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巨大先天性黑素细胞痣(GCMN)中的DNA含量与细胞增殖。图像细胞术分析

DNA content and cell proliferation in giant congenital melanocytic naevi (GCMN). An analysis by image cytometry.

作者信息

Fromont Hankard G, Fraitag S, Wolter M, Brousse N, Masood S

机构信息

Department of Pathology, University Medical Center, Jacksonville, Florida, USA.

出版信息

J Cutan Pathol. 1998 Sep;25(8):401-6. doi: 10.1111/j.1600-0560.1998.tb01765.x.

Abstract

GCMN may be precursors of melanoma, and it has been suggested that the presence of atypical foci could increase the risk of malignant transformation. In order to better define atypical GCMN, we analyzed DNA content and proliferative activity in 21 samples of GCMN, with (n=13) or without (n=8) cytologic atypia. Six benign acquired naevi (AN) and 6 malignant melanoma (MM) were used as controls. DNA content was determined with the CAS 200 image analyzer, and DNA histograms were classified according to the Auer classification. The proliferative indices (PI) were measured after Ki 67 immunostaining using the CAS 200 system. All AN and GCMN without atypia showed class I histograms (normal DNA content) and low PI (mean 1.9 and 2.1). Atypical GCMN showed in 10 cases an abnormal DNA content (class III or IV histograms) with low PI (mean 2.7), and in 3 cases a normal DNA content (class I histograms) with higher PI (mean 16.2). All MM displayed abnormal DNA content and high PI (mean 32.6). In conclusion, abnormal DNA content seems to correlate with cytologic atypia in GCMN. Atypical GCMN exhibit an overall pattern of DNA content and cell proliferation intermediate between non-atypical naevi and MM.

摘要

巨大先天性黑素细胞痣(GCMN)可能是黑色素瘤的前体,有人提出非典型病灶的存在可能会增加恶性转化的风险。为了更好地定义非典型GCMN,我们分析了21例GCMN样本的DNA含量和增殖活性,其中13例有细胞学非典型性,8例无细胞学非典型性。6例良性获得性痣(AN)和6例恶性黑色素瘤(MM)用作对照。使用CAS 200图像分析仪测定DNA含量,并根据奥尔分类法对DNA直方图进行分类。使用CAS 200系统在Ki 67免疫染色后测量增殖指数(PI)。所有无非典型性的AN和GCMN均显示I类直方图(正常DNA含量)和低PI(平均值分别为1.9和2.1)。10例非典型GCMN显示DNA含量异常(III类或IV类直方图)且PI低(平均值为2.7),3例显示DNA含量正常(I类直方图)但PI较高(平均值为16.2)。所有MM均显示DNA含量异常和高PI(平均值为32.6)。总之,DNA含量异常似乎与GCMN中的细胞学非典型性相关。非典型GCMN表现出DNA含量和细胞增殖的总体模式,介于非典型痣和MM之间。

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