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首页> 外文期刊>American Journal of Dermatopathology >A proposal for improving multicolor fish sensitivity in the diagnosis of malignant melanoma using new combined criteria
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A proposal for improving multicolor fish sensitivity in the diagnosis of malignant melanoma using new combined criteria

机译:使用新的联合标准提高对多色鱼敏感性的恶性黑色素瘤诊断的建议

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Fluorescence in situ hybridization (FISH) for the diagnosis of melanoma makes use of specific fluorescent probes to detect selected chromosomal alterations on paraffin-embedded tissue samples. To date, interpretation of FISH data has been based on numerical values generated by 2 different computational algorithms that of Abbott and that of Gerami. To further evaluate the value of FISH in the diagnosis of malignant melanoma, we selected 163 clinically and histologically unequivocal cases of malignant melanoma in a cohort of 575 melanocytic tumors and analyzed FISH data using the criteria of Abbott, Gerami, and new combined criteria. Depending on the used criteria, FISH was positive in the unequivocal malignant melanoma in 69.3% (113/163) of cases using the Abbott criteria, 74.2% (121/163) of cases using the Gerami criteria, and 82.2% (134/163) of cases using the combined criteria of Abbott and Gerami. Although use of all 3 criteria was associated with 100% FISH negativity in a cohort of 30 unequivocal benign melanocytic nevi, use of the combined criteria revealed more FISH-positive cases in ambiguous benign melanocytic lesions than the criteria of Abbott or Gerami alone: Abbott, 125 of 367; Gerami, 146 of 367; combined, 161 of 367. Furthermore, we show that 66% (8/12) of FISH-negative cases of unequivocal melanoma are positive when analyzed by array comparative genomic hybridization (aCGH), demonstrating that false-negative results remain despite the usage of the combined criteria for evaluation of FISH data. In these 8 FISH-negative aCGH-positive cases, copy number alterations were often located on chromosomes 9p, a chromosomal locus that is not targeted by the FISH probes currently used. In conclusion, the existing criteria for the evaluation of multicolor melanocytic FISH are limited by a nonnegligeable rate of false negativity that can be reduced by using newly proposed combined criteria but at the cost of increased detection of FISH positivity in ambiguous benign melanocytic lesions.
机译:用于诊断黑素瘤的荧光原位杂交(FISH)利用特定的荧光探针来检测石蜡包埋的组织样本上的选定染色体改变。迄今为止,FISH数据的解释是基于由Abbott和Gerami的2种不同计算算法生成的数值。为了进一步评估FISH在恶性黑色素瘤诊断中的价值,我们在575名黑素细胞性肿瘤队列中选择了163例临床和组织学明确的恶性黑色素瘤病例,并使用Abbott,Gerami和新的合并标准对FISH数据进行了分析。根据所使用的标准,使用雅培标准的FISH在明确的恶性黑色素瘤中分别为69.3%(113/163),使用Gerami标准的74.2%(121/163)和82.2%(134/163) )使用雅培和Gerami的合并标准的案例。尽管在所有30个明确的良性黑素细胞痣中,所有这三个标准的使用均与100%FISH阴性相关,但综合标准的使用显示,歧义性良性黑素细胞病变的FISH阳性病例多于单独的Abbott或Gerami标准:Abbott, 367中的125;热拉米(Gerami),第367个,共146个;结合起来,共367个样本中的161个。此外,我们通过阵列比较基因组杂交(aCGH)分析显示,在明确的黑色素瘤FISH阴性病例中,有66%(8/12)是阳性的,这表明尽管使用了评估FISH数据的综合标准。在这8例FISH阴性aCGH阳性病例中,拷贝数变化通常位于9p染色体上,9p染色体是目前使用的FISH探针未靶向的染色体位点。总之,现有的评估多色黑素细胞性FISH的标准受到假阴性率不可忽略的限制,可以通过使用新提出的组合标准来降低假阴性率,但以增加对歧义良性黑素细胞病变中FISH阳性的检测为代价。

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