的网膜阑尾在一个spiegelian疝,随后通过机器人辅助手术方法治疗。病例描述:这是一个52岁的男性患者,表现为恶心和两周的左下腹疼痛加重史。经检查,患者有一个不可还原的左下腹肿块。计算机断层扫描显示左侧螺旋疝的网膜阑尾炎。患者成功接受了机器人经腹腹膜前疝修补术,并于当天出院回家。结论:机器人平台是一种安全有效的治疗方法,无术后并发症。
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引用次数: 0
Mixed Adeno-Neuroendocrine Neoplasms: Two Cases, One Institution. 混合性腺神经内分泌肿瘤:一个机构,两个病例。
Pub Date : 2023-01-15 eCollection Date: 2023-10-01 DOI: 10.4293/CRSLS.2023.00045
Casey Paterson, Gabrielle Perrotti, Bakhtawar Mushtaq, Jaclyn Heilman, Steven Fassler

Epithelial tumors with neuroendocrine and nonendocrine components constitute the rare yet aggressive entity of neoplasms of the gastro-entero-pancreatic tract. These tumors were first named "mixed adeno-neuroendocrine carcinomas" (MANECs) by the World Health Organization in 2010 and in 2017 renamed "mixed neuroendocrine non-neuroendocrine neoplasms" (MiNENs). Combined adenocarcinoma and neuroendocrine carcinoma neoplasms are a rare occurrence within the gastrointestinal tract. In this report, we describe two separate cases of mixed rectal adeno-neuroendocrine carcinomas and their treatment. We describe two cases at one institution of mixed neuroendocrine non-neuroendocrine rectal neoplasms. Given the rarity of diagnosis and inconsistencies in both nomenclature and treatment recommendations in the literature, mixed adeno-neuroendocrine carcinoma epidemiology and prognosis are not yet fully understood. Future prospective trials with a focus in management of MiNENs will offer valuable insight into these rare mixed carcinomas.

具有神经内分泌和非内分泌成分的上皮性肿瘤构成了胃-肠-胰腺道肿瘤中罕见但具有侵袭性的实体。世界卫生组织于 2010 年首次将这些肿瘤命名为 "混合腺癌-神经内分泌癌"(MANECs),并于 2017 年更名为 "混合神经内分泌-非神经内分泌肿瘤"(MiNENs)。腺癌和神经内分泌癌的合并肿瘤在胃肠道中较为罕见。在本报告中,我们分别描述了两例直肠腺癌-神经内分泌癌混合瘤病例及其治疗方法。我们描述了一家医疗机构的两例神经内分泌与非神经内分泌混合型直肠肿瘤。鉴于诊断的罕见性以及文献中命名和治疗建议的不一致性,混合型腺神经内分泌癌的流行病学和预后尚未完全明了。未来以治疗混合腺内分泌癌为重点的前瞻性试验将为了解这些罕见的混合腺内分泌癌提供有价值的信息。
{"title":"Mixed Adeno-Neuroendocrine Neoplasms: Two Cases, One Institution.","authors":"Casey Paterson, Gabrielle Perrotti, Bakhtawar Mushtaq, Jaclyn Heilman, Steven Fassler","doi":"10.4293/CRSLS.2023.00045","DOIUrl":"10.4293/CRSLS.2023.00045","url":null,"abstract":"<p><p>Epithelial tumors with neuroendocrine and nonendocrine components constitute the rare yet aggressive entity of neoplasms of the gastro-entero-pancreatic tract. These tumors were first named \"mixed adeno-neuroendocrine carcinomas\" (MANECs) by the World Health Organization in 2010 and in 2017 renamed \"mixed neuroendocrine non-neuroendocrine neoplasms\" (MiNENs). Combined adenocarcinoma and neuroendocrine carcinoma neoplasms are a rare occurrence within the gastrointestinal tract. In this report, we describe two separate cases of mixed rectal adeno-neuroendocrine carcinomas and their treatment. We describe two cases at one institution of mixed neuroendocrine non-neuroendocrine rectal neoplasms. Given the rarity of diagnosis and inconsistencies in both nomenclature and treatment recommendations in the literature, mixed adeno-neuroendocrine carcinoma epidemiology and prognosis are not yet fully understood. Future prospective trials with a focus in management of MiNENs will offer valuable insight into these rare mixed carcinomas.</p>","PeriodicalId":72723,"journal":{"name":"CRSLS : MIS case reports from SLS","volume":"10 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10789440/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139473137","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
Multiple Internal Hernias: A Complication of Laparoscopic Roux-en-Y Gastric Bypass. 多发性内疝:腹腔镜 Roux-en-Y 胃旁路术并发症。
Pub Date : 2023-01-15 eCollection Date: 2023-10-01 DOI: 10.4293/CRSLS.2023.00040
Annika G Samuelson, Leland F Damron, Zaid Haddadin, Sakib M Adnan, Marc Neff

Introduction: Internal hernias are the most common cause of small bowel obstruction following laparoscopic Roux-en-Y gastric bypass surgery (LRYGBP) with four distinct types. Herein, we report the clinical course of a patient with two independent hernias at the Petersen's space and a rarer subtype at the jejunojejunal window. A high index of suspicion for less common subtypes of internal hernias and the possibility of multiple, simultaneous internal hernias is critical.

Case description: We describe the case of a 52-year-old female with a history of LRYGBP who presented with abdominal pain and emesis due to an internal hernia at Peterson's defect, requiring subsequent laparoscopic repair. On postoperative day three, the patient presented again with recurrent abdominal pain and emesis. Repeat exploratory laparoscopy found a separate internal hernia involving the jejunojejunal window with the previously repaired Petersen's defect intact.

Discussion: This case illustrates a unique scenario of a patient post-LRYGBP with multiple internal hernias at the Peterson's space and the less common jejunojejunal window, which was missed during the index surgery. Failure to identify simultaneous hernias may result in additional invasive intervention and further morbidity.

Conclusion: Multiple less-common variants of internal hernias may present simultaneously following LRYGBP.

导言:内疝是腹腔镜鲁-恩-Y 胃旁路手术(LRYGBP)后导致小肠梗阻的最常见原因,有四种不同类型。在此,我们报告了一名患者的临床病程,该患者在彼得森间隙处有两个独立的疝,在空肠空肠窗处有一个较罕见的亚型。高度怀疑不常见的亚型内疝以及同时发生多个内疝的可能性至关重要:我们描述了一例 52 岁女性的病例,她有 LRYGBP 病史,因 Peterson's 缺口处的内疝而出现腹痛和呕吐,随后需要进行腹腔镜修补术。术后第三天,患者再次出现腹痛和呕吐。再次进行探查性腹腔镜检查发现了一个单独的内疝,涉及空肠空肠窗,而之前修补过的彼得森缺损完好无损:本病例说明了一种独特的情况,即一名 LRYGBP 术后患者在彼得森间隙和较少见的空肠空肠窗处有多个内疝,但在索引手术中却漏诊了。如果不能同时发现疝气,可能会导致额外的侵入性干预和进一步的发病:结论:LRYGBP术后可能会同时出现多种不常见的内疝。
{"title":"Multiple Internal Hernias: A Complication of Laparoscopic Roux-en-Y Gastric Bypass.","authors":"Annika G Samuelson, Leland F Damron, Zaid Haddadin, Sakib M Adnan, Marc Neff","doi":"10.4293/CRSLS.2023.00040","DOIUrl":"10.4293/CRSLS.2023.00040","url":null,"abstract":"<p><strong>Introduction: </strong>Internal hernias are the most common cause of small bowel obstruction following laparoscopic Roux-en-Y gastric bypass surgery (LRYGBP) with four distinct types. Herein, we report the clinical course of a patient with two independent hernias at the Petersen's space and a rarer subtype at the jejunojejunal window. A high index of suspicion for less common subtypes of internal hernias and the possibility of multiple, simultaneous internal hernias is critical.</p><p><strong>Case description: </strong>We describe the case of a 52-year-old female with a history of LRYGBP who presented with abdominal pain and emesis due to an internal hernia at Peterson's defect, requiring subsequent laparoscopic repair. On postoperative day three, the patient presented again with recurrent abdominal pain and emesis. Repeat exploratory laparoscopy found a separate internal hernia involving the jejunojejunal window with the previously repaired Petersen's defect intact.</p><p><strong>Discussion: </strong>This case illustrates a unique scenario of a patient post-LRYGBP with multiple internal hernias at the Peterson's space and the less common jejunojejunal window, which was missed during the index surgery. Failure to identify simultaneous hernias may result in additional invasive intervention and further morbidity.</p><p><strong>Conclusion: </strong>Multiple less-common variants of internal hernias may present simultaneously following LRYGBP.</p>","PeriodicalId":72723,"journal":{"name":"CRSLS : MIS case reports from SLS","volume":"10 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10789439/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139473138","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
In Vitro Fertilization Cycle Outcomes for a Patient Undergoing Oocyte Retrieval following Ovarian Torsion. 卵巢扭转后接受卵母细胞回收的患者体外受精周期结果。
Pub Date : 2023-01-01 DOI: 10.4293/CRSLS.2022.00092
Roisin M Mortimer, Catherine Gordon, Serene Srouji

Introduction: To report a case of ovarian torsion following ovarian hyperstimulation with subsequent detorsion and oocyte retrieval.

Case description: The patient was diagnosed with torsion following acute onset abdominal pain following her leuprolide acetate trigger injection. The patient underwent diagnostic laparoscopy which confirmed right ovarian torsion. Following detorsion, the patient underwent oocyte retrieval as planned with 72 total oocytes and 70 mature oocytes retrieved. Thirty-six mature oocytes were cryopreserved; 34 were inseminated with conventional in vitro fertilization, of which 27 (79.4%) were fertilized. Sixteen blastocyst stage embryos were cryopreserved.

Discussion: Ovarian torsion during ovarian hyperstimulation is a rare event, but consideration should be given to detorsion first, followed by oocyte retrieval. We demonstrate that mature oocytes can be retrieved even after temporary vascular compromise to the ovary with subsequent excellent fertilization and blastocyst conversion rates.

简介:报告一例卵巢过度刺激后卵巢扭转,随后卵巢扭转和卵母细胞取出。病例描述:患者被诊断为扭转后急性发作腹痛后,她的醋酸左uprolide触发注射。患者行诊断性腹腔镜检查,证实右侧卵巢扭转。变形后,患者按计划进行卵母细胞回收,共获得72个总卵母细胞和70个成熟卵母细胞。冷冻保存成熟卵母细胞36个;常规体外受精34例,受精率27例(79.4%)。16个囊胚期胚胎冷冻保存。讨论:卵巢过度刺激时卵巢扭转是一种罕见的事件,但应首先考虑卵巢扭转,然后再考虑卵母细胞回收。我们证明,成熟的卵母细胞可以在卵巢血管暂时受损后恢复,随后具有良好的受精和囊胚转化率。
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引用次数: 0
Multidisciplinary Management of Cutaneous Gluteus Vaginal Fistula After Sacrospinous Ligament Fixation. 骶棘韧带固定后皮肤臀阴道瘘的多学科治疗。
Pub Date : 2023-01-01 DOI: 10.4293/CRSLS.2022.00085
Veronica Kim, Shadi Seraji, Bogdan A Grigorescu, Man Hon, Daniel H Hunt, Farr R Nezhat

Introduction: Cutaneous gluteal vaginal fistula is a rare but significant postoperative complication which may present years after sacrospinous ligament fixation (SSLF) surgery There is limited data on the management of cutaneous vaginal fistula following SSLF.

Case description: This case report describes a 77-year-old who presents twenty years after SSLF with cutaneous gluteal vaginal abscess and fistula. She underwent successful management with CT-guided percutaneous drainage of gluteal abscess and placement of guiding cutaneous vaginal catheter, laparoscopic pelvic wall dissection and evaluation, and transvaginal localization and removal of the infected permanent suture.

Discussion: Multi-disciplinary approach should be considered in the treatment of chronic fistula status post SSLF, including interventional radiology, urogynecology, and minimally invasive gynecologic surgery.

摘要:臀皮阴道瘘是骶棘韧带固定(SSLF)手术后一种罕见但重要的术后并发症,关于骶棘韧带固定(SSLF)术后皮肤阴道瘘的处理资料有限。病例描述:这个病例报告描述了一个77岁的病人,在SSLF后20年出现皮肤臀阴道脓肿和瘘管。她成功地接受了ct引导下的经皮臀脓肿引流术和引导阴道导管的放置,腹腔镜盆腔壁剥离和评估,以及经阴道定位和拆除感染的永久缝线。讨论:SSLF后慢性瘘管状态的治疗应考虑多学科方法,包括介入放射学、泌尿妇科和微创妇科手术。
{"title":"Multidisciplinary Management of Cutaneous Gluteus Vaginal Fistula After Sacrospinous Ligament Fixation.","authors":"Veronica Kim,&nbsp;Shadi Seraji,&nbsp;Bogdan A Grigorescu,&nbsp;Man Hon,&nbsp;Daniel H Hunt,&nbsp;Farr R Nezhat","doi":"10.4293/CRSLS.2022.00085","DOIUrl":"https://doi.org/10.4293/CRSLS.2022.00085","url":null,"abstract":"<p><strong>Introduction: </strong>Cutaneous gluteal vaginal fistula is a rare but significant postoperative complication which may present years after sacrospinous ligament fixation (SSLF) surgery There is limited data on the management of cutaneous vaginal fistula following SSLF.</p><p><strong>Case description: </strong>This case report describes a 77-year-old who presents twenty years after SSLF with cutaneous gluteal vaginal abscess and fistula. She underwent successful management with CT-guided percutaneous drainage of gluteal abscess and placement of guiding cutaneous vaginal catheter, laparoscopic pelvic wall dissection and evaluation, and transvaginal localization and removal of the infected permanent suture.</p><p><strong>Discussion: </strong>Multi-disciplinary approach should be considered in the treatment of chronic fistula status post SSLF, including interventional radiology, urogynecology, and minimally invasive gynecologic surgery.</p>","PeriodicalId":72723,"journal":{"name":"CRSLS : MIS case reports from SLS","volume":"10 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/c9/50/e2022.00085.PMC10065752.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9326373","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: 1
Laparoscopic Repair of a Congenital Diaphragmatic Hernia Presenting with a Small Bowel Obstruction. 以小肠梗阻为表现的先天性膈疝腹腔镜修补术。
Pub Date : 2023-01-01 DOI: 10.4293/CRSLS.2022.00091
Roberto Torres-Aguiar, Victor Cabrera-Bou, Luis F Serrano

Diaphragmatic hernias are uncommon, and can appear secondary to trauma or as a congenital defect. These hernias can be asymptomatic or have various clinical presentations. One of the clinical scenarios is incarceration of bowel through the diaphragmatic defect. A bowel obstruction from an incarcerated diaphragmatic hernia is a rare occurrence. We present a case of a small bowel obstruction caused by a congenital diaphragmatic hernia that was successfully managed with laparoscopy.

膈疝并不常见,可继发于创伤或先天性缺陷。这些疝气可以是无症状的或有各种临床表现。其中一种临床情况是通过横膈膜缺损导致肠嵌顿。嵌顿性膈疝引起的肠梗阻是很少见的。我们提出了一个由先天性膈疝引起的小肠梗阻的病例,并成功地进行了腹腔镜检查。
{"title":"Laparoscopic Repair of a Congenital Diaphragmatic Hernia Presenting with a Small Bowel Obstruction.","authors":"Roberto Torres-Aguiar,&nbsp;Victor Cabrera-Bou,&nbsp;Luis F Serrano","doi":"10.4293/CRSLS.2022.00091","DOIUrl":"https://doi.org/10.4293/CRSLS.2022.00091","url":null,"abstract":"<p><p>Diaphragmatic hernias are uncommon, and can appear secondary to trauma or as a congenital defect. These hernias can be asymptomatic or have various clinical presentations. One of the clinical scenarios is incarceration of bowel through the diaphragmatic defect. A bowel obstruction from an incarcerated diaphragmatic hernia is a rare occurrence. We present a case of a small bowel obstruction caused by a congenital diaphragmatic hernia that was successfully managed with laparoscopy.</p>","PeriodicalId":72723,"journal":{"name":"CRSLS : MIS case reports from SLS","volume":"10 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/27/fa/e2022.00091.PMC9912997.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9324885","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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CRSLS : MIS case reports from SLS
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