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Foreign body in infant hard palate: A report of a rare case and literature review 婴儿硬腭异物:罕见病例报告和文献综述
IF 0.4 Q4 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2024-05-02 DOI: 10.1016/j.ajoms.2024.04.015
Shohei Takaoka , Kenji Yamagata , Satoshi Fukuzawa , Fumihiko Uchida , Naomi Ishibashi-Kanno , Hiroki Bukawa
Infants tend to place anything in their mouths; however, foreign bodies embedded in the hard palate of infants are extremely rare in clinical practice. Infants are often difficult to examine, and foreign bodies in the hard palate are misdiagnosed as neoplastic or inflammatory lesions in some cases. We present a rare case of a foreign body that was not diagnosed until its removal from the hard palate of an infant under general anesthesia. A healthy 12-month-old girl with a protruding foreign body on the hard palate was referred for close investigation. A white-yellow protruding foreign body measuring approximately 10 mm was found on the palate. Computed tomography revealed a radiopaque foreign body at the border. It was decided to examine and performed biopsy under general anesthesia, and the foreign body removed easily was an obviously plastic object with a semicircular shape and a brim around it. The histopathological examination of the abnormal gingiva under the foreign body revealed inflammatory granulation tissue. This report highlights the difficulty in diagnosing an infant with a foreign body in the hard palate and the safety of its removal under general anesthesia. Clinicians must consider the possibility of foreign bodies causing lesions on an infant’s hard palate. Therefore, careful examination and safe removal are necessary to prevent serious aspiration complications.
婴儿倾向于将任何东西放入口中,但在临床实践中,嵌入婴儿硬腭的异物极为罕见。婴儿通常很难进行检查,硬腭异物有时会被误诊为肿瘤或炎症病变。我们介绍了一例罕见病例,该病例是在全身麻醉下从婴儿硬腭取出异物后才确诊的。一名 12 个月大的健康女孩因硬腭上有异物突出而被转诊接受仔细检查。在腭部发现了一个约 10 毫米的白黄色突出异物。计算机断层扫描显示边界处有一个不透射线的异物。医生决定进行检查,并在全身麻醉的情况下进行了活组织检查,轻松取出的异物是一个明显的塑料制品,呈半圆形,周围有帽檐。对异物下的异常牙龈进行组织病理学检查后发现有炎症性肉芽组织。该报告强调了诊断婴儿硬腭异物的难度以及在全身麻醉下取出异物的安全性。临床医生必须考虑到异物导致婴儿硬腭病变的可能性。因此,必须仔细检查并安全取出异物,以防发生严重的吸入并发症。
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引用次数: 0
Anti-BP230 type mucous membrane pemphigoid with desquamative gingivitis: A case report 抗 BP230 型粘膜丘疹并伴有脱屑性牙龈炎:病例报告
IF 0.4 Q4 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2024-04-27 DOI: 10.1016/j.ajoms.2024.04.013
Seiichiro Oda , Hirofumi Okada , Atsushi Kihara , Norito Ishii , Hiroshi Koga , Yoshiyuki Mori , Tadahide Noguchi
Mucous membrane pemphigoid (MMP) is an autoimmune subepithelial/subepidermal blistering disease characterized by linear deposition of immunoglobulin G (IgG), IgA, and/or C3 in the basement membrane zone (BMZ) and predominant mucosal lesions involving the oral cavity and conjunctivae. Here, we describe a case of a 58-year-old Japanese man with MMP. Intraoral examination revealed desquamative gingivitis in the upper and lower gingivae. No conjunctival or cutaneous lesions were observed. Histopathological examination revealed a subepithelial split with inflammatory cell infiltration of the epithelial and connective tissues. Direct immunofluorescence revealed a linear deposition of C3 in the BMZ. IgG autoantibodies against BP230 were detected using an enzyme-linked immunosorbent assay. Indirect immunofluorescence using 1 mol/L NaCl-split skin sections revealed no reactivity for serum IgG or IgA. Immunoblotting using normal human epidermal extract as a substrate did not detect IgG reactivity against the 230-kDa antigen. Based on the above results, the definitive diagnosis of MMP with anti-BP230 antibody alone was established. Our case was categorized as low-risk MMP. The patient was treated with 0.1% triamcinolone acetonide ointment, oral minocycline, and oral nicotinamide, which improved the oral erosions. However, the mechanism underlying IgG autoantibody production against intracellular BP230 remains unclear. Further research and more such case studies are necessary to elucidate the mechanism of anti-BP230 antibody production and the clinical feature of anti-BP230 type MMP.
粘膜丘疹性类风湿(MMP)是一种自身免疫性上皮下/表皮下大疱性疾病,其特征是免疫球蛋白 G(IgG)、IgA 和/或 C3 在基底膜区(BMZ)线性沉积,主要粘膜病变涉及口腔和结膜。在此,我们描述了一例 58 岁的日本男性 MMP 患者。口腔内部检查发现,上牙龈和下牙龈出现脱屑性牙龈炎。未发现结膜或皮肤病变。组织病理学检查发现上皮下分裂,上皮和结缔组织有炎症细胞浸润。直接免疫荧光显示,C3在BMZ呈线状沉积。使用酶联免疫吸附试验检测到了针对 BP230 的 IgG 自身抗体。使用 1 mol/L NaCl 分层皮肤切片进行间接免疫荧光检测,未发现血清 IgG 或 IgA 反应。使用正常人表皮提取物作为底物进行免疫印迹,未检测到针对 230 kDa 抗原的 IgG 反应。根据上述结果,仅用抗 BP230 抗体就可明确诊断为 MMP。我们的病例被归类为低风险 MMP。患者接受了 0.1% 曲安奈德醋酸氨溴索软膏、口服米诺环素和口服烟酰胺的治疗,口腔糜烂有所改善。然而,针对细胞内 BP230 的 IgG 自身抗体产生的机制仍不清楚。要阐明抗 BP230 抗体产生的机制和抗 BP230 型 MMP 的临床特征,还需要进一步研究和更多此类病例研究。
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引用次数: 0
Evaluation of the changes in trabecular bone density of angle and condyle regions of the mandible before and after COVID-19 contraction using fractal analysis 利用分形分析评估 COVID-19 收缩前后下颌角和髁状突区域骨小梁密度的变化
IF 0.4 Q4 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2024-04-24 DOI: 10.1016/j.ajoms.2024.04.011
Farzad Esmaeili , Narges Bayat , Amir Ebrahimpour Tolouei , Mohammad Azimzadeh , Mehrdad Nateghi , Kasra Rahimipour
This study aimed to investigate the impact of COVID-19 on the trabecular bone thickness in the mandible using fractal analysis. The researchers selected 82 healthy patients who had previously been infected with COVID-19 and had dental panoramic radiographs (DPRs) prior to contracting the virus. DPRs were obtained again after infection, and the trabecular thickness was analyzed before and after COVID-19 using statistical tests. The results revealed that the average trabecular thickness of the mandible at the angle and condyle regions decreased significantly after contracting COVID-19. The mean thickness before infection was 1.479 ± 0.128 at the angle point and 1.469 ± 0.124 at the condylar region, while after infection, it decreased to 1.200 ± 0.123 and 1.159 ± 0.114, respectively. The reduction in trabecular thickness was found to be statistically significant. This study underscores the importance of monitoring bone density in COVID-19 patients. The findings suggest that COVID-19 can have extrapulmonary effects on skeletal health, specifically the mandibular bone. The results highlight the need for preventive interventions to mitigate pathological bone loss in individuals affected by COVID-19. Overall, this research emphasizes the significance of considering skeletal manifestations and implementing appropriate measures for COVID-19 patients to safeguard their bone health.
这项研究旨在利用分形分析法研究 COVID-19 对下颌骨骨小梁厚度的影响。研究人员选取了 82 名健康患者,这些患者曾感染过 COVID-19,并在感染病毒前拍摄了牙科全景X光片(DPR)。感染后再次拍摄了牙科全景X光片,并使用统计检验分析了COVID-19感染前后的小梁厚度。结果显示,感染 COVID-19 病毒后,下颌角和髁状突区域的平均骨小梁厚度明显下降。感染前,角点的平均厚度为 1.479 ± 0.128,髁状突区域的平均厚度为 1.469 ± 0.124,而感染后则分别降至 1.200 ± 0.123 和 1.159 ± 0.114。小梁厚度的减少具有统计学意义。这项研究强调了监测 COVID-19 患者骨密度的重要性。研究结果表明,COVID-19 会对骨骼健康(尤其是下颌骨)产生肺外影响。研究结果强调,有必要采取预防性干预措施,以减轻 COVID-19 患者的病理性骨质流失。总之,这项研究强调了考虑骨骼表现并采取适当措施保护 COVID-19 患者骨骼健康的重要性。
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引用次数: 0
Maroteaux-lamy syndrome (mucopolysaccharidosis VI) with abnormal coronoid and condylar processes of the mandible: Report of a case with surgical intervention 马罗托-拉米综合征(粘多糖病 VI)伴下颌骨冠状突和髁状突异常:一例手术干预病例的报告
IF 0.4 Q4 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2024-04-23 DOI: 10.1016/j.ajoms.2024.04.012

Maroteaux-Lamy syndrome (mucopolysaccharidoses VI) is a rare genetic disease results in functional deficiency of arylsulfatase B and accumulation of dermatan sulfate within lysosomes in various tissues. Here we present an 8-year-old male who was referred for treatment of limited mouth opening. The patient had been diagnosed with mucopolysaccharidoses VI at age of 6 months. He had received bone marrow transplantation at age of 3.5 years, developed graft-versus-host disease and subsequent vitiligo-like changes. The patient presented with short stature, and some skeletal anomalies. In radiographic images bilateral hyperplasia of the coronoid process, underdeveloped condyles, and dentigerous cyst-like follicles in the jaws were noted. Bilateral coronoidectomy was performed to improve the maximum opening of the mouth. Post-op follow-up examinations in 5 years showed moderate improvement. Abnormal coronoid and condylar processes are unusual in MPS VI. Proper management is needed to improve patients’ oral and general health for the remainder of their lives.

Maroteaux-Lamy 综合征(粘多糖病 VI)是一种罕见的遗传性疾病,会导致芳基硫酸酯酶 B 功能性缺乏,并在各种组织的溶酶体中积累硫酸皮质酯。我们在此介绍一名因张口受限而转诊治疗的 8 岁男性患者。患者在 6 个月大时被诊断出患有粘多糖病 VI。他在 3.5 岁时接受了骨髓移植,后来患上了移植物抗宿主病,并出现了白癜风样改变。患者表现为身材矮小和一些骨骼异常。放射影像显示,患者双侧冠状突增生,髁状突发育不全,下颌有齿状囊肿样滤泡。为了改善口腔的最大张开度,医生对他进行了双侧冠状突切除术。术后5年的随访检查显示病情有适度改善。冠状突和髁突异常在 MPS VI 中并不常见。需要进行适当的治疗,以改善患者余生的口腔和全身健康状况。
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引用次数: 0
Artificial intelligence in dentistry — A scoping review 人工智能在牙科中的应用--范围审查
IF 0.4 Q3 Dentistry Pub Date : 2024-04-21 DOI: 10.1016/j.ajoms.2024.04.009
Ruchi Vashisht , Aaina Sharma , Tanvi Kiran , Satnam Singh Jolly , Prabhleen Kaur Brar , Jay Veer Puri

Introduction

In dentistry, AI technologies are revolutionizing diagnosis, treatment planning, and patient care. From image analysis for detecting cavities and fractures to personalized treatment recommendations based on patient data, AI is enhancing efficiency and accuracy in dental practices, leading to improved outcomes and patient satisfaction.

Objectives

This scoping review was done to assess the use of artificial intelligence in various fields of dentistry.

Methods

The electronic databases were searched for scientific research articles in electronic search engines like PubMed, Scopus, Web of science etc. and 87 articles fulfilled the eligibility criteria. Various artificial intelligence, machine learning and deep learning tools and techniques used in various fields of dentistry were studied and their accuracy and precision were noted.

Results

We have various artificial intelligence models being used in various fields of dentistry with high accuracy, sensitivity and specificity.

Conclusion

This data would be helpful for dental practitioners in reducing their workload and improve precision and accuracy in various treatments.

导言在牙科领域,人工智能技术正在彻底改变诊断、治疗计划和患者护理。从检测龋齿和骨折的图像分析到基于患者数据的个性化治疗建议,人工智能正在提高牙科临床实践的效率和准确性,从而改善治疗效果,提高患者满意度。方法在电子数据库中搜索PubMed、Scopus、Web of science等电子搜索引擎中的科学研究文章,共有87篇文章符合资格标准。研究了牙科各领域使用的各种人工智能、机器学习和深度学习工具和技术,并记录了它们的准确性和精确性。结果我们发现牙科各领域使用的各种人工智能模型具有很高的准确性、灵敏度和特异性。
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引用次数: 0
Non-calcifying/Langerhans cell-rich variant of calcifying epithelial odontogenic tumor: A case report and review 非钙化/富含朗格汉斯细胞的钙化上皮性牙本质肿瘤变体:病例报告和综述
IF 0.4 Q4 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2024-04-17 DOI: 10.1016/j.ajoms.2024.04.010
Reo Fukushima , Dai Nakashima , Shusaku Yoshimura , Yutaro Kase , Ryunosuke Nozaki , Tomoaki Saito , Atsushi Kasamatsu , Katsuhiro Uzawa
A calcifying epithelial odontogenic tumor (CEOT) is a rare benign epithelial odontogenic tumor. Histologically, CEOTs are commonly composed of polygonal epithelial cells, eosinophilic amyloid deposits, and calcifications. The non-calcifying/Langerhans cell-rich variant, one of the three variants of CEOTs according to the 2022 World Health Organization classification of head and neck tumors, is rare with few cases reported to date. We present an additional case of a non-calcifying/Langerhans cell-rich CEOT. A 76-year-old woman was referred to our department for painless swelling of the mandibular incisor. Computed tomography showed a 33 × 10 × 18 mm well-defined bone resorption lesion without distention, radiopaque spots, or unerupted teeth in the mandible. Tissue biopsy showed that the tumor was composed of atypical cells with oval nuclei and eosinophilic cytoplasm and many amorphous eosinophilic amyloid-like deposits, which led to the diagnosis of CEOT. Marginal mandibulectomy was performed under general anesthesia from the right mandibular first premolar to the left mandibular canine. The tumor was composed of small nests and strands of odontogenic epithelial cells and many amorphous eosinophilic amyloid-like deposits; however, there was no area of calcification in any tissue section. Immunohistochemical examination showed that the tumor epithelial cells were positive for S-100 protein. Based on these histopathological and immunohistochemical findings, the tumor was diagnosed as a non-calcifying/Langerhans cell-rich CEOT. No local recurrence was detected over the 4 years of follow up.
钙化上皮性牙本质肿瘤(CEOT)是一种罕见的良性上皮性牙本质肿瘤。组织学上,CEOT 通常由多角形上皮细胞、嗜酸性淀粉样沉积和钙化组成。非钙化/朗格汉斯细胞丰富变异型是 2022 年世界卫生组织头颈部肿瘤分类中 CEOT 的三种变异型之一,但迄今为止鲜有报道。我们又发现了一例非钙化/朗格汉斯细胞丰富型CEOT。一名 76 岁的妇女因下颌切牙无痛性肿胀而被转诊至我科。计算机断层扫描显示,下颌骨内有一个 33 × 10 × 18 毫米的骨吸收病灶,界限清楚,没有膨胀、不透射线的斑点或未萌出的牙齿。组织活检显示,肿瘤由非典型性细胞组成,细胞核呈椭圆形,细胞质嗜酸性,并有许多无定形的嗜酸性淀粉样沉积物,因此诊断为 CEOT。在全身麻醉的情况下,对右侧下颌第一前磨牙至左侧下颌犬齿进行了下颌骨边缘切除术。肿瘤由细小的牙源性上皮细胞巢和股以及许多无定形的嗜酸性淀粉样沉积物组成,但任何组织切片中都没有钙化区域。免疫组化检查显示,肿瘤上皮细胞的 S-100 蛋白呈阳性。根据这些组织病理学和免疫组化检查结果,该肿瘤被诊断为非钙化/朗格汉斯细胞丰富的 CEOT。4 年的随访未发现局部复发。
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引用次数: 0
A case of treatment-related myelodysplastic syndrome in the early stage after radiotherapy in a patient with cancer of the oral floor 一例口腔底癌患者放疗后早期出现的与治疗相关的骨髓增生异常综合征
IF 0.4 Q4 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2024-04-13 DOI: 10.1016/j.ajoms.2024.04.004

Therapy-related myelodysplastic syndrome (t-MDS) is a rare but potentially fatal adverse event caused by chemotherapy or radiotherapy. We report a case of t-MDS diagnosed 8 months after radiotherapy for recurrent carcinoma of the floor of the mouth and cervical lymph node metastases after surgical treatment. A 74-year-old man visited our department with the chief complaint of pain in the lower part of the tongue. Tumor resection and right radical neck dissection (RND) were performed based on the diagnosis of carcinoma of the floor of the mouth (cT1N2bM0). A computed tomography scan at 10 months postoperatively showed metastatic lymph nodes in the left neck, right hyoid bone, right parotid subpolar, and anterior trachea. Therefore, the patient underwent left RND and excision of the right hyoid bone, subpolar right parotid and anterior tracheal metastatic lymph nodes. Postoperative radiation therapy (70 Gy) was administered to the neck bilaterally. An upper gastrointestinal examination revealed a carcinoma in situ in the lower esophagus, and endoscopic submucosal dissection of the esophagus was performed. He had pancytopenia preoperatively, which progressed postoperatively; therefore, a bone marrow examination was performed to rule out a hematological malignancy. Bone marrow smear and flow cytometric analyses indicated the development of t-MDS. He received supportive transfusion therapy but died 8 months after the diagnosis of t-MDS. During post-treatment follow-up, clinicians should be aware of t-MSD, in addition to cancer recurrence and metastasis.

治疗相关骨髓增生异常综合征(t-MDS)是化疗或放疗引起的一种罕见但可能致命的不良反应。我们报告了一例因口腔底癌复发和手术治疗后颈淋巴结转移而接受放疗8个月后确诊的t-MDS病例。一名 74 岁的男性来我科就诊,主诉为舌头下部疼痛。根据口底癌(cT1N2bM0)的诊断,医生为其进行了肿瘤切除和右侧颈部根治性切除术(RND)。术后 10 个月的计算机断层扫描显示,左颈部、右舌骨、右腮腺下极和气管前部出现转移淋巴结。因此,患者接受了左侧 RND 和右舌骨、右腮腺下极和气管前转移淋巴结切除术。术后对双侧颈部进行了放疗(70 Gy)。上消化道检查发现食道下段有原位癌,于是进行了内镜下食道黏膜下剥离术。他术前有全血细胞减少,术后病情恶化,因此进行了骨髓检查以排除血液恶性肿瘤。骨髓涂片和流式细胞分析表明他患上了 t-MDS。他接受了输血支持治疗,但在确诊为 t-MDS 8 个月后死亡。在治疗后的随访中,除了癌症复发和转移外,临床医生还应注意 t-MDS。
{"title":"A case of treatment-related myelodysplastic syndrome in the early stage after radiotherapy in a patient with cancer of the oral floor","authors":"","doi":"10.1016/j.ajoms.2024.04.004","DOIUrl":"10.1016/j.ajoms.2024.04.004","url":null,"abstract":"<div><p><span>Therapy-related myelodysplastic syndrome<span><span> (t-MDS) is a rare but potentially fatal adverse event caused by chemotherapy or radiotherapy. We report a case of t-MDS diagnosed 8 months after radiotherapy for </span>recurrent carcinoma<span><span><span> of the floor of the mouth and cervical lymph node metastases<span> after surgical treatment. A 74-year-old man visited our department with the chief complaint of pain in the lower part of the tongue. Tumor resection and right </span></span>radical neck dissection<span><span> (RND) were performed based on the diagnosis of carcinoma of the floor of the mouth (cT1N2bM0). A </span>computed tomography scan<span><span> at 10 months postoperatively showed metastatic lymph nodes in the left neck, right </span>hyoid bone<span><span>, right parotid subpolar, and anterior trachea. Therefore, the patient underwent left RND and excision of the right hyoid bone, subpolar right parotid and anterior tracheal metastatic lymph nodes. Postoperative radiation therapy (70 Gy) was administered to the neck bilaterally. An upper gastrointestinal examination revealed a </span>carcinoma in situ<span> in the lower esophagus, and endoscopic submucosal dissection of the esophagus was performed. He had </span></span></span></span></span>pancytopenia preoperatively, which progressed postoperatively; therefore, a </span></span></span>bone marrow examination<span> was performed to rule out a hematological malignancy<span>. Bone marrow smear<span> and flow cytometric analyses indicated the development of t-MDS. He received supportive transfusion therapy but died 8 months after the diagnosis of t-MDS. During post-treatment follow-up, clinicians should be aware of t-MSD, in addition to cancer recurrence and metastasis.</span></span></span></p></div>","PeriodicalId":45034,"journal":{"name":"Journal of Oral and Maxillofacial Surgery Medicine and Pathology","volume":"36 6","pages":"Pages 860-865"},"PeriodicalIF":0.4,"publicationDate":"2024-04-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140787117","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
The role of the cartilage guanylyl cyclase-B receptor in craniofacial skeletal development 软骨鸟苷酸环化酶-B 受体在颅面骨骼发育中的作用
IF 0.4 Q4 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2024-04-12 DOI: 10.1016/j.ajoms.2024.04.005
Marina Kashiwagi , Shigeki Yamanaka , Keita Asai , Takuma Watanabe , Takehiro Watanabe , Mariko Yamamoto-Kawai , Kazumasa Nakao

Objective

C-type natriuretic peptide (CNP), a member of the natriuretic peptide family, is a potent endochondral bone growth factor that exerts its biological effects via the guanylate cyclase B (GC-B) receptor. We previously demonstrated that CNP knockout (KO) mice exhibited midfacial hypoplasia along the sagittal plane; however, the effects of GC-B (the receptor for CNP) on endochondral ossification in the maxillofacial region remain unclear, and the mechanism of the CNP/GC-B system has not been elucidated.

Methods

We investigated the physiological significance of GC-B in the cartilage of the craniofacial region through analysis of cartilage-specific GC-B KO mice. Morphological assessments were performed at 12 weeks old, with histological analyses performed at 2 weeks old.

Results

GC-B-KO mice exhibited sagittal midfacial hypoplasia, foramen magnum stenosis, and spinal canal stenosis. Histological examination revealed reduced thickness in the spheno-occipital synchondrosis (SOS), a critical growth center in cranio-maxillofacial skeletal development. The hypertrophic zone of the SOS exhibited reduced thickness, accompanied by a reduction in cell count in this area.

Conclusions

This study highlights the essential role of GC-B receptors in craniofacial morphology contributing to our understanding of the mechanisms underlying facial morphological abnormalities, foramen magnum stenosis, and spinal canal stenosis.
目的C型钠尿肽(CNP)是钠尿肽家族的一员,它是一种强效的软骨内骨生长因子,通过鸟苷酸环化酶B(GC-B)受体发挥其生物效应。我们曾证实 CNP 基因敲除(KO)小鼠表现出沿矢状面的中面部发育不良;然而,GC-B(CNP 的受体)对颌面部内软骨骨化的影响仍不清楚,CNP/GC-B 系统的机制也尚未阐明。结果GC-B-KO小鼠表现出矢状面中部发育不良、枕骨大孔狭窄和椎管狭窄。组织学检查显示,颅颌面骨骼发育的关键生长中心--椎枕骨突(SOS)的厚度减少。结论这项研究强调了 GC-B 受体在颅颌面形态中的重要作用,有助于我们了解面部形态异常、枕骨大孔狭窄和椎管狭窄的发病机制。
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引用次数: 0
A new sliding rotation flap for functional lip reconstruction after cancer ablation: A technical note 用于癌症消融术后唇部功能重建的新型滑动旋转皮瓣:技术说明
IF 0.4 Q4 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2024-04-11 DOI: 10.1016/j.ajoms.2024.04.007
Yoshihiro Sawaki , Masaki Saito , Hajime Mizuno , Tadashi Sawaki , Masahiro Omori , Hirokazu Mizuno

Objective

To establish a new technique for ensuring preservation of orbicularis oris muscle continuity and facial nerve for the lip reconstruction after moderate lower lip cancer ablation.

Methods

The surgical procedure consists of three steps. First, a Z-shaped skin flap is created around the nasolabial groove. The incision is made on the skin and muscular side, but not down to the oral mucosa. The angle of the mouth, orbicularis oris muscle, and facial nerve are not affected by this approach. Next, a careful obtuse dissection is performed to preserve the facial artery, facial nerve and mental nerve and to allow freedom of the flap. Finally, changing of the flap allows sliding rotation of the perioral tissue to reconstruct the lip defect.

Results

The replaced flap pulled new mouth angle outward, and a good morphology was formed. Opening the mouth was sufficiently to wear the dentures. The sphincter movement of the lips was good, and the patient's pronunciation and eating were good.

Conclusion

This method may be a useful option for the reconstruction of lower lip after cancer ablation because the resection with safety margins creates a large lip defect.
目的 确立一种新技术,以确保中度下唇癌消融术后唇部重建时保留口轮匝肌连续性和面神经。 方法 手术过程包括三个步骤。首先,在鼻唇沟周围制作 Z 形皮瓣。切口位于皮肤和肌肉一侧,但不深入口腔粘膜。这种方法不会影响口角、口轮匝肌和面神经。接下来,进行仔细的钝性剥离,以保留面动脉、面神经和精神神经,并使皮瓣自由活动。最后,更换皮瓣,使口周组织滑动旋转,重建唇缺损。结果更换后的皮瓣将新的口角向外拉,形成了良好的形态。张开嘴巴即可佩戴假牙。结论这种方法可能是癌症消融术后重建下唇的有效选择,因为带有安全边缘的切除术会造成较大的唇缺损。
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引用次数: 0
Reestablishing disc-condyle-mandibular fossa alignment and condylar repair following self-care for the temporomandibular joint closed lock with osteoarthritis: A case report 骨关节炎颞下颌关节闭锁自我护理后重建椎间盘-髁状突-下颌窝对齐和髁状突修复:病例报告
IF 0.4 Q4 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2024-04-10 DOI: 10.1016/j.ajoms.2024.04.001

Temporomandibular joint (TMJ) disc displacement without reduction, often referred to as closed lock, is a debilitating condition characterized by a sudden decrease in mouth opening capacity, accompanied by TMJ pain. Over time, this closed lock can lead to the development of TMJ osteoarthritis (OA). While conservative treatments effectively alleviate TMJ pain and improve jaw function in most patients, they seldom restore normal TMJ structures. In this case report, we present a rare case of a 39-year-old woman who experienced the restoration of a normal disc-condyle-mandibular fossa relationship and the repair of OA changes following self-care for chronic TMJ closed lock with OA. She initially presented with a 7-month history of left TMJ pain and limited mouth opening persisting. Magnetic resonance imaging (MRI) of the left TMJ showed anterior disc displacement without reduction and OA changes including erosion, subchondral cyst, and sclerosis of the subchondral bone in the left condyle. Self-care, including parafunction control and stretching exercises, relieved the TMJ pain and increased the range of mouth opening. A follow-up MRI obtained 13 months following the initial MRI revealed a normal disc-condyle-mandibular fossa relationship and repair of the surface erosion with the subchondral cyst. Our clinical findings indicate that although rare, restoration of the normal disc-condyle-mandibular fossa relationship and condylar repair are possible through self-care for chronic closed lock with OA.

颞下颌关节(TMJ)椎间盘移位而不缩小,通常被称为闭锁,是一种使人衰弱的病症,其特点是张口能力突然下降,并伴有颞下颌关节疼痛。随着时间的推移,闭锁可导致颞下颌关节骨关节炎(OA)的发展。虽然保守治疗能有效缓解大多数患者的颞下颌关节疼痛并改善下颌功能,但很少能恢复正常的颞下颌关节结构。在本病例报告中,我们介绍了一例罕见的病例,患者是一名 39 岁的女性,她在对伴有 OA 的慢性颞下颌关节闭锁进行自我护理后,椎间盘-髁状突-下颌窝关系恢复正常,OA 病变也得到修复。她最初因左侧颞下颌关节疼痛和张口受限持续 7 个月而就诊。左侧颞下颌关节的磁共振成像(MRI)显示椎间盘前移位,但未缩小,OA 病变包括侵蚀、软骨下囊肿和左侧髁突软骨下骨硬化。包括副功能控制和伸展运动在内的自我护理缓解了颞下颌关节疼痛,并增加了张口范围。在初次核磁共振成像检查后 13 个月进行的后续核磁共振成像检查显示,椎间盘-髁状突-下颌窝关系正常,软骨下囊肿的表面侵蚀得到修复。我们的临床研究结果表明,对于患有 OA 的慢性闭锁患者来说,通过自我护理恢复正常的椎间盘-髁突-下颌窝关系和髁突修复是可能的,尽管这种情况很少见。
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Journal of Oral and Maxillofacial Surgery Medicine and Pathology
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