腺样成釉细胞瘤的诊断难题:基于文献回顾的证据认为它是一种新的成釉细胞瘤亚型。

IF 4.1
Head and neck pathology Pub Date : 2022-06-01 Epub Date: 2021-07-19 DOI:10.1007/s12105-021-01358-w
Primali R Jayasooriya, W A M Udari L Abeyasinghe, R L Pemith R Liyanage, Gunandahandi N Uthpali, Wanninayake M Tilakaratne
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引用次数: 17

摘要

腺样成釉细胞瘤是一种混合的牙源性肿瘤,具有成釉细胞瘤和腺瘤样牙源性肿瘤(AOT)的组织病理学特征,文献中报道了大约40例。本报告的目的是用三个新病例说明腺样成釉细胞瘤的诊断挑战,并分析文献证据,认为腺样成釉细胞瘤是一种新的成釉细胞瘤亚型。以“腺样成釉细胞瘤”、“混合型/复合型牙源性肿瘤”、“混合型成釉细胞瘤与腺瘤样牙源性肿瘤”、“诱导改变的成釉细胞瘤”、“牙本质样和牙本质瘤”为关键词进行文献综述,选择符合腺样成釉细胞瘤诊断的病例。在文献报道的40例病例中,有充分资料的31例和新病例3例进行分析。在34例腺样成釉细胞瘤中,大多数肿瘤(76.5%)发生在25至55岁的成年人中。有轻微的女性偏好,男女比例为0.9:1。大约64.7%发生在下颌骨。放射学上,82.4%的腺样成釉细胞瘤表现为放射透明病变,而47.1%的腺样成釉细胞瘤在诊断时伴有边界不清和皮质穿孔。组织病理学上,70.8%的肿瘤表现为丛状成釉细胞瘤,而管状结构/腺状结构是支持腺瘤样牙源性肿瘤的最常见特征,绝大多数腺样成釉细胞瘤在95.9%的腺样成釉细胞瘤中观察到。91.6%的肿瘤表现为牙本质样形态的诱导改变。此外,45.4%的肿瘤在手术切除后至少复发一次。本报告以文献综述为基础,证明腺样体成釉细胞瘤的存在,其人口学特征与常规成釉细胞瘤相似,但在组织病理学上存在差异,且具有较高的复发率/多次复发率,表明其生物侵袭性。因此,我们建议将腺样成釉细胞瘤作为成釉细胞瘤的一个亚型纳入下一版WHO牙源性肿瘤分类。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Diagnostic Enigma of Adenoid Ameloblastoma: Literature Review Based Evidence to Consider It as a New Sub Type of Ameloblastoma.

Diagnostic Enigma of Adenoid Ameloblastoma: Literature Review Based Evidence to Consider It as a New Sub Type of Ameloblastoma.

Diagnostic Enigma of Adenoid Ameloblastoma: Literature Review Based Evidence to Consider It as a New Sub Type of Ameloblastoma.

Adenoid ameloblastoma is a hybrid odontogenic tumour showing histopathological features of both ameloblastoma and adenomatoid odontogenic tumour (AOT), with approximately 40 cases reported in the literature. The aims of the report are to illustrate the diagnostic challenges of adenoid ameloblastoma using three new cases and to analyze evidence in literature to consider adenoid ameloblastoma as a new sub type of ameloblastoma. A literature review was performed with the key words-adenoid ameloblastoma, hybrid/composite odontogenic tumours, hybrid ameloblastoma and adenomatoid odontogenic tumour, ameloblastoma with inductive changes, dentinoid and dentinoma to select the cases compatible with the diagnosis of adenoid ameloblastoma. Out of the 40 cases reported in literature, 31 cases with sufficient information and 3 new cases were analyzed. Out of the 34 adenoid ameloblastomas majority of tumours (76.5%) occurred in adults with age ranging from 25 to 55 years. Slight female predilection with a male:female ratio of 0.9:1 was observed. Approximately, 64.7% occurred in the mandible. Radiologically, 82.4% of adenoid ameloblastomas presented as radiolucent lesions while 47.1% occurred with ill-defined margins and cortical perforation at diagnosis. Histopathologically, 70.8% of tumours presented as plexiform ameloblastomas, while duct like structures/glandular structures were the commonest feature supportive of adenomatoid odontogenic tumour observed in overwhelming majority of 95.9% of adenoid ameloblastomas. 91.6% of tumours showed inductive change in the form of dentinoid. Further, 45.4% of the tumours developed at least one recurrence following surgical excision. The report presents literature review based evidence to show the existence of adenoid ameloblastoma, which is demographically similar to conventional ameloblastoma but with histopathological differences and presenting with higher rate/multiple recurrences, indicating its biological aggressiveness. Thus, we would like to propose the inclusion of adenoid ameloblastoma as a sub type of ameloblastoma in the next revision of the WHO odontogenic tumour classification.

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