Gao H W, Ho J Y, Lee H S, Yu C P
Department of Pathology, Tri-Service General Hospital and National Defense Medical Center, Taipei, Taiwan.
Oral Dis. 2009 May;15(4):259-64. doi: 10.1111/j.1601-0825.2009.01518.x. Epub 2009 Feb 11.
To describe sequential changes in Merkel cells (MC), and CD10(+) and CD34(+) stromal cells (SC) during the transition from benign to malignant oral lesions and correlate with clinicopathologic parameters.
Changes in cytokeratin 20-positive (CK20(+)) Merkel cells, CD10(+) and CD34(+) SC were immunohistochemically examined in specimens of 28 oral verrucous carcinomas (VC), 32 squamous cell carcinomas (SCC) and 36 benign squamous lesions (BSL). Immunoreactivity and localized inflammation were measured quantitatively and/or semiquantitatively, and between-group results were statistically compared.
The mean number of CD34(+) SC was significantly lower in VC (57.36) and SCC (33.81) than BSL (351.56, P < 0.001). However, the three tumor types had similar staining level and number of CD10(+) SC. We found a significant difference in the density of MC between BSL and VC (P < 0.001) or SCC (P < 0.001). The number of CK20(+) MC was significantly lower in highly inflamed specimens than mildly inflamed specimens (P = 0.001).
CD34(+) SC and to a lesser extent MC, but not CD10(+) SC, reveal statistically different density during the transition from benign to malignant oral lesions. The correlations between the CD34(+) SC expression and squamous lesions may be associated with epithelial dysplasia and/or tumor invasion.
描述从良性口腔病变转变为恶性口腔病变过程中默克尔细胞(MC)、CD10(+)和CD34(+)基质细胞(SC)的序列变化,并与临床病理参数相关联。
采用免疫组织化学方法检测28例口腔疣状癌(VC)、32例鳞状细胞癌(SCC)和36例良性鳞状病变(BSL)标本中细胞角蛋白20阳性(CK20(+))的默克尔细胞、CD10(+)和CD34(+)的基质细胞。对免疫反应性和局部炎症进行定量和/或半定量测量,并对组间结果进行统计学比较。
VC组(57.36)和SCC组(33.81)中CD34(+)基质细胞的平均数量显著低于BSL组(351.56,P < 0.001)。然而,三种肿瘤类型的CD10(+)基质细胞染色水平和数量相似。我们发现BSL与VC(P < 0.001)或SCC(P < 0.001)之间的默克尔细胞密度存在显著差异。高度炎症标本中CK20(+)默克尔细胞的数量显著低于轻度炎症标本(P = 0.001)。
从良性口腔病变转变为恶性口腔病变过程中,CD34(+)基质细胞以及程度较轻的默克尔细胞,但不包括CD10(+)基质细胞,显示出统计学上的不同密度。CD34(+)基质细胞表达与鳞状病变之间的相关性可能与上皮发育异常和/或肿瘤侵袭有关。