Upadhyaya Jasbir D, Bhattacharyya Indraneel, Fitzpatrick Sarah G, Cohen Donald M, Islam Mohammed N
Resident, Department of Oral and Maxillofacial Diagnostic Sciences, College of Dentistry, University of Florida, Gainesville, FL.
Professor and Interim Division Director, Department of Oral and Maxillofacial Pathology, College of Dentistry, University of Florida, Gainesville, FL.
J Oral Maxillofac Surg. 2018 May;76(5):996-1004. doi: 10.1016/j.joms.2017.11.020. Epub 2017 Nov 23.
Peripheral ameloblastoma (PA) is a rare odontogenic tumor arising in the mucosa of tooth-bearing areas of the jaws that typically shows no radiographic evidence of bone involvement. It bears close histologic resemblance to intraoral basal cell carcinoma (IOBCC), an extremely rare entity. In our experience from previous published data, 3 cases of IOBCC were initially misdiagnosed as PA and were later differentiated from PA on the basis of Ber-EP4 protein expression. This unusual but significant experience set the premise for us to rule out a diagnosis of IOBCC by evaluating Ber-EP4 expression in all previously diagnosed cases of PA from the University of Florida Oral Pathology (UFOP) biopsy service archives.
With institutional review board approval, 18 cases of PA were retrieved from the UFOP biopsy service archives. We describe the clinicopathologic features of these cases and discuss the Ber-EP4 immunohistochemical staining performed to rule out a potential diagnosis of IOBCC. In addition, we conducted calretinin and epithelial membrane antigen staining for 1 case of PA.
Most PAs presented in the lingual gingiva of the posterior mandible. Men were affected twice as often as women, and the average age at the diagnosis was 59 ± 21.5 years. Of the 18 lesions, 13 showed no reactivity to Ber-EP4, 4 displayed patchy membranous immunoreactivity, and 1 demonstrated nonspecific reactivity.
We have concluded that all cases of PA that present with histologic overlap with basal cell carcinoma, especially those from incisional biopsies, those that appear significantly infiltrative, and those that appear ulcerated and/or demonstrate recurrence should be evaluated with Ber-EP4 to rule out IOBCC.
外周型成釉细胞瘤(PA)是一种罕见的牙源性肿瘤,发生于颌骨牙列区的黏膜,通常影像学检查无骨受累证据。它在组织学上与口腔基底细胞癌(IOBCC)极为相似,而IOBCC是一种极其罕见的实体。根据我们以往发表的数据经验,3例IOBCC最初被误诊为PA,后来根据Ber-EP4蛋白表达与PA区分开来。这一不同寻常但意义重大的经验为我们通过评估佛罗里达大学口腔病理学(UFOP)活检服务档案中所有先前诊断为PA的病例的Ber-EP4表达来排除IOBCC的诊断奠定了基础。
经机构审查委员会批准,从UFOP活检服务档案中检索出18例PA病例。我们描述了这些病例的临床病理特征,并讨论了为排除潜在的IOBCC诊断而进行的Ber-EP4免疫组化染色。此外,我们对1例PA进行了钙视网膜蛋白和上皮膜抗原染色。
大多数PA发生在下颌后牙区的舌侧牙龈。男性受累频率是女性的两倍,诊断时的平均年龄为59±21.5岁。在这18个病变中,13个对Ber-EP4无反应,4个显示斑片状膜免疫反应,1个显示非特异性反应。
我们得出结论,所有组织学表现与基底细胞癌重叠的PA病例,尤其是那些来自切开活检的病例、表现为明显浸润性的病例、出现溃疡和/或复发的病例,均应进行Ber-EP4评估以排除IOBCC。