Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/16159
Full metadata record
DC FieldValueLanguage
dc.contributor.authorPoon, Carolin-
dc.contributor.authorHyde, Simon-
dc.contributor.authorGrant, Peter-
dc.contributor.authorNewman, Marsali R-
dc.contributor.authorIreland Jenkin, Kerryn-
dc.date2016-08-03-
dc.date.accessioned2016-08-26T00:01:46Z-
dc.date.available2016-08-26T00:01:46Z-
dc.date.issued2016-08-03-
dc.identifier.citationInternational Journal of Gynecological Cancer 2016; 26(8): 1415-1420en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/16159-
dc.description.abstractOBJECTIVE: Risk reducing salpingooophorectomy is recommended to women with a BReast CAncer susceptibility gene (BRCA) 1 or 2 germline mutation to reduce the risk of ovarian cancer. The incidence of unsuspected neoplasia varies in the literature. The purpose of this study was to identify the rate of unsuspected neoplasia in a high-risk Australian population, discuss their management, and assess the clinical outcome. METHOD: This is a retrospective review of all women undergoing risk reductive salpingooophorectomy between January 2006 and December 2014. The medical, operative, and pathology results were reviewed. The specimens were assessed using the Sectioning and Extensively Examining the Fimbriated End protocol to the fallopian tube, and the ovary was also examined using 2 to 3 mm sectioning. RESULTS: During the study period, 138 patients underwent risk-reducing salpingooophorectomy for a known BRCA 1 or 2 germline mutation or a high-risk personal or family history of ovarian cancer. Five patients with neoplasia were identified, 2 with invasive tubal carcinoma and 3 with serous tubal intraepithelial carcinoma (STIC), giving an overall incidence of 3.62%. Invasive tubal carcinoma occurred in 1 woman with a BRCA 1 mutation and 1 woman with a BRCA 2 mutation. The incidence of carcinoma in women with either a BRCA 1 or 2 germline mutation was subsequently 2.78%. STIC occurred in 2 women with a BRCA 1 germline mutation and 1 woman carrying a BRCA 2 germline mutation. The incidence of STIC in women with either a BRCA 1 or 2 germline mutation was subsequently 4.17%. Of the patients with STIC, all 3 remain disease free at an average follow-up period of 79.33 months. CONCLUSIONS: In this retrospective review, we found the incidence of neoplasia within a high-risk Australian population undergoing risk-reducing bilateral salpingo-oophorectomy to be 3.62%. The incidence of STIC was 2.17%. During our follow-up period, all patients with STIC remained disease free.en_US
dc.subjectRisk reductive bilateral salpingooophorectomyen_US
dc.subjectBRCA 1en_US
dc.subjectBRCA 2en_US
dc.subjectOvarian carcinomaen_US
dc.subjectFallopian tube carcinomaen_US
dc.subjectSerous tubal intraepithelial carcinomaen_US
dc.subjectCarcinoma in Situ-
dc.subjectFallopian Tube Neoplasms-
dc.subjectOvarian Neoplasms-
dc.titleIncidence and characteristics of unsuspected neoplasia discovered in high-risk women undergoing risk reductive bilateral salpingoo-ophorectomyen_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleInternational Journal of Gynecological Canceren_US
dc.identifier.affiliationAustin Health, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Gynaecology Oncology, Mercy Hospital for Women, Heideberg, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Anatomical Pathology, Austin Health, Heidelberg, Victoria, Australiaen_US
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/27488216en_US
dc.identifier.doi10.1097/IGC.0000000000000791en_US
dc.type.contentTexten_US
dc.type.austinJournal Articleen_US
local.name.researcherNewman, Marsali R
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
crisitem.author.deptPathology-
Appears in Collections:Journal articles
Show simple item record

Page view(s)

12
checked on Oct 1, 2024

Google ScholarTM

Check


Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.