Journal of Surgical Case Reports最新文献_第5页

Late-onset esophagogastric anastomotic fistula managed without continuous fasting: a case report. 无连续禁食治疗迟发型食管胃吻合口瘘1例。

IF 0.5

Journal of Surgical Case Reports Pub Date : 2025-10-06 eCollection Date: 2025-10-01 DOI: 10.1093/jscr/rjaf796

Yuhui Gong, Yu Zhang, Haitao Ma, Wei Jiang, Jiangjiang Liu, Yunteng Kang, Jialiang Liu, Xiaojun Yu

引用次数: 0

Delayed pancreatic metastasis from renal cell carcinoma managed with pazopanib and stereotactic ablative body radiotherapy. 帕唑帕尼联合立体定向消融体放疗治疗肾细胞癌延迟性胰腺转移。

IF 0.5

Journal of Surgical Case Reports Pub Date : 2025-10-06 eCollection Date: 2025-10-01 DOI: 10.1093/jscr/rjaf798

Mutahar A Tunio, Wael Mohamed, Sing-Yu Moorcraft, Basil Mary Eldo, Waqas Mehmood, Tawfik Elazzabi

引用次数: 0

Revision total knee arthroplasty with long-stem prosthesis following primary knee replacement for giant cell tumor with fracture: a case report. 原发性巨细胞瘤合并骨折行全膝关节置换术后长柄假体改良全膝关节置换术1例。

IF 0.5

Journal of Surgical Case Reports Pub Date : 2025-10-06 eCollection Date: 2025-10-01 DOI: 10.1093/jscr/rjaf789

Dung A Vu, Nhat D Vu, Tien T Nguyen, Tien T Pham, Ngoc B Thai

引用次数: 0

Porto-spleno-mesenteric thrombosis secondary to medroxyprogesterone acetate as a treatment for abnormal uterine bleeding: a case report. 醋酸甲孕酮继发于门脾肠系膜血栓形成治疗子宫异常出血1例。

IF 0.5

Journal of Surgical Case Reports Pub Date : 2025-10-06 eCollection Date: 2025-10-01 DOI: 10.1093/jscr/rjaf791

David J Alvarez Chavez, Javier A Maciel Urzua, Maria C Torres González, Carlos A Bautista López, Carla M Cruz Rocha, Esther A Casado De La Torre, Daniela I Sánchez Lozano

{"title":"Porto-spleno-mesenteric thrombosis secondary to medroxyprogesterone acetate as a treatment for abnormal uterine bleeding: a case report.","authors":"David J Alvarez Chavez, Javier A Maciel Urzua, Maria C Torres González, Carlos A Bautista López, Carla M Cruz Rocha, Esther A Casado De La Torre, Daniela I Sánchez Lozano","doi":"10.1093/jscr/rjaf791","DOIUrl":"10.1093/jscr/rjaf791","url":null,"abstract":"Acute mesenteric venous thrombosis is a rare and potentially lethal cause of intestinal ischemia. We report a 38-year-old woman with abnormal uterine bleeding, with anemia, and prolonged use of medroxyprogesterone acetate. She presented severe abdominal pain, peritoneal signs, and systemic inflammatory response. Computed tomography revealed thrombosis of the portal, splenic, and superior mesenteric veins with jejunal wall thickening. Initial laparotomy showed a viable bowel; full anticoagulation was started. She later developed perforation requiring jejunal resection and subsequent reoperation for anastomotic dehiscence. Extensive workup revealed no prothrombotic disorder other than progestin use. This case highlights the need to consider hormonal agents as potential triggers of porto-spleno-mesenteric thrombosis, even in young women without comorbidities, and to pursue multidisciplinary, individualized management to balance timely surgery with preservation of bowel length.","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2025 10","pages":"rjaf791"},"PeriodicalIF":0.5,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12499917/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145245288","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 case of metastatic myxofibrosarcoma to the right colon. 右结肠转移性黏液纤维肉瘤1例。

IF 0.5

Journal of Surgical Case Reports Pub Date : 2025-10-06 eCollection Date: 2025-10-01 DOI: 10.1093/jscr/rjaf635

Timothy K Farrell, Matthew A Carnell, Vincent J Obias

引用次数: 0

Neuroendocrine tumor of the appendix associated with an appendiceal mucocele: an incidental discovery during breast tumor surveillance. 阑尾神经内分泌肿瘤伴阑尾黏液囊肿：在乳腺肿瘤监测中偶然发现。

IF 0.5

Journal of Surgical Case Reports Pub Date : 2025-10-04 eCollection Date: 2025-10-01 DOI: 10.1093/jscr/rjaf787

Yassine Hamdaoui, Mohamed El Hammouti, Zakaria Saber, Mohammed Doumar, Ayoub Kharkhach, Tariq Bouhout, Badr Serji

引用次数: 0

Lymphoepithelioma-like carcinoma of the distal urethra: a case report and management strategies. 尿道远端淋巴上皮瘤样癌1例报告及治疗策略。

IF 0.5

Journal of Surgical Case Reports Pub Date : 2025-10-03 eCollection Date: 2025-10-01 DOI: 10.1093/jscr/rjaf785

Ramiro Fonseca, José Ignacio Perez Reggeti, Cristina Ferreiro Pareja, Gabriela Paganini, Marcial Berrios-Quinteros, Gilberto Eduardo Chechile, Nahuel Paesano

引用次数: 0

Fetus-in-fetu in an 11-day-old female infant with descriptive histopathological insights: a case report. 一个11天大的女婴的胎中胎与描述性的组织病理学见解：一个病例报告。

IF 0.5

Journal of Surgical Case Reports Pub Date : 2025-10-03 eCollection Date: 2025-10-01 DOI: 10.1093/jscr/rjaf611

Rem Ehab Abdelkader, Mohamed Elsherbiny, Adham Elsaied, Momen Abdelglil, Khadiga M Ali

{"title":"Fetus-in-fetu in an 11-day-old female infant with descriptive histopathological insights: a case report.","authors":"Rem Ehab Abdelkader, Mohamed Elsherbiny, Adham Elsaied, Momen Abdelglil, Khadiga M Ali","doi":"10.1093/jscr/rjaf611","DOIUrl":"10.1093/jscr/rjaf611","url":null,"abstract":"Fetus-in-fetu (FIF), a rare congenital anomaly, involves a malformed fetus within its twin. It typically presents as an asymptomatic abdominal mass discovered postnatally, with an incidence of 1/500000 births. An 11-day-old Arab female infant presented with progressive abdominal distention. General physical examinations were normal. Abdominal examination revealed an ill-defined fixed lump in the right upper quadrant. Imaging revealed a 8 × 6 cm retroperitoneal mass containing skeletal elements. Surgical exploration via laparotomy confirmed diagnosis. Careful dissection was necessary due to its vascular and anatomical complexity. Histopathological examination revealed tissues from all three germ layers, excluding teratoma. FIF is distinguished from teratomas by the presence of a vertebral column with organized development of surrounding tissues, and typically manifests without malignant potential. Surgical excision is curative, with minimal risk of recurrence. Long-term follow-up with imaging and tumor markers is recommended to monitor for complications, despite its benign nature.","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2025 10","pages":"rjaf611"},"PeriodicalIF":0.5,"publicationDate":"2025-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12494229/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145233764","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 torsion in polysplenia syndrome: a rare cause of acute abdomen in a paediatric patient. 脾扭转在多脾综合征：一个罕见的原因急性腹部在儿科患者。

IF 0.5

Journal of Surgical Case Reports Pub Date : 2025-10-03 eCollection Date: 2025-10-01 DOI: 10.1093/jscr/rjaf771

Shaima Osman Mohamed Ali Alaraby, Sara Y Mukhtar, Mohamed Y Ibrahim, Eman Mohamed, Shima Abdalraheem Elnadeef Hussein, Mohamed Osman Mohamed Idres

{"title":"Splenic torsion in polysplenia syndrome: a rare cause of acute abdomen in a paediatric patient.","authors":"Shaima Osman Mohamed Ali Alaraby, Sara Y Mukhtar, Mohamed Y Ibrahim, Eman Mohamed, Shima Abdalraheem Elnadeef Hussein, Mohamed Osman Mohamed Idres","doi":"10.1093/jscr/rjaf771","DOIUrl":"10.1093/jscr/rjaf771","url":null,"abstract":"Acute abdominal pain in children presents a significant diagnostic challenge due to its broad differential, including rare congenital anomalies. Torsion of an accessory spleen is a rare but important cause, particularly in the context of polysplenia syndrome. We report the case of a 6-year-old boy with polysplenia syndrome who presented with severe abdominal pain, vomiting, and diarrhea. Imaging revealed multiple splenic masses, and exploratory laparotomy identified a torsed accessory spleen with a twisted vascular pedicle. Resection of the infarcted splenule and correction of associated intestinal malrotation were performed. The patient recovered uneventfully and was discharged on the third postoperative day. Splenic torsion in polysplenia syndrome should be considered in the differential diagnosis of acute abdomen in children with congenital anomalies. Prompt imaging and surgical intervention are essential for favourable outcomes, and increased awareness may aid in early diagnosis and management of this rare condition.","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2025 10","pages":"rjaf771"},"PeriodicalIF":0.5,"publicationDate":"2025-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12494201/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145233584","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

Monomicrobial necrotizing soft tissue infection of upper extremity caused by Eggerthia catenaformis. 链状埃及杆菌致上肢单菌性坏死性软组织感染。

IF 0.5

Journal of Surgical Case Reports Pub Date : 2025-10-03 eCollection Date: 2025-10-01 DOI: 10.1093/jscr/rjaf769

Nadeem Chaudhry, Abid Qureshi, Dhipthika Srinivasan, Michael Davrayev, Natasha Vo, Heidi Wallour, Minnah Chaudhry

{"title":"Monomicrobial necrotizing soft tissue infection of upper extremity caused by Eggerthia catenaformis.","authors":"Nadeem Chaudhry, Abid Qureshi, Dhipthika Srinivasan, Michael Davrayev, Natasha Vo, Heidi Wallour, Minnah Chaudhry","doi":"10.1093/jscr/rjaf769","DOIUrl":"10.1093/jscr/rjaf769","url":null,"abstract":"Necrotizing soft tissue infections are characterized by fulminant tissue destruction that are rapidly progressive in nature, occurring as a result of trauma, minor skin lesions, nonpenetrating injuries, as well as in post-surgical and immunocompromised patients. Eggerthia catenaformis has mostly been reported linked to dental abscesses but this report presents a case of a poor controlled diabetic with E. catenaformis induced necrotizing infection. Forty nine-year-old male presented to the emergency department with left arm pain and swelling, associated with foul smelling drainage. Physical examination exhibited left upper extremity tenderness, erythema, fluctuance, and crepitus. Patient was taken to the operating room for forearm fasciotomy, amputation of third digit, and washout. Cultures were positive for E. catenaformis. The pathogenicity and severity of E. catenaformis is mostly unknown. Clinicians should be aware of this rare entity for its complexity and management worldwide.","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2025 10","pages":"rjaf769"},"PeriodicalIF":0.5,"publicationDate":"2025-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12494214/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145233726","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