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Deferring gonadectomy in patients with turner syndrome with a genetic Y component is not a safe practice
Sameer Mittal1, John Weaver1, Aznive Aghababian1
1Division of Urology, Children's Hospital of Philadelphia, 3401 Civic Center Blvd, Philadelphia, PA 19104, USA.
Introduction:
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.
Hypothesis/Objective:
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.
Study Design:
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.
Results:
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).
Discussion:
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.
Conclusion:
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.
Insights
Patients with Turner syndrome and Y chromosome material (TSY) have a high risk of germ cell tumors. Early gonadectomy at diagnosis is recommended due to a 33.3% tumor incidence and safe surgical outcomes.
Area of Science:
- Reproductive Endocrinology
- Oncology
- Genetics
Background:
- Patients with Turner syndrome (TS) and Y chromosome material (TSY) are at increased risk for germ cell neoplasms.
- The optimal timing for prophylactic gonadectomy in TSY patients remains undefined.
Purpose of the Study:
- To evaluate the outcomes of gonadectomy in TSY patients.
- To determine if gonadectomy can be safely performed at diagnosis rather than deferred.
Main Methods:
- Retrospective, single-center study of TSY patients who underwent gonadectomy between 2012 and 2021.
- Electronic health records were queried to identify eligible patients.
Main Results:
- Eighteen TSY patients underwent gonadectomy.
- Tumors were identified in 6 patients (33.3%), including 4 with dysgerminoma and 2 with gonadoblastoma.
- The youngest patient diagnosed with gonadoblastoma was 40 days old.
Conclusions:
- TSY patients have a high incidence of germ cell tumors, necessitating prompt intervention.
- Gonadectomy is a safe procedure with low morbidity and no tumor recurrence in the follow-up period.
- Bilateral gonadectomy at the time of diagnosis is recommended for all TSY patients.
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