Deferring gonadectomy in patients with turner syndrome with a genetic Y component is not a safe practice
Patients with Turner syndrome who harbor Y chromosome material are known to be at increased risk of developing germ cell neoplasms. The optimal timing to perform gonadectomy to reduce the risk of cancer development in these patients is not well defined. We present outcomes of Turner with a Y compone...
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Veröffentlicht in: | Journal of pediatric urology 2023-06, Vol.19 (3), p.294.e1-294.e5 |
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creator | Mittal, Sameer Weaver, John Aghababian, Aznive Edwins, Rebecca Godlewski, Karl Fischer, Katherine Siu, Sharmayne Gruccio, Denise Van Batavia, Jason Srinivasan, Arun Long, Christopher Bamba, Vaneeta Batra, Vandana Bhatti, Tricia Kolon, Thomas |
description | Patients with Turner syndrome who harbor Y chromosome material are known to be at increased risk of developing germ cell neoplasms. The optimal timing to perform gonadectomy to reduce the risk of cancer development in these patients is not well defined. We present outcomes of Turner with a Y component (TSY) patients who underwent gonadectomy at our institution.
We hypothesized that tumors could occur in a significant portion of TSY patients at any age and gonadectomy can be safely performed at diagnosis rather than deferred.
We performed an IRB-approved retrospective single center study in which we queried our institutions electronic health record to identify all patients with TSY who underwent gonadectomy at our institution from 2012 to 2021.
In our series of 18 consecutive TSY patients, a tumor was identified in 6 patients (33.3%): 4 (22.2%) with dysgerminoma (DG) [Fig. 1] and 2 (11.1%) with gonadoblastoma (GB).
Our cohort of 18 consecutive TSY who underwent gonadectomy over a 9-year period is the largest published single site cohort to date. Additionally, our patient who was found to have GB at 40 days is to our knowledge the youngest TSY patient to be diagnosed with GB in the literature. This patient's remarkably early incidence of tumor occurrence illustrates the urgency of protective gonadectomy. Given the high incidence of tumor formation in this population and the minimal morbidity associated with gonadectomy, we do not recommend delaying gonadectomy in this population for any reason. Our study is vulnerable to selection bias and confounding innate to any retrospective study. There was variation with respect to the frequency and timing of pre-operative imaging as a strict preoperative imaging protocol with sequential studies was not in place at our institution. Additionally, we do not have a comparison cohort of patients who are being followed without operative intervention as all TSY patients at our institution have undergone gonadectomy.
TSY patients cannot be safely observed for tumor formation based on clinical factors such as imaging or age. Gonadectomy is safe with a low complication rate and without tumor recurrence during three-year follow-up. We continue to recommend bilateral gonadectomy in this patient population at the time of diagnosis. [Display omitted] |
doi_str_mv | 10.1016/j.jpurol.2022.12.012 |
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We hypothesized that tumors could occur in a significant portion of TSY patients at any age and gonadectomy can be safely performed at diagnosis rather than deferred.
We performed an IRB-approved retrospective single center study in which we queried our institutions electronic health record to identify all patients with TSY who underwent gonadectomy at our institution from 2012 to 2021.
In our series of 18 consecutive TSY patients, a tumor was identified in 6 patients (33.3%): 4 (22.2%) with dysgerminoma (DG) [Fig. 1] and 2 (11.1%) with gonadoblastoma (GB).
Our cohort of 18 consecutive TSY who underwent gonadectomy over a 9-year period is the largest published single site cohort to date. Additionally, our patient who was found to have GB at 40 days is to our knowledge the youngest TSY patient to be diagnosed with GB in the literature. This patient's remarkably early incidence of tumor occurrence illustrates the urgency of protective gonadectomy. Given the high incidence of tumor formation in this population and the minimal morbidity associated with gonadectomy, we do not recommend delaying gonadectomy in this population for any reason. Our study is vulnerable to selection bias and confounding innate to any retrospective study. There was variation with respect to the frequency and timing of pre-operative imaging as a strict preoperative imaging protocol with sequential studies was not in place at our institution. Additionally, we do not have a comparison cohort of patients who are being followed without operative intervention as all TSY patients at our institution have undergone gonadectomy.
TSY patients cannot be safely observed for tumor formation based on clinical factors such as imaging or age. Gonadectomy is safe with a low complication rate and without tumor recurrence during three-year follow-up. We continue to recommend bilateral gonadectomy in this patient population at the time of diagnosis. [Display omitted]</description><identifier>ISSN: 1477-5131</identifier><identifier>EISSN: 1873-4898</identifier><identifier>DOI: 10.1016/j.jpurol.2022.12.012</identifier><identifier>PMID: 36740540</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Castration ; Chromosomes, Human, Y ; Female ; Gonadectomy ; Gonadoblastoma - genetics ; Gonadoblastoma - surgery ; Humans ; Minimally invasive surgery ; Neoplasm Recurrence, Local ; Ovarian Neoplasms - genetics ; Ovarian Neoplasms - pathology ; Ovarian Neoplasms - surgery ; Pediatric laparoscopic surgery ; Retrospective Studies ; Turner syndrome ; Turner Syndrome - complications ; Turner Syndrome - diagnosis ; Turner Syndrome - genetics</subject><ispartof>Journal of pediatric urology, 2023-06, Vol.19 (3), p.294.e1-294.e5</ispartof><rights>2022 Journal of Pediatric Urology Company</rights><rights>Copyright © 2022 Journal of Pediatric Urology Company. Published by Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c362t-37676f47cc3f4f113ec7e39e9aa94518c6fa04e8ff150de93958f64231d13c723</citedby><cites>FETCH-LOGICAL-c362t-37676f47cc3f4f113ec7e39e9aa94518c6fa04e8ff150de93958f64231d13c723</cites><orcidid>0000-0002-7150-2740 ; 0000-0002-6193-2819 ; 0000-0002-4734-1094 ; 0000-0002-8740-5021 ; 0000-0002-7841-5383 ; 0000-0001-7284-1907 ; 0000-0001-9386-6855</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jpurol.2022.12.012$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,46000</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36740540$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mittal, Sameer</creatorcontrib><creatorcontrib>Weaver, John</creatorcontrib><creatorcontrib>Aghababian, Aznive</creatorcontrib><creatorcontrib>Edwins, Rebecca</creatorcontrib><creatorcontrib>Godlewski, Karl</creatorcontrib><creatorcontrib>Fischer, Katherine</creatorcontrib><creatorcontrib>Siu, Sharmayne</creatorcontrib><creatorcontrib>Gruccio, Denise</creatorcontrib><creatorcontrib>Van Batavia, Jason</creatorcontrib><creatorcontrib>Srinivasan, Arun</creatorcontrib><creatorcontrib>Long, Christopher</creatorcontrib><creatorcontrib>Bamba, Vaneeta</creatorcontrib><creatorcontrib>Batra, Vandana</creatorcontrib><creatorcontrib>Bhatti, Tricia</creatorcontrib><creatorcontrib>Kolon, Thomas</creatorcontrib><title>Deferring gonadectomy in patients with turner syndrome with a genetic Y component is not a safe practice</title><title>Journal of pediatric urology</title><addtitle>J Pediatr Urol</addtitle><description>Patients with Turner syndrome who harbor Y chromosome material are known to be at increased risk of developing germ cell neoplasms. The optimal timing to perform gonadectomy to reduce the risk of cancer development in these patients is not well defined. We present outcomes of Turner with a Y component (TSY) patients who underwent gonadectomy at our institution.
We hypothesized that tumors could occur in a significant portion of TSY patients at any age and gonadectomy can be safely performed at diagnosis rather than deferred.
We performed an IRB-approved retrospective single center study in which we queried our institutions electronic health record to identify all patients with TSY who underwent gonadectomy at our institution from 2012 to 2021.
In our series of 18 consecutive TSY patients, a tumor was identified in 6 patients (33.3%): 4 (22.2%) with dysgerminoma (DG) [Fig. 1] and 2 (11.1%) with gonadoblastoma (GB).
Our cohort of 18 consecutive TSY who underwent gonadectomy over a 9-year period is the largest published single site cohort to date. Additionally, our patient who was found to have GB at 40 days is to our knowledge the youngest TSY patient to be diagnosed with GB in the literature. This patient's remarkably early incidence of tumor occurrence illustrates the urgency of protective gonadectomy. Given the high incidence of tumor formation in this population and the minimal morbidity associated with gonadectomy, we do not recommend delaying gonadectomy in this population for any reason. Our study is vulnerable to selection bias and confounding innate to any retrospective study. There was variation with respect to the frequency and timing of pre-operative imaging as a strict preoperative imaging protocol with sequential studies was not in place at our institution. Additionally, we do not have a comparison cohort of patients who are being followed without operative intervention as all TSY patients at our institution have undergone gonadectomy.
TSY patients cannot be safely observed for tumor formation based on clinical factors such as imaging or age. Gonadectomy is safe with a low complication rate and without tumor recurrence during three-year follow-up. We continue to recommend bilateral gonadectomy in this patient population at the time of diagnosis. [Display omitted]</description><subject>Castration</subject><subject>Chromosomes, Human, Y</subject><subject>Female</subject><subject>Gonadectomy</subject><subject>Gonadoblastoma - genetics</subject><subject>Gonadoblastoma - surgery</subject><subject>Humans</subject><subject>Minimally invasive surgery</subject><subject>Neoplasm Recurrence, Local</subject><subject>Ovarian Neoplasms - genetics</subject><subject>Ovarian Neoplasms - pathology</subject><subject>Ovarian Neoplasms - surgery</subject><subject>Pediatric laparoscopic surgery</subject><subject>Retrospective Studies</subject><subject>Turner syndrome</subject><subject>Turner Syndrome - complications</subject><subject>Turner Syndrome - diagnosis</subject><subject>Turner Syndrome - genetics</subject><issn>1477-5131</issn><issn>1873-4898</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1vFSEUhonR2Fr9B8awdDMjB5hhZtPE9EuTJm7ahSuCzOGWmzswBUZz_31pprp0dcjheXnDQ8hHYC0w6L_s2_2ypnhoOeO8Bd4y4K_IKQxKNHIYh9f1LJVqOhBwQt7lvGdMKMbHt-RE9EqyTrJT8nCJDlPyYUd3MZgJbYnzkfpAF1M8hpLpH18eaFlTwETzMUwpzrgtDd1hwOIt_UltnJcYaoD6TEMs9TIbh3RJxlYC35M3zhwyfniZZ-T--uru4ltz--Pm-8XX28aKnpdGqF71TiprhZMOQKBVKEYcjRllB4PtnWESB-egYxOOYuwG10suYAJhFRdn5PP27pLi44q56Nlni4eDCRjXrLlSQlVlICoqN9SmmHNCp5fkZ5OOGph-dqz3enOsnx1r4Lo6rrFPLw3rrxmnf6G_UitwvgFY__nbY9LZVpUWJ5-qXz1F__-GJ56MkCQ</recordid><startdate>202306</startdate><enddate>202306</enddate><creator>Mittal, Sameer</creator><creator>Weaver, John</creator><creator>Aghababian, Aznive</creator><creator>Edwins, Rebecca</creator><creator>Godlewski, Karl</creator><creator>Fischer, Katherine</creator><creator>Siu, Sharmayne</creator><creator>Gruccio, Denise</creator><creator>Van Batavia, Jason</creator><creator>Srinivasan, Arun</creator><creator>Long, Christopher</creator><creator>Bamba, Vaneeta</creator><creator>Batra, Vandana</creator><creator>Bhatti, Tricia</creator><creator>Kolon, Thomas</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-7150-2740</orcidid><orcidid>https://orcid.org/0000-0002-6193-2819</orcidid><orcidid>https://orcid.org/0000-0002-4734-1094</orcidid><orcidid>https://orcid.org/0000-0002-8740-5021</orcidid><orcidid>https://orcid.org/0000-0002-7841-5383</orcidid><orcidid>https://orcid.org/0000-0001-7284-1907</orcidid><orcidid>https://orcid.org/0000-0001-9386-6855</orcidid></search><sort><creationdate>202306</creationdate><title>Deferring gonadectomy in patients with turner syndrome with a genetic Y component is not a safe practice</title><author>Mittal, Sameer ; Weaver, John ; Aghababian, Aznive ; Edwins, Rebecca ; Godlewski, Karl ; Fischer, Katherine ; Siu, Sharmayne ; Gruccio, Denise ; Van Batavia, Jason ; Srinivasan, Arun ; Long, Christopher ; Bamba, Vaneeta ; Batra, Vandana ; Bhatti, Tricia ; Kolon, Thomas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c362t-37676f47cc3f4f113ec7e39e9aa94518c6fa04e8ff150de93958f64231d13c723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Castration</topic><topic>Chromosomes, Human, Y</topic><topic>Female</topic><topic>Gonadectomy</topic><topic>Gonadoblastoma - genetics</topic><topic>Gonadoblastoma - surgery</topic><topic>Humans</topic><topic>Minimally invasive surgery</topic><topic>Neoplasm Recurrence, Local</topic><topic>Ovarian Neoplasms - genetics</topic><topic>Ovarian Neoplasms - pathology</topic><topic>Ovarian Neoplasms - surgery</topic><topic>Pediatric laparoscopic surgery</topic><topic>Retrospective Studies</topic><topic>Turner syndrome</topic><topic>Turner Syndrome - complications</topic><topic>Turner Syndrome - diagnosis</topic><topic>Turner Syndrome - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mittal, Sameer</creatorcontrib><creatorcontrib>Weaver, John</creatorcontrib><creatorcontrib>Aghababian, Aznive</creatorcontrib><creatorcontrib>Edwins, Rebecca</creatorcontrib><creatorcontrib>Godlewski, Karl</creatorcontrib><creatorcontrib>Fischer, Katherine</creatorcontrib><creatorcontrib>Siu, Sharmayne</creatorcontrib><creatorcontrib>Gruccio, Denise</creatorcontrib><creatorcontrib>Van Batavia, Jason</creatorcontrib><creatorcontrib>Srinivasan, Arun</creatorcontrib><creatorcontrib>Long, Christopher</creatorcontrib><creatorcontrib>Bamba, Vaneeta</creatorcontrib><creatorcontrib>Batra, Vandana</creatorcontrib><creatorcontrib>Bhatti, Tricia</creatorcontrib><creatorcontrib>Kolon, Thomas</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pediatric urology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mittal, Sameer</au><au>Weaver, John</au><au>Aghababian, Aznive</au><au>Edwins, Rebecca</au><au>Godlewski, Karl</au><au>Fischer, Katherine</au><au>Siu, Sharmayne</au><au>Gruccio, Denise</au><au>Van Batavia, Jason</au><au>Srinivasan, Arun</au><au>Long, Christopher</au><au>Bamba, Vaneeta</au><au>Batra, Vandana</au><au>Bhatti, Tricia</au><au>Kolon, Thomas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Deferring gonadectomy in patients with turner syndrome with a genetic Y component is not a safe practice</atitle><jtitle>Journal of pediatric urology</jtitle><addtitle>J Pediatr Urol</addtitle><date>2023-06</date><risdate>2023</risdate><volume>19</volume><issue>3</issue><spage>294.e1</spage><epage>294.e5</epage><pages>294.e1-294.e5</pages><issn>1477-5131</issn><eissn>1873-4898</eissn><abstract>Patients with Turner syndrome who harbor Y chromosome material are known to be at increased risk of developing germ cell neoplasms. The optimal timing to perform gonadectomy to reduce the risk of cancer development in these patients is not well defined. We present outcomes of Turner with a Y component (TSY) patients who underwent gonadectomy at our institution.
We hypothesized that tumors could occur in a significant portion of TSY patients at any age and gonadectomy can be safely performed at diagnosis rather than deferred.
We performed an IRB-approved retrospective single center study in which we queried our institutions electronic health record to identify all patients with TSY who underwent gonadectomy at our institution from 2012 to 2021.
In our series of 18 consecutive TSY patients, a tumor was identified in 6 patients (33.3%): 4 (22.2%) with dysgerminoma (DG) [Fig. 1] and 2 (11.1%) with gonadoblastoma (GB).
Our cohort of 18 consecutive TSY who underwent gonadectomy over a 9-year period is the largest published single site cohort to date. Additionally, our patient who was found to have GB at 40 days is to our knowledge the youngest TSY patient to be diagnosed with GB in the literature. This patient's remarkably early incidence of tumor occurrence illustrates the urgency of protective gonadectomy. Given the high incidence of tumor formation in this population and the minimal morbidity associated with gonadectomy, we do not recommend delaying gonadectomy in this population for any reason. Our study is vulnerable to selection bias and confounding innate to any retrospective study. There was variation with respect to the frequency and timing of pre-operative imaging as a strict preoperative imaging protocol with sequential studies was not in place at our institution. Additionally, we do not have a comparison cohort of patients who are being followed without operative intervention as all TSY patients at our institution have undergone gonadectomy.
TSY patients cannot be safely observed for tumor formation based on clinical factors such as imaging or age. Gonadectomy is safe with a low complication rate and without tumor recurrence during three-year follow-up. We continue to recommend bilateral gonadectomy in this patient population at the time of diagnosis. [Display omitted]</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>36740540</pmid><doi>10.1016/j.jpurol.2022.12.012</doi><orcidid>https://orcid.org/0000-0002-7150-2740</orcidid><orcidid>https://orcid.org/0000-0002-6193-2819</orcidid><orcidid>https://orcid.org/0000-0002-4734-1094</orcidid><orcidid>https://orcid.org/0000-0002-8740-5021</orcidid><orcidid>https://orcid.org/0000-0002-7841-5383</orcidid><orcidid>https://orcid.org/0000-0001-7284-1907</orcidid><orcidid>https://orcid.org/0000-0001-9386-6855</orcidid></addata></record> |
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subjects | Castration Chromosomes, Human, Y Female Gonadectomy Gonadoblastoma - genetics Gonadoblastoma - surgery Humans Minimally invasive surgery Neoplasm Recurrence, Local Ovarian Neoplasms - genetics Ovarian Neoplasms - pathology Ovarian Neoplasms - surgery Pediatric laparoscopic surgery Retrospective Studies Turner syndrome Turner Syndrome - complications Turner Syndrome - diagnosis Turner Syndrome - genetics |
title | Deferring gonadectomy in patients with turner syndrome with a genetic Y component is not a safe practice |
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