complex odontoma

  • 文章类型: Journal Article
    背景:牙瘤是最常见的牙源性肿瘤,通常被认为是错构瘤性牙源性病变。根据其组成,这些肿瘤在组织病理学上可分为复杂牙瘤和复合牙瘤。牙瘤表现出生长缓慢的行为,通常缺乏特征性症状。大型牙源性肿瘤的标准手术治疗是下颌(连续性)切除术,然后进行原发性或继发性塑料重建。
    方法:一名22岁的男性出现在颌面外科,左侧下颌骨的压力越来越大。正像图显示了一个大型复杂的牙瘤rg038。代替下颌骨连续性切除术,采用梯形骨瓣的另一种微创技术/方法(口内)进行了下颌角的牙瘤摘除,随后进行了皮瓣植入和骨合成。
    结论:通过口外入路进行连续切除的大型下颌骨瘤的手术摘除是该实体的手术标准治疗方法。本病例报告描述了一种替代的微创技术/方法。这种技术可以通过口外入路(神经损伤,疤痕),并可以通过骨保存来提高下颌骨的长期稳定性。
    BACKGROUND: Odontomas are among the most common odontogenic tumors and are generally considered as hamartomatous odontogenic lesions. These tumors can be histopathologically divided into complex odontomas and compound odontomas based on their composition. Odontomas show a slow growing behavior and typically lack characteristic symptoms. The standard surgical treatment for large odontogenic tumors is a mandibular (continuity) resection followed by primary or secondary plastic reconstruction.
    METHODS: A 22-year-old male presented to the Department of maxillofacial surgery with an increasing feeling of pressure in the left mandible. An orthopantomogram revealed a large complex odontoma rg 038. Instead of mandible continuity resection an alternative minimally invasive technique/approach (intraoral) with a trapezoidal bone flap for the enucleation of an odontoma of the mandibular angle with subsequent flap reimplantation and osteosynthesis was performed.
    CONCLUSIONS: Surgical enucleation of large mandibular odontoma with a continuity resection through an extraoral approach represents the surgical standard treatment of this entity. The present case report describes an alternative minimally invasive technique/approach. This technique may reduce surgical risks of the continuity resection through an extraoral approach (nerve damage, scarring) and can improve the long-term stability of the mandible by bone preservation.
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  • 文章类型: Case Reports
    此病例报告的目的是提供对位于15岁男性上颌骨前的扩张性复合牙瘤的见解。重点放在早期发现和逐步理解牙瘤的重要性上。
    牙瘤是常见的牙源性病变,在检查延迟的牙齿萌出时经常发现。牙瘤-复合牙瘤和复杂牙瘤有两种不同的分类。每一套都有自己的特点。及时诊断对于避免并发症至关重要。
    一名15岁的男性表现出位于上颌骨前的扩张性复合牙瘤。临床检查显示延迟的牙齿萌出和无症状的肿胀。射线照相图像显示不透射线的团块,具有齿状结构和射线可透边界,影响周围的牙列。进行了手术切除,随后进行组织病理学检查,确认诊断为复合牙瘤。随访1年后,患者继续正畸治疗,无复发。
    此案例强调了定期牙科检查在早期发现牙瘤中的重要性。这一观察结果还强调了对牙瘤作为错构瘤性牙源性畸形的日益理解以及临床诊断它们的挑战。需要额外的分子研究来促进遗传因素的分类和阐明。
    AlhazmiYA。揭开谜底:青少年上颌骨前部的膨胀性复合牙瘤。IntJClinPediatrDent2024;17(1):82-85。
    UNASSIGNED: The objective of this case report is to offer insight into an expansive compound-complex odontoma located in the anterior maxilla of a 15-year-old male. The focus is placed on the importance of early detection and the progressive comprehension of odontomas.
    UNASSIGNED: Odontomas are common odontogenic lesions that are frequently discovered during examinations for delayed tooth eruption. There are two distinct classifications for odontomas-compound odontomas and complex odontomas. With its own each set of characteristics. A timely diagnosis is critical for avoiding complications.
    UNASSIGNED: A male individual aged 15 years exhibited an expansive compound-complex odontoma located in the anterior maxilla. The clinical examination showed delayed tooth eruption and asymptomatic swelling. The radiographic images showed a radiopaque mass with tooth-like structures and radiolucent borders affecting the surrounding dentition. A surgical excision procedure was conducted, followed by a subsequent histopathological examination confirming the diagnosis of compound-complex odontoma. The patient continued orthodontic treatment after a 1-year follow-up without recurrence.
    UNASSIGNED: This case emphasizes the importance of regular dental exams in detecting odontomas early. This observation also highlights the growing understanding of odontomas as hamartomatous odontogenic malformations and the challenges of diagnosing them clinically. Additional molecular investigations are required to facilitate the classification and elucidation of genetic factors.
    UNASSIGNED: Alhazmi YA. The Enigma Unveiled: Expansile Compound-complex Odontoma in the Anterior Maxilla of a Teenager. Int J Clin Pediatr Dent 2024;17(1):82-85.
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  • 文章类型: Journal Article
    牙瘤被认为是错构瘤性病变,是颌骨两种最常见的牙源性肿瘤之一。牙瘤被分类为化合物或复合物。最近,成釉细胞纤维牙本质瘤(AFO)和成釉细胞纤维牙本质瘤被重新分类为发展中的牙本质瘤。尽管临床上的牙瘤通常无症状,它们对相邻的牙齿有不良影响,如牙齿嵌塞,延迟喷发,牙齿的位移,牙齿的过度保留,并可在颌骨内产生牙源性囊肿。我们试图通过收集和分析临床,射线照相,2013年至2022年在我院诊断的牙瘤病理资料。在这10年的时间里,242例患者的组织病理学和/或影像学诊断为牙瘤.没有性别偏爱,年龄在3至101岁之间(中位数,14年)。生命的第二个十年是最普遍的(57.4%)。没有下巴偏爱;然而,前颌是最常见的位置。94例(38.8%)有临床表现。最常见的发现是牙齿嵌塞(n=83)。9例(3.7%)经组织病理学证实与其他病变有关,例如牙质囊肿(n=8)和鼻腭管囊肿(n=1)。被诊断为与囊肿相关的牙瘤患者的中位年龄(25岁)比没有相关囊肿的牙瘤患者(14岁)大。与复杂和AFO相比,复合牙瘤是最常见的牙瘤类型,占71.4%,26.6%,2%,分别。大多数复合牙瘤涉及前颌(69.3%)和下颌骨(54.9%),而大多数复杂牙瘤涉及后颌(59.6%)和上颌骨(54.7%)。四个AFO位于后颌,75%涉及上颌骨。诊断为AFO的患者的中位年龄(12岁)与诊断为化合物(13岁)和复杂(16岁)的患者相比是最年轻的。总之,我们分析了临床,射线照相,242例新发牙瘤的病理特征。我们的研究重申,牙列瘤经常影响儿科人群,并可能破坏他们的牙列。根据这项研究的结果,我们的临床建议是防止牙瘤对相邻牙齿的问题是,牙医应易于诊断牙瘤,以确保及时通过手术切除牙瘤。
    Odontomas are considered hamartomatous lesions and are one of the two most common odontogenic tumors of the jaw. Odontomas are classified as compound or complex. Recently, ameloblastic fibro-odontoma (AFO) and ameloblastic fibro-dentinoma were reclassified as developing odontomas. Though clinically odontomas are usually asymptomatic, they have adverse effects on adjacent teeth such as tooth impaction, delayed eruption, displacement of teeth, over-retention of teeth, and can give rise to odontogenic cysts within the jaw. We sought to evaluate the clinicoradiopathologic presentations of odontomas by collecting and analyzing the clinical, radiographic, and pathologic data of odontomas diagnosed in our institution from 2013 to 2022. Over this 10-year period, there were 242 patients with a histopathological and/or radiographic diagnosis of odontoma. There was no gender predilection and ages ranged from 3 to 101 years (median, 14 years). The second decade of life was the most prevalent (57.4%). There was no jaw predilection; however, the anterior jaw was the most common location. Ninety-four (38.8%) cases presented with clinical findings. The most common finding was tooth impaction (n = 83). Nine (3.7%) cases were histopathologically confirmed to be associated with other lesions such as dentigerous cysts (n = 8) and nasopalatine duct cyst (n = 1). The median age (25 years) of patients diagnosed with odontomas associated with cysts was older than patients with odontomas (14 years) without associated cysts. Compound odontomas were the most common type of odontoma compared to complex and AFOs with 71.4%, 26.6%, and 2%, respectively. The majority of compound odontomas involved the anterior jaw (69.3%) and mandible (54.9%) while the majority of complex odontomas involved the posterior jaw (59.6%) and maxilla (54.7%). The four AFOs were in the posterior jaw and 75% involved the maxilla. The median age (12 years) of patients diagnosed with AFO was the youngest compared to patients diagnosed with compound (13 years) and complex (16 years). In conclusion, we analyzed the clinical, radiographic, and pathologic features of 242 new cases of odontomas. Our study reaffirms that odontomas frequently affect the pediatric population and can disrupt their dentition. Based on the result of this study, our clinical recommendation to prevent problems to adjacent teeth from odontomas is for dentists to be apt in the diagnose of odontomas to ensure that they are surgically removed in a timely manner.
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  • 文章类型: Case Reports
    牙瘤是最常见的牙源性肿瘤。它们通常很小且无症状。本文介绍了一个不寻常的巨大上颌复杂牙瘤,掩盖了上颌窦的一部分并影响了牙齿。这是在颌面部蜂窝织炎发作期间发现的。在这种情况下,病灶的手术切除是在全身麻醉下进行的,用脂肪垫带蒂皮瓣闭合。对文献进行了简要回顾,以分析该临床实体的特征及其在治疗中的意义。
    Odontomas are the most common odontogenic neoplasms. They are generally small and asymptomatic. This article presents an unusual case of a giant maxillary complex odontoma, which obscured a part of the maxillary antrum and impacted a tooth. This was discovered during an episode of maxillofacial cellulitis. In this case, surgical excision of the lesion was performed under general anesthesia, and the closure was performed with a fat pad pedicled flap. A brief review of the literature was performed to analyze the characteristics of this clinical entity and their implication in the treatment.
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  • 文章类型: Journal Article
    未经授权:牙瘤是最常见的牙源性肿瘤。文献综述显示,台湾牙列切除术的数据有限。这项研究评估了国立台湾大学儿童医院(NTUCH)1280例患者的牙齿切除的影像学特征。
    UNASSIGNED:这项回顾性研究主要基于对NTUCH中1280例患者的全景X射线照片和相关X射线照片的检查,分析了牙瘤。趋势分析采用卡方检验。
    未经评估:在1280名患者(710名男孩和570名女孩)中,共发现16例牙瘤患者(10名男孩和6名女孩)。有14个化合物和2个复杂的牙瘤。患者的平均年龄为10.38岁,大多数牙瘤发生在生命的第一个十年(37.5%)和第二个十年(62.5%)。牙瘤对下颌骨(56.25%)和颌骨前部(75%)有明显的好感,特别是前上颌骨(43.75%)。10个牙齿切除(62.5%)与受影响的相应恒牙有关。牙瘤的矢状位置和牙瘤与相应恒牙的垂直关系与相应恒牙的萌出率显着相关(P<0.05)。
    UNASSIGNED:牙瘤最常见于男性患者,男女比例为1.67:1。在我们的1280例患者中,牙瘤的发生率为1.25%。牙瘤患者的年龄范围为6-17岁。牙瘤最常见的位置是上颌前区域。牙瘤经常与受影响的相应恒牙相关。
    UNASSIGNED: Odontoma is the most common odontogenic tumor. A literature review revealed limited data for odontomas in Taiwan. This study evaluated the radiographic characteristics of odontomas in 1280 patients in the National Taiwan University Children\'s Hospital (NTUCH).
    UNASSIGNED: This retrospective study analyzed the odontomas based on examination of mainly panoramic radiographs and related radiographs of 1280 patients in the NTUCH. Chi-square test was used for trend analysis.
    UNASSIGNED: Among 1280 patients (710 boys and 570 girls), a total of 16 patients with odontomas (10 boys and 6 girls) were identified. There were 14 compound and 2 complex odontomas. The mean age of the patients was 10.38 years with the majority of odontomas occurring in the first (37.5%) and second decade (62.5%) of life. Odontomas had a marked predilection for the mandible (56.25%) and for the anterior region of the jaws (75%), particularly for the anterior maxilla (43.75%). Ten odontomas (62.5%) were associated with the impacted corresponding permanent teeth. The sagittal position of odontomas and vertical relation of odontomas to the corresponding permanent teeth were significantly correlated with the eruption rate of corresponding permanent teeth (P < 0.05).
    UNASSIGNED: The odontomas occur most commonly in male patients with a male to female ratio of 1.67:1. The incidence of odontomas in our 1280 patients is 1.25%. The age range of patients with odontomas is 6-17 years. The most frequent location of odontomas is the anterior maxillary region. Odontoma is frequently associated with an impacted corresponding permanent tooth.
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  • 文章类型: Journal Article
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  • 文章类型: Case Reports
    背景:和重要性:复杂牙瘤是代表所有牙齿组织聚集的错构瘤。开发时,他们很少成为巨人,甚至更罕见的儿童成为巨人。该报告在非常年轻的患者中提出了一个不寻常的巨大的下颌复合体牙瘤。它还提供了文献分析,并更好地了解了下颌骨中此类巨大病变的临床特征。
    方法:一名8岁男孩表现为下颌骨右侧肿胀。经过临床和放射学检查,对巨大的复合牙瘤进行了临时诊断。这个病变导致颌骨扩张,不对称的脸,和牙齿萌出改变。对病灶进行了手术切除,组织病理学检查证实了诊断。患者随访显示,正常的颌骨大小和面部对称性恢复,3年无复发迹象。
    UNASSIGNED:对已报道的下颌大型牙瘤进行了文献综述。所有已发表的报告都报道了下颌骨巨大的牙瘤病例,无论有无疼痛,都会引起骨扩张。根据文献,本文描述了最年轻的下颌骨巨大复杂牙瘤患者。这也是叙利亚报告的首例病例。
    结论:下颌骨的巨大复杂复合牙瘤可以在任何年龄发展,导致面部不对称,然而,具有良好的预后和可预测的手术治疗。
    BACKGROUND: and importance: Complex odontomas are hamartomas representing a conglomeration of all dental tissues. When developed, they rarely become giant and even more rare to become giant in children. This report presented an unusual giant mandibular complex odontoma in very young patient. It also provided a literature analysis and better understanding of clinical features of such giant lesions in the mandible.
    METHODS: An 8-year-old boy presented with swelling in the right side of the mandible. After clinical and radiological exams, a provisional diagnosis of giant composite odontoma was made. This lesion led to jaw expansion, asymmetrical face, and teeth eruption alterations. Surgical excision of the lesion was performed, and histopathological examination confirmed the diagnosis. The patient\'s follow-up showed that normal jaw size and facial symmetry was restored with no evidence of recurrence for 3 years.
    UNASSIGNED: A literature review of reported mandibular large odontomas was made. All published reported cases of giant odontoma in the mandible caused bone expansion with or without pain. According to the literature, this paper described the youngest patient with giant complex odontoma in the mandible. This was also the first reported case from Syria.
    CONCLUSIONS: Giant complex composite odontoma of the mandible can develop at any age causing facial asymmetry, however, with good prognosis and predictable surgical treatment.
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  • 文章类型: Journal Article
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  • 文章类型: Case Reports
    Odontomas are known as the most common odontogenic tumor and usually present without clinical symptoms. It can be divided into compound odontoma and complex odontoma. Compound odontomas are calcified tissue and they bear similarity to the teeth, whereas complex odontomas do not show similarity to the tooth. Diagnosis of the odontomas is usually accidental on radiographic examination. Complex odontomas are commonly seen in the posterior mandible. Apart from the few case reports regarding the complex odontoma of the anterior mandibular region, reported occurrence in this site is rare. Here, authors described a case of a child who presented with a chief complaint of swelling in the anterior mandibular canine region. After clinical examination and required investigations, provisionally, it was diagnosed as complex odontoma. It was surgically removed and histopathological examination confirmed the provisional diagnosis. How to cite this article: Ahammed H, Seema T, Cheranjeevi J. Complex Odontoma at an Unusual Site in a Child: A Case Report. Int J Clin Pediatr Dent 2021;14(3):438-440.
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  • 文章类型: Case Reports
    成釉细胞纤维牙瘤是一种罕见的肿瘤,影响儿科人群和年轻人。世界卫生组织(WHO)在2005年将其定义为“一种由细胞外胚间充质组织中增殖的牙源性上皮组成的肿瘤,具有不同程度的诱导性变化和牙齿硬组织形成。“在其组织起源上存在争议,将其指定为错构瘤(发展中的复杂牙瘤[CO])或真正的肿瘤,因为两种病变在组织学上看起来相似。最近,2017年,WHO将这两种病变归为同一实体.大多数病例在男性和下颌骨中报告,而上颌骨的病例很少。本文描述了先前报道的成釉细胞纤维瘤病例的复发,该病例显示在上颌骨后部6岁的女孩中成熟为AFO或CO。由于罕见,该病例被报道,并对鉴别诊断进行了简要回顾。
    Ameloblastic fibro-odontoma is a rare tumor affecting the pediatric population and young adults. The World Health Organization (WHO) in 2005 defined it as \"A neoplasm composed of proliferating odontogenic epithelium in a cellular ectomesenchymal tissue with varying degrees of inductive changes and dental hard tissue formation.\" There exists a controversy on its histogenesis designating it as a hamartoma (developing complex odontoma [CO]) or a true neoplasm since both the lesions appear similar histologically. Recently, the WHO in 2017 has clubbed both these lesions as the same entity. Most cases are reported in males and in mandible, while cases in maxilla are scarce. This article describes a recurrence of a previously reported case of ameloblastic fibroma which showed maturation into AFO or CO in a girl aged 6 years in the posterior maxilla. This case is reported due to its rarity and a brief review with differential diagnosis is also discussed.
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