发布求助
文献互助 智能选刊 最新文献

Journal of Surgical Case Reports最新文献

筛选
英文 中文
Progressive dysphagia from an esophageal liposarcoma, a complex problem in a challenging setting. 食管脂肪肉瘤引起的进行性吞咽困难，这是一个具有挑战性的复杂问题。
IF 0.4
Journal of Surgical Case Reports Pub Date : 2024-10-29 eCollection Date: 2024-10-01 DOI: 10.1093/jscr/rjae670
Santiago A Endara, Gerardo A Dávalos, Ana G Finke, Veronica Ayala, Nelson A Montalvo, Santiago Munoz-Palomeque, Gabriel A Molina
{"title":"Progressive dysphagia from an esophageal liposarcoma, a complex problem in a challenging setting.","authors":"Santiago A Endara, Gerardo A Dávalos, Ana G Finke, Veronica Ayala, Nelson A Montalvo, Santiago Munoz-Palomeque, Gabriel A Molina","doi":"10.1093/jscr/rjae670","DOIUrl":"https://doi.org/10.1093/jscr/rjae670","url":null,"abstract":"<p><p>Esophageal lipomatous tumors are extremely rare, and due to their nonspecific clinical manifestations, distinguishing them is nearly impossible without the aid of histopathology, immunohistochemistry, and molecular analysis. Complete resection with clear margins is the treatment of choice to avert metastasis, improve prognosis, and prevent complex complications due to the polyp growth and location. We present the case of a 70-year-old male who presented in 2023 with dysphagia due to an esophageal polyp; surgery was recommended. However, he did not accept any treatment due to fear. One year later, and since his symptoms worsened, he finally decided to undergo endoscopic treatment at another medical institution. However, during that procedure, he suffered severe asphyxia, which caused a cardiopulmonary arrest. Once he partially recovered and because he continued with dysphagia, surgery was completed, and the polyp was removed. The final diagnosis was esophageal liposarcoma.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2024 10","pages":"rjae670"},"PeriodicalIF":0.4,"publicationDate":"2024-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11520925/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142548277","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
Incidental aortic valve papillary fibroelastoma diagnosed by transesophageal echocardiography in a patient undergoing coronary artery bypass surgery: a case report. 在一名接受冠状动脉搭桥手术的患者中通过经食道超声心动图诊断出意外的主动脉瓣乳头纤维瘤：病例报告。
IF 0.4
Journal of Surgical Case Reports Pub Date : 2024-10-29 eCollection Date: 2024-10-01 DOI: 10.1093/jscr/rjae679
Nael Al-Sarraf, Adel Maher, Yuldash Agzamov, Mohammed Hasan, Ali Alhumaidan
{"title":"Incidental aortic valve papillary fibroelastoma diagnosed by transesophageal echocardiography in a patient undergoing coronary artery bypass surgery: a case report.","authors":"Nael Al-Sarraf, Adel Maher, Yuldash Agzamov, Mohammed Hasan, Ali Alhumaidan","doi":"10.1093/jscr/rjae679","DOIUrl":"https://doi.org/10.1093/jscr/rjae679","url":null,"abstract":"<p><p>Papillary fibroelastoma of aortic valve is a rare benign tumor that can present with symptoms of obstruction or embolization and can be asymptomatic. The main stay of diagnosis is echocardiography. The size of the tumor affects the sensitivity of transthoracic echocardiography which can miss small size tumors. The treatment is surgical resection. Here, we report a case of papillary fibroelastoma of aortic valve that was detected intraoperatively by transesophageal echocardiography and was missed by transthoracic echocardiography in a patient undergoing coronary artery surgery. The tumor was resected successfully with preservation of aortic valve with no complication. This case highlights importance of intraoperative transesophageal echocardiography in making the diagnosis.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2024 10","pages":"rjae679"},"PeriodicalIF":0.4,"publicationDate":"2024-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11520927/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142548274","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
Peritoneal invagination hernia in the virgin abdomen. 处女腹膜嵌顿疝。
IF 0.4
Journal of Surgical Case Reports Pub Date : 2024-10-28 eCollection Date: 2024-10-01 DOI: 10.1093/jscr/rjae666
Evan A Thomas, Adam S Harris
{"title":"Peritoneal invagination hernia in the virgin abdomen.","authors":"Evan A Thomas, Adam S Harris","doi":"10.1093/jscr/rjae666","DOIUrl":"https://doi.org/10.1093/jscr/rjae666","url":null,"abstract":"<p><p>Hernias are a common cause of small bowel obstruction. Many different classifications of hernias exist, all differing by location throughout the abdomen and hernia contents. We present a case report that describes a unique hernia-a peritoneal invagination hernia-which may lead to small bowel obstruction. The peritoneal invagination hernia is a defect in the peritoneum, in this case located on the right anterolateral abdominal wall, allowing small bowel to enter and become incarcerated. In our patient, the peritoneal defect was circular with smooth, rolled borders. The defect contained intact peritoneum overlying intact transversalis fascia. The patient had no prior abdominal surgeries. This hernia differs by location and etiology from preperitoneal interparietal hernias, which are found in the inguinal and femoral regions. This case describes a newly characterized abdominal hernia which is hypothesized to be due to a prior intra-abdominal inflammatory process.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2024 10","pages":"rjae666"},"PeriodicalIF":0.4,"publicationDate":"2024-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11520227/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142548275","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
Rare case of concomitant coronary artery bypass grafting and open abdominal aortic aneurysm repair. 罕见的同时进行冠状动脉旁路移植术和开放式腹主动脉瘤修补术的病例。
IF 0.4
Journal of Surgical Case Reports Pub Date : 2024-10-28 eCollection Date: 2024-10-01 DOI: 10.1093/jscr/rjae672
Dakota Pastore, Sabrina Higgins, Taylor James, Zamaan Hooda, Pasha Shenasen, Alexios Therionos, John Paul Bustamante, Jagbir Beniwal, Mark Connolly, John Danks
{"title":"Rare case of concomitant coronary artery bypass grafting and open abdominal aortic aneurysm repair.","authors":"Dakota Pastore, Sabrina Higgins, Taylor James, Zamaan Hooda, Pasha Shenasen, Alexios Therionos, John Paul Bustamante, Jagbir Beniwal, Mark Connolly, John Danks","doi":"10.1093/jscr/rjae672","DOIUrl":"https://doi.org/10.1093/jscr/rjae672","url":null,"abstract":"<p><p>Coronary artery disease occurs when coronary vessels are unable to supply adequate oxygen to the myocardium, while an abdominal aortic aneurysm (AAA) is a dilatation of the abdominal aorta. Both conditions have similar risk factors such as smoking and hypertension. If these disease processes become severe and are left untreated, life-threatening consequences may occur. We present a 71-year-old male with prior myocardial infarction and an infrarenal AAA that underwent a rare combined procedure of coronary artery bypass grafting (CABG) and open AAA repair surgery. The CABG involved grafting the left internal mammary artery and saphenous vein to coronary arteries while the AAA repair used an 18-mm bifurcated aortic graft. Combined CABG and open AAA repair is complex and rare, but aims to reduce mortality and prevent aneurysm rupture in patients with severe comorbid conditions. The patient's positive postoperative outcome highlights the procedure's efficacy in select cases.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2024 10","pages":"rjae672"},"PeriodicalIF":0.4,"publicationDate":"2024-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11520231/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142548278","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
Postoperative chylothorax following video-assisted mediastinoscopic lymphadenectomy (VAMLA) for early-stage non-small cell lung carcinoma. 早期非小细胞肺癌视频辅助纵隔镜淋巴腺切除术（VAMLA）术后出现乳糜胸。
IF 0.4
Journal of Surgical Case Reports Pub Date : 2024-10-28 eCollection Date: 2024-10-01 DOI: 10.1093/jscr/rjae665
Kayleigh A M van Dam, Yvonne L J Vissers, Karel W E Hulsewé, Erik R de Loos
{"title":"Postoperative chylothorax following video-assisted mediastinoscopic lymphadenectomy (VAMLA) for early-stage non-small cell lung carcinoma.","authors":"Kayleigh A M van Dam, Yvonne L J Vissers, Karel W E Hulsewé, Erik R de Loos","doi":"10.1093/jscr/rjae665","DOIUrl":"https://doi.org/10.1093/jscr/rjae665","url":null,"abstract":"<p><p>Chylothorax is a rare condition in which chylous fluid accumulates in the pleural cavity, most often due to iatrogenic injury of the thoracic duct. This paper reports a case of a woman in her 50s presenting with chyle leakage after a video-assisted mediastinoscopic lymphadenectomy (VAMLA) for staging of a nodule suspected of non-small cell lung carcinoma. After the VAMLA, a Uniportal Video Assisted Thoracoscopic Surgery lobectomy was scheduled during which the chylothorax was observed. The chyle was evacuated and the planned resection was conducted. The chest drain could be removed after 6 days while the patient followed a medium-chain triglyceride diet for 4 weeks. The purpose of this case report is to raise awareness for this very rare complication after VAMLA and discuss treatment options.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2024 10","pages":"rjae665"},"PeriodicalIF":0.4,"publicationDate":"2024-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11520229/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142548276","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
Successful surgical treatment of a right atrial myxoma with hypothermic circulatory arrest and venous cannulation in pulmonary artery. 通过低体温循环停滞和肺动脉静脉插管手术成功治疗右心房肌瘤。
IF 0.4
Journal of Surgical Case Reports Pub Date : 2024-10-28 eCollection Date: 2024-10-01 DOI: 10.1093/jscr/rjae677
Takao Miki, Satoshi Ohki, Ryo Yamaguchi, Ayako Nagasawa, Shuichi Okonogi, Kiyomitsu Yasuhara, Tamiyuki Obayashi
{"title":"Successful surgical treatment of a right atrial myxoma with hypothermic circulatory arrest and venous cannulation in pulmonary artery.","authors":"Takao Miki, Satoshi Ohki, Ryo Yamaguchi, Ayako Nagasawa, Shuichi Okonogi, Kiyomitsu Yasuhara, Tamiyuki Obayashi","doi":"10.1093/jscr/rjae677","DOIUrl":"https://doi.org/10.1093/jscr/rjae677","url":null,"abstract":"<p><p>Myxomas are the most common type of benign cardiac tumors, and the right atrium is the second most common location among them, with an incidence ranging from 8.6% to 20% of all cardiac myxomas. Herein, we described a rare case of right atrial myxoma originating from the inferior vena cava orifice. In this case, main pulmonary artery cannulation and moderate hypothermic circulatory arrest were helpful to obtain a clear and simple view of the operative field without blood, which led to complete resection of the tumor with safety and better outcomes with no future recurrence.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2024 10","pages":"rjae677"},"PeriodicalIF":0.4,"publicationDate":"2024-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11520226/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142548279","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
The conundrum of the giant condyloma: is it carcinoma? 巨大尖锐湿疣的难题：是癌吗？
IF 0.4
Journal of Surgical Case Reports Pub Date : 2024-10-22 eCollection Date: 2024-10-01 DOI: 10.1093/jscr/rjae668
Hyung C Kim, James D Schlenker, Amber B Post, Nicholas S Agoff, Timothy Feldmann, Vlad V Simianu
{"title":"The conundrum of the giant condyloma: is it carcinoma?","authors":"Hyung C Kim, James D Schlenker, Amber B Post, Nicholas S Agoff, Timothy Feldmann, Vlad V Simianu","doi":"10.1093/jscr/rjae668","DOIUrl":"https://doi.org/10.1093/jscr/rjae668","url":null,"abstract":"<p><p>Perineal verrucous carcinoma is a rare variant of squamous cell carcinoma that is mainly treated with surgical excision. In this case report, we present a 58-year-old man with human immunodeficiency virus who presented with an extraordinarily large perineal mass that was ultimately found to be verrucous carcinoma in association with giant condyloma acuminata. He was treated with a wide local excision followed by staged abdominoperineal resection and fasciocutaneous flap reconstruction. In the post-operative course, the patient developed relatively short interval recurrence which was successfully managed with salvage radiotherapy. He is now post-radiation without evidence of recurrence.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2024 10","pages":"rjae668"},"PeriodicalIF":0.4,"publicationDate":"2024-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11495325/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142510296","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
Postsurgical pyoderma gangrenosum after mastectomy with a familial component. 乳房切除术后的脓疱疮与家族遗传有关。
IF 0.4
Journal of Surgical Case Reports Pub Date : 2024-10-22 eCollection Date: 2024-10-01 DOI: 10.1093/jscr/rjae667
Christine Courtney Rogers, Jordyn Nepper, Kassandra E Holzem, Chandler S Cortina
{"title":"Postsurgical pyoderma gangrenosum after mastectomy with a familial component.","authors":"Christine Courtney Rogers, Jordyn Nepper, Kassandra E Holzem, Chandler S Cortina","doi":"10.1093/jscr/rjae667","DOIUrl":"https://doi.org/10.1093/jscr/rjae667","url":null,"abstract":"<p><p>Postsurgical pyoderma gangrenosum (PSPG) is a rare, ulcerative skin condition that presents a diagnostic challenge due to its similar presentation to infectious etiologies in the postsurgical period-often leading to gratuitous and unnecessary surgery and antibiotic use. We report a 37-year-old female with breast cancer who received neoadjuvant chemotherapy and immunotherapy and underwent bilateral skin-sparing mastectomies who developed delayed bilateral mastectomy skin flap necrosis secondary to PSPG. This case had rare factors associated with the development of PSPG such as preoperative systemic therapy and a familial component. This case underscores the importance of early recognition of this rare disease and appropriate management of PSPG to prevent unnecessary interventions and ensure an optimal outcome.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2024 10","pages":"rjae667"},"PeriodicalIF":0.4,"publicationDate":"2024-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11495327/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142510294","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
Surgical intervention of a giant bronchogenic cyst in the right middle lobe with recurrent infections: a case report. 右肺中叶巨大支气管源性囊肿合并反复感染的手术治疗：病例报告。
IF 0.4
Journal of Surgical Case Reports Pub Date : 2024-10-22 eCollection Date: 2024-10-01 DOI: 10.1093/jscr/rjae664
Quan Qiao, Hongmei Wen, Xiande Chen, Chao Tu, Xiuxiong Zhang, Xing Wei
{"title":"Surgical intervention of a giant bronchogenic cyst in the right middle lobe with recurrent infections: a case report.","authors":"Quan Qiao, Hongmei Wen, Xiande Chen, Chao Tu, Xiuxiong Zhang, Xing Wei","doi":"10.1093/jscr/rjae664","DOIUrl":"https://doi.org/10.1093/jscr/rjae664","url":null,"abstract":"<p><p>Bronchogenic cysts, a rare congenital pulmonary disorder, typically affect young adults and are often managed conservatively. However, large cysts with recurrent infections require surgical intervention. This case study highlights the successful management of a large bronchogenic cyst. A 53-year-old female presented with a decade-long history of recurrent respiratory infections manifesting as cough, yellow purulent sputum, and shortness of breath. Chest computed tomography revealed a large bronchogenic cyst in the right middle lobe, causing cardiac compression. Despite conservative management, the recurrent symptoms persisted. After multidisciplinary consultation, a thoracoscopic right middle lobectomy was planned. Severe pleural adhesions and bleeding complicated the procedure; therefore, thoracotomy was performed. Postoperatively, the patient developed transient fever and elevated white blood cell count, both of which resolved with appropriate antibiotic therapy. The patient was discharged in stable condition, with no recurrence of symptoms at follow-up. Large, symptomatic bronchogenic cysts that cause recurrent infections require surgical resection.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2024 10","pages":"rjae664"},"PeriodicalIF":0.4,"publicationDate":"2024-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11495328/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142510295","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 finding of pulmonary nodules in a middle ear neuroendocrine tumor: a case report and review of the literature. 中耳神经内分泌肿瘤罕见的肺结节：病例报告和文献综述。
IF 0.4
Journal of Surgical Case Reports Pub Date : 2024-10-21 eCollection Date: 2024-10-01 DOI: 10.1093/jscr/rjae662
Nader Alharbi, Ghadah Alotaibi, Saleh Alabood, Ibrahim AlSulaiman, Essa Bakry
{"title":"A rare finding of pulmonary nodules in a middle ear neuroendocrine tumor: a case report and review of the literature.","authors":"Nader Alharbi, Ghadah Alotaibi, Saleh Alabood, Ibrahim AlSulaiman, Essa Bakry","doi":"10.1093/jscr/rjae662","DOIUrl":"10.1093/jscr/rjae662","url":null,"abstract":"<p><p>Neuroendocrine tumors (NETs) are usually found in the gastrointestinal tract and pancreas; however, they are rare in the middle ear. The presentation of vague symptoms, such as tinnitus and conductive hearing loss, complicates the diagnosis. We present a 46-year-old male with a history of right ear discharge and a previous canal wall-down mastoidectomy, suspected to have cholesteatoma recurrence. Imaging and surgery demonstrated a well-differentiated G1 NET in the middle ear. Postoperative metastatic workup revealed few pulmonary nodules needing ongoing observation. Middle-ear NETs are difficult to diagnose due to their rarity. This case underscores the importance of histological and immunohistochemical evaluation and the need for systemic assessment to rule out metastasis due to pulmonary nodules. We contribute to the limited literature highlighting the need to include NETs in the differential of middle ear masses and the usefulness of interdisciplinary teamwork.</p>","PeriodicalId":47321,"journal":{"name":"Journal of Surgical Case Reports","volume":"2024 10","pages":"rjae662"},"PeriodicalIF":0.4,"publicationDate":"2024-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11491658/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142477550","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
首页 上一页 下一页 尾页
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整，为了账户安全，请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
请完成安全验证×
相关产品
×
本文献相关产品
联系我们：info@booksci.cn Book学术提供免费学术资源搜索服务，方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号：481959085
Book学术官方微信