Journal of Surgical Case Reports最新文献_第7页

Is it a hemangioma? A combined case report of soft tissue sarcomas mimicking infantile hemangioma. 是血管瘤吗？模拟婴儿血管瘤的软组织肉瘤合并1例报告。

IF 0.5

Journal of Surgical Case Reports Pub Date : 2025-09-24 eCollection Date: 2025-09-01 DOI: 10.1093/jscr/rjaf748

Shaden Almutairi, Wed AlWabel, Saud Aljadaan, Norah Alsabty, Afnan Alshehri, Faten Alrobian

引用次数: 0

Adenomyoma of the round ligament of the uterus in the inguinal canal: a case report. 腹股沟管子宫圆韧带腺肌瘤1例。

IF 0.5

Journal of Surgical Case Reports Pub Date : 2025-09-24 eCollection Date: 2025-09-01 DOI: 10.1093/jscr/rjaf421

Linhan Dai, Jin Wang, Yuhan Chen, Lvjia Cheng, Xiaoshen Zhang, Wenbin Zhang

引用次数: 0

Laparoscopic management of a Gharbi type II hepatic hydatid cyst after failed pair. 腹腔镜下处理Gharbi型肝包虫囊肿失败后。

IF 0.5

Journal of Surgical Case Reports Pub Date : 2025-09-24 eCollection Date: 2025-09-01 DOI: 10.1093/jscr/rjaf665

Luis Francisco Llerena Freire, Majerlly Anahí Gallardo, Ivonne Carolina Córdova

{"title":"Laparoscopic management of a Gharbi type II hepatic hydatid cyst after failed pair.","authors":"Luis Francisco Llerena Freire, Majerlly Anahí Gallardo, Ivonne Carolina Córdova","doi":"10.1093/jscr/rjaf665","DOIUrl":"10.1093/jscr/rjaf665","url":null,"abstract":"Hepatic hydatidosis, caused by Echinococcus granulosus, remains prevalent in endemic regions. Surgery is the cornerstone of treatment, although laparoscopic approaches have gained prominence in selected cases in the past decade. We present a case of a Gharbi-type II hepatic hydatid cyst successfully treated via laparoscopy. A 19-year-old man from a rural endemic area, presented with right upper quadrant pain. Imaging revealed a Gharbi type 2 hydatid cyst in the posterior segment VII of the liver. Laparoscopic evacuation of the cyst content was performed with strict preventive measures to avoid dissemination. The patient had a favorable outcome without complications. Laparoscopy offers a safe alternative for peripheral cysts without biliary communication and in experienced centers. Proper patient selection and technical proficiency are essential to minimize risks. This report highlights the feasibility of laparoscopic management of Gharbi type II cysts in carefully selected patients and illustrates the role of laparoscopy as a salvage strategy following failed PAIR.","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2025 9","pages":"rjaf665"},"PeriodicalIF":0.5,"publicationDate":"2025-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12459247/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145151461","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

Tension gastrothorax in a late-presenting congenital diaphragmatic hernia: a case report and review of the literature. 迟发性膈疝张力性胃胸一例报告及文献复习。

IF 0.5

Journal of Surgical Case Reports Pub Date : 2025-09-24 eCollection Date: 2025-09-01 DOI: 10.1093/jscr/rjaf750

Ziad A Bataineh, Abdullah S Al-Darwish, Sumaiah Alkhulaifi, Thekraiat M Al Quran

{"title":"Tension gastrothorax in a late-presenting congenital diaphragmatic hernia: a case report and review of the literature.","authors":"Ziad A Bataineh, Abdullah S Al-Darwish, Sumaiah Alkhulaifi, Thekraiat M Al Quran","doi":"10.1093/jscr/rjaf750","DOIUrl":"10.1093/jscr/rjaf750","url":null,"abstract":"Congenital diaphragmatic hernia (CDH), a rare but potentially life-threatening anomaly resulting from incomplete diaphragm closure during fetal development, typically presents neonatally but can rarely manifest later in infancy as tension gastrothorax-a critical condition of intrathoracic gastric herniation and distension causing severe respiratory distress and mediastinal shift; we describe a 2-month-old male infant who developed sudden dyspnea and mediastinal shift due to a left-sided Bochdalek hernia with a distended stomach occupying the thoracic cavity, requiring emergent laparotomy with gastric decompression and defect repair using non-absorbable sutures, leading to full lung re-expansion and recovery; this case highlights the diagnostic and therapeutic challenges of late-presenting CDH complicated by tension gastrothorax, the importance of distinguishing it from other causes of respiratory distress, and emphasizes that prompt recognition, timely decompression, and surgical repair are vital for favorable outcomes, urging clinicians to maintain high suspicion when imaging reveals an air-filled hemithorax in distressed infants.","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2025 9","pages":"rjaf750"},"PeriodicalIF":0.5,"publicationDate":"2025-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12459967/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145151496","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

Genomic profiling guided therapy for synchronous SCC and CLL of the parotid gland: a rare case report. 基因组图谱指导治疗同步SCC和CLL腮腺：一个罕见的病例报告。

IF 0.5

Journal of Surgical Case Reports Pub Date : 2025-09-24 eCollection Date: 2025-09-01 DOI: 10.1093/jscr/rjaf752

Rockey Dahiya, Natalie Weiss, Prishae Wilson, Bastien A Valencia-Sanchez, Phillip Pirgousis

{"title":"Genomic profiling guided therapy for synchronous SCC and CLL of the parotid gland: a rare case report.","authors":"Rockey Dahiya, Natalie Weiss, Prishae Wilson, Bastien A Valencia-Sanchez, Phillip Pirgousis","doi":"10.1093/jscr/rjaf752","DOIUrl":"10.1093/jscr/rjaf752","url":null,"abstract":"Synchronous squamous cell carcinoma (SCC) and chronic lymphocytic leukemia (CLL) in the parotid gland is rare, with limited evidence on personalized treatment. We report a 75-year-old male with prior cutaneous SCC who presented with a hypermetabolic parotid mass and cervical lymphadenopathy; fine needle aspiration confirmed SCC. Surgery revealed poorly differentiated SCC and CLL in multiple lymph nodes. He underwent radiotherapy but developed regional SCC relapse without systemic CLL symptoms. Recurrence in the ear required extensive surgical resection and reconstruction. Genetic profiling showed high tumor mutational burden (>50 mutations/Mb) and mutations in ARID1B, CDKN2A, MSH2, PMS2, and TP53. He received six cycles of cemiplimab followed by cetuximab-based targeted therapy, based on rising circulating DNA levels. This case emphasizes the value of genetic profiling and tools like TMB, FISH, and immunohistochemistry for risk stratification and personalized treatment in managing advanced or complex parotid malignancies, including synchronous SCC and CLL, to optimize patient outcomes.","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2025 9","pages":"rjaf752"},"PeriodicalIF":0.5,"publicationDate":"2025-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12459969/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145151418","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

Malignant triton tumor of the bladder with fatal outcome: a rare case report. 膀胱恶性triton肿瘤致死亡：罕见病例报告。

IF 0.5

Journal of Surgical Case Reports Pub Date : 2025-09-24 eCollection Date: 2025-09-01 DOI: 10.1093/jscr/rjaf756

El Mehdi Bouayad, Taha Yassine Aaboudech, Sabrine Derqaoui, Hamza Bouayad, Siham Mesmoudi, Kaoutar Znati, Zakia Bernoussi, Ahmed Jahid

{"title":"Malignant triton tumor of the bladder with fatal outcome: a rare case report.","authors":"El Mehdi Bouayad, Taha Yassine Aaboudech, Sabrine Derqaoui, Hamza Bouayad, Siham Mesmoudi, Kaoutar Znati, Zakia Bernoussi, Ahmed Jahid","doi":"10.1093/jscr/rjaf756","DOIUrl":"10.1093/jscr/rjaf756","url":null,"abstract":"Malignant triton tumors (MTTs) are a rare subtype of malignant peripheral nerve sheath tumors characterized by rhabdomyoblastic differentiation, often associated with neurofibromatosis type 1 (NF-1). Primary MTTs of the bladder are exceptionally uncommon, with few documented cases. We report a case of a 75-year-old male without neurofibromatosis type 1 history presenting with hematuria and urinary obstruction. Imaging revealed a 6.5 × 4 × 2 cm invasive bladder mass, and histopathology confirmed a high-grade spindle cell neoplasm with biphasic neurogenic (S100-positive) and rhabdomyoblastic (desmin- and myogenin-positive) differentiation, consistent with a diagnosis of MTT. Despite radical cystoprostatectomy, the patient succumbed to postoperative complications. This case highlights the aggressive behavior, diagnostic challenges, and poor prognosis of bladder MTTs, emphasizing the critical role of immunohistochemistry in distinguishing them from other spindle cell neoplasms. The rarity of this presentation underscores the need for further research to elucidate its pathogenesis and optimize therapeutic strategies.","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2025 9","pages":"rjaf756"},"PeriodicalIF":0.5,"publicationDate":"2025-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12459258/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145151441","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

Late human immunodeficiency virus presenting as necrotizing anal ulceration due to cytomegalovirus. 晚期人类免疫缺陷病毒表现为巨细胞病毒引起的坏死性肛门溃疡。

IF 0.5

Journal of Surgical Case Reports Pub Date : 2025-09-24 eCollection Date: 2025-09-01 DOI: 10.1093/jscr/rjaf763

Katherine L Szeliga, Jenny C McCloskey, Abdallah Elsabagh, Gawri Rajakaruna

引用次数: 0

Jejunal lipoma presenting as small bowel intussusception in an adult: diagnostic and surgical challenges-a case report. 成人空肠脂肪瘤表现为小肠肠套叠：诊断和手术挑战- 1例报告。

IF 0.5

Journal of Surgical Case Reports Pub Date : 2025-09-24 eCollection Date: 2025-09-01 DOI: 10.1093/jscr/rjaf551

Midani Touati, Faiez Boughanmi, Hiba Ben Hassine, Hanene Zenati, Leith Limayem, Faouzi Noomen

引用次数: 0

Multidisciplinary management of intracranial migration of a fractured dental needle through the foramen ovale: a case report. 多学科治疗牙针骨折经卵圆孔颅内移位1例。

IF 0.5

Journal of Surgical Case Reports Pub Date : 2025-09-23 eCollection Date: 2025-09-01 DOI: 10.1093/jscr/rjaf662

Josep Rubio-Palau, Ferran Escrigas-Cañameras, Adaia Valls-Ontañon, Albert Malet-Contreras, Maria Victoria Becerra-Castro, Jordi Muchart-López, José Hinojosa-Bernal

{"title":"Multidisciplinary management of intracranial migration of a fractured dental needle through the foramen ovale: a case report.","authors":"Josep Rubio-Palau, Ferran Escrigas-Cañameras, Adaia Valls-Ontañon, Albert Malet-Contreras, Maria Victoria Becerra-Castro, Jordi Muchart-López, José Hinojosa-Bernal","doi":"10.1093/jscr/rjaf662","DOIUrl":"10.1093/jscr/rjaf662","url":null,"abstract":"Local anaesthesia and nerve block are common practices in dental therapy. Although they are associated with low rate of complications, local events such as needle fracture could entail life threatening consequences. We present a case of a needle fracture in a 4 year old girl who underwent a minor dental procedure. The needle migrated intracranially through the foramen ovale. She required a multidisciplinary management with a final neurosurgical intervention in order to remove it. In addition to an initial diagnostic computerized tomography (CT), it was of utmost importance to have access to an intraoperative imaging tools (preferably low radiation CT in paediatric population) to monitor the potential risk of needle migration. This report demonstrates that a broken needle may migrate intracranially, among other complications, underscoring the importance of managing these cases in a tertiary referral hospital with the appropriate equipment and specialists.","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2025 9","pages":"rjaf662"},"PeriodicalIF":0.5,"publicationDate":"2025-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12454255/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145138997","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

Pedicled transverse rectus abdominis myocutaneous flap removal after 21 years: a case report. 21年后带蒂腹横直肌肌皮瓣切除1例。

IF 0.5

Journal of Surgical Case Reports Pub Date : 2025-09-21 eCollection Date: 2025-09-01 DOI: 10.1093/jscr/rjaf654

Natasha Lim, Lee Chee Meng, Marissa Teo, Allen Wei-Jiat Wong

引用次数: 0