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, Supritha Nilam, Alexander McMahon, Brennan Leininger, 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":"10 1","pages":"Article 100341"},"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}
{"title":"Case reporting in cleft and craniofacial surgery","authors":"Ashley E. Manlove , Daniel Setzke , 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":"10 1","pages":"Article 100338"},"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}
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 , 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","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":"10 1","pages":"Article 100340"},"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}
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, David Seratelli DMD, 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":"9 4","pages":"Article 100337"},"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}
{"title":"Surgical and biochemical outcomes of phosphaturic mesenchymal tumors causing tumor-induced osteomalacia in the head and neck region","authors":"Yusuke Tsuda , Yoichi Yasunaga , Masanobu Abe , Kazuto Hoshi , Nobuaki Ito , Kenji Kondo , Koichi Okajima , Liuzhe Zhang , Hajime Kato , Naoko Hidaka , Sakae Tanaka , 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":"9 4","pages":"Article 100335"},"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}
{"title":"MALT lymphoma of the palatal minor salivary Grand in patient with Sjögren's syndrome: A case report","authors":"Harusachi Kanazawa , Kohei Kawasaki , Isao Miyamoto , Atsusi Kasamatsu , Katsuhiro Uzawa , 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":"9 4","pages":"Article 100336"},"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}
{"title":"Total scalp avulsion reconstruction with acellular dermal matrix and split thickness skin graft: A case report","authors":"Stuart Allyn , Rachel Lim , Andrea Burke","doi":"10.1016/j.omsc.2023.100324","DOIUrl":"10.1016/j.omsc.2023.100324","url":null,"abstract":"<div><p>Full thickness total scalp avulsion injuries present a complex reconstructive challenge. Here we present a case of a 32-year-old female with an extensive full thickness scalp avulsion injury from a fishing boat engine accident that led to a unique injury pattern and loss of pericranium. This case report demonstrates the effectiveness of acellular dermal matrix and split thickness skin grafting in reconstruction of full thickness scalp avulsion injuries where there is significant loss of pericranium. After this patient's reconstruction, six-month postoperative follow up demonstrated an acceptable functional and esthetic outcome.</p></div>","PeriodicalId":38030,"journal":{"name":"Oral and Maxillofacial Surgery Cases","volume":"9 3","pages":"Article 100324"},"PeriodicalIF":0.0,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43199716","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}
Dini Widiarni Widodo , Febriani Endiyarti , Amanda Siagian , Respati W. Ranakusuma , Mirta Hediyati Reksodiputro
{"title":"Reconstruction of a huge frontal defect caused by a mucocele with a combination of autologous graft and titanium mesh: A case report","authors":"Dini Widiarni Widodo , Febriani Endiyarti , Amanda Siagian , Respati W. Ranakusuma , Mirta Hediyati Reksodiputro","doi":"10.1016/j.omsc.2023.100328","DOIUrl":"10.1016/j.omsc.2023.100328","url":null,"abstract":"<div><h3>Introduction</h3><p>Reconstruction of frontal deformities is challenging for surgeons, with the search for materials and techniques that offer a more comfortable and optimal result being a significant issue. This report describes the reconstruction of a large frontal defect caused by a mucocele using a titanium mesh and rib cartilage.</p></div><div><h3>Case</h3><p>A 44-year-old female with a left frontal ethmoid mass was suspected of having a mucocele with a frontal defect and optic nerve compression. The patient underwent drainage, endoscopic marsupialization of the mucocele, and reconstruction of the frontal defect using a combination of a rib graft and titanium mesh. The patient showed no complications or functional or esthetic complaints over one year of follow-up.</p></div><div><h3>Discussion</h3><p>Autologous bony cartilage has great growth potential and functions best when integrated into the natural bone, indicating a reduced risk of graft loss. Titanium is a non-inflammatory, biocompatible metal that is helpful for the quick repair of large cranial defects. In the present case, the frontal defect was large. Therefore, we decided to use a rib graft combined with a titanium mesh as a bridge to close the defect.</p></div><div><h3>Conclusion</h3><p>Reconstruction of a frontal defect using a combination of autologous rib grafts and titanium mesh showed excellent results in the current case.</p></div>","PeriodicalId":38030,"journal":{"name":"Oral and Maxillofacial Surgery Cases","volume":"9 3","pages":"Article 100328"},"PeriodicalIF":0.0,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48289936","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}
Artem Krutyansky , Steven Halepas , Elie M. Ferneini
{"title":"Cosmetic surgery","authors":"Artem Krutyansky , Steven Halepas , Elie M. Ferneini","doi":"10.1016/j.omsc.2023.100322","DOIUrl":"10.1016/j.omsc.2023.100322","url":null,"abstract":"<div><p>Facial cosmetic surgery has a long and rich history, dating back to ancient times when people attempted to improve their appearance through various methods such as using makeup, wigs, and even undergoing rudimentary surgical procedures. With the advancement of medical knowledge and technology, facial cosmetic surgery has evolved into a sophisticated and specialized field that aims to enhance the aestheticfeatures of the face while also ensuring functional outcomes. This chapter will review the history of facial cosmetic surgery and present some of the most influential case reports that have contributed to the development of facial cosmetic surgery as we know it today.</p></div>","PeriodicalId":38030,"journal":{"name":"Oral and Maxillofacial Surgery Cases","volume":"9 3","pages":"Article 100322"},"PeriodicalIF":0.0,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41855092","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}
Andrew C. Jenzer , Victoria Wickenheisser , Diana Marcella Cardona , David B. Powers
{"title":"Osteoblastoma of the orbit: A rare case report and review of the literature","authors":"Andrew C. Jenzer , Victoria Wickenheisser , Diana Marcella Cardona , David B. Powers","doi":"10.1016/j.omsc.2023.100326","DOIUrl":"10.1016/j.omsc.2023.100326","url":null,"abstract":"<div><p>Osteoblastoma is a benign tumor of bone representing less than 1% of all primary bone tumors [1]. Osteoblastomas are primarily reported in long bones and the spinal column, with craniofacial cases representing about 15% of the literature (Meli et al., 2008; Kroon and Schurmans, 1990) [1,2]. Osteoblastoma with orbital involvement is exceedingly rare, with less than twenty-five documented cases (Akhaddar et al., 2004; Meli et al., 2008; Bilkay et al., 2004; Hafidi and Daoudi, 2013) [3,1,4,5]. The mainstay of treatment for osteoblastoma is surgical excision with consideration for resection depending on the lesion, size, location, involved structures, and clinical presentation. The authors present a case of an orbital osteoblastoma presenting with globe subluxation in a pediatric patient.</p></div>","PeriodicalId":38030,"journal":{"name":"Oral and Maxillofacial Surgery Cases","volume":"9 3","pages":"Article 100326"},"PeriodicalIF":0.0,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47402509","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}