结缔组织增生成釉细胞瘤:18个病例的多中心研究并文献复习

Madhusudan Astekar , Roopa Rao , Karpagaselvi Sanjai , Krishna Sireesha Sundaragiri , Gaurav Sapra , Shylaja Sanjeevareddygari , Srikant Natarajan , Sima P. Odedra
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引用次数: 0

摘要

成釉细胞瘤是第二常见的牙源性肿瘤,也是最常见的组织病理学报告。成釉细胞瘤的六种组织学变异在成釉细胞瘤的诊断中得到了很好的确立,其中结缔组织增生型仍是临床医生面临的挑战。在这个多中心的病例系列中,我们遵循了各种临床、放射学和组织病理学参数,以更好地了解1993年至2023年诊断的病例的独特变异。在本病例系列中,计算出的成釉细胞瘤的平均年龄为55.5岁,女性的偏好更高,三分之二的病例发生在前颌骨。放射学上,I型和II型为主要表现。组织病理学上可见间质透明化和骨增生。61.1 %的病例伴有另一亚型成釉细胞瘤。不同的表现需要重新考虑使用新的放射技术进行早期诊断,治疗计划和新定义的“杂交”成釉细胞瘤的组织病理学标准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Desmoplastic ameloblastoma: A multicentric study of 18 case series with literature review
Ameloblastoma is the second most common odontogenic tumour and the most common one to be reported histopathologically. The six histological variants of ameloblastoma are well established in the diagnosis of ameloblastoma, among which desmoplastic type still presents challenges to clinicians. In this multi-centric case series, we have complied with various clinical, radiological and histopathological parameters to better understand a unique variant from cases diagnosed between 1993 and 2023. The calculated mean age for desmoplastic ameloblastoma in the present case series was 55.5 years, with a higher female predilection and two-thirds of cases in the anterior mandible. Radiologically, Type I and II were the predominant presentation. Histopathologically, stromal hyalinization and osteoplasia were noted. The 61.1 % of cases were associated with another sub-type of ameloblastoma. The varied presentation has necessitated a rethink of using newer radiological techniques for early diagnosis, treatment planning and newly defined histopathological criteria for ‘Hybrid’ ameloblastoma.
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