Oral lesions

口腔病变
  • 文章类型: Case Reports
    Tori是牙槽骨的反应性或发育性局部过度生长,不是癌性的。一个瘦,弱血管化的粘膜围绕着密集的皮质,低密度骨髓块称为托里或外生骨。Tori在中年时更常见。上颌骨(Toruspalatinus)和下颌骨(Torusmandibularis)都表现出Tori。说话困难和其他问题是与托里相关的常见障碍。Tori的直径范围从几毫米到几厘米。托里手术切除是治疗大托里妨碍言语的主要方法,咀嚼,或舌头的位置。以下病例研究包括一名36岁的男性患者,其下颌犬和前磨牙区域与骨生长有关。
    Tori are reactive or developmental localized overgrowths of alveolar bone that are not cancerous. A thin, weakly vascularized mucosa surrounds a densely cortical, low-density mass of bone marrow known as tori or exostosis. Tori are more frequently observed in middle age. Both the maxilla (torus palatinus) and the mandible (torus mandibularis) exhibit tori. Difficulty in speaking and other issues are common obstacles associated with tori. Tori range in diameter from a few millimeters to several centimeters. Surgical excision of tori is the mainstay of treatment for large tori obstructing speech, mastication, or tongue position. The following case study includes a 36-year-old male patient with an association of mandibular canine and premolar regions with bony outgrowth.
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  • 文章类型: Journal Article
    目标:几个因素,如专家不到位,牙科恐惧症,经济困难可能会导致接收口腔放射学报告和咨询牙医之间的延迟。这项研究的主要目的是根据放射科医生的锥形束计算机断层扫描(CBCT)图像报告区分高风险和低风险口腔病变。这种设施可以由牙医或他/她的助手采用,以使患者了解口腔病变的严重程度和等级,并转诊以进行立即治疗或其他后续护理。
    方法:收集了设拉子医科大学拥有的1134份CBCT摄影报告。每个样本的严重程度由三位专家指定,并相应地进行了注释。对数据进行预处理后,一个深度学习模型,被称为CNN-LSTM,被开发,其目的是根据对放射科医生报告的分析来检测问题的严重程度。与通常使用简单单词集合的传统模型不同,提出的深度模型使用嵌入在密集向量表示中的单词,这使得它能够有效地捕捉语义相似性。
    结果:结果表明,所提出的模型在精度方面优于其对应物,召回,和F1标准。这表明其作为早期估计口腔病变严重程度的可靠工具的潜力。
    结论:这项研究显示了深度学习在分析文本报告和准确区分高风险和低风险病变方面的有效性。采用所提出的模型,可以提供及时的警告,需要跟进和及时治疗,可以保护患者免受与延误相关的风险。
    结论:我们合作收集和专家注释的数据集作为探索性研究的宝贵资源。结果表明,我们的深度学习模型可以在评估牙科报告中口腔病变的严重程度方面发挥关键作用。
    OBJECTIVE: Several factors such as unavailability of specialists, dental phobia, and financial difficulties may lead to a delay between receiving an oral radiology report and consulting a dentist. The primary aim of this study was to distinguish between high-risk and low-risk oral lesions according to the radiologist\'s reports of cone beam computed tomography (CBCT) images. Such a facility may be employed by dentist or his/her assistant to make the patient aware of the severity and the grade of the oral lesion and referral for immediate treatment or other follow-up care.
    METHODS: A total number of 1134 CBCT radiography reports owned by Shiraz University of Medical Sciences were collected. The severity level of each sample was specified by three experts, and an annotation was carried out accordingly. After preprocessing the data, a deep learning model, referred to as CNN-LSTM, was developed, which aims to detect the degree of severity of the problem based on analysis of the radiologist\'s report. Unlike traditional models which usually use a simple collection of words, the proposed deep model uses words embedded in dense vector representations, which empowers it to effectively capture semantic similarities.
    RESULTS: The results indicated that the proposed model outperformed its counterparts in terms of precision, recall, and F1 criteria. This suggests its potential as a reliable tool for early estimation of the severity of oral lesions.
    CONCLUSIONS: This study shows the effectiveness of deep learning in the analysis of textual reports and accurately distinguishing between high-risk and low-risk lesions. Employing the proposed model which can Provide timely warnings about the need for follow-up and prompt treatment can shield the patient from the risks associated with delays.
    CONCLUSIONS: Our collaboratively collected and expert-annotated dataset serves as a valuable resource for exploratory research. The results demonstrate the pivotal role of our deep learning model could play in assessing the severity of oral lesions in dental reports.
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  • 文章类型: Case Reports
    系统性红斑狼疮(SLE)是一种自身免疫性疾病,具有各种口腔表现,包括溃疡,白色角化斑块,口腔盘状红斑狼疮,口腔扁平苔藓(OLP)样病变,非特异性红斑,紫癜,瘀斑,和唇炎,类似于其他系统性疾病的病变。认识到SLE的口腔表现对于全面的患者管理至关重要。本研究报告4例SLE伴各种口腔病变,基本条件和诊断方法。2019年9月,在口腔医学诊所咨询了2名成年SLE患者和2名青少年SLE患者。全身性疾病的评估由内科和儿科住院医师进行,而口腔医学住院医师进行了口内检查。病史,对临床结果和实验室检查结果进行分析以确定诊断。第一位患者是一名38岁的女性,在整个粘膜上有多个白色角化斑块,右侧颊粘膜有OLP样病变,硬腭上的瘀点,上肢和下肢有瘀点和紫癜。第二例是一名24岁女性,她患有黄斑皮疹,朱红色区有多处溃疡,左侧颊粘膜有OLP样病变,和腭部溃疡.第三和第四例是16岁的女性,有明显的蝴蝶皮疹。患者出现急性假膜性念珠菌病,口疮样溃疡和角化斑。他们接受了口腔内病变的抗菌治疗,并显示了有希望的结果。成年和青少年发病的SLE患者的口腔病变根据疾病的严重程度和接受的治疗而有所不同。
    Systemic lupus erythematosus (SLE) is an autoimmune disease with various oral manifestations, including ulceration, white keratotic plaques, oral discoid lupus erythematosus, oral lichen planus (OLP)-like lesions, non-specific erythema, purpura, petechiae, and cheilitis, which resemble lesions of other systemic diseases. Recognizing the oral manifestation of SLE is essential for comprehensive patient management. This study reports 4 cases of SLE with various oral lesions, underlying conditions and diagnostic methods.In September 2019, 2 adult SLE patients and 2 juvenile SLE patients were consulted at the Oral Medicine Clinic. The assessment of systemic diseases was conducted by the Internal Medicine and Pediatrics resident, whereas the Oral Medicine resident performed the intraoral examinations. The medical history, clinical findings and laboratory results were analyzed to establish the diagnosis.The first patient was a 38-year-old female presenting with multiple white keratotic plaques throughout the mucosa, an OLP-like lesion on the right buccal mucosa, petechiae on the hard palate, and petechiae and purpura on the upper and lower extremities. The second case was a 24-year-old female with a malar rash and multiple ulcerations on the vermilion zone, an OLP-like lesion on the left buccal mucosa, and a palatal ulcer. The third and fourth cases were 16-year-old females with a prominent butterfly rash. The patients presented with acute pseudomembranous candidiasis, an aphthous-like ulcer and keratotic plaques. They received antimicrobial therapy for the intraoral lesions and showed promising results.The oral lesions in adultand juvenile-onset SLE patients varied depending on the disease severity and treatment received.
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  • 文章类型: Case Reports
    Cowden综合征(CS)是一种与PTEN基因突变相关的罕见遗传性疾病。它的特点是大头畸形,特定的粘膜皮肤特征,和良性和恶性肿瘤的易感性。主要表现为口腔临床表现的CS病例相对少见。
    我们报告了一例41岁的男性先证者,表现为双侧连合和舌外突出对称病变超过两年。先证者还表现出其他特征,包括大头畸形,沟通困难,和肥胖。在家庭成员中观察到类似的口腔临床表现。全外显子组测序分析显示,先证者和他的弟弟的PTEN基因突变与CS相关。此病例提醒人们注意CS在口腔临床实践中的不同表现,并强调了基因检测对指导诊断和治疗的重要性。
    很少报道以口腔病变为主的CS病例。这一发现有助于进一步了解CS发病机理的某些方面,并增强了对主要表现为口腔临床表现的CS病例的认识。
    UNASSIGNED: Cowden syndrome (CS) is a rare genetic disorder associated with PTEN gene mutations. It is characterized by macrocephaly, specific mucocutaneous features, and a predisposition to benign and malignant tumors. Cases of CS primarily presenting with oral clinical manifestations are relatively uncommon.
    UNASSIGNED: We report the case of a 41-year-old male proband who presented with bilateral commissural and lingual externally projecting symmetric lesions for over two years. The proband also exhibited other features, including macrocephaly, communication difficulties, and obesity. Similar oral clinical manifestations were observed in family members. Whole exome sequencing analysis revealed PTEN gene mutations associated with CS in both the proband and his younger brother. This case serves as a reminder to be aware of the diverse presentations of CS in oral clinical practice and highlights the importance of genetic testing for guiding diagnosis and treatment.
    UNASSIGNED: There are few reported cases of CS primarily presenting with oral lesions. This finding contributes to further understanding of certain aspects of the pathogenesis of CS and enhances awareness of CS cases primarily exhibiting oral clinical manifestations.
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  • 文章类型: Multicenter Study
    寻常型天疱疮(PV)是一种慢性自身免疫性皮肤粘膜起泡疾病。自身抗体针对桥粒蛋白,导致上皮内大疱的形成。PV,与其他口腔自身免疫性皮肤粘膜疾病一样,提出了诊断和治疗的挑战。大约50-70%的病例首先出现口腔病变。病变通常以快速破裂的囊泡或大疱开始,导致糜烂和溃疡。腭,牙龈,颊,和唇粘膜是最常见的受影响的部位。口腔肺静脉可以模仿其他几种导致粘膜糜烂和/或溃疡的疾病,包括多形性红斑(EM)。EM是急性的,免疫介导的,主要与单纯疱疹感染有关的自限性超敏反应。口腔病变可以是可变的,但是唇部出血性糜烂的一个非常典型的表现,溃疡和结痂是常见的。在这个系列中,我们介绍了6例PV:1例男性患者和5例女性患者,年龄在34至65岁之间。所有患者除了多次口内糜烂和溃疡外,还表现为嘴唇出血和结痂。3例患者出现口腔和皮肤病变。所有患者都接受了活检,诊断为PV。所有患者均接受类固醇(局部和全身)和可变的类固醇保护剂治疗。该病例系列强调,在存在持续唇出血和结痂的患者亚组中,口腔PV可能被误诊为EM。因此,全面的历史,此类患者应考虑进行临床检查和切开活检.
    Pemphigus vulgaris (PV) is a chronic autoimmune mucocutaneous blistering disease. Autoantibodies are directed against desmogleins, leading to the formation of intraepithelial bullae. PV, as with other autoimmune mucocutaneous disorders of the oral cavity, presents diagnostic and therapeutic challenges. Approximately 50-70% of cases present first with oral lesions. The lesions commonly start as vesicles or bullae that rapidly rupture, leading to erosions and ulcerations. The palatal, gingival, buccal, and labial mucosa are the most commonly affected sites. Oral PV can mimic several other diseases that cause mucosal erosions and/or ulcerations, including erythema multiforme (EM). EM is an acute, immune-mediated, self-limited hypersensitivity condition primarily associated with herpes simplex infection. Oral lesions can be variable, but a very characteristic presentation with labial hemorrhagic erosions, ulcerations and crusting is commonly seen. In this case series, we present six cases of PV: one male patient and five female patients whose ages ranged from 34 to 65 years old. All patients presented with hemorrhage and crusting of the lips in addition to multiple intraoral erosions and ulcerations. Three patients presented with oral and skin lesions. All patients underwent biopsies, and a diagnosis of PV was confirmed. All patients were treated with steroids (topical and systemic) and variable steroid-sparing agents. This case series emphasizes that oral PV may be misdiagnosed as EM in a subgroup of patients who present with persistent lip hemorrhage and crusting. Therefore, a comprehensive history, clinical examination and incisional biopsies should be considered in such patients.
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  • 文章类型: Case Reports
    背景:银屑病是一种常见的皮肤病;有关银屑病相关口腔粘膜病变的信息在文献中很少。
    方法:我们报告一例73岁男性患者,皮肤和口腔腭改变。这些病变的切开活检显示牛皮癣。
    结论:本病例强调了对银屑病患者进行口腔系统检查对于控制这些病变的适当诊断和治疗的重要性。
    BACKGROUND: Psoriasis is a common cutaneous disease; however, information about psoriasis-related oral mucosal lesions is scarce in the literature.
    METHODS: We report a case of a 73-year-old male patient with cutaneous and oral palatal alterations. An incisional biopsy of these lesions revealed psoriasis.
    CONCLUSIONS: The current case highlights the importance of a systematic examination of the oral cavity in psoriasis patients for the appropriate diagnosis and management on the control of these lesions.
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  • 文章类型: Case Reports
    文献中已经报道了COVID-19患者的口腔表现。确定这些病例的口腔表现是否与SARS-CoV-2感染直接相关一直是临床医生和研究人员的挑战。虽然目前还无法证明。COVID-19患者口腔病变的发展有几种可能的原因,其中包括,机会性感染,药物反应,医源性和与病毒感染直接相关的那些。本工作描述了10例严重COVID-19住院患者口腔表现的主要特征。通过分析报告患者的特点,以及文献中发表的内容,我们得出的结论是,对于这一系列病例,这些表现与SARS-CoV-2没有直接关系,但是,这是所有患者都应该考虑的可能性。
    Oral manifestations in patients with COVID-19 have already been reported in the literature. Determining whether the oral manifestations in these cases are directly related to SARS-CoV-2 infection or not has been challenging for both clinicians and researchers, although at present it has not been possible to prove. There are several possible causes for the development of the oral lesions in patients with COVID-19, among them are, opportunistic infections, drug reactions, iatrogenic and those directly related to viral infection. The present work describes the main characteristics of 10 severe COVID-19 hospitalized patients with oral manifestations. By analyzing the characteristics of the reported patients, and what is published in the literature, we conclude that for this series of cases the manifestations are not directly related to SARS-CoV-2, however, it is a possibility that should be considered for all patients.
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  • 文章类型: Case Reports
    背景:Behçet病(BD)是一种罕见的慢性自身炎症性全身性疾病,具有非特异性口腔表现,归类为一般可变血管血管炎,由于其表型异质性,需要跨学科的方法来诊断。虽然BD中复发的口腔病变是复杂诊断过程的基础,在本文总结的病例报告中强调了牙科专业人员的关键作用。我们介绍了一例47岁的男性,该男性在先前因a静脉和下腔静脉血栓形成而住院后,由风湿病学家转诊至口腔科。他的炎性C反应蛋白生物标志物升高,红细胞沉降率增加。毛囊炎反复发作,报告了口腔和生殖器溃疡。临床检查发现口腔粘膜有多处溃疡。互补的,进行组织病理学分析以排除其他疾病,基于切除活检,显示非角化的复层鳞状上皮,具有胞吐和溃疡区域。结缔组织表现出强烈的混合炎症浸润,血管充血,出血,血管炎,和HLA-B基因分型鉴定了HLA-B15的表达,进一步支持BD诊断。开始用秋水仙碱治疗,泼尼松龙,每周皮下注射甲氨蝶呤,并导致口腔病变完全缓解,其他表现无复发。
    结论:这份BD病例报告强调了多学科方法在诊断BD中的重要性。包括使用组织病理学评估和遗传谱分析。它强调了彻底的口内评估和转诊给多学科小组进行诊断的重要性。作为主要症状的BD的口腔表现通常表明潜在的主要全身性病变。作者强调需要一种结构化的诊断算法,以促进对BD的及时有效管理。
    BACKGROUND: Behçet\'s disease (BD) is a rare chronic auto-inflammatory systemic disease with non-specific oral manifestations, categorised as generalised variable vessel vasculitis that requires an interdisciplinary approach to diagnose due to its phenotypic heterogeneity. Whilst the oral lesions that reoccur in BD underpin the complex diagnostic process, the crucial role of dental professionals is highlighted in a case report summarised herein. We present a case of a 47-year-old male referred to the Oral Medicine Department by a rheumatologist after previous hospitalization for thrombosis of the iliac vein and inferior vena cava. He had elevated inflammatory C-reactive protein biomarker and an increased erythrocyte sedimentation rate. Recurrent episodes of folliculitis, oral and genital ulcers were reported. Clinical examination revealed multiple ulcerations in the oral mucosa. The complementary, histopathological analysis performed to rule out other disorders, based on excisional biopsy, showed non-keratinised stratified squamous epithelium with areas of exocytosis and ulceration. The connective tissue presented an intense mixed inflammatory infiltrate, congested blood vessels, haemorrhage, vasculitis, and HLA-B genotyping identified the expression of HLA-B15, further supporting the BD diagnosis. Treatment was initiated with colchicine, prednisolone, and weekly subcutaneous administration of methotrexate and resulted in the complete remission of oral lesions and no recurrence of other manifestations.
    CONCLUSIONS: This BD case report emphasizes the importance of a multidisciplinary approach in diagnosing BD, including the use of histopathological assessment and genetic profiling. It highlights the significance of thorough intraoral assessment and referral to a multidisciplinary team for diagnosis. The oral manifestations of BD as the primary symptoms often indicate underlying major systemic pathologies. The authors stress the need for a structured diagnostic algorithm to facilitate timely and effective management of BD.
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  • 文章类型: Case Reports
    疼痛管理在口腔粘膜疾病的治疗中变得重要,因为它会损害生活质量。光生物调节(PBM)作为替代疗法,具有通过靶向靶组织中的周围神经的几种机制来减轻疼痛的效力。
    探讨PBM治疗4例口腔黏膜病的效果。
    四个病人,两个雌性和两个雄性,年龄从24岁到63岁不等,来到口腔科,抱怨口腔有疼痛的病变。3例显示口腔粘膜溃疡,并被诊断为复发性口疮性口炎,顽固性慢性溃疡,和非特异性慢性唾液腺炎。一名患者抱怨面部右侧剧烈疼痛和肿胀,被诊断为疱疹后神经痛(PHN)。
    在所有四种情况下均给予PBM(976nm二极管激光,3例斑点尺寸为0.01cm2,流畅性为10J/cm2,1例斑点尺寸为0.5cm2;流畅性为3J/cm2)。每次就诊时在PBM前后进行视觉模拟量表(VAS)控制。记录的VAS结果显示在激光后时间开始的疼痛减轻,PBM之前的VAS范围从5到7,PBM之后的VAS范围从0到4。3例患者给予曲安奈德0.1%,葡萄糖酸氯己定0.2%漱口水,凡士林,和多种维生素。一名患者给予甲芬那酸和多种维生素。
    PBM由于具有减轻疼痛强度的能力,可以成为缓解口腔粘膜疾病疼痛的有用辅助治疗方法。
    UNASSIGNED: Pain management becomes important in the treatment of oral mucosal diseases since it can impair the quality of life. Photobiomodulation (PBM) as an alternative therapy, has potency in reducing pain through several mechanisms targeting peripheral nerves in the target tissue.
    UNASSIGNED: To discuss the effectiveness of PBM in the management of four cases of oral mucosal diseases.
    UNASSIGNED: Four patients, two females and two males, with an age ranging from 24 to 63 years came to the Oral Medicine Department complaining of painful lesions in their oral cavity. Three cases showed ulceration of the oral mucosa and had been diagnosed with recurrent aphthous stomatitis, recalcitrant chronic ulcer, and non-specific chronic sialadenitis. One patient who complained of intense pain and swelling on the right side of the face was diagnosed with post-herpetic neuralgia (PHN).
    UNASSIGNED: PBM was administered in all four cases (976 nm diode laser, three cases with spot size 0.01 cm2, fluency 10 J/cm2, and one case with spot size 0.5 cm2; fluency 3 J/cm2). Visual analog scale (VAS) control was performed before and after the PBM at each visit. The recorded VAS results show a reduction in pain that started at the post-laser time, with VAS before PBM ranging from 5 to 7 and after PBM ranging from 0 to 4. Three patients were given triamcinolone acetonide 0.1%, chlorhexidine gluconate 0.2% mouthwash, petroleum jelly, and multivitamins. One patient was given mefenamic acid and multivitamins.
    UNASSIGNED: PBM can be a useful adjunctive treatment to relieve the pain of oral mucosal diseases due to its ability to reduce pain intensity.
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  • 文章类型: Case Reports
    世界卫生组织最近将痘病毒感染(MPXV)确认为突发公共卫生事件。虽然一些研究已经描述了MPXV口腔病变的临床特征,关于组织学和超微结构口腔发现的信息仍然缺乏。一名24岁的HIV阳性男性出现浅层溃疡,被纤维蛋白膜覆盖,周围有一个红斑晕在硬腭和软腭。病变的临床表现引起了对病毒感染的怀疑;因此,诊断基于组织学和电子显微镜检查结果,并通过皮肤标本的RT-PCR检测证实.本病例报告旨在提供对临床,组织病理学,以及HIV感染者中MPXV引起的口腔病变的超微结构特征。本报告提供了有关口腔粘膜MPXV感染特征的有价值的信息,特别是艾滋病毒感染者。
    Mpox virus infection (MPXV) has recently been recognized as a public health emergency by the World Health Organization. While several studies have described the clinical characteristics of MPXV-oral lesions, there remains a dearth of information regarding the histological and ultrastructural oral findings. A 24-year-old HIV-positive man presented with a shallow ulcer, covered by a fibrinoid membrane, and surrounded by an erythematous halo in the hard and soft palate. The clinical appearance of the lesion raised suspicion of a viral infection; thus, the diagnosis was based on histological and electronic microscopy findings and confirmed by RT-PCR testing in the skin specimen. This case report aims to offer comprehensive insights into the clinical, histopathological, and ultrastructural features of oral lesions caused by MPXV in an individual with HIV. This report provides valuable information about the characteristics of MPXV infection in the oral mucosa, particularly in people living with HIV.
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