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Clinical Presentation and Surgical Management of a Grynfelt Hernia: Report of a Clinical Case and Literature Review.
IF 0.6 Q4 SURGERY Pub Date : 2025-03-27 eCollection Date: 2025-01-01 DOI: 10.1155/cris/5634242
Pabel Ruben Carbajal Cabrera, Ruben Daniel Pérez López, Yunuen Ailyn Morales Tercero, Itzel Ocampo Barrero

Background: Grynfelt's lumbar hernia is the rarest of all abdominal wall hernias, accounting for between 1.5% and 2% of cases, with only 300-350 instances described to date. Lumbar hernias can be congenital or acquired, often triggered by trauma or surgery (iatrogenic). Diagnosis is clinical and confirmed via computed tomography. Surgical intervention is required for resolution, with repair performed either through open or laparoscopic surgery. Material and Methods: We present the case of a young female with no prior surgical or traumatic history, in whom the diagnosis of Grynfelt's hernia was made. Results: The patient underwent elective left lumbotomy surgery with hernioplasty using a supra-aponeurotic polypropylene mesh. Postsurgical recovery was adequate, and she was discharged 4 h after surgery. Follow-up in the general surgery outpatient clinic occurred at 20 days, 1, 3, and 6 months, with no recurrence, complications, or incidents. Conclusion: Grynfelt's hernia is a rare entity that requires a high index of suspicion for accurate diagnosis. Although cases are often asymptomatic, untreated hernias can lead to significant morbidity. Early recognition and timely surgical intervention are crucial for symptom relief and prevention of complications. In this case report, surgical management involved hernioplasty through a left lumbotomy approach, repairing the hernia defect and reducing the hernia content. Supra-aponeurotic mesh was placed to ensure adequate closure. Given the rarity of this pathology, no specific management guidelines exist in the literature. Therefore, the decision for this type of repair was based on intraoperative findings. Further research is needed to clarify management strategies and optimize outcomes for patients with Grynfelt's hernia.

背景:Grynfelt 腰疝是所有腹壁疝中最罕见的一种,占病例的 1.5% 到 2%,迄今为止仅描述过 300 到 350 例。腰疝可以是先天性的,也可以是后天性的,通常由外伤或手术(先天性)引发。诊断依据临床表现,并通过计算机断层扫描确诊。需要进行手术治疗,通过开腹或腹腔镜手术进行修补。材料与方法:本病例为一名年轻女性,既往无手术史,也无外伤史,诊断为 Grynfelt 疝。手术结果患者接受了选择性左腰部切除手术,并使用腹膜上聚丙烯网片进行了疝成形术。术后恢复良好,术后 4 小时即可出院。普外科门诊分别在 20 天、1 个月、3 个月和 6 个月进行了随访,没有发现复发、并发症或事故。结论Grynfelt疝是一种罕见病,需要高度怀疑才能准确诊断。虽然病例通常没有症状,但未经治疗的疝气可导致严重的发病率。早期识别和及时手术治疗对于缓解症状和预防并发症至关重要。在本病例报告中,手术治疗包括通过左腰部切开术进行疝成形术,修补疝缺损并缩小疝内容物。为确保充分闭合,还放置了上腹膜网片。鉴于这种病症的罕见性,文献中没有具体的治疗指南。因此,这种类型的修补术是根据术中发现决定的。需要进一步开展研究,以明确管理策略,优化 Grynfelt 疝患者的治疗效果。
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引用次数: 0
Post-Traumatic Diaphragmatic Hernia Presenting as Bowel Obstruction 12 Years After a Chest Gunshot Wound: A Rare Delayed Diagnosis.
IF 0.6 Q4 SURGERY Pub Date : 2025-03-26 eCollection Date: 2025-01-01 DOI: 10.1155/cris/2527619
Papa Mamadou Faye, Ulrich Igor Mbessoh Kengne, Ousmane Thiam, Mouhamadou Laye Diop, Joël Gabin Konlack Mekontso, Mouhamed Moustapha Gueye, Seydy Ly, Amacoumba Fall, Mame Dieme Diop, Christophe Mbueda, Naomi Makam, Alpha Oumar Toure, Mamadou Cisse

Post-traumatic diaphragmatic hernia (PTDH) is defined as the migration of intra-abdominal organs into the chest through a pathological defect in the diaphragm caused by trauma. PTDH is a rare condition, occurring in 3%-7% of all thoracoabdominal injuries. Approximately 14.6% of PTDH cases present months to years after the initial trauma. Cases of delayed PTDH complicated by bowel obstruction and perforation are exceedingly uncommon, with a reported prevalence of 0.17%-6%. In Africa, fewer than 10 cases of delayed PTDH have been documented over the past three decades. Despite the availability of published reports, there are no established practice guidelines for managing PTDH. Here, we present a case of delayed PTDH that manifested as acute bowel obstruction 12 years after a gunshot wound to the chest. The condition led to a fatal postoperative outcome. This case highlights the critical need for clinicians to consider PTDH in patients with a history of trauma presenting with acute bowel obstruction and underscores the importance of urgent surgical management to prevent fatal complications.

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引用次数: 0
Successful Management of Complicated Burst Abdomen With Open Abdomen Using Only Simple Saline Dressing.
IF 0.6 Q4 SURGERY Pub Date : 2025-03-25 eCollection Date: 2025-01-01 DOI: 10.1155/cris/6862550
Dionizi Muganga, Francis Basimbe, Irene Nayiga, Amanda Ategeka, Paddy Malinga, Twaha Muwanga

Introduction: Necrosis of the rectus or lateral abdominal wall investing fascia may be associated with invasive infections or closure under extreme tension. This can lead to fascial dehiscence and evisceration of the intra-abdominal contents. Globally, abdominal wound dehiscence varies from 0.4% to 3.5% with associated mortalities reaching up to 45% in the perioperative period. Redo surgical operations and infectious complications are the major risk factors for abdominal wound dehiscence, but also presence of low albumin, glucocorticoid use, chest infections, and emergency surgeries have been also implicated. Open abdomen has been employed in incidences of trauma where a second look operation may be necessary, loss of abdominal wall, sepsis after penetrating abdominal trauma, and in cases of severe secondary peritonitis and acute pancreatitis. Patients with open abdomen are at a risk of fistula formation, sepsis, and loss of abdominal domain due to lateral fascial retraction. To reduce the mentioned complications mesh and nonmediated techniques to bridge fascia defects have been recommended with particular emphasis on biologic meshes with or without negative pressure wound therapy, component separation, or planned ventral hernia. Methods: We report a case of necrosis of the rectus and abdominal wound dehiscence and its management in a sub-Saharan setting, highlighting the challenges encountered and lessons learned. Conclusion: Retention sutures should be used cautiously in the management of wound dehiscence as it increases the risk of fascial necrosis in cases of intra-abdominal hypertension, as seen in our patient. In the absence of a VAC dressing, the utilization of routine saline gauze dressing promotes epithelialization over the exposed bowel and is a viable alternative to temporary abdominal closure modes of managing an open abdomen in a resource-limited setting.

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引用次数: 0
An Early Presentation of Tricuspid Valve Rupture in a Trauma Patient With Congenital Heart Disease.
IF 0.6 Q4 SURGERY Pub Date : 2025-01-30 eCollection Date: 2025-01-01 DOI: 10.1155/cris/6711702
Justus Boever, Rishi Batra, Hason Khan, Zachary M Bauman

Tricuspid valve regurgitation/rupture is a rare complication of trauma, with only around 150 cases reported in the literature, though this prevalence may be underestimated due to subtle clinical manifestations. The tricuspid valve is the most frequently affected heart valve following blunt chest trauma due to its anterior anatomical position between the sternum and the vertebrae. The diagnosis of tricuspid regurgitation is often delayed in the traumatic setting due to the subtlety of clinical manifestations. Many trauma patients also present with distracting injuries. The subsequent treatment delay can result in development of irreversible dilatation of right-sided heart chambers, making it imperative to have a high index of suspicion for tricuspid regurgitation as a cause of acute hemodynamic instability in the setting of blunt trauma to the chest. In this report, we present a unique case of traumatic tricuspid valve regurgitation in a patient with a history of congenital atrial septal defect (ASD)/partial anomalous pulmonary venous return (PAPVR).

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引用次数: 0
Unusual Surgical Resection of Asymptomatic Schwannoma of the Cervical Vagus Nerve With Risk of Stroke: Case Report.
IF 0.6 Q4 SURGERY Pub Date : 2025-01-23 eCollection Date: 2025-01-01 DOI: 10.1155/cris/9443139
Roberto Sérgio Martins, Adilson J M de Oliveira, Evander Lucas, Mario Gilberto Siqueira

Schwannomas are the most common tumors of the peripheral nerves, originating from their support cells, the Schwann cells. The location of the tumor in the vagus nerve is rare. Vagus schwannomas usually present as a solitary, slow-growing, asymptomatic mass that rarely causes neurological alterations. The differential diagnosis of vagus nerve schwannomas includes other tumors of the parapharyngeal space or neoplasms of the jugular foramen. We report the case of a patient with an asymptomatic schwannoma of the vagus nerve involving important neck structures, with radiological compression of the carotid artery with a high risk of stroke; because of this, we underwent surgery using a transcervical approach with intracapsular excision of the tumor. The patient has a good outcome. In asymptomatic patients' surgical indication is not an easy decision; in this case, the main reason for surgical indication was the risk of stroke with potential neurological sequels.

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引用次数: 0
Intramural Intestinal Metastasis of Malignant Melanoma as a Rare Cause of Ileoileal Intussusception: A Case Report and Review of the Literature.
IF 0.6 Q4 SURGERY Pub Date : 2025-01-16 eCollection Date: 2025-01-01 DOI: 10.1155/cris/5556332
Gary Amseian, Alexandre Soler, Alba Torroella, Lia Sisuashvili, Paula Escarcena, Gerard Rafart

Intussusception in adults is rare and poses a diagnostic challenge, often due to neoplastic causes. Metastatic melanoma is known to spread to the gastrointestinal tract, especially the small intestine. We report the case of a patient with obstructive symptoms and a history of metastatic melanoma. An emergency abdominal computed tomography (CT) scan identified an obstruction caused by ileoileal intussusception located at the site of a previously described enteric metastasis. Following palliative surgery with ileal resection, two nodular lesions causing intussusception were identified, and pathological examination confirmed intramural metastases from melanoma. In adult patients with obstructive symptoms and a history of melanoma, intussusception secondary to intestinal metastases should be considered in the differential diagnosis.

{"title":"Intramural Intestinal Metastasis of Malignant Melanoma as a Rare Cause of Ileoileal Intussusception: A Case Report and Review of the Literature.","authors":"Gary Amseian, Alexandre Soler, Alba Torroella, Lia Sisuashvili, Paula Escarcena, Gerard Rafart","doi":"10.1155/cris/5556332","DOIUrl":"10.1155/cris/5556332","url":null,"abstract":"<p><p>Intussusception in adults is rare and poses a diagnostic challenge, often due to neoplastic causes. Metastatic melanoma is known to spread to the gastrointestinal tract, especially the small intestine. We report the case of a patient with obstructive symptoms and a history of metastatic melanoma. An emergency abdominal computed tomography (CT) scan identified an obstruction caused by ileoileal intussusception located at the site of a previously described enteric metastasis. Following palliative surgery with ileal resection, two nodular lesions causing intussusception were identified, and pathological examination confirmed intramural metastases from melanoma. In adult patients with obstructive symptoms and a history of melanoma, intussusception secondary to intestinal metastases should be considered in the differential diagnosis.</p>","PeriodicalId":9600,"journal":{"name":"Case Reports in Surgery","volume":"2025 ","pages":"5556332"},"PeriodicalIF":0.6,"publicationDate":"2025-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11756941/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143028041","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
A Case of Radical Resection of Esophageal Basaloid Cell Carcinoma After Hemostasis by Transarterial Embolization.
IF 0.6 Q4 SURGERY Pub Date : 2025-01-10 eCollection Date: 2025-01-01 DOI: 10.1155/cris/7736573
Keita Sato, Koji Takahashi

Esophageal bleeding management typically involves endoscopy but becomes challenging with large or hemorrhagic tumors, especially in cases of rare basal cell carcinoma. This malignancy, with a poorer prognosis than squamous cell carcinoma, often requires definitive surgery. A 78-year-old man with severe hematemesis underwent transarterial embolization (TAE) after failed endoscopic hemostasis for a middle thoracic esophageal tumor. Subsequently, he successfully underwent radical tumor resection on the seventh day of hospitalization. While emergency surgery is an option, its invasiveness may be a limitation, especially for patients in poor general condition. TAE is effective for hemostasis and serves as a crucial bridge to radical esophageal tumor resection.

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引用次数: 0
A Rare Case of Linear Phlebolith: Foreign Body Discovered in the Femoral Vein.
IF 0.6 Q4 SURGERY Pub Date : 2025-01-10 eCollection Date: 2025-01-01 DOI: 10.1155/cris/8824786
Tariq Alanezi, Abdulmajeed Altoijry, Kaisor Iqbal, Saeed Alabduljabbar, Mohammed Yousef Aldossary, Sultan AlSheikh

Introduction: Phlebolith is a term that refers to round-shaped calcified thrombi commonly located in the pelvic region. The occurrence of dense, linear calcifications or phlebolith-like formations within the soft tissues of the lower extremities, particularly in the superficial femoral, greater saphenous, or popliteal veins, is rare. Patient Concerns: This study presents the case of a 73-year-old woman who was being evaluated for postmenopausal bleeding. During the patient's diagnostic workup, an incidental linear-shaped phlebolith was discovered. She had a positive history of deep vein thrombosis (DVT) for 36 years following her previous vaginal delivery. Diagnosis: Upon further examination and imaging, the patient was found to have a chronic calcified thrombus in the iliofemoral, popliteal, great saphenous, and superficial femoral veins, which was initially reported as a foreign body in the femoral vein on computed tomography (CT). Interventions and Outcomes: Conservative management was undertaken, with no worsening of her condition upon further follow-up. Conclusion: This study showcased a rare form of a radiographically visible calcified thrombus in the veins of the lower extremities of our patient. Calcified venous thrombosis in the lower extremities is rare, as previously documented cases of venous calcifications have been observed in the pelvis with round shapes or as phleboliths. The common presentations differ from those in our case, making it important to consider such cases when formulating a differential diagnosis. While the precise mechanisms behind the formation of calcified thrombi remain unclear, this study emphasizes the significance of further exploration and future case studies to shed light on this enigmatic phenomenon.

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引用次数: 0
A Large Thoracolumbosacral Meningomyelocele From Northern Tanzania: A Case Report. 坦桑尼亚北部大胸腰骶部脊膜膨出1例。
IF 0.6 Q4 SURGERY Pub Date : 2025-01-09 eCollection Date: 2025-01-01 DOI: 10.1155/cris/5662565
Mujaheed Suleman, Happiness Rabiel, Kerry Vaughan, Mathayo Shadrack, Goodluck Ndibalema, Raghav Lodhia, Jay Lodhia

Meningomyelocele and meningocele are types of neural tube defects, which are congenital abnormalities of the spine and spinal cord. These conditions are frequently encountered by pediatric neurosurgeons worldwide and represent a significant public health concern due to their association with a range of collateral conditions, other malformations, and increased morbidity. While many cases can be identified during prenatal ultrasound screenings, this is often challenging in resource-limited settings with poor health-seeking behaviors. Surgical intervention is the primary treatment for these defects, and while various methods are described in the literature, larger defects require complex flaps and techniques, with limited options available. Beyond early surgical intervention, patients require lifelong care involving multidisciplinary medical teams.

脊膜脊膜膨出和脑膜膨出是神经管缺陷的一种,是脊柱和脊髓的先天性异常。这些情况是世界各地的儿科神经外科医生经常遇到的,由于它们与一系列附带条件、其他畸形和发病率增加有关,因此代表了一个重大的公共卫生问题。虽然许多病例可以在产前超声筛查中发现,但在资源有限且就医行为不良的环境中,这往往具有挑战性。手术干预是这些缺陷的主要治疗方法,虽然文献中描述了各种方法,但较大的缺陷需要复杂的皮瓣和技术,可供选择的方法有限。除了早期手术干预,患者还需要多学科医疗团队的终身护理。
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引用次数: 0
Iatrogenic Proximal Urethro-Rectal Perforation During Foley Catheter Insertion. Foley导尿管置入期间医源性近端尿道直肠穿孔。
IF 0.6 Q4 SURGERY Pub Date : 2025-01-08 eCollection Date: 2025-01-01 DOI: 10.1155/cris/4784527
Claude Tayar, Ali Alameh, Rawan Abdallah, Jamil Boufarah, Yehya Tlaiss, Hadi Farhat

Iatrogenic urethral-rectal perforation represents a rare but severe complication arising from medical interventions, notably highlighted in the context of Foley catheter insertion. This case report outlines the presentation, diagnosis, management, and outcomes of a 71-year-old male patient who experienced iatrogenic rectal perforation during the routine insertion of a Foley catheter, against the backdrop of several predisposing factors, such as atrial fibrillation, valvular disease, benign prostatic hyperplasia, urethral stenosis, and colorectal cancer with liver metastasis. The inadvertent creation of a rectourethral fistula during the procedure led to an urgent multidisciplinary approach involving surgery and postoperative management, including fecal and urine diversion and antibiotic therapy. The case highlights the critical importance of meticulous technique and comprehensive preoperative patient assessment in minimizing the risk of such iatrogenic complications. It further discusses the management strategies for rectourethral fistulas, ranging from conservative approaches to surgical interventions, and emphasizes the role of fecal diversion, urine diversion, and the potential of robotic surgery in enhancing outcomes for complex cases. The report concludes by reflecting on the intricate balance between routine medical procedures and the potential for severe complications, highlighting the need for heightened awareness and skill in the prevention and management of iatrogenic rectal perforation.

医源性尿道直肠穿孔是一种罕见但严重的并发症,由医疗干预引起,特别是在Foley导尿管插入的情况下。本病例报告概述了一位71岁男性患者的表现、诊断、处理和结果,他在常规插入Foley导管时经历了医源性直肠穿孔,背景是几个易感因素,如心房颤动、瓣膜疾病、良性前列腺增生、尿道狭窄和结直肠癌伴肝转移。在手术过程中无意中产生的直肠尿道瘘导致了紧急的多学科方法,包括手术和术后处理,包括粪便和尿液转移和抗生素治疗。该病例强调了细致的技术和全面的术前患者评估对于最大限度地减少此类医源性并发症的风险至关重要。它进一步讨论了直肠尿道瘘的治疗策略,从保守方法到手术干预,并强调了粪便转移、尿液转移的作用,以及机器人手术在提高复杂病例预后方面的潜力。报告最后反思了常规医疗程序与潜在严重并发症之间的复杂平衡,强调需要提高预防和管理医源性直肠穿孔的认识和技能。
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引用次数: 0
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Case Reports in Surgery
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