Aravindan Vedha, Kumar Santhosh P, Murugan P Senthil, Krishnan Murugesan, Sneha Alladi
Oral and Maxillofacial Surgery, Saveetha Institute of Medical and Technical Sciences, Chennai, IND.
Cureus. 2023 May 7;15(5):e38685. doi: 10.7759/cureus.38685. eCollection 2023 May.
Benign fibro-osseous lesions are a group of pathological conditions characterized by the replacement of normal bone with cellular fibrous connective tissue that undergoes mineralization. The most common types of benign fibro-osseous lesions include fibrous dysplasia, ossifying fibroma, and osseous dysplasia. However, diagnosing these lesions can be challenging due to their overlapping clinical, radiological, and histological features, which can cause a diagnostic dilemma for surgeons, radiologists, and pathologists. One rare type of benign fibro-osseous lesion is the cemento-ossifying fibroma (COF), which is a definitive form of a benign fibro-osseous tumor that affects the craniofacial region, particularly the jaws (70%). Here, we present a case of COF in a 61-year-old female patient in the maxillary anterior region. Due to a clear distinction between the lesion and healthy bone, the lesion was treated with conservative surgical excision followed by curettage and primary closure. However, differential diagnosis of COF can be highly challenging for clinicians due to its overlapping features with other fibro-osseous lesions like Paget's disease and fibrous dysplasia. Ossifying fibroma and fibrous dysplasia often present a histopathological, clinical, and radiological overlap. The post-operative follow-up after eight months was unpredictable, with a radiological picture showing the increased thickness of the frontal bone, parietal bone, and maxilla with obliteration of marrow spaces, alteration of the trabecular pattern with a cotton wool/ground glass appearance, and reduced maxillary sinus space. Proper evaluation and diagnosis of fibro-osseous lesions are necessary before arriving at a final conclusion. Cemento-ossifying fibroma in the maxillofacial skeleton is uncommon, and after eight months, the recurrence rate is rare. This case highlights the importance of considering COF as a differential diagnosis for fibro-osseous lesions in the maxillofacial region and the necessity for proper evaluation and diagnosis to determine the appropriate treatment plan and prognosis. In summary, the diagnosis of benign fibro-osseous lesions can be challenging due to their overlapping features, but early diagnosis and proper evaluation are essential for successful treatment outcomes. COF is a rare type of benign fibro-osseous lesion where other fibro-osseous lesions in the maxillofacial region should be considered as a differential diagnosis, and the necessary steps should be taken to confirm the diagnosis before arriving at a final conclusion.
良性纤维-骨病变是一组病理状况,其特征是正常骨被经历矿化的细胞性纤维结缔组织所替代。最常见的良性纤维-骨病变类型包括骨纤维异常增殖症、骨化性纤维瘤和骨发育异常。然而,由于这些病变在临床、放射学和组织学特征上存在重叠,诊断起来可能具有挑战性,这会给外科医生、放射科医生和病理科医生带来诊断难题。一种罕见的良性纤维-骨病变是牙骨质-骨化性纤维瘤(COF),它是一种影响颅面部区域,尤其是颌骨(70%)的良性纤维-骨肿瘤的明确形式。在此,我们报告一例61岁女性患者上颌前部区域的COF病例。由于病变与健康骨之间界限清晰,该病变采用保守性手术切除,随后刮除并一期缝合进行治疗。然而,COF的鉴别诊断对临床医生来说极具挑战性,因为它与其他纤维-骨病变如佩吉特病和骨纤维异常增殖症有重叠特征。骨化性纤维瘤和骨纤维异常增殖症常常在组织病理学、临床和放射学上存在重叠。八个月后的术后随访情况难以预测,放射影像显示额骨、顶骨和上颌骨厚度增加,骨髓腔消失,小梁模式改变呈棉絮状/磨砂玻璃样外观,上颌窦空间减小。在得出最终结论之前,对纤维-骨病变进行恰当的评估和诊断是必要的。上颌面部骨骼中的牙骨质-骨化性纤维瘤并不常见,八个月后复发率很低。该病例凸显了将COF作为上颌面部区域纤维-骨病变鉴别诊断的重要性,以及进行恰当评估和诊断以确定合适治疗方案和预后的必要性。总之,由于良性纤维-骨病变特征重叠,其诊断可能具有挑战性,但早期诊断和恰当评估对于成功的治疗结果至关重要。COF是一种罕见的良性纤维-骨病变,上颌面部区域的其他纤维-骨病变应被视为鉴别诊断对象,在得出最终结论之前应采取必要步骤以确诊。