TY - JOUR
T1 - Current update on the molecular genetics and management of hereditary ovarian cancers
T2 - a primer for radiologists
AU - Itani, Malak
AU - Lalwani, Neeraj
AU - Ganeshan, Dhakshinamoorthy
AU - Zulfiqar, Maria
AU - Siegel, Cary
N1 - Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2021/6
Y1 - 2021/6
N2 - 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.
AB - 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.
KW - BRCA mutation
KW - Gorlin syndrome
KW - Hereditary ovarian cancer
KW - Lynch syndrome
KW - Peutz-Jeghers syndrome
UR - http://www.scopus.com/inward/record.url?scp=85104672256&partnerID=8YFLogxK
U2 - 10.1007/s00261-020-02911-x
DO - 10.1007/s00261-020-02911-x
M3 - Article
C2 - 33847772
AN - SCOPUS:85104672256
SN - 2366-004X
VL - 46
SP - 2281
EP - 2292
JO - Abdominal Radiology
JF - Abdominal Radiology
IS - 6
ER -