Ihrler S, Weiler C, Hirschmann A, Sendelhofert A, Lang S, Guntinas-Lichius O, Arnold G, Zietz C, Harrison J D
Institute of Pathology, Ludwig Maximilian University, Munich, Germany.
Histopathology. 2007 Sep;51(3):362-71. doi: 10.1111/j.1365-2559.2007.02736.x. Epub 2007 Jun 25.
Although intraductal carcinoma has been demonstrated in intracapsular carcinoma ex pleomorphic adenoma (CEPA), the morphological and genetic stages of transformation of pleomorphic adenoma (PA) to CEPA are not fully understood. The aim of this study was to investigate the morphology of intracapsular CEPA.
The largest series of intracapsular CEPA studied was subject to immunohistochemical double-staining to detect p53 protein and cellular proliferation in different types of cell combined with mutational analysis of the p53 gene in laser-microdissected material. Intraductal carcinoma with high-grade cellular atypia and frequent accumulation of p53 protein was found in 15/19 cases. Purely intraductal carcinoma was found in eight cases. Mutation of p53 was found in 7/19 cases, of which it was found in intraductal carcinoma in 5/15 cases.
The frequent demonstration of intraductal carcinoma indicates that this preinvasive lesion is likely to be a constant feature in the malignant transformation of PA to CEPA. It appears to be a feature of CEPA developing from both primary and recurrent PA. The combined immunohistochemical and genetic data show that 14/19 cases of CEPA and 11/15 cases with intraductal carcinoma showed genetic or morphological evidence of dysfunctional p53, indicating that this is an early event in malignant transformation.
尽管在多形性腺瘤囊内癌(CEPA)中已证实存在导管内癌,但多形性腺瘤(PA)向CEPA转变的形态学和遗传学阶段尚未完全明了。本研究的目的是调查囊内CEPA的形态学。
对研究的最大系列囊内CEPA进行免疫组织化学双重染色,以检测不同类型细胞中的p53蛋白和细胞增殖,并结合激光显微切割材料中p53基因的突变分析。19例中有15例发现具有高级别细胞异型性和p53蛋白频繁积聚的导管内癌。8例发现单纯性导管内癌。19例中有7例发现p53突变,其中15例中有5例在导管内癌中发现。
导管内癌的频繁出现表明这种侵袭前病变可能是PA向CEPA恶性转化的一个恒定特征。它似乎是原发性和复发性PA发展而来的CEPA的一个特征。免疫组织化学和遗传学数据相结合显示,19例CEPA中有14例以及15例导管内癌中有11例显示出p53功能失调的遗传学或形态学证据,表明这是恶性转化中的一个早期事件。