Current update on the molecular genetics and management of hereditary ovarian cancers: a primer for radiologists

被引:1
作者
Itani, Malak [1 ]
Lalwani, Neeraj [2 ]
Ganeshan, Dhakshinamoorthy [3 ]
Zulfiqar, Maria [1 ]
Siegel, Cary [1 ]
机构
[1] Washington Univ, Mallinckrodt Inst Radiol, St Louis, MO 63110 USA
[2] Virginia Commonwealth Univ, Sch Med, Med Coll Virginia Campus, Richmond, VA 23298 USA
[3] Univ Texas MD Anderson Canc Ctr, Div Diagnost Imaging, Houston, TX 77030 USA
关键词
Hereditary ovarian cancer; BRCA mutation; Lynch syndrome; Peutz-Jeghers syndrome; Gorlin syndrome; LYNCH SYNDROME; MISMATCH REPAIR; CELL CARCINOMA; BREAST-CANCER; BRCA MUTATION; STROMAL TUMOR; DNA-DAMAGE; RISK; FEATURES; WOMEN;
D O I
10.1007/s00261-020-02911-x
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
More than one-fifth of ovarian cancers are hereditary, with most of them caused by BRCA genes. Malignant ovarian neoplasms are primarily epithelial tumors, a heterogeneous group of tumors with variable genetic backgrounds that translate into different biologic behaviors and morphologic features. Radiologists play an increasingly important role in the diagnosis and management of oncology patients. Familiarity with hereditary ovarian cancers will have a positive impact on patient management and radiologists' involvement in the multidisciplinary approach needed for this delicate patient population. In this paper, we review the basic histologic and genetic backgrounds of ovarian tumors with an emphasis on hereditary ovarian cancers, as well as the effects that these factors have on patient workup, primarily with regard to imaging studies.
引用
收藏
页码:2281 / 2292
页数:12
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