Calcifying odontogenic cyst with ameloblastic fibroma: Report of three cases
Calcifying odontogenic cyst with ameloblastic fibroma: Report of three cases
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DOI：
10.1016/j.tripleo.2004.01.010
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发表时间：
2004-10-01
期刊：
影响因子：
--
通讯作者：
Ellis, E
中科院分区：
文献类型：
--
作者：
Lin, CC;Chen, CH;Ellis, E
虽然这是一种罕见的事件，但牙源性肿瘤如成釉细胞瘤、成釉纤维纤维瘤（AF）、成釉纤维牙瘤和牙瘤已被报道与钙化牙源性囊肿（COC）相关。在英文文献中，COC合并AF的病例仅有4例。然而，这四个病例中的三个要么被纳入一系列病例的综述中，要么作为摘要报道，并且提供了有限的临床和组织学信息。我们提出了另外三例COC合并房颤的病例，并讨论了这种合并病变的处理。由于COC以其组织学多样性和可变的临床行为而闻名，并且COC与房颤关联的临床意义尚不清楚，因此我们认为有详细的临床和病理记录来报道COC与房颤是有价值的。
Although it is a rare event, odontogenic tumors such as ameloblastoma, ameloblastic fibroma (AF), ameloblastic fibro-odontoma, and odontoma have been reported associated with calcifying odontogenic cyst (COC). There are only four cases of COC with AF cited in the English literature. However, three of these four cases were either included in a review of a series of cases or reported as an abstract, and limited clinical and histological information was provided. We present three additional cases of COC with AF and discuss the management for this combined lesion. Because COC is known for its histologic diversity and variable clinical behavior, and the clinical significance of an association of COC with AF is still unknown, we think it is valuable to report COC with AF with detailed clinical and pathological documentation.