Hansen L S, Ficarra G
Division of Oral Pathology, University of California, San Francisco 94143-0424.
Head Neck Surg. 1988 May-Jun;10(5):330-43. doi: 10.1002/hed.2890100508.
The ameloblastic fibroma, ameloblastic fibrodentinoma, and ameloblastic fibro-odontoma are mixed odontogenic tumors that are considered to arise from both epithelial and mesenchymal elements of the tooth germ. This article presents the clinical and histopathologic characteristics of 23 new cases. The patients' ages ranged from 3 to 19 years (median 9). Most tumors were asymptomatic and were associated with an unerupted tooth or teeth. All patients were treated with simple enucleation of the tumor. We found that histologically these lesions comprise a spectrum. Some were probably benign odontogenic tumors (neoplasms) and others were odontomas undergoing maturation (hamartomas); however, in any given case we were, on histologic grounds, unable to differentiate the two. The majority, if not all, of our cases were nonaggressive with little or no tendency to recur, whereas some reported cases have exhibited local aggressiveness and recurrence, suggestive of neoplasia. In our opinion, it is clinically important to distinguish the mixed odontogenic tumors from ameloblastoma since the mixed tumors, found mostly in children, are relatively benign when compared to ameloblastoma, which is found in all age groups (usually adults). The usually innocuous behavior of these lesions does not justify aggressive treatment initially, and simple enucleation should be appropriate in most cases.
成釉细胞纤维瘤、成釉细胞纤维牙本质瘤和成釉细胞纤维牙瘤是混合性牙源性肿瘤,被认为起源于牙胚的上皮和间充质成分。本文介绍了23例新病例的临床和组织病理学特征。患者年龄在3至19岁之间(中位数为9岁)。大多数肿瘤无症状,与一颗或多颗未萌出的牙齿有关。所有患者均接受了肿瘤单纯摘除术。我们发现,从组织学上看,这些病变构成一个谱系。有些可能是良性牙源性肿瘤(新生物),而另一些是正在成熟的牙瘤(错构瘤);然而,在任何特定病例中,基于组织学依据,我们无法区分这两者。我们的大多数病例(如果不是全部的话)不具侵袭性,很少或没有复发倾向,而一些报道的病例表现出局部侵袭性和复发,提示为肿瘤形成。我们认为,将混合性牙源性肿瘤与成釉细胞瘤区分开来在临床上很重要,因为混合性肿瘤大多发生于儿童,与各年龄组(通常为成年人)均可发生的成釉细胞瘤相比,其相对良性。这些病变通常无害的行为并不足以证明一开始就采取积极治疗是合理的,在大多数情况下单纯摘除术应该是合适的。