Venugopal Reshma, Makarla Soumya, Muniswammappa Sudhakara, Ramachandra Prashanth, Bavle Radhika, Bhattacharya Soumita
Department of Oral and Maxillofacial Pathology, Krishnadevaraya College of Dental Sciences and Hospital, Bangalore, IND.
Cureus. 2025 Apr 18;17(4):e82484. doi: 10.7759/cureus.82484. eCollection 2025 Apr.
Aneurysmal bone cyst (ABC) is rarely a clinical diagnosis on first take; hence, data pertaining to primary ABC assists in differentiating lesions from related pathologies. The cases of primary ABCs were managed by curettage even with extensive cortical plate expansion, whereas secondary ABCs were managed according to primary pathology. The present review retrospectively studies the case reports of primary ABCs affecting the jaws, reported from the year 2000 (the time when USP6 to CDH 11 gene translocation was detected) to date, to identify cases that were diagnostically confirmed with gene analysis. Confirmed primary ABCs of jaws as defined by the World Health Organization (WHO) 2020 classification were included after a thorough literature search. In cases where gene analysis was not done, criteria considered to diagnose as primary ABC (clinical-radiological characteristics and histopathological features) were studied. Recurrence rate and prognosis were analyzed. A male predominance was noted with a ratio of 2:1. The age group between 10 and 20 years and the mandibular posterior region, followed by the temporomandibular joint (TMJ), were mainly affected. Around 22 of 33 cases showed both buccal and lingual cortical plate expansion. Blown-out cortices, fluid levels on magnetic resonance imaging (MRI) or contrast computed tomography (CT), altered blood, and the key histopathological feature of large blood-filled spaces surrounded by fibrovascular septa were the main clues for diagnosis. Around 28 of 33 cases showed giant cells, and 14 of 33 cases showed calcifications/ossifications. Recurrence was noted in 6 of 13 cases treated by curettage. A majority of primary ABCs are believed to exhibit gene mutations; however, genetic analysis was infrequently performed in the reviewed cases. Since the gene analysis may not be feasible in all cases, studies on histopathological analysis and immunohistochemical (IHC) markers to find clues for confirmatory diagnosis are in need.
动脉瘤样骨囊肿(ABC)很少能在初次诊断时就明确;因此,有关原发性ABC的数据有助于将病变与相关病理情况区分开来。原发性ABC病例即使伴有广泛的皮质板扩张也采用刮除术治疗,而继发性ABC则根据原发性病变进行处理。本综述回顾性研究了2000年(检测到USP6至CDH 11基因易位的时间)至今报道的影响颌骨的原发性ABC病例报告,以确定经基因分析确诊的病例。在全面检索文献后,纳入了世界卫生组织(WHO)2020年分类定义的确诊颌骨原发性ABC病例。对于未进行基因分析的病例,研究了被认为可诊断为原发性ABC的标准(临床-放射学特征和组织病理学特征)。分析了复发率和预后情况。发现男性占优势,比例为2:1。主要受累的年龄组为10至20岁,主要受累部位是下颌后区,其次是颞下颌关节(TMJ)。33例病例中约22例显示颊侧和舌侧皮质板均有扩张。皮质板膨出、磁共振成像(MRI)或增强计算机断层扫描(CT)上的液平、血液改变以及被纤维血管间隔围绕的大血腔的关键组织病理学特征是主要诊断线索。33例病例中约28例显示有巨细胞,33例病例中14例显示有钙化/骨化。刮除术治疗的13例病例中有6例出现复发。大多数原发性ABC被认为存在基因突变;然而,在本综述病例中很少进行基因分析。由于基因分析并非在所有病例中都可行,因此需要开展关于组织病理学分析和免疫组织化学(IHC)标志物的研究,以寻找确诊的线索。