Ameloblastic fibroma and BRAF V600E immunohistochemistry staining pattern: case report and review of a rare entity.

D de Gracia Hahn, G Gupta, S Mukhopadhyay, L Greaney
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Abstract

Ameloblastic fibroma is a rare, benign, biphasic odontogenic tumour that typically presents in young patients and is treated conservatively with an excellent prognosis. An important differential is ameloblastoma, a more common odontogenic neoplasm that shares many of the clinical, radiological, and histological features, but requires more extensive surgery due to its potentially destructive nature. Both tumours demonstrate BRAF V600E mutations. While epithelial staining with BRAF V600E-specific immunohistochemistry is considered a surrogate marker for mutation and is supportive of the diagnosis of ameloblastoma, the staining pattern in ameloblastic fibroma has not been defined previously because of the rarity of the lesion. This report describes a case of ameloblastic fibroma in a 13-year-old, in which BRAF V600E immunohistochemistry showed cytoplasmic staining in both the stromal and epithelial components of the tumour. On review of the literature, this was interpreted to be concordant with the biphasic nature of the lesion.

成釉细胞纤维瘤和BRAF V600E免疫组化染色模式:一个罕见实体的病例报告和回顾。
成釉细胞纤维瘤是一种罕见的良性双期牙源性肿瘤,通常出现在年轻患者中,保守治疗预后良好。一个重要的区别是成釉细胞瘤,这是一种更常见的牙源性肿瘤,具有许多临床、放射学和组织学特征,但由于其潜在的破坏性,需要更广泛的手术。两种肿瘤均表现出BRAF V600E突变。虽然BRAF v600e特异性免疫组化上皮染色被认为是突变的替代标记物,并支持成釉细胞瘤的诊断,但由于病变罕见,成釉细胞瘤的染色模式尚未明确。本报告描述了一例13岁的成釉细胞纤维瘤,其BRAF V600E免疫组织化学显示肿瘤的间质和上皮成分均有细胞质染色。回顾文献,这被解释为与病变的双相性一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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