Reviewing the Unicystic Ameloblastoma : a Clinicopathologically Distinct Entity
Reviewing the Unicystic Ameloblastoma : a Clinicopathologically Distinct Entity
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单囊性成釉细胞瘤回顾：临床病理学上独特的实体
DOI：
10.3353/omp.2.61
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发表时间：
1997
期刊：
影响因子：
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通讯作者：
M. Kitano
中科院分区：
文献类型：
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作者：
Tie‐Jun Li;M. Kitano
根据成釉细胞瘤的生物学行为，成釉细胞瘤可分为实性或多囊型、单囊型和周围型。综述了自1977年首次描述以来有关单囊成釉细胞瘤的英文文献。总共检索了182例病例，以评估该变异的不同临床和病理方面。与传统的成釉细胞瘤相比，肿瘤的发病年龄较小(平均25.5岁)，摘除或刮除后复发率较低(13.8%)。根据近期的研究兴趣和进展，还讨论了这种造釉细胞瘤的组织学谱的变异性、诊断问题和治疗方法的选择。
Classification of ameloblastoma into solid or multicystic, unicystic and peripheral types based on the biological behavior has gained recent recognition. Available English-language literature on unicystic ameloblastoma since its first description in 1977 was reviewed. A total number of 182 cases was retrieved to evaluate various clinical and pathological aspects of this variant. The tumor tends to occur at an younger age (mean: 25.5 years) and exhibits a low rate of recurrence (13.8%) following enucleation or curettage in comparison to the conventional ameloblastoma. The variability of histological spectrum, diagnostic problems and choice of treatment for this form of ameloblastoma were also discussed in the light of recent research interest and progress.