Department of Urology, University Medical Center, Lessingstrasse 1, 07743, Jena, Germany.
World J Urol. 2010 Jun;28(3):329-34. doi: 10.1007/s00345-010-0541-7. Epub 2010 Apr 3.
There are often problems in differentiating between benign and malignant adrenal gland tumors by imaging and histopathology. Fine-needle biopsy is possible but not used owing to problems in histopathological differentiation. On account of considerable differences in the therapy and aftercare of benign and malignant adrenal tumors, correct classification of tumor type is of greatest importance. The purpose of this study was to define specific genetic alterations differentiating between adenomas and carcinomas.
DNA was isolated from tumor areas in paraffin sections and amplified by a modified protocol for DOP-PCR. After labeling of tumor-DNA and normal DNA with biotin-dUTP and digoxigenin-dUTP, respectively, comparative genomic hybridization (CGH) was carried out according to standard protocols. Retrospectively, 26 (16 adenomas and 10 carcinomas) tumors of the adrenal cortex were analyzed.
Genetic alterations were found in 5/16 adenomas (31.25%) and in all adrenocortical carcinomas. The mean number of genetic changes per tumor was 8.7 (range 6-12) in carcinomas. The benign cortical tumors present 1.6 changes (range 0-3) per tumor. Only a moderate correlation between number of alterations and size of tumor was seen. Furthermore, specific chromosomal alterations of carcinomas were identified.
Genetic evaluation facilitates differentiation between adrenal gland tumors. Genetic tests should be used in routine diagnostics of adrenal specimens. Potentially, fine-needle biopsy can be established as standard diagnostics of adrenal tumors with unknown genesis.
通过影像学和组织病理学方法常常难以区分肾上腺良恶性肿瘤。细针活检是可行的,但由于组织病理学上的差异,并不常用。由于良性和恶性肾上腺肿瘤的治疗和后续护理存在显著差异,因此正确分类肿瘤类型至关重要。本研究的目的是确定能够区分腺瘤和腺癌的特定遗传改变。
从石蜡切片的肿瘤区域中分离 DNA,并用改良的 DOP-PCR 方案进行扩增。用生物素-dUTP 和地高辛-dUTP 分别标记肿瘤 DNA 和正常 DNA 后,按照标准方案进行比较基因组杂交(CGH)。回顾性地分析了 26 例(16 例腺瘤和 10 例癌)肾上腺皮质肿瘤。
在 16 例腺瘤中的 5 例(31.25%)和所有肾上腺皮质癌中均发现了遗传改变。每例肿瘤的遗传改变平均数为 8.7(范围 6-12),良性皮质肿瘤每例有 1.6 个改变(范围 0-3)。仅观察到肿瘤大小与改变数量之间存在中度相关性。此外,还确定了癌的特定染色体改变。
遗传评估有助于区分肾上腺肿瘤。遗传检测应在常规肾上腺标本的诊断中使用。潜在地,可以将细针活检确立为具有未知起源的肾上腺肿瘤的标准诊断方法。