Cemento-ossifying fibroma

骨水泥骨化性纤维瘤
  • 文章类型: Journal Article
    良性纤维骨性病变(BFOL)包括骨骼疾病的异质集合,其特征在于用类骨质或编织骨的纤维胶原组织代替正常骨骼,和水泥。尽管它们具有临床意义,沙特阿拉伯的BFOL频率仍需评估。
    这项回顾性研究调查了利雅得BFOL的频率和人口统计学,沙特阿拉伯,通过从单个口腔病理学实验室档案中检索1984年1月至2013年1月期间记录的所有病例。
    共有64例被归类为BFOL,女性占主导地位(67.2%),中位年龄为21.5岁。确定的最普遍的疾病是纤维发育不良(45.31%),其次是骨水泥骨化性纤维瘤(26.56%)。BFOLs之间存在显著的性别差异,p值为0.03。FD主要位于上颌骨(65.5%),而COF主要存在于下颌骨(82.3%)。在17.2%的FD患者中观察到复发,与COF患者未报告复发相反。
    这项研究代表了利雅得首次探索BFOL频率和人口统计学,沙特阿拉伯,强调需要进一步调查,以全面了解我们人群中这些病变的性质。
    UNASSIGNED: Benign fibroosseous lesions (BFOLs) encompass a heterogenous collection of bone conditions characterized by replacing normal bone with fibro-collagenous tissue with osteoid or woven bone, and cementicles. Despite their clinical significance, the frequency of BFOLs in Saudi Arabia still needs to be assessed.
    UNASSIGNED: This retrospective study investigated the frequency and demographics of BFOLs in Riyadh, Saudi Arabia, by retrieving all cases recorded between January 1984 and January 2013 from a single Oral Pathology Laboratory archive.
    UNASSIGNED: A total of 64 cases were classified as BFOLs, with a predominance in females (67.2 %) and a median age of 21.5 years. The most prevalent condition identified was fibrous dysplasia (45.31 %), followed by cemento-ossifying fibroma (26.56 %). There were significant sex differences between BFOLs, with a p-value of 0.03. FD was predominantly located in the maxilla (65.5 %), whereas COF was predominantly found in the mandible (82.3 %). Recurrence was observed in 17.2 % of patients with FD, in contrast to no reported recurrence in patients with COF.
    UNASSIGNED: This study represents the first exploration of BFOL frequency and demographics in Riyadh, Saudi Arabia, highlighting the need for further investigations to comprehensively understand the nature of these lesions in our population.
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  • 文章类型: Case Reports
    骨化性纤维瘤(COF)是一种间充质良性牙源性肿瘤,这可能导致阻生或异位恒牙。自体牙齿移植是一个手术过程,其中一颗牙齿从同一个人的一个位置移植到另一个位置。该方法能有效恢复患者的咀嚼和美观,在更换缺牙方面是可行的。本研究报告1例同期COF切除联合异位犬自体移植修复牙列缺损,有效促进骨骼连续性和稳定性的恢复,达到即时和长期的美学功能要求。
    Cemento-ossifying fibroma (COF) is a mesenchymal benign odontogenic tumor, which may lead to impacted or ectopic permanent teeth. Autotransplantation of teeth is a surgical process, in which a tooth is transplanted from one position to another in the same individual. This method can effectively restore the patient\'s mastication and aesthetics and is feasible in replacing missing teeth. This study reports a case of simultaneous COF resection combined with heterotopic canine autotransplantation to repair dentition defect, which effectively promotes the restoration of bone continuity and stability and achieves immediate and long-term aesthetic function requirements.
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  • 文章类型: Case Reports
    Cemento-ossifying fibroma (COF) is a benign mesenchymal odontogenic tumor that commonly occurs in the tooth-bearing areas of the maxilla and mandible. This study reports a COF case located under the left buccal mucosa. The classification and differential diagnosis of this COF case were discussed based on the diagnosis and treatment of this case and previous literature.
    牙骨质-骨化纤维瘤作为间充质来源的良性牙源性肿瘤,主要发生于颌骨的牙承载区。本文报道1例位于左侧颊黏膜下的牙骨质-骨化纤维瘤病变,结合该病例的诊治情况及既往相关文献,对其分类以及鉴别诊断进行讨论。.
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  • 文章类型: Case Reports
    包括在纤维骨病变组中的中胚层起源的良性骨性肿瘤包括牙骨质骨化性纤维瘤(COF)。这些疾病的纤维细胞成分起源于牙周膜,将骨骼和牙骨质沉积在纤维组织中。它通常出现在下颌骨中,表现为孤立的,非侵略性,缓慢发展,无症状,扩张性损伤,很少发生在上颌骨。唯一被证明能成功产生优异结果并可被视为最终治疗选择的干预措施是完全手术切除COF。本文提供的病例报告描述了左下颌区域的无痛且可膨胀的肿块,组织病理学诊断为COF。
    Benign osseous tumors of mesodermal origin that are included within the group of fibro-osseous lesions include cemento-ossifying fibromas (COFs). The fibrocellular component of these diseases originates from the periodontal ligament, which deposits bone and cementum encased in fibrous tissue. It typically appears in the mandible and presents as a solitary, nonaggressive, slowly developing, asymptomatic, expansile lesion, rarely occurring in the maxilla. The only intervention that proved to be successful in producing excellent outcomes and that may be regarded as a final therapeutic option is the complete surgical removal of COFs. Presenting herein is a case report describing a painless and expansile mass in the left mandibular region, histopathologically diagnosed as COF.
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  • 文章类型: Journal Article
    骨化性纤维瘤(COF)和青少年骨化性纤维瘤(JOF)被认为是纤维骨性病变类别中的不同实体。本研究旨在通过研究骨吸收标志物来评估COF和JOF中的成骨细胞和破骨细胞活性。特别是核因子-kB(RANK)的受体激活剂,RANK配体(RANKL),及其抑制剂骨保护素(OPG)。对所有病变进行了这些标记的比较分析。免疫组织化学用于评估和定量20例水泥骨化性纤维瘤(COF)样本中这些生物标志物的表达。青少年骨化性纤维瘤(PsJOF)15例,10例青少年骨化性纤维瘤(TrJOF)。骨水泥骨化性纤维瘤(33.9±13.0)中的骨保护素表达明显高于幼年骨化性纤维瘤(27.3±9.2)和类骨化性纤维瘤(25.2±14.9),COF表达最高,其次是后两者(p=0.037)。考虑到阳性表达得分为3(p=0.024),与沙瘤样幼年骨化性纤维瘤(PsJOF)(33.3%)和小梁幼年骨化性纤维瘤(TrJOF)(30.0%)相比,基质成纤维细胞在骨骨化性纤维瘤(COF)中显示RANKL阳性表达的百分比更高(80%)。骨化性纤维瘤显示骨保护素和RANKL阳性基质成纤维细胞的最高表达,其次是沙瘤样青少年骨化纤维瘤和骨小梁青少年骨化纤维瘤。这些发现为这些病变的发病机理提供了有价值的见解。
    Cemento-ossifying fibroma (COF) and juvenile ossifying fibroma (JOF) have been considered distinct entities within the category of fibro-osseous lesions. This study aimed to assess osteoblast and osteoclast activity in COF and JOF by investigating bone resorption markers, specifically receptor activator of nuclear factor-kB (RANK), RANK ligand (RANKL), and its inhibitor osteoprotegerin (OPG). A comparative analysis of these markers was performed on all lesions. Immunohistochemistry was employed to evaluate and quantify the expression of these biomarkers in a sample of 20 cases of cemento-ossifying fibroma (COF), 15 cases of psammomatoid juvenile ossifying fibroma (PsJOF), and 10 cases of trabecular juvenile ossifying fibroma (TrJOF). The expression of osteoprotegerin was significantly higher in cemento-ossifying fibroma (33.9±13.0) compared to trabecular juvenile ossifying fibroma (27.3±9.2) and psammatoid ossifying fibroma (25.2±14.9), with the COF showing the highest expression followed by the latter two (p=0.037). There was a higher percentage (80%) of stromal fibroblast cells that showed positive expression of RANKL in cemento-ossifying fibroma (COF) compared to psammomatoid juvenile ossifying fibroma (PsJOF) (33.3%) and trabecular juvenile ossifying fibroma (TrJOF) (30.0%) when considering a positive expression score of 3 (p=0.024). Cemento-ossifying fibroma demonstrated the highest expression of osteoprotegerin and RANKL-positive stromal fibroblast cells, followed by psammomatoid juvenile ossifying fibroma and trabecular juvenile ossifying fibroma. These findings provide valuable insights into the pathogenesis of these lesions.
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  • 文章类型: Case Reports
    骨化性纤维瘤是由牙周膜引起的良性纤维骨病变,有可能在牙周膜中形成牙骨质和骨。骨化性纤维瘤是无痛的,有花梗,或无柄,附着在牙龈组织上的光滑外生体生长。我们介绍了一名52岁的女性患者,在手术切除病灶的情况下,上颌骨后部的牙骨质骨化性纤维瘤与26至27区域之间的齿间牙龈相连,拔除受累的牙齿,刮宫,全麻下的腭闭孔。患者术后随访,愈合是令人满意的,没有感染的迹象,在6个月的随访期内没有发现复发.
    Cemento-ossifying fibroma is a benign fibro-osseous lesion arising from the periodontal ligament and has the potential to form cementum and bone in the periodontal ligament. Cemento-ossifying fibroma is a painless, pedunculated, or sessile, smooth exophytic growth arising attached to the gingival tissues. We present a case of cemento-ossifying fibroid epulis in the posterior maxilla attached to the interdental gingiva between the 26 and 27 region buccally in a 52-year-old female patient managed with surgical excision of the lesion, extraction of the involved teeth, curettage, and palatal obturator while under general anesthesia. The patient was followed up post-operatively, healing was satisfactory, there were no signs of infection, and no recurrence was noted in the six-month follow-up period.
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  • 文章类型: Case Reports
    骨化性纤维瘤是一种罕见的牙齿支撑颌骨良性牙源性肿瘤。其伴随发生与骨肉瘤,恶性颌面部骨肿瘤,以前从未描述过。我们介绍了一例罕见的43岁女性病例,其中右上颌骨骨骨化性纤维瘤通过使用深回旋动脉皮瓣切除和重建来治疗。在手术后一年的假肢康复手术中,在旋足深动脉皮瓣中偶然发现了从对侧上颌骨延伸的骨肉瘤。本病例报告的目的是提高对极其罕见但可能同时发生的骨水泥骨化性纤维瘤和骨肉瘤的认识。
    Cemento-ossifying fibroma is a rare benign odontogenic tumour of the tooth-bearing jaws. Its concomitant occurrence with osteosarcoma, a malignant maxillofacial bone tumour, has never been described before. We present an uncommon case of a 43-year-old woman in whom a cemento-ossifying fibroma in the right maxilla was treated by resection and reconstruction using a deep circumflex iliac artery flap. During surgical prosthetic rehabilitation one-year post-operative, an osteosarcoma extending from the contralateral maxilla was coincidentally discovered in the deep circumflex iliac artery flap. The aim of this case report is to raise awareness on the extremely rare but possible simultaneous and independent occurrence of a cemento-ossifying fibroma and an osteosarcoma.
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  • 文章类型: Journal Article
    具有两种或多种形态上不同成分的杂合牙源性病变的发生是一种罕见现象,并提出了诊断挑战。我们的目的是研究临床,放射学,以及杂合牙源性病变的病理特征和行为,提高对这些罕见病变的认识.
    回顾了2012年1月1日至2020年12月31日之间诊断的混合牙源性病变的苏木精和伊红载玻片。从患者的医疗记录中获得人口统计学和放射学信息。
    8例诊断为平均年龄19.1岁,男女比例为1:1.7。与上颌骨(n=3)相比,下颌骨的受累更为普遍(n=5)。所有患者出现肿胀,持续时间平均为9.75个月(3-25个月)。出血,牙齿松动,5、3、3和2例报告了疼痛和面部不对称,分别。放射学上,7例分界良好,75%的病例(n=6)是射线可透的,平均放射学大小为4.8cm。所有患者均仅接受手术治疗。5例(62.5%)行摘除术和刮宫术,而局部切除,全块切除术和节段性下颌骨切除术各1例。组织学上,骨化性纤维瘤/骨质骨化纤维瘤是最多的病变,5例(62%),其次是巨细胞肉芽肿样病变(GCG),中央和外周巨细胞肉芽肿(n=3),腺瘤样牙源性肿瘤(AOT)(n=2),和DC(n=2),成釉细胞纤维瘤(AF)(n=1),成釉细胞瘤(n=1),牙源性钙化囊肿(COC)(n=1),和复杂的牙瘤(n=1)。在有可用数据的情况下(n=7),手术4-99个月后(平均:32.9)没有发现复发的证据。长期主诉包括面部不对称(n=2)和疼痛(n=1)。
    大多数混合牙源性病变会在生命的第二个十年中影响年轻女性,并且通常显示COF和OF为混合成分。保守的管理方法似乎足够了。
    UNASSIGNED: The occurrence of hybrid odontogenic lesions with two or more morphologically distinct components is a rare phenomenon and poses a diagnostic challenge. We aimed to study the clinical, radiological, and pathological features and behavior of hybrid odontogenic lesions, to enhance awareness about these rare lesions.
    UNASSIGNED: Hematoxylin and Eosin slides of hybrid odontogenic lesions diagnosed between January 01, 2012 and December 31, 2020, were reviewed. Demographic and radiological information were obtained from the patient\'s medical records.
    UNASSIGNED: 8 cases were diagnosed with a mean age of 19.1 years and male to female ratio of 1:1.7. Involvement of mandible was more common (n = 5) as compared to maxilla (n = 3). All patients presented with swelling for an average of 9.75 months (3-25 months) duration. Bleeding, loose teeth, pain and facial asymmetry were reported in 5,3, 3, and 2 cases, respectively. Radiologically, 7 cases were well demarcated, 75% cases (n = 6) were radiolucent, and average radiological size was 4.8 cm. All patients were managed with surgery alone. 5 cases (62.5%) underwent enucleation and curettage, while local excision, en-block resection and segmental mandibulectomy were performed in 1 case each. Histologically, ossifying fibroma/cemento-ossifyiong fibroma were the most lesion, occurring in 5 cases (62%), followed by giant cell granuloma like lesions (GCG) i.e., central and peripheral giant cell granuloma (n = 3), Adenomatoid Odontogenic tumor (AOT) (n = 2), and DC (n = 2), ameloblastic fibroma (AF) (n = 1), Ameloblastoma (n = 1), calcifying odontogenic cyst (COC) (n = 1), and complex odontoma (n = 1). No evidence of recurrence was noted after 4-99 months of surgery (mean: 32.9) in cases with available data (n = 7). Long-term complaints included facial asymmetry (n = 2) and pain (n = 1).
    UNASSIGNED: Most hybrid odontogenic lesions affect young females in the second decade of life and commonly show COF and OF as hybrid components. A conservative approach to management appears adequate.
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  • 文章类型: Case Reports
    颌骨的纤维骨病变包括纤维发育不良,骨化性纤维瘤(OF),骨质骨化性纤维瘤,植物性骨性发育不良,和局灶性骨发育不良.OF是最常见的纤维骨性肿瘤,表现为生长缓慢,包裹良好的良性肿瘤,由与相邻正常骨界限良好的纤维基质中不同数量的骨或水泥样组织组成。OF在颌骨中最常见,对下颌骨有偏爱。OF通常作为患者的孤立性病变发生,很少作为多发性病变发生。我们介绍临床和放射学特征,组织病理学,以及对下颌骨和上颌骨中大量同步OF的罕见病例的手术治疗,并简要回顾了文献。
    Fibro-osseous lesions in the jaw bones include fibrous dysplasia, ossifying fibroma (OF), cemento-ossifying fibroma, florid osseous dysplasia, and focal osseous dysplasia. OF is the most common fibro-osseous tumor that presents as a slow-growing well-encapsulated benign neoplasm composed of varying amounts of bone or cement-like tissue in a fibrous stroma well-demarcated from the adjacent normal bone. OF is most common in the jaw bones, with a predilection for the mandible. OF usually occur as solitary lesions and rarely as multiple lesions in a patient. We present clinical and radiologic features, histopathology, and surgical management of a rare case with large synchronous OFs in the mandible and maxilla and a brief review of the literature.
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  • 文章类型: Journal Article
    方法:成牙本质瘤(CB)在牙源性肿瘤中是独特的,因为它的大体病理解剖在大多数情况下是病理性的,即,一种圆形的钙化生长物,融合到牙齿的根部,完全被纤维组织包裹。由此产生的射线照相外观是明确定义的,球状混合不透射线/透明或完全不透射线的质量消除了根部的一些细节,中央不透明周围有一个薄的射线可透区域。尽管数百篇出版物涵盖了CB的临床病理特征,对它的真实历史几乎一无所知。此外,对于术语“CB”最初是如何作为病理实体引入的,似乎知之甚少。本报告涵盖了一些可追溯到19世纪的关于CB的被忽视的论文,包括1888年的第一次完整描述和1906年的第一次射线照相演示。
    METHODS: Cementoblastoma (CB) is unique among odontogenic tumors because its gross pathological anatomy is pathognomonic in most cases, i.e., a rounded calcified growth that is fused to the root of a tooth and completely encapsulated by fibrous tissue. The resulting radiographic appearance is a well-defined, globular mixed radiopaque/lucent or completely radiopaque mass obliterating some details of the root, with a thin radiolucent zone surrounding the central opacity. Although hundreds of publications have covered the clinicopathologic features of CB, almost nothing is known about its true history. Also it seems there is little understanding about how the term \"CB\" was originally introduced as a pathologic entity. This report covers some overlooked papers on CB dating back to the 19th century, including the first complete description in 1888 and the first radiographic presentation in 1906.
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