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首页> 外文期刊>Journal of Oral and Maxillofacial Pathology >Ameloblastic carcinoma: Secondary dedifferentiated carcinoma of the mandible: Report of a rare entity with a brief review
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Ameloblastic carcinoma: Secondary dedifferentiated carcinoma of the mandible: Report of a rare entity with a brief review

机译:潮气母细胞癌:下颌骨继发性去分化癌:简要回顾的罕见实体报告

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摘要

Epithelial odontogenic tumors arise from odontogenic epithelial structures. Malignant epithelial odontogenic tumors are extremely rare. Ameloblastic carcinomas may present denovo, ex ameloblastoma or ex odontogenic cyst. Most ameloblastic carcinomas are presumed to present denovo. To date less than 45 cases of ameloblastoma with metastasis have been reported. It occurs primarily in the mandible in a wide range of age groups; no sex or race predilection has been noted. It may present as a cystic lesion with benign clinical features or as a large tissue mass with ulceration, significant bone resorption, and tooth mobility. The lesion is usually found unexpectedly after an incisional biopsy or the removal of a cyst. Histologic features of ameloblastic carcinoma shows tumor cells that resemble the cells seen in ameloblastoma, but they show cytologic atypia. Moreover, they lack the characteristic arrangement seen in ameloblastoma. The clinical course of ameloblastic carcinoma is typically aggressive, with extensive local destruction. Here we describe a rare case of ameloblastic carcinoma (secondary dedifferentiated carcinoma) of mandible in a 40-year-old female patient. Ameloblastic carcinoma: Secondary dedifferentiated carcinoma of the mandible.Keywords: Ameloblastic carcinoma, cytologic atypia, de novo
机译:上皮牙源性肿瘤源自牙源性上皮结构。恶性上皮牙源性肿瘤极为罕见。潮气母细胞癌可表现为牙本质,前成釉细胞瘤或前牙源性囊肿。推测大多数釉母细胞癌均表现为牙本质癌。迄今为止,已报道不到45例转移性成釉细胞瘤病例。它主要发生在下颌骨的各个年龄段中;尚未发现性别或种族偏爱。它可能表现为具有良性临床特征的囊性病变,也可能表现为具有溃疡,明显的骨吸收和牙齿活动性的大组织块。通常在切开活检或去除囊肿后意外发现病变。成釉细胞癌的组织学特征显示肿瘤细胞类似于成釉细胞瘤中见到的细胞,但它们显示出细胞学上的异型性。而且,它们缺乏成釉细胞瘤所见的特征性排列。成釉细胞癌的临床过程通常是侵袭性的,具有广泛的局部破坏。在这里,我们描述了40岁女性患者下颌骨成釉细胞癌(继发性去分化癌)的罕见病例。潮红细胞癌:下颌骨继发性去分化癌。关键词:潮红细胞癌,细胞学非典型性,从新

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