Classification of adrenal cortical tumors: What limits for the pathological approach?

被引:25
作者
Tissier, Frederique [1 ,2 ]
机构
[1] Paris Descartes Univ, Cochin Hosp, AP HP, Pathol Dept,INSERM U1016, Paris, France
[2] INCa COMETE Network, Endocrinol Metab Canc Dept, Cochin Inst, CNRS UMR 8104, Paris, France
关键词
adrenal; adrenal cortex; adrenocortical adenoma; adrenocortical carcinoma; adrenocortical tumor; Wnt/beta-catenin signaling pathway; IGF-II; cyclin E; Ki-67; p53; immunohistochemistry; ADRENOCORTICAL TUMORS; RENAL-CELL; DIFFERENTIAL-DIAGNOSIS; MOLECULAR MARKERS; WEISS SYSTEM; PROGNOSTIC-SIGNIFICANCE; PROLIFERATION MARKER; BETA-CATENIN; CYCLIN-E; EXPRESSION;
D O I
10.1016/j.beem.2010.10.011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Most adrenocortical tumors are benign; adrenocortical carcinomas are rare but their prognosis is poor and their therapeutics are sparse. In most adrenocortical tumors, the morphological approach in particular by Weiss system, brings sufficient elements to establish the differential diagnosis between a benign and a malignant tumor. But some tumors of Weiss score of 2 or 3 can raise problems: are they benign, malignant or are they of uncertain malignant potential? On the other hand, some Weiss criteria are difficult to evaluate as, for example, sinusoidal invasion. These observations led to the development of other approaches, in particular genetic approaches. These genetics findings already have repercussions for the patients in the development of molecular markers for diagnosis and prognosis and in the future they could help in the development of new morphological approaches, in particular immunohistochemical approaches. (C)2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:877 / 885
页数:9
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