颌骨成釉细胞癌:文献综述

R. Braimah, C. Uguru, K. Ndukwe
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引用次数: 10

摘要

成釉细胞癌是一种罕见的牙源性恶性肿瘤,即使在没有转移的情况下,也具有成釉细胞瘤的组织学特征和细胞学非典型性。主要的预后因素是疾病的临床病程,包括其侵袭性、局部破坏和远处转移性扩散,如果被忽视,优先通过血液途径。组织学上,成釉细胞癌保留成釉细胞分化的特征,在原发性或复发性肿瘤中表现出恶性肿瘤的细胞学特征。因为它是一种非常罕见的病变,它给诊断带来很大的困难。整体切除1-2厘米的正常骨缘被认为是确保无病生存的最安全的手术方式。在PubMed上使用布尔算子“And”在成釉细胞瘤和癌之间进行文献检索。我们对检索到的文章进行了广泛的回顾,以了解成釉细胞癌的流行病学、病因学、诊断、治疗方案和预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ameloblastic carcinoma of the jaws: Review of the literature
Ameloblastic carcinoma is a rare odontogenic malignancy that combines the histological features of ameloblastoma with cytological atypia, even in the absence of metastases. The major prognostic factor is the clinical course of the disease which includes its aggressiveness, local destruction, and distant metastatic spread preferentially through hematologic route if neglected. Histologically, ameloblastic carcinoma retains the features of ameloblastic differentiation and exhibits cytological features of malignancy in a primary or recurrent tumor. Because it is a very rare lesion, it poses a great difficulty in diagnosis. En bloc removal with 1–2 cm of normal bone margin has been regarded as the safest surgical modality to ensure disease-free survival. Literature search was carried out using the Boolean operator “And” between ameloblastoma and carcinoma on PubMed. Retrieved articles were extensively reviewed for epidemiology, etiology, diagnosis, treatment options, and prognosis of ameloblastic carcinoma.
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