Oral and Maxillofacial Surgery Cases最新文献

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Combined mandibular inverted L osteotomy and total mandibular subapical osteotomy 下颌倒 L 型截骨术和下颌角下全切骨术联合应用
Oral and Maxillofacial Surgery Cases Pub Date : 2024-01-10 DOI: 10.1016/j.omsc.2023.100343
Anson Grant Fisher , Jacob Johnson , Soyoung Shin , Chang Min Richard Yim
{"title":"Combined mandibular inverted L osteotomy and total mandibular subapical osteotomy","authors":"Anson Grant Fisher ,&nbsp;Jacob Johnson ,&nbsp;Soyoung Shin ,&nbsp;Chang Min Richard Yim","doi":"10.1016/j.omsc.2023.100343","DOIUrl":"10.1016/j.omsc.2023.100343","url":null,"abstract":"<div><p>This case report documents a patient with a Class II skeletal malocclusion and suspected obstructive sleep apnea who underwent a combined mandibular inverted L osteotomy and total subapical osteotomy. The surgery involved a single-piece Lefort 1 osteotomy of the maxilla, bilateral inverted L osteotomies of the mandible, and a total mandibular subapical osteotomy. After the patient's pre-surgical orthodontic phase was completed, a traditional bilateral sagittal split osteotomy (BSSO) was initially planned to achieve mandibular advancement. However, the large horizontal and yaw correction required for the patient's mandibular teeth made a BSSO alone unrealistic. The virtual surgical plan (VSP) indicated that a subapical osteotomy was necessary, and due to the extension of the total subapical segment, an inverted L osteotomy was added to benefit the subapical osteotomy. The patient's surgery was successful, and the results were satisfactory.</p></div>","PeriodicalId":38030,"journal":{"name":"Oral and Maxillofacial Surgery Cases","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214541923000524/pdfft?md5=fc174ede1fd432c4126fc902acdaa50d&pid=1-s2.0-S2214541923000524-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139457076","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 traumatic temporomandibular joint ankylosis: A case report 外伤性颞下颌关节强直的治疗:病例报告
Oral and Maxillofacial Surgery Cases Pub Date : 2024-01-07 DOI: 10.1016/j.omsc.2023.100344
Cheng-Han He
{"title":"Management of traumatic temporomandibular joint ankylosis: A case report","authors":"Cheng-Han He","doi":"10.1016/j.omsc.2023.100344","DOIUrl":"10.1016/j.omsc.2023.100344","url":null,"abstract":"<div><p>Ankylosis of temporomandibular joint (TMJ) is a complicated condition which impairs jaw function and nutrition. Post-traumatic joint ankylosis could be treated with various surgical techniques. However, no standard surgery guarantees symptom-free success. Treating post-traumatic TMJ thus remains a challenging task to oral and maxillofacial surgeons. This paper is a case of a bilateral post-traumatic TMJ ankylosis. The 27-year-old young man sustained mid-face and mandible fractures including bilateral condyles due to a road accident and was treated 7 years ago. The injured condyles are managed conservatively. He presented with limited mouth opening (13mm) along with bite changes. Conservative treatments failed to restore normal jaw movement. Preoperative cone beam CT revealed ankyloses joint of both sides. An arthroplasty with the interpositional umbilical fat grafting was performed. Follow-up course was uneventful with up to 40mm mouth opening. Arthroplasty with interpositional fat grafting is an effective technique to restore jaw function and to prevent relapse.</p></div>","PeriodicalId":38030,"journal":{"name":"Oral and Maxillofacial Surgery Cases","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214541923000536/pdfft?md5=d6356f76640e3c2e37c565340c702fa1&pid=1-s2.0-S2214541923000536-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139456858","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
Submandibular gland amyloidosis: A rare manifestation of extranodal marginal lymphoma – A case report and literature review 颌下腺淀粉样变性:结节外边缘淋巴瘤的罕见表现--病例报告和文献综述
Oral and Maxillofacial Surgery Cases Pub Date : 2023-12-20 DOI: 10.1016/j.omsc.2023.100342
N. Chargi , T. Verhoeven , E. Dik , C. Coppen , L.L. van den Hoogen , W.B.C. Stevens , K.M. Hebeda , W. Weijs
{"title":"Submandibular gland amyloidosis: A rare manifestation of extranodal marginal lymphoma – A case report and literature review","authors":"N. Chargi ,&nbsp;T. Verhoeven ,&nbsp;E. Dik ,&nbsp;C. Coppen ,&nbsp;L.L. van den Hoogen ,&nbsp;W.B.C. Stevens ,&nbsp;K.M. Hebeda ,&nbsp;W. Weijs","doi":"10.1016/j.omsc.2023.100342","DOIUrl":"10.1016/j.omsc.2023.100342","url":null,"abstract":"<div><p>Amyloidosis of the submandibular gland is a rare manifestation of extranodal marginal zone lymphoma (eMZL). Here, we present a case-report of a 62-year-old female patient with a history of eMZL, limited stage IIEA. The patient was initially treated with radiotherapy; however large glands remained with lack of clinical response to the radiotherapy. Consequently, a surgical excision of the submandibular glands was performed, and histology revealed massive amyloid deposits in the gland tissue next to eMZL. This case report highlights the importance of considering amyloidosis as a possible cause of submandibular gland enlargement in patients with a history of lymphoma and emphasizes the need for a histological diagnosis to direct appropriate treatment.</p></div>","PeriodicalId":38030,"journal":{"name":"Oral and Maxillofacial Surgery Cases","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214541923000512/pdfft?md5=e47109060c328ad5cec397221ab8ee88&pid=1-s2.0-S2214541923000512-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139013038","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
Low-grade central osteosarcoma of the maxilla: A diagnostic dilemma 上颌骨低级别中心性骨肉瘤:诊断难题
Oral and Maxillofacial Surgery Cases Pub Date : 2023-12-03 DOI: 10.1016/j.omsc.2023.100339
Tushar Bhosale, Kalyani Bhate, Shilpa Bawane, Uday Londhe
{"title":"Low-grade central osteosarcoma of the maxilla: A diagnostic dilemma","authors":"Tushar Bhosale,&nbsp;Kalyani Bhate,&nbsp;Shilpa Bawane,&nbsp;Uday Londhe","doi":"10.1016/j.omsc.2023.100339","DOIUrl":"https://doi.org/10.1016/j.omsc.2023.100339","url":null,"abstract":"","PeriodicalId":38030,"journal":{"name":"Oral and Maxillofacial Surgery Cases","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214541923000482/pdfft?md5=40577e866422505ce35077cb7b137ca9&pid=1-s2.0-S2214541923000482-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138577675","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
Case report: Rare latent postoperative pseudoaneurysm of internal maxillary artery after Le Fort osteotomy 病例报告:Le Fort截骨术后罕见的潜伏性上颌内动脉假性动脉瘤
Oral and Maxillofacial Surgery Cases Pub Date : 2023-11-28 DOI: 10.1016/j.omsc.2023.100341
Victoria Chen, Supritha Nilam, Alexander McMahon, Brennan Leininger, Nora Kahenasa
{"title":"Case report: Rare latent postoperative pseudoaneurysm of internal maxillary artery after Le Fort osteotomy","authors":"Victoria Chen,&nbsp;Supritha Nilam,&nbsp;Alexander McMahon,&nbsp;Brennan Leininger,&nbsp;Nora Kahenasa","doi":"10.1016/j.omsc.2023.100341","DOIUrl":"https://doi.org/10.1016/j.omsc.2023.100341","url":null,"abstract":"<div><h3>Background</h3><p>The Le Fort I osteotomy is a commonly employed and predictable surgical technique used to treat maxillofacial deformities. While considered technically safe, orthognathic surgery can cause significant vascular complications. Presentation: This case report describes a 20-year old male who had undergone a routine Le Fort I osteotomy to treat maxillo-mandibular discrepancy, and subsequently developed an internal maxillary artery pseudoaneurysm that caused uncontrolled hemorrhage and hemodynamic instability. The patient ultimately required interventional radiology coil embolization for source control.</p></div><div><h3>Discussion</h3><p>Although rare, internal maxillary artery pseudoaneurysms continue to be reported as postoperative complications in Le Fort I osteotomies, wherein coil-embolization technique remains a viable option for treatment. Additionally, the presentation of temporal swelling and retrobulbar pain may be useful in diagnosing the existence of a maxillary artery pseudoaneurysm. Conclusion: Pseudoaneurysm of the internal maxillary artery is a possible sequela of orthognathic surgery, and proper monitoring and management can avoid morbid outcomes.</p></div>","PeriodicalId":38030,"journal":{"name":"Oral and Maxillofacial Surgery Cases","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214541923000500/pdfft?md5=121bdb21831f657defcf82ae07a59782&pid=1-s2.0-S2214541923000500-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138474941","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
Case reporting in cleft and craniofacial surgery 唇裂与颅面外科病例报告
Oral and Maxillofacial Surgery Cases Pub Date : 2023-11-20 DOI: 10.1016/j.omsc.2023.100338
Ashley E. Manlove , Daniel Setzke , Knika Sethi
{"title":"Case reporting in cleft and craniofacial surgery","authors":"Ashley E. Manlove ,&nbsp;Daniel Setzke ,&nbsp;Knika Sethi","doi":"10.1016/j.omsc.2023.100338","DOIUrl":"https://doi.org/10.1016/j.omsc.2023.100338","url":null,"abstract":"","PeriodicalId":38030,"journal":{"name":"Oral and Maxillofacial Surgery Cases","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214541923000470/pdfft?md5=2d5a8b337abec88e900ae9ce723086b9&pid=1-s2.0-S2214541923000470-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138436836","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
Treatment of the median mandibular cleft in Richieri-Costa-Pereira syndrome with a customized total mandibular prosthesis: A case report 定制全下颌假体治疗Richieri-Costa-Pereira综合征下颌正中裂1例报告
Oral and Maxillofacial Surgery Cases Pub Date : 2023-11-17 DOI: 10.1016/j.omsc.2023.100340
Ryuichi Hoshi , Paula Marcella Silva Drago , Henrique Mascarenhas Villela , Gabriela Gayer Sheibler , Daniel Serra Cassano , Fernanda Barros Silva de Pedreira Barbosa , Lissa Hoshi , Isadora dos Santos Lima
{"title":"Treatment of the median mandibular cleft in Richieri-Costa-Pereira syndrome with a customized total mandibular prosthesis: A case report","authors":"Ryuichi Hoshi ,&nbsp;Paula Marcella Silva Drago ,&nbsp;Henrique Mascarenhas Villela ,&nbsp;Gabriela Gayer Sheibler ,&nbsp;Daniel Serra Cassano ,&nbsp;Fernanda Barros Silva de Pedreira Barbosa ,&nbsp;Lissa Hoshi ,&nbsp;Isadora dos Santos Lima","doi":"10.1016/j.omsc.2023.100340","DOIUrl":"https://doi.org/10.1016/j.omsc.2023.100340","url":null,"abstract":"<div><p>Richieri-Costa-Pereira syndrome (RCPS) is a rare genetic disease with an autosomal recessive inheritance pattern characterized by craniofacial alterations such as microsomia, Pierre-Robin sequence, mandibular cleft, absence of lower central incisors, short stature, and changes in the upper and lower limbs. Mandibular clefts are rare and can vary from a slight notch in the lower lip or mandibular alveolus to a complete mandibular cleavage. Only three cases of total mandibular rehabilitation with a customized prosthesis have been published, and none have described a patient born with a mandibular cleft. With the aid of computer-aided design/computer-aided manufacturing technology, virtual surgical planning, and customized manufacturing of surgical materials, the rehabilitation of this case became attainable. In this study, we describe the case of a patient with RCPS and median mandibular cleft treated with a customized total mandibular prosthesis.</p></div>","PeriodicalId":38030,"journal":{"name":"Oral and Maxillofacial Surgery Cases","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214541923000494/pdfft?md5=970b59ccb97bbb938ec9b40c0d69f6ce&pid=1-s2.0-S2214541923000494-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138391184","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
Case Review: Lower Blepharoplasty with Autogenous Fat Transpositioning 病例回顾:自体脂肪转位下睑成形术
Oral and Maxillofacial Surgery Cases Pub Date : 2023-10-19 DOI: 10.1016/j.omsc.2023.100337
Mina A. Ayoub DMD, David Seratelli DMD, Vincent B. Ziccardi DDS, MD, FACS
{"title":"Case Review: Lower Blepharoplasty with Autogenous Fat Transpositioning","authors":"Mina A. Ayoub DMD,&nbsp;David Seratelli DMD,&nbsp;Vincent B. Ziccardi DDS, MD, FACS","doi":"10.1016/j.omsc.2023.100337","DOIUrl":"https://doi.org/10.1016/j.omsc.2023.100337","url":null,"abstract":"","PeriodicalId":38030,"journal":{"name":"Oral and Maxillofacial Surgery Cases","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214541923000469/pdfft?md5=e61aef5be65763625a6800bd0740aec8&pid=1-s2.0-S2214541923000469-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"92147957","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 and biochemical outcomes of phosphaturic mesenchymal tumors causing tumor-induced osteomalacia in the head and neck region 头颈部磷化间充质肿瘤引起肿瘤性骨软化症的手术和生化结果
Oral and Maxillofacial Surgery Cases Pub Date : 2023-10-02 DOI: 10.1016/j.omsc.2023.100335
Yusuke Tsuda , Yoichi Yasunaga , Masanobu Abe , Kazuto Hoshi , Nobuaki Ito , Kenji Kondo , Koichi Okajima , Liuzhe Zhang , Hajime Kato , Naoko Hidaka , Sakae Tanaka , Hiroshi Kobayashi
{"title":"Surgical and biochemical outcomes of phosphaturic mesenchymal tumors causing tumor-induced osteomalacia in the head and neck region","authors":"Yusuke Tsuda ,&nbsp;Yoichi Yasunaga ,&nbsp;Masanobu Abe ,&nbsp;Kazuto Hoshi ,&nbsp;Nobuaki Ito ,&nbsp;Kenji Kondo ,&nbsp;Koichi Okajima ,&nbsp;Liuzhe Zhang ,&nbsp;Hajime Kato ,&nbsp;Naoko Hidaka ,&nbsp;Sakae Tanaka ,&nbsp;Hiroshi Kobayashi","doi":"10.1016/j.omsc.2023.100335","DOIUrl":"https://doi.org/10.1016/j.omsc.2023.100335","url":null,"abstract":"<div><h3>Objectives</h3><p>We aimed to report the surgical outcomes of phosphaturic mesenchymal tumors causing tumor-induced osteomalacia in the head and neck.</p></div><div><h3>Methods</h3><p>This study analyzed nine patients who underwent surgical excision of phosphaturic mesenchymal tumors in the head and neck region. The primary sites were two in the maxilla and ethmoid sinus, and one in the intracranial, skull, parotid gland, maxillary sinus, and nasal cavity in each patient. Outcomes were compared with those in the extremities and trunk (n = 32).</p></div><div><h3>Results</h3><p>Five of nine patients (56%) developed residual disease/local recurrence associated with low serum phosphate level after initial surgical excision. At the last follow-up, the biochemical parameters were normalized in four of the five patients after re-excision without any medication. The local recurrence/residual disease risk was significantly higher for the head and neck compared with the extremities and trunk (56% vs. 25%, p = 0.048). The rate of remission (normalized serum phosphate without medication) at final follow-up was similar in both groups after re-excision (head and neck vs. extremities and trunk, 86% vs. 73%, p = 0.827).</p></div><div><h3>Conclusions</h3><p>Phosphaturic mesenchymal tumor resection in the head and neck region was challenging because of its complex anatomy and proximity to the brain or other crucial organs, which was associated with high local recurrence/residual disease rate. However, biological remission was achieved in the majority of the patients after re-excision.</p></div>","PeriodicalId":38030,"journal":{"name":"Oral and Maxillofacial Surgery Cases","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49744966","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
MALT lymphoma of the palatal minor salivary Grand in patient with Sjögren's syndrome: A case report Sjögren综合征患者腭小唾液腺MALT淋巴瘤1例
Oral and Maxillofacial Surgery Cases Pub Date : 2023-09-30 DOI: 10.1016/j.omsc.2023.100336
Harusachi Kanazawa , Kohei Kawasaki , Isao Miyamoto , Atsusi Kasamatsu , Katsuhiro Uzawa , Masashi Fukuyama
{"title":"MALT lymphoma of the palatal minor salivary Grand in patient with Sjögren's syndrome: A case report","authors":"Harusachi Kanazawa ,&nbsp;Kohei Kawasaki ,&nbsp;Isao Miyamoto ,&nbsp;Atsusi Kasamatsu ,&nbsp;Katsuhiro Uzawa ,&nbsp;Masashi Fukuyama","doi":"10.1016/j.omsc.2023.100336","DOIUrl":"https://doi.org/10.1016/j.omsc.2023.100336","url":null,"abstract":"<div><p>We present a quite rare case of MALT lymphoma originating from the palatal minor salivary gland in a 37-year-old woman with Sjögren's syndrome (SS). She underwent an excision biopsy and definite diagnosis of MALT lymphoma was obtained on the basis of microscopic finding with lymphoepithelial lesion, immunohistochemistry positive for CD20 and negative for CD3, CD5, cycclinD1, and detection of immunoglobulin light chain restriction with kappa light-chain restricted monoclonality. MALT lymphoma is considered in the differential diagnosis of a painless, non-ulcerative palatal swelling. In this case, SS remained undiagnosed until after MALT lymphoma diagnosis. Patients with MALT lymphoma in the minor salivary glands need to be investigated for SS even if there is no clinical symptom of SS. Surgical excision can be recommended in case of limited stages resulting in good prognosis.</p></div>","PeriodicalId":38030,"journal":{"name":"Oral and Maxillofacial Surgery Cases","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49757732","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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