Oral and Maxillofacial Surgery Cases最新文献

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A case of spindle cell hemangioma of the upper lip 上唇梭形细胞血管瘤1例
Oral and Maxillofacial Surgery Cases Pub Date : 2023-07-01 DOI: 10.1016/j.omsc.2023.100327
Takeshi Yoshida, Shuu Inoue, Tatsuto Kuramoto, A. Yamaguchi
{"title":"A case of spindle cell hemangioma of the upper lip","authors":"Takeshi Yoshida, Shuu Inoue, Tatsuto Kuramoto, A. Yamaguchi","doi":"10.1016/j.omsc.2023.100327","DOIUrl":"https://doi.org/10.1016/j.omsc.2023.100327","url":null,"abstract":"","PeriodicalId":38030,"journal":{"name":"Oral and Maxillofacial Surgery Cases","volume":"39 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"55344430","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
Multidisciplinary management of an advanced mandibular ameloblastoma: Etiopathogenesis, surgical management and prosthetic rehabilitation 晚期下颌成釉细胞瘤的多学科治疗:发病机制、手术治疗和假肢康复
Oral and Maxillofacial Surgery Cases Pub Date : 2023-06-01 DOI: 10.1016/j.omsc.2023.100296
Jeffrey W. Chadwick , Sonia Ruo Chen Huang , Ali Khadivi , Karl K. Cuddy
{"title":"Multidisciplinary management of an advanced mandibular ameloblastoma: Etiopathogenesis, surgical management and prosthetic rehabilitation","authors":"Jeffrey W. Chadwick ,&nbsp;Sonia Ruo Chen Huang ,&nbsp;Ali Khadivi ,&nbsp;Karl K. Cuddy","doi":"10.1016/j.omsc.2023.100296","DOIUrl":"10.1016/j.omsc.2023.100296","url":null,"abstract":"<div><h3>Background</h3><p>The ameloblastoma is a benign but locally aggressive epithelial odontogenic neoplasm. Although rare, the ameloblastoma is the most common odontogenic tumor associated with the maxillofacial complex which possesses a significant propensity for local recurrence in the setting of conservative treatment. Concordantly, definitive therapy is predicated on wide surgical excision with reconstruction of ablative defects dictated by the resultant tissue defects. The purpose of this report is to highlight specific treatment and reconstructive challenges, emphasizing the essential need for collaborative patient care within a large multidisciplinary team.</p></div><div><h3>Case description</h3><p>A 31-year-old Vietnamese-speaking male was referred for management of an extensive ameloblastoma associated with the left mandible. Management consisted of a bilateral composite mandibular resection and reconstruction via free tissue transfer utilizing an osteocutaneous fibular free flap. Histopathologic analysis confirmed the diagnosis of a conventional ameloblastoma. Delayed oral rehabilitation employing virtual surgical planning to facilitate the placement of endosseous implants with immediate loading of a fixed acrylic prosthesis was accomplished in the post-operative period without any evidence of recurrence.</p></div><div><h3>Practical implications</h3><p>Multidisciplinary collaboration in the setting of advanced odontogenic tumors is paramount in enhancing treatment outcomes. This case strengthens the need for accurate and rapid diagnosis in the primary care setting with collaborative interprofessional management utilizing advances in digital technologies to optimize both functional and aesthetic outcomes which have significant influence over long-term quality-of-life.</p></div>","PeriodicalId":38030,"journal":{"name":"Oral and Maxillofacial Surgery Cases","volume":"9 2","pages":"Article 100296"},"PeriodicalIF":0.0,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46938652","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
Hypoglossal nerve injury following local anesthetic injection: A case report and literature review 局麻注射后舌下神经损伤1例并文献复习
Oral and Maxillofacial Surgery Cases Pub Date : 2023-06-01 DOI: 10.1016/j.omsc.2023.100300
Andrew J. Deek , Christopher Scott , Michael Foster , Jack E. Gotcher Jr.
{"title":"Hypoglossal nerve injury following local anesthetic injection: A case report and literature review","authors":"Andrew J. Deek ,&nbsp;Christopher Scott ,&nbsp;Michael Foster ,&nbsp;Jack E. Gotcher Jr.","doi":"10.1016/j.omsc.2023.100300","DOIUrl":"10.1016/j.omsc.2023.100300","url":null,"abstract":"<div><p>Hypoglossal nerve injury is a known complication of oral intubation, otolaryngology procedures, and trauma. More rarely, hypoglossal nerve injury has been described as a complication of dental procedures. While iatrogenic damage to the inferior alveolar nerve has been extensively described in the oral and maxillofacial surgery literature, a paucity of literature can be found related to 12th cranial nerve complications. This case report aims to describe a case presenting to our office and the available treatment for patients suffering from this pathology.</p></div>","PeriodicalId":38030,"journal":{"name":"Oral and Maxillofacial Surgery Cases","volume":"9 2","pages":"Article 100300"},"PeriodicalIF":0.0,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46734315","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
Rosai-Dorfman disease of the submandibular gland 下颌下腺Rosai dorfman病
Oral and Maxillofacial Surgery Cases Pub Date : 2023-06-01 DOI: 10.1016/j.omsc.2023.100308
Peng Chen, Jun Li, Bingju Gao, Yu Qiu, Lisong Lin
{"title":"Rosai-Dorfman disease of the submandibular gland","authors":"Peng Chen,&nbsp;Jun Li,&nbsp;Bingju Gao,&nbsp;Yu Qiu,&nbsp;Lisong Lin","doi":"10.1016/j.omsc.2023.100308","DOIUrl":"10.1016/j.omsc.2023.100308","url":null,"abstract":"<div><h3>Background</h3><p>Only 8 cases of Rosai-Dorfman disease (RDD) involving the submandibular gland (SMG) have been reported. We report one more such case, involving a 51-year-old man, thus, adding to the available body of knowledge for this specific pathology.</p></div><div><h3>Methods</h3><p>The patient presented with a growing mass in the right SMG. Along with physical examination, hematologic and imaging-based diagnostic techniques were used. A diagnosis of the right SMG tumor was made and, thus, resection of the right SMG along with the lesion was carried out.</p></div><div><h3>Results</h3><p>Post-operative pathology was found to correspond to that of RDD. After 24 months of observation, the patient remained healthy.</p></div><div><h3>Conclusion</h3><p>RDD involving the SMG is rare, but not improbable, and hence, should be considered during diagnosis, especially when accompanied by neck lymph node enlargement. This is imperative because RDD is generally benign and self-limiting, and thus, a correct diagnosis may prevent SMG resection.</p></div>","PeriodicalId":38030,"journal":{"name":"Oral and Maxillofacial Surgery Cases","volume":"9 2","pages":"Article 100308"},"PeriodicalIF":0.0,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42835018","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
Case reporting in oral and maxillofacial pathology: Requisite among rare diseases 口腔颌面病理学病例报告:罕见病中必不可少的
Oral and Maxillofacial Surgery Cases Pub Date : 2023-06-01 DOI: 10.1016/j.omsc.2023.100309
Thomas Schlieve
{"title":"Case reporting in oral and maxillofacial pathology: Requisite among rare diseases","authors":"Thomas Schlieve","doi":"10.1016/j.omsc.2023.100309","DOIUrl":"10.1016/j.omsc.2023.100309","url":null,"abstract":"<div><p>Oral and maxillofacial pathology is replete with rare diseases that by their very nature, are difficult to study. Adequately powered, randomized controlled trials cannot be performed when cases are rare and spread across a large geographic area among numerous institutions. For example, there are approximately 500 ameloblastoma tumors diagnosed in the United States each year and these necessarily represent a heterogenous group with maxillary, mandibular, anterior/posterior, old and young all part of this group. To detect a treatment outcome difference of 5% at 80% power would require a sample size of over 3000 Ameloblastoma tumors. The specific aim of this manuscript is to highlight several of these rare diseases and the case reports that have contributed to our evolving knowledge to emphasize the significance of case reporting in oral and maxillofacial pathology.</p></div>","PeriodicalId":38030,"journal":{"name":"Oral and Maxillofacial Surgery Cases","volume":"9 2","pages":"Article 100309"},"PeriodicalIF":0.0,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44172831","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
Granular cell ameloblastoma in maxilla: A report of rare case 上颌骨颗粒细胞成釉细胞瘤一例报告
Oral and Maxillofacial Surgery Cases Pub Date : 2023-06-01 DOI: 10.1016/j.omsc.2023.100299
Siwakorn Rattanakuntee , Wacharaporn Thosaporn , Natnicha Ketchaikosol , Napatsorn Imerb
{"title":"Granular cell ameloblastoma in maxilla: A report of rare case","authors":"Siwakorn Rattanakuntee ,&nbsp;Wacharaporn Thosaporn ,&nbsp;Natnicha Ketchaikosol ,&nbsp;Napatsorn Imerb","doi":"10.1016/j.omsc.2023.100299","DOIUrl":"10.1016/j.omsc.2023.100299","url":null,"abstract":"<div><p>Ameloblastoma is the most common odontogenic tumor found at the posterior region of mandible. Granular cell ameloblastoma is one of the histological subtypes of ameloblastoma, mainly characterized by nests of large eosinophilic granular cell. Here, we reported a rare case of 75-year-old female patient presented with granular cell ameloblastoma in maxilla region. The conventional surgery was performed by upper lip-splitting technique and partial maxillectomy. The prosthetic obturators were delivered to rehabilitate a maxillofacial integrity, improving facial appearance and functional abilities. Long-term follow up revealed a favorable outcome without an evidence of tumor recurrence.</p></div>","PeriodicalId":38030,"journal":{"name":"Oral and Maxillofacial Surgery Cases","volume":"9 2","pages":"Article 100299"},"PeriodicalIF":0.0,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47131847","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
COVID-related mucormycosis mimicking dental infection 与新冠肺炎相关的毛霉菌病,模仿牙齿感染。
Oral and Maxillofacial Surgery Cases Pub Date : 2023-06-01 DOI: 10.1016/j.omsc.2023.100310
Saja A. Alramadhan , Sumita S. Sam , Shaun Young , Donald M. Cohen , Mohammed N. Islam , Indraneel Bhattacharyya
{"title":"COVID-related mucormycosis mimicking dental infection","authors":"Saja A. Alramadhan ,&nbsp;Sumita S. Sam ,&nbsp;Shaun Young ,&nbsp;Donald M. Cohen ,&nbsp;Mohammed N. Islam ,&nbsp;Indraneel Bhattacharyya","doi":"10.1016/j.omsc.2023.100310","DOIUrl":"10.1016/j.omsc.2023.100310","url":null,"abstract":"<div><h3>Background</h3><p>A recent increase in the prevalence of mucormycosis of the head and neck in patients who have recovered from COVID-19 following hospitalization has been reported. A Majority of the cases have been reported from India. Conditions such as diabetes mellitus, use of corticosteroids for other autoimmune conditions, organ transplant, immunosuppression, immunodeficiency, and malignancies especially hematologic ones, are all known risk factors for mucormycosis. Recently, hospitalization for COVID-19 has been added to the list of risk factors for opportunistic mucormycosis infection. This is likely attributable to the high doses and prolonged use of corticosteroids in the treatment of hospitalized COVID-19 patients. <strong>Case Description</strong>: Two patients with post-COVID-19 associated rhinocerebral mucormycosis presented with profound unexplained dental disease including tooth mobility and dental abscess mimicking periodontal disease. The patients were previously hospitalized for COVID-19 and received prolonged treatment with high doses of corticosteroids. The patients responded well to the surgical debridement with or without antifungal therapy. <strong>Conclusion</strong>: Oral healthcare providers including oral and maxillofacial surgeons, dentists, dental hygienists, and other dental practitioners can play a vital role in the recognition and early diagnosis of rhinocerebral mucormycosis given the large number of patients with severe COVID-19 infection who have recovered following hospitalization and/or received long-term high doses of immunosuppressive treatment.</p></div>","PeriodicalId":38030,"journal":{"name":"Oral and Maxillofacial Surgery Cases","volume":"9 2","pages":"Article 100310"},"PeriodicalIF":0.0,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10163790/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9642782","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 bilateral multifocal nodular oncocytic hyperplasia of the parotid gland 一例罕见的双侧腮腺多灶结节性嗜酸细胞增生
Oral and Maxillofacial Surgery Cases Pub Date : 2023-06-01 DOI: 10.1016/j.omsc.2023.100312
Wauters Lauri , Geers Caroline , Büttner Michael
{"title":"A rare case of bilateral multifocal nodular oncocytic hyperplasia of the parotid gland","authors":"Wauters Lauri ,&nbsp;Geers Caroline ,&nbsp;Büttner Michael","doi":"10.1016/j.omsc.2023.100312","DOIUrl":"10.1016/j.omsc.2023.100312","url":null,"abstract":"<div><p>Multifocal nodular oncocytic hyperplasia (MNOH) is an extremely rare pathological entity occurring in the parotid gland, even more rarely described in the submandibular gland. We report a case of bilateral parotid MNOH in a 71-year-old woman and perform a search of the existing literature that is compiled in a table. Fifty-nine cases are described in 34 publications. Half of the published cases presented as bilateral lesions, either synchronous or metachronous. Other lesions of the oncocyte-spectrum such as oncocytomas are frequently described on the ground of oncocytic hyperplasia. MNOH rarely occurs before the age of 40 years and mean age of the described cases is 62 years. The condition is considered as benign by all authors, but surgery was performed in nearly all cases, most often due to a lack of diagnostic certainty. Nevertheless, the radiologic presentation of MNOH is often highly suggestive. Based on the existing literature, recommendations for the management of MNOH are formulated.</p></div>","PeriodicalId":38030,"journal":{"name":"Oral and Maxillofacial Surgery Cases","volume":"9 2","pages":"Article 100312"},"PeriodicalIF":0.0,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43691674","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
A hard nodule of the upper lip 上唇硬结
Oral and Maxillofacial Surgery Cases Pub Date : 2023-06-01 DOI: 10.1016/j.omsc.2023.100315
Dries Govaerts , Esther Hauben , Constantinus Politis
{"title":"A hard nodule of the upper lip","authors":"Dries Govaerts ,&nbsp;Esther Hauben ,&nbsp;Constantinus Politis","doi":"10.1016/j.omsc.2023.100315","DOIUrl":"10.1016/j.omsc.2023.100315","url":null,"abstract":"<div><p>In this case report, we present a pleomorphic adenoma that presented as a hard nodule on the upper lip in a man in his 30s. Differential diagnosis is necessary, as there are multiple causes of a nodule in the lip. The nodule was excised extracapsularly and a histopathological examination was performed. Although the tumor was found to be benign, there is a risk of late malignant conversion, which underscores the importance of prompt treatment.</p></div>","PeriodicalId":38030,"journal":{"name":"Oral and Maxillofacial Surgery Cases","volume":"9 2","pages":"Article 100315"},"PeriodicalIF":0.0,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42035966","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
Reconstruction of frontal bone using patient specific implant poly-ether-ketone-ketone via a lateral nasal/lynch incision 采用患者特异性种植体聚醚酮酮经鼻/鼻侧切口重建额骨
Oral and Maxillofacial Surgery Cases Pub Date : 2023-06-01 DOI: 10.1016/j.omsc.2023.100293
Dana Jackson, Temidayo Obayomi, Francis Mir
{"title":"Reconstruction of frontal bone using patient specific implant poly-ether-ketone-ketone via a lateral nasal/lynch incision","authors":"Dana Jackson,&nbsp;Temidayo Obayomi,&nbsp;Francis Mir","doi":"10.1016/j.omsc.2023.100293","DOIUrl":"10.1016/j.omsc.2023.100293","url":null,"abstract":"<div><p>Trauma to the craniofacial structures can result in both functional and aesthetic defects. Mucosa lines the frontal sinus outflow tract (FSOT) from the frontal sinus to the nasal cavity and any obstruction to the flow of mucus can lead to complications such as mucocele formation or chronic frontal sinusitis. If the FSOT or posterior cranial vault is not damaged, reestablishment of the aesthetic contour of the frontal bandeau becomes the primary concern. There are several materials that have been proposed for treatment of frontal bone defects. Technological advances such as computed tomography (CT) scan, computer assisted design (CAD), and computer assisted manufacturing (CAM), have led to the development of three-dimensionally printed patient-specific implants. Poly-Ether-Ketone-Ketone (PEKK) is a biocompatible material from the same polyaromatic semicrystalline polymer family as Poly-Ether-Ether-Ketone (PEEK). Patient specific implants have given way to smaller surgical incisions that enable the implant to be slipped into the bony defect to reestablish contour of the frontal bandeau and secured with lag screws. The aim of this study is to describe a case of frontal bone defect reconstruction with PEKK implant via a lateral nasal/Lynch incision.</p></div>","PeriodicalId":38030,"journal":{"name":"Oral and Maxillofacial Surgery Cases","volume":"9 2","pages":"Article 100293"},"PeriodicalIF":0.0,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45946305","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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