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Hereditary Gynecologic Cancer Syndromes-A Narrative Review

Journal

ONCOTARGETS AND THERAPY
Volume 15, Issue -, Pages 381-405

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/OTT.S353054

Keywords

syndromes beyond hereditary gynecologic cancer syndromes; pathogenesis; diagnosis; pathology; screening

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Hereditary cancer syndromes, which result from low penetrant polymorphisms or single gene disorders, account for approximately 5-10% of all cancers. Significant progress has been made in the evaluation and management of these syndromes in the past decade. However, hereditary syndromes associated with gynecologic malignancies present a challenge for oncogynecologists, who tend to focus more on staging, histological type, and treatment options rather than considering inherited cancers and obtaining detailed family histories.
Hereditary cancer syndromes are defined as syndromes, where the genetics of cancer are the result of low penetrant polymorphisms or of a single gene disorder inherited in a mendelian fashion. During the last decade, compelling evidence has accumulated that approximately 5-10% of all cancers could be attributed to hereditary cancer syndromes. A tremendous progress has been made over the last decade in the evaluation and management of these syndromes. However, hereditary syndromes associated with gynecologic malignancies still present significant challenge for oncogynecologists. Oncogynecologists tend to pay more attention to staging, histological type and treatment options of gynecological cancers than thinking of inherited cancers and taking a detailed family history. Moreover, physicians should also be familiar with screening strategies in patients with inherited gynecological cancers. Lynch syndrome and hereditary breast-ovarian cancer syndrome are the most common and widely discussed syndromes in medical literature. The aim of the present review article is to delineate and emphasize the majority of hereditary gynecological cancer syndromes, even these, which are rarely reported in oncogynecology. The following inherited cancers are briefly discussed: Lynch syndrome; site-specific ovarian cancer and hereditary breast-ovarian cancer syndrome; Cowden syndrome; Li-Fraumeni syndrome; neoplasia type I, II; hereditary small cell carcinoma of the ovary, hypercalcemic type and hereditary undifferentiated uterine sarcoma; hereditary diffuse gastric cancer and MUTYH-associated polyposis. Epidemiology, pathogenesis, diagnosis, pathology and screening of these syndromes are discussed. General treatment recommendations are beyond the scope of this review.

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