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Journal of Surgical Case Reports最新文献

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Acute avulsion fracture of the ischial tuberosity in an adolescent athlete treated by suture anchor fixation using the suture bridge technique: a case report. 使用缝合桥技术进行缝合锚固定治疗青少年运动员骶骨结节急性撕脱性骨折：病例报告。
IF 0.4
Journal of Surgical Case Reports Pub Date : 2024-11-25 eCollection Date: 2024-11-01 DOI: 10.1093/jscr/rjae748
Yasuyuki Omichi, Tomohiro Goto, Kaori Momota, Michihiro Takai, Ryosuke Sato, Tetsuya Enishi, Shunji Nakano, Koichi Sairyo
{"title":"Acute avulsion fracture of the ischial tuberosity in an adolescent athlete treated by suture anchor fixation using the suture bridge technique: a case report.","authors":"Yasuyuki Omichi, Tomohiro Goto, Kaori Momota, Michihiro Takai, Ryosuke Sato, Tetsuya Enishi, Shunji Nakano, Koichi Sairyo","doi":"10.1093/jscr/rjae748","DOIUrl":"10.1093/jscr/rjae748","url":null,"abstract":"<p><p>This is the first report of acute avulsion fracture of the ischial tuberosity (AFIT) treated by suture anchor fixation using the suture bridge technique. A 13-year-old boy developed sudden, severe right hip pain while running a short distance. Pelvic images revealed the avulsion fracture of the right ischial tuberosity with displacement of the avulsed fragment by 35 mm. We performed open reduction and reconstruction fixation 5 days after the injury using the subgluteal approach with longitudinal skin incision. Four suture anchors were set at the ischial tuberosity, and the avulsed fragment was repositioned and fixed using the suture bridge technique. At 1 year postoperatively, the avulsion fracture was bony fused, and he had returned to his preinjury competitive level. Use of multiple suture anchors increases the strength of fixation, which overcomes the problem of anchor loosening and makes open reduction and reconstruction fixation an effective treatment for acute avulsion fracture of the ischial tuberosity.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2024 11","pages":"rjae748"},"PeriodicalIF":0.4,"publicationDate":"2024-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11587889/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142717337","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
Spontaneous sigmoid perforation and subsequent ruptured hepatic aneurysms in suspected vascular type Ehlers-Danlos syndrome: a case report and comprehensive literature review. 疑似血管型埃勒斯-丹洛斯综合征（Ehlers-Danlos syndrome）的自发性乙状结肠穿孔和随后的肝动脉瘤破裂：病例报告和综合文献综述。
IF 0.4
Journal of Surgical Case Reports Pub Date : 2024-11-25 eCollection Date: 2024-11-01 DOI: 10.1093/jscr/rjae726
SaeRam Oh, Aaron D Hudnall, Caitlin A Fitzgerald
{"title":"Spontaneous sigmoid perforation and subsequent ruptured hepatic aneurysms in suspected vascular type Ehlers-Danlos syndrome: a case report and comprehensive literature review.","authors":"SaeRam Oh, Aaron D Hudnall, Caitlin A Fitzgerald","doi":"10.1093/jscr/rjae726","DOIUrl":"10.1093/jscr/rjae726","url":null,"abstract":"<p><p>Ehlers-Danlos syndrome (EDS) is an inherited disorder of collagen creation and function which can affect many organs. Surgical management of EDS spectrum remains a significant challenge for surgeons, including the vascular type of EDS (vEDS). There do not exist specific guidelines for the management of vEDS, which proves difficulty given the devastating pathology and potential outcomes. This case report emphasizes the need for further research in many areas including the need for certain screenings to identify any vascular aneurysms or dissections prior to rupture, as well as asking should there be a screen for this gene mutation in COL3A1 included at birth. Our case report is one of few reports that link the spontaneous colonic rupture that may trigger the subsequent vascular catastrophe leading to devastating mortality.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2024 11","pages":"rjae726"},"PeriodicalIF":0.4,"publicationDate":"2024-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11587892/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142717407","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
Lung resection from wedge to pneumonectomy as surgical options for pulmonary mucormycosis. 从楔形肺切除术到肺切除术，作为肺粘液瘤病的手术选择。
IF 0.4
Journal of Surgical Case Reports Pub Date : 2024-11-25 eCollection Date: 2024-11-01 DOI: 10.1093/jscr/rjae753
Alexander Pohlman, Mohammad Nizamuddin, Fritzie S Albarillo, Zaid M Abdelsattar
{"title":"Lung resection from wedge to pneumonectomy as surgical options for pulmonary mucormycosis.","authors":"Alexander Pohlman, Mohammad Nizamuddin, Fritzie S Albarillo, Zaid M Abdelsattar","doi":"10.1093/jscr/rjae753","DOIUrl":"10.1093/jscr/rjae753","url":null,"abstract":"<p><p>Pulmonary mucormycosis (PM) is a rare and life-threatening condition, most prevalent in immunocompromised patients. Early signs and symptoms are often nonspecific. A high index of suspicion in at risk patients should prompt early infectious work-up, including bronchoscopy, followed by aggressive antifungal therapy and early surgical resection when indicated. We demonstrate these core tenants of diagnosis and management of PM via two patient presentations, the first involving a kidney transplant recipient who presented with a mild cough, found to have a lung lesion with rapid growth over a few weeks; the second involving a patient with acute lymphoblastic leukemia who presented with hemoptysis and imaging revealing a 5 cm perihilar mass obliterating the left pulmonary artery. Both patients were managed with aggressive surgical therapy.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2024 11","pages":"rjae753"},"PeriodicalIF":0.4,"publicationDate":"2024-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11588314/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142717370","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
Sleeve resection of a typical carcinoid tumour in a case of aberrant anatomy. 对一例解剖异常的典型类癌进行袖状切除。
IF 0.4
Journal of Surgical Case Reports Pub Date : 2024-11-25 eCollection Date: 2024-11-01 DOI: 10.1093/jscr/rjae756
Jeesoo J Choi, Abigail A Palmares
{"title":"Sleeve resection of a typical carcinoid tumour in a case of aberrant anatomy.","authors":"Jeesoo J Choi, Abigail A Palmares","doi":"10.1093/jscr/rjae756","DOIUrl":"10.1093/jscr/rjae756","url":null,"abstract":"<p><p>Neuroendocrine tumours of bronchial origin account for ~1%-2%. They can be typical or atypical in nature and are likely to be endobronchial in growth. We report a case of a 37-year-old woman with a carcinoid tumour in the bronchus intermedius with a background of aberrant bronchial anatomy. The tumour was removed by sleeve resection and histopathology confirmed a typical carcinoid tumour. This report describes successful surgical management of this carcinoid tumour despite aberrant bronchial anatomy.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2024 11","pages":"rjae756"},"PeriodicalIF":0.4,"publicationDate":"2024-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11588313/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142717393","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
Splenic artery pseudoaneurysm rupture post-laparoscopic sleeve gastrectomy. 腹腔镜袖状胃切除术后脾动脉假性动脉瘤破裂。
IF 0.4
Journal of Surgical Case Reports Pub Date : 2024-11-25 eCollection Date: 2024-11-01 DOI: 10.1093/jscr/rjae752
Stephanie M Babic, Roshan N Ramachandran
{"title":"Splenic artery pseudoaneurysm rupture post-laparoscopic sleeve gastrectomy.","authors":"Stephanie M Babic, Roshan N Ramachandran","doi":"10.1093/jscr/rjae752","DOIUrl":"10.1093/jscr/rjae752","url":null,"abstract":"<p><p>A splenic artery pseudoaneurysm (SAP) is a rare vascular entity that is becoming increasingly recognized as a potential complication of bariatric surgery. This is a case of a 36-year-old woman brought by ambulance to a regional emergency department with abdominal pain, collapse, and gross haemodynamic instability 2 years post-laparoscopic sleeve gastrectomy. She received aggressive resuscitation in the emergency department but could not be stabilized and so underwent an emergency laparotomy. Intra-operatively, she was found to have a ruptured SAP with active bleeding, which was managed with a splenectomy. A high index of suspicion is required in any patient presenting with abdominal pain and circulatory collapse in the context of previous bariatric surgery. In rural or regional settings without immediate access to interventional radiology services, the most appropriate management option will almost invariably be an emergency laparotomy and splenectomy due to the risk of deterioration during patient transfer.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2024 11","pages":"rjae752"},"PeriodicalIF":0.4,"publicationDate":"2024-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11587890/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142717400","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 rare complication of infantile hemangioma: Kasabach-Merritt phenomenon. 婴儿血管瘤的罕见并发症：卡萨巴赫-梅里特现象。
IF 0.4
Journal of Surgical Case Reports Pub Date : 2024-11-25 eCollection Date: 2024-11-01 DOI: 10.1093/jscr/rjae721
Ricardo A Caravantes, José Manuel Toralla, Daniela Saenz
{"title":"A rare complication of infantile hemangioma: Kasabach-Merritt phenomenon.","authors":"Ricardo A Caravantes, José Manuel Toralla, Daniela Saenz","doi":"10.1093/jscr/rjae721","DOIUrl":"10.1093/jscr/rjae721","url":null,"abstract":"<p><p>Infantile hemangiomas are the most common type of vascular tumors, affecting ~5% of infants within the first weeks of life. In rare instances, these tumors can lead to Kasabach-Merritt phenomenon (KMP), a life-threatening consumptive coagulopathy characterized by thrombocytopenia, microangiopathic hemolytic anemia, and hypofibrinogenemia. In the present case, a 20-month-old patient is diagnosed with KMP. This case report highlights the challenges in diagnosis and management, reinforcing the importance of multidisciplinary approach.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2024 11","pages":"rjae721"},"PeriodicalIF":0.4,"publicationDate":"2024-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11587558/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142717334","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
Fulminant amoebic colitis: a challenging diagnosis for the surgeon. 暴发性阿米巴结肠炎：外科医生的挑战性诊断。
IF 0.4
Journal of Surgical Case Reports Pub Date : 2024-11-25 eCollection Date: 2024-11-01 DOI: 10.1093/jscr/rjae724
David Rafael Barrón-Díaz, Javier Meza-Hernández, Erika Hernández-Montiel, Orlando Solis-Coronado, Jessica Jazmín Betancourt-Ferreyra, Alejandra Núñez-Venzor, Mario Trejo-Ávila, Francisco E Alvarez-Bautista
{"title":"Fulminant amoebic colitis: a challenging diagnosis for the surgeon.","authors":"David Rafael Barrón-Díaz, Javier Meza-Hernández, Erika Hernández-Montiel, Orlando Solis-Coronado, Jessica Jazmín Betancourt-Ferreyra, Alejandra Núñez-Venzor, Mario Trejo-Ávila, Francisco E Alvarez-Bautista","doi":"10.1093/jscr/rjae724","DOIUrl":"10.1093/jscr/rjae724","url":null,"abstract":"<p><p>Fulminant amoebic colitis is a rare complication of amoebiasis that carries a high mortality rate. Its diagnosis is challenging and requires a high index of suspicion, and its early recognition is a priority to provide timely medical and surgical treatment. We present the case of a male patient who came to the emergency department with unspecific clinical presentation of abdominal pain, systemic inflammatory response and imaging study showing intestinal perforation of the right colon. Fecal peritonitis and perforation at the level of the hepatic flexure were observed, so a right hemicolectomy with terminal ileostomy was performed. Despite adequate medical and surgical treatment, the patient presented progressive deterioration and died. Colon perforation due to <i>Entamoeba histolytica</i> was the final diagnosis.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2024 11","pages":"rjae724"},"PeriodicalIF":0.4,"publicationDate":"2024-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11587891/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142717343","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
Primary pulmonary follicular lymphoma. 原发性肺滤泡淋巴瘤
IF 0.4
Journal of Surgical Case Reports Pub Date : 2024-11-25 eCollection Date: 2024-11-01 DOI: 10.1093/jscr/rjae730
Sarah E Kim, Daniel Steeno, Alexander P Lynch, Francis J Podbielski
{"title":"Primary pulmonary follicular lymphoma.","authors":"Sarah E Kim, Daniel Steeno, Alexander P Lynch, Francis J Podbielski","doi":"10.1093/jscr/rjae730","DOIUrl":"10.1093/jscr/rjae730","url":null,"abstract":"<p><p>Primary pulmonary follicular lymphoma is an extremely rare subset of extra-nodal non-Hodgkin's lymphoma. We present a successful work-up and surgical management of this disease entity. The patient is a 74-year-old man who presented with an enlarging ground glass opacity on his computed tomography scan. Percutaneous biopsy was not diagnostic for malignancy, but given the underlying malignant potential, he underwent definitive operative resection rather than additional invasive diagnostic testing. Our case highlights challenges in the management of nondiagnostic preliminary pathology as well as the role of a multidisciplinary approach to treatment of a rare lung pathology.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2024 11","pages":"rjae730"},"PeriodicalIF":0.4,"publicationDate":"2024-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11588351/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142717388","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
Management of retained endoscopy capsule: a case series and literature review. 内镜胶囊滞留的处理：病例系列和文献综述。
IF 0.4
Journal of Surgical Case Reports Pub Date : 2024-11-25 eCollection Date: 2024-11-01 DOI: 10.1093/jscr/rjae749
Preston H Palm, Madison M Patrick, Claudia A Cruz, Udayakumar Navaneethan, Antonio Caycedo, Marco Ferrara
{"title":"Management of retained endoscopy capsule: a case series and literature review.","authors":"Preston H Palm, Madison M Patrick, Claudia A Cruz, Udayakumar Navaneethan, Antonio Caycedo, Marco Ferrara","doi":"10.1093/jscr/rjae749","DOIUrl":"10.1093/jscr/rjae749","url":null,"abstract":"<p><p>Video capsule endoscopy has become the gold standard for the evaluation of small bowel pathology. Capsular retention remains the most significant risk of this intervention. Here, we present two cases of retained capsules and our minimally invasive approach to retrieval. We also review the literature pertaining to retained endoscopy capsules and highlight a range of medical, surgical, and preventative strategies utilized in its management.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2024 11","pages":"rjae749"},"PeriodicalIF":0.4,"publicationDate":"2024-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11587894/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142717375","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
Mature cystic teratoma mimicking a tailgut cyst in an adolescent female: a case report. 模仿尾肠囊肿的成熟囊性畸胎瘤：一份病例报告。
IF 0.4
Journal of Surgical Case Reports Pub Date : 2024-11-25 eCollection Date: 2024-11-01 DOI: 10.1093/jscr/rjae719
Safaa Abatli, Yazan AlHabil, Mohammed Shawkat Hamad, Yousef Abulibdeh
{"title":"Mature cystic teratoma mimicking a tailgut cyst in an adolescent female: a case report.","authors":"Safaa Abatli, Yazan AlHabil, Mohammed Shawkat Hamad, Yousef Abulibdeh","doi":"10.1093/jscr/rjae719","DOIUrl":"10.1093/jscr/rjae719","url":null,"abstract":"<p><p>Presacral tumors are uncommon, particularly in the pediatric population, and can arise from various germ cell types during embryologic development. Tailgut cysts, or retrorectal cystic hamartomas, represent rare congenital anomalies resulting from defective regression of hindgut remnants. We present a unique case of a 13-year-old female with pelvic symptoms, initially suspected to have a tailgut cyst based on imaging findings. However, surgical exploration revealed a mature cystic teratoma, a rare occurrence in this age group. Surgical excision was performed using an anterior approach, revealing adhesions and necessitating meticulous dissection for complete removal. Histopathological examination of the mass unexpectedly confirmed a mature cystic teratoma, characterized by a fibrovascular cyst wall containing smooth muscle and lobules resembling salivary acini, the cyst's surface exhibited squamous and respiratory-type epithelium. The accurate diagnosis of presacral masses, rather than relying solely on diagnostic measures, underscores the importance of prioritizing surgical exploration for definitive assessment and management.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2024 11","pages":"rjae719"},"PeriodicalIF":0.4,"publicationDate":"2024-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11588352/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142717381","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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