Journal of Surgical Case Reports最新文献

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Rare presentation of hydrocephalus occlusus caused by membranous obstruction of the foramina of Magendie and Luschka: a case report. 罕见的由Magendie和Luschka椎间孔膜性阻塞引起的脑积水闭塞:1例报告。
IF 0.5
Journal of Surgical Case Reports Pub Date : 2026-10-19 eCollection Date: 2026-10-01 DOI: 10.1093/jscr/rjag931
Sergio Calero Martinez, Lydia Karamani, Heike de Vries, Paul-Christian Krüger, Christian Senft, Nazeer Aboud
{"title":"Rare presentation of hydrocephalus occlusus caused by membranous obstruction of the foramina of Magendie and Luschka: a case report.","authors":"Sergio Calero Martinez, Lydia Karamani, Heike de Vries, Paul-Christian Krüger, Christian Senft, Nazeer Aboud","doi":"10.1093/jscr/rjag931","DOIUrl":"10.1093/jscr/rjag931","url":null,"abstract":"<p><p>Fourth ventricle outlet obstruction is a rare cause of obstructive hydrocephalus in children. Although surgical management has been reported, the diagnostic challenges, differential considerations, and therapeutic strategies remain debated. We report a 5-year-old boy with progressive vomiting, severe headache, gait instability, and incontinence. High-resolution magnetic resonance imaging with T2-CISS sequences confirmed a membranous obstruction at the foramina of Magendie and Luschka. The patient underwent microsurgical fenestration via suboccipital craniotomy, with histopathological confirmation of arachnoid membranes without signs of infection or malignancy. The postoperative course was favorable with complete symptom resolution. Notably, persistent papilledema was observed at 2-month follow-up despite clinical improvement, but showed gradual regression during subsequent visits, underlining the need for cautious postoperative monitoring.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2026 10","pages":"rjag931"},"PeriodicalIF":0.5,"publicationDate":"2026-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13679811/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149229195","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
Diffuse stimulant-associated vasculopathy presenting with acute limb ischemia, compartment syndrome, and multifocal visceral infarction. 弥漫性兴奋剂相关血管病变表现为急性肢体缺血、室室综合征和多灶性内脏梗死。
IF 0.5
Journal of Surgical Case Reports Pub Date : 2026-10-19 eCollection Date: 2026-10-01 DOI: 10.1093/jscr/rjag930
Syed Azaan Adnan, Julianne Wanner, Syed Moaiz Adnan, Christopher Thompson
{"title":"Diffuse stimulant-associated vasculopathy presenting with acute limb ischemia, compartment syndrome, and multifocal visceral infarction.","authors":"Syed Azaan Adnan, Julianne Wanner, Syed Moaiz Adnan, Christopher Thompson","doi":"10.1093/jscr/rjag930","DOIUrl":"10.1093/jscr/rjag930","url":null,"abstract":"<p><p>Stimulant-induced vasculopathy typically presents as localized ischemia secondary to vasospasm and thrombosis. Diffuse involvement of multiple vascular territories is uncommon and may result in severe, multisystem complications and increased morbidity. We report a 40-year-old female with polysubstance exposure, including cocaine and amphetamines, who presented with acute right lower extremity ischemia and compartment syndrome. Computed tomographic angiography demonstrated distal tibial, peroneal, and posterior tibial arterial occlusion. The patient underwent emergent four-compartment fasciotomy, allowing Doppler signals to return. Postoperative complications included rhabdomyolysis, acute kidney injury, bilateral adrenal infarctions, left renal infarction, and persistent foot drop. This case highlights the need to consider stimulant-associated vasculopathy in patients with acute limb ischemia without an embolic source and to evaluate for concurrent renal and visceral ischemic injuries. Early recognition and multidisciplinary management are essential to reduce morbidity.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2026 10","pages":"rjag930"},"PeriodicalIF":0.5,"publicationDate":"2026-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13679815/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149228991","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
Non-traumatic acute mediastinitis secondary to acute phlegmonous esophagitis: a rare case report. 非外伤性急性纵隔炎继发于急性痰性食管炎1例。
IF 0.5
Journal of Surgical Case Reports Pub Date : 2026-10-19 eCollection Date: 2026-10-01 DOI: 10.1093/jscr/rjag947
Meron H Biza, Eyerusalem K Degife, Selamawit Z Tadesse, Chernet T Mengistie, Ephrem M Atsbha, Biruk T Mengistie
{"title":"Non-traumatic acute mediastinitis secondary to acute phlegmonous esophagitis: a rare case report.","authors":"Meron H Biza, Eyerusalem K Degife, Selamawit Z Tadesse, Chernet T Mengistie, Ephrem M Atsbha, Biruk T Mengistie","doi":"10.1093/jscr/rjag947","DOIUrl":"10.1093/jscr/rjag947","url":null,"abstract":"<p><p>Acute mediastinitis secondary to acute phlegmonous esophagitis (APE) is an exceptionally rare, life-threatening condition with high morbidity. We report a 75-year-old diabetic female with recent severe pneumonia who presented with pleuritic chest pain, dyspnea, and elevated inflammatory markers. Computed tomography pulmonary angiography excluded embolism but revealed diffuse long-segment esophageal wall thickening with mediastinal fat stranding, aortic encasement, and pleural effusion, features consistent with APE and secondary non-traumatic mediastinitis without overt perforation. Given clinical stability, endoscopy was deferred to avoid disrupting a possible contained micro-perforation. The patient was successfully managed with 14 days of empiric broad-spectrum intravenous antibiotics (vancomycin, cefepime, metronidazole), achieving complete clinical and radiographic resolution. This case underscores that in hemodynamically stable patients without free perforation or large abscess, conservative antimicrobial therapy can be definitive. It also highlights the importance of considering APE in non-surgical patients presenting with acute chest pain.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2026 10","pages":"rjag947"},"PeriodicalIF":0.5,"publicationDate":"2026-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13679810/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149229120","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 novel pattern of complex bile duct injury characterized by distal ligation and proximal perforation: temporary T-tube drainage as a bridge to definitive reconstruction-a case report and literature review. 以远端结扎和近端穿孔为特征的新型复杂胆管损伤:临时t管引流作为最终重建的桥梁-一个病例报告和文献综述。
IF 0.5
Journal of Surgical Case Reports Pub Date : 2026-10-19 eCollection Date: 2026-10-01 DOI: 10.1093/jscr/rjag940
Mirwais Safi, Muhibullah Saifi, Nasrullah Shefayee, Hamidullah Hamid, Ehsanullah Safi, Nasratullah Nasrat, Maihan Abdullah
{"title":"A novel pattern of complex bile duct injury characterized by distal ligation and proximal perforation: temporary T-tube drainage as a bridge to definitive reconstruction-a case report and literature review.","authors":"Mirwais Safi, Muhibullah Saifi, Nasrullah Shefayee, Hamidullah Hamid, Ehsanullah Safi, Nasratullah Nasrat, Maihan Abdullah","doi":"10.1093/jscr/rjag940","DOIUrl":"10.1093/jscr/rjag940","url":null,"abstract":"<p><p>Bile duct injury (BDI) is a serious complication of cholecystectomy. We report a previously unrecognized pattern of complex BDI in a 30-year-old man who presented one week after open cholecystectomy with biliary peritonitis. Endoscopic retrograde cholangiopancreatography demonstrated an abrupt common bile duct (CBD) cutoff, while magnetic resonance cholangiopancreatography revealed a biloma with features suggestive of biliary peritonitis. Exploratory laparotomy confirmed distal CBD ligation with proximal common hepatic duct perforation. Because of severe inflammation and friable tissues, definitive reconstruction was deferred, and temporary T-tube drainage was established. The T-tube was maintained for ~3 months before removal. The established tract remained temporarily patent after removal, permitting transient bile drainage during progressive fibrosis and closure. The patient was closely monitored clinically, with serial liver function tests and ultrasonography. After adequate biliary-tree dilatation, Roux-en-Y hepaticojejunostomy was performed. At 2-year follow-up, he remained asymptomatic without recurrent biliary complications.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2026 10","pages":"rjag940"},"PeriodicalIF":0.5,"publicationDate":"2026-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13679809/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149229058","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
Traumatic transfemoral bowel evisceration following bull horn injury: a case report and review of literature. 牛角损伤后外伤性经股肠切除一例报告及文献复习。
IF 0.5
Journal of Surgical Case Reports Pub Date : 2026-10-18 eCollection Date: 2026-06-01 DOI: 10.1093/jscr/rjag901
Venkata Avinash Kumar Vegi, Meraj Ahmed, Afzal Anees
{"title":"Traumatic transfemoral bowel evisceration following bull horn injury: a case report and review of literature.","authors":"Venkata Avinash Kumar Vegi, Meraj Ahmed, Afzal Anees","doi":"10.1093/jscr/rjag901","DOIUrl":"10.1093/jscr/rjag901","url":null,"abstract":"<p><p>Bull horn injuries produce complex shearing and penetrating forces capable of causing occult abdominal wall disruption with visceral herniation. We report a rare case of bowel evisceration through the thigh following bull horn injury associated with pelvic fractures and traumatic inguino-femoral disruption. A 55-year-old female presented to the emergency with bowel loops protruding through a lacerated wound over the anterolateral aspect of the right thigh following a bull horn injury. Contrast-enhanced computed tomography of the abdomen and pelvis revealed herniation of ileal loops with mesentery through a large right lower abdominal wall defect with possible femoral canal involvement. Exploratory laparotomy revealed mesenteric tears and traumatic disruption of the inguinal region allowing bowel migration into the thigh. Reduction of bowel loops, repair of mesentery, peritoneal lavage and inguinal ligament repair were performed successfully. This case highlights the importance of suspecting occult abdominal wall and inguino-femoral disruption in atypical bowel evisceration patterns following animal-inflicted trauma.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2026 6","pages":"rjag901"},"PeriodicalIF":0.5,"publicationDate":"2026-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13677062/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149221062","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
Correction to: The utility of endoscopic ultrasound-guided fine-needle aspiration and robotic surgery for submucosal-type metastatic rectal cancer with persistent descending mesocolon. 修正:超声内镜引导下细针穿刺和机器人手术治疗伴有持续降系结肠系膜的粘膜下型转移性直肠癌的应用。
IF 0.5
Journal of Surgical Case Reports Pub Date : 2026-10-16 eCollection Date: 2026-10-01 DOI: 10.1093/jscr/rjag851
{"title":"Correction to: The utility of endoscopic ultrasound-guided fine-needle aspiration and robotic surgery for submucosal-type metastatic rectal cancer with persistent descending mesocolon.","authors":"","doi":"10.1093/jscr/rjag851","DOIUrl":"https://doi.org/10.1093/jscr/rjag851","url":null,"abstract":"<p><p>[This corrects the article DOI: 10.1093/jscr/rjag512.].</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2026 10","pages":"rjag851"},"PeriodicalIF":0.5,"publicationDate":"2026-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13672077/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149217144","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
Chemotherapy-induced secondary sclerosing cholangitis mimicking primary sclerosing cholangitis: a case report. 化疗诱导的继发性硬化性胆管炎模拟原发性硬化性胆管炎1例报告。
IF 0.5
Journal of Surgical Case Reports Pub Date : 2026-10-14 eCollection Date: 2026-10-01 DOI: 10.1093/jscr/rjag553
Neşe Demirhan, Kasım Çağlayan
{"title":"Chemotherapy-induced secondary sclerosing cholangitis mimicking primary sclerosing cholangitis: a case report.","authors":"Neşe Demirhan, Kasım Çağlayan","doi":"10.1093/jscr/rjag553","DOIUrl":"10.1093/jscr/rjag553","url":null,"abstract":"<p><p>Secondary sclerosing cholangitis (SSC) is a rare condition that may mimic primary sclerosing cholangitis. Chemotherapy-related biliary injury is an emerging cause. We present a 72-year-old male with gastric carcinoma who developed cholestatic liver injury following oxaliplatin-based chemotherapy. Imaging revealed intrahepatic biliary dilatation without an obstructing lesion. Percutaneous transhepatic cholangiography confirmed biliary abnormalities. The patient was managed with biliary drainage and supportive care, resulting in gradual clinical and biochemical improvement. Chemotherapy-induced SSC should be considered in patients with cholestatic liver injury after oxaliplatin-based regimens, and early recognition is essential.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2026 10","pages":"rjag553"},"PeriodicalIF":0.5,"publicationDate":"2026-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13668418/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149197107","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
Myofibrosarcoma of the maxillary sinus with orbital floor involvement: a case report. 上颌窦肌纤维肉瘤累及眶底1例。
IF 0.5
Journal of Surgical Case Reports Pub Date : 2026-10-14 eCollection Date: 2026-10-01 DOI: 10.1093/jscr/rjag920
Adam El Hassouni, Rajae Borki, Aymene Benmansour, Omar Rami, Ilham Rkain, Hicham Mimouni
{"title":"Myofibrosarcoma of the maxillary sinus with orbital floor involvement: a case report.","authors":"Adam El Hassouni, Rajae Borki, Aymene Benmansour, Omar Rami, Ilham Rkain, Hicham Mimouni","doi":"10.1093/jscr/rjag920","DOIUrl":"10.1093/jscr/rjag920","url":null,"abstract":"<p><p>Myofibrosarcoma is a rare spindle-cell malignancy with myofibroblastic differentiation, and primary maxillary sinus involvement is exceptional. A 36-year-old woman presented with progressive unilateral nasal obstruction, purulent rhinorrhea, and hemifacial pain. Computed tomography and magnetic resonance imaging demonstrated a destructive 44 × 45 × 57 mm right maxillary sinus mass involving the orbital floor and extending into the nasal cavity, ethmoid cells, and pterygopalatine fossa. Histology and immunohistochemistry supported the diagnosis of myofibrosarcoma. Partial maxillectomy with titanium orbital floor reconstruction was performed. Several soft-tissue margins were positive, whereas gingival and bony margins were clear. Postoperative radiotherapy delivered 66 Gy in 33 fractions. This case illustrates the diagnostic complexity of sinonasal spindle-cell tumors and the individualized role of radiotherapy when local control is threatened by anatomically constrained positive-margin disease.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2026 10","pages":"rjag920"},"PeriodicalIF":0.5,"publicationDate":"2026-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13668423/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149197134","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
Nerve-sparing resection of cervical vagal schwannoma with complete functional recovery: a case report. 保留神经切除颈迷走神经鞘瘤并功能完全恢复1例。
IF 0.5
Journal of Surgical Case Reports Pub Date : 2026-10-14 eCollection Date: 2026-10-01 DOI: 10.1093/jscr/rjag916
Zaid A Alzaghal, Faryal Imran, Mohammad Aamir Qayyum Sarguroh Khan, Aafreen A Nyaz, Gyanendra Jora, Safwan A Alzaghal, Hutham K Aliessa, Husam M Saleh
{"title":"Nerve-sparing resection of cervical vagal schwannoma with complete functional recovery: a case report.","authors":"Zaid A Alzaghal, Faryal Imran, Mohammad Aamir Qayyum Sarguroh Khan, Aafreen A Nyaz, Gyanendra Jora, Safwan A Alzaghal, Hutham K Aliessa, Husam M Saleh","doi":"10.1093/jscr/rjag916","DOIUrl":"10.1093/jscr/rjag916","url":null,"abstract":"<p><p>Vagal schwannomas are rare benign neoplasms arising from the Schwann cells of the vagus nerve, representing 2%-5% of all peripheral nerve tumors and ~10% of head and neck schwannomas. They typically present as slow-growing, asymptomatic lateral neck masses and pose significant diagnostic and surgical challenges due to their proximity to critical neurovascular structures. We report a case of a 28-year-old Asian male who presented with a right-sided neck swelling. Imaging workup including ultrasound, magnetic resonance imaging, and computed tomography angiography identified a well-defined mass in the right carotid space at the level of C4-C5, displacing adjacent vascular structures. The tumor was surgically excised en bloc via a lateral transverse approach with full preservation of vagal nerve function, confirmed by intraoperative nerve monitoring. Histopathology confirmed the diagnosis of vagal schwannoma. This case highlights the importance of a multidisciplinary approach, thorough preoperative imaging, and meticulous intraoperative technique in achieving complete resection with minimal morbidity.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2026 10","pages":"rjag916"},"PeriodicalIF":0.5,"publicationDate":"2026-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13668425/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149197145","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
Cough-induced rectus sheath hematoma in an adolescent without external abdominal findings: a case report. 青少年咳嗽引起的直肌鞘血肿,无腹部外表现:1例报告。
IF 0.5
Journal of Surgical Case Reports Pub Date : 2026-10-14 eCollection Date: 2026-10-01 DOI: 10.1093/jscr/rjag915
Yujin Kaneko, Haruhisa Ozawa, Ayane Tachiki, Kensuke Sakamoto, Genki Takei, Yukiko Kouchi, Naoto Yoshida, Toyoaki Sawano, Tetsuya Tanimoto, Akihiko Ozaki, Hiroaki Shimmura
{"title":"Cough-induced rectus sheath hematoma in an adolescent without external abdominal findings: a case report.","authors":"Yujin Kaneko, Haruhisa Ozawa, Ayane Tachiki, Kensuke Sakamoto, Genki Takei, Yukiko Kouchi, Naoto Yoshida, Toyoaki Sawano, Tetsuya Tanimoto, Akihiko Ozaki, Hiroaki Shimmura","doi":"10.1093/jscr/rjag915","DOIUrl":"10.1093/jscr/rjag915","url":null,"abstract":"<p><p>Rectus sheath hematoma (RSH) is an uncommon cause of acute abdominal pain that predominantly affects older, anticoagulated adults and usually presents with a palpable abdominal-wall mass. We report a 17-year-old previously healthy male who developed midline lower abdominal pain after 6 days of severe coughing, without anticoagulation, trauma, or bleeding disorder, and with no visible swelling, ecchymosis, or palpable mass; Carnett's sign was positive. Ultrasonography, magnetic resonance imaging, and contrast-enhanced computed tomography confirmed a hematoma confined to the lower rectus sheath without active extravasation, and he recovered fully with conservative management. In a review of recent cough-induced RSH reports, all prior patients had a predisposing condition or external abdominal findings; our patient is the youngest reported and had neither. RSH should be considered in adolescents with persistent abdominal pain after severe coughing, even when examination is unremarkable.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2026 10","pages":"rjag915"},"PeriodicalIF":0.5,"publicationDate":"2026-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13668420/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149197143","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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