Philipsen H P, Reichart P A
Oral Biology Unit, Faculty of Dentistry, University of Hong Kong, Hong Kong.
Oral Oncol. 1998 Sep;34(5):317-25. doi: 10.1016/s1368-8375(98)00012-8.
Based on a world-wide literature survey of 193 published cases of unicystic ameloblastomas (UA), data have been produced allowing the presentation of a revised concept of this much debated lesion. UA is a variant of the solid or multicystic ameloblastoma. Radiographically, the unilocular pattern is more common that the multilocular, especially in cases associated with tooth impaction. However, it is stressed that although the lesion is pathomorphologically unicystic, it will far from always produce a unilocular radiolucency. The mean age at the time of diagnosis of UA is closely related to an association with an impacted tooth. Almost 20 years separate the mean age of the 'dentigerous' variant from the 'non-dentigerous' (16.5 years versus 35.2 years) The male:female ratio for the 'dentigerous' type is 1.5:1, but for the 'non-dentigerous' type it is reversed (1:1.8). Location favours greatly the mandible (mandible to maxilla = 3 to 13:1). Between 50 and 80% of cases are associated with tooth impaction, the mandibular third molar being most often involved. The 'dentigerous' type occurs on average 8 years earlier than the 'non-dentigerious' variant. The mean age for unilocular, impaction-associated UAs is 22 years, whereas the mean age for the multilocular lesion unrelated to an impacted tooth is 33 years. Histologically, the minimum criterion for diagnosing a lesion as UA is the demonstration of a single cystic sac lined by odontogenic (ameloblastomatous) epithelium often seen only in focal areas. This simple type of UA (according to the authors' modification of the classification by Ackermann et al. (Journal of Oral Pathology 1988; 17:541-546)), is one of four UA subtypes, the others being (1) simple with intralumenal proliferations; (2) simple with both intralumenal and intramural proliferations; and (3) simple with intramural proliferations only. All four subtypes occur in both the 'dentigerous' and 'non-dentigerous' variants. The simple subtype with and without intralumenal proliferations may be treated conservatively (enucleation), whereas subtypes showing intramural growths must be treated radically, i.e. as a solid or multicystic ameloblastoma. Finally, the authors disclose areas and issues pertaining to UA that still need to be addressed.
基于对193例已发表的单囊型成釉细胞瘤(UA)的全球文献调查,已得出相关数据,从而能够呈现对这一备受争议病变的修订概念。UA是实性或多囊型成釉细胞瘤的一种变体。在影像学上,单房型比多房型更常见,尤其是在与牙齿阻生相关的病例中。然而,需要强调的是,尽管该病变在病理形态学上为单囊型,但它远非总是产生单房性透射区。UA诊断时的平均年龄与牙齿阻生密切相关。“含牙”型与“非含牙”型的平均年龄相差近20岁(分别为16.5岁和35.2岁)。“含牙”型的男女比例为1.5:1,但“非含牙”型则相反(1:1.8)。病变部位极多见于下颌骨(下颌骨与上颌骨的比例为3:13至1:1)。50%至80%的病例与牙齿阻生有关,下颌第三磨牙最常受累。“含牙”型平均比“非含牙”型早8年出现。单房性、与阻生相关的UA的平均年龄为22岁,而与牙齿阻生无关的多房型病变的平均年龄为33岁。在组织学上,将病变诊断为UA的最低标准是证明存在单个囊腔,其内衬牙源性(成釉细胞瘤样)上皮,且通常仅在局部区域可见。这种简单类型的UA(根据作者对Ackermann等人分类法(《口腔病理学杂志》1988年;17:541 - 546)的修改)是四种UA亚型之一,其他三种亚型分别为:(1)伴有腔内增殖的简单型;(2)伴有腔内和壁内增殖的简单型;(3)仅伴有壁内增殖的简单型。所有四种亚型在“含牙”型和“非含牙”型中均有出现。伴有或不伴有腔内增殖的简单亚型可采用保守治疗(摘除术),而显示壁内生长的亚型必须采用根治性治疗,即如同实性或多囊型成釉细胞瘤那样治疗。最后,作者揭示了与UA相关的仍需解决的领域和问题。